Form 10-K
Table of Contents

 

 

UNITED STATES

SECURITIES AND EXCHANGE COMMISSION

Washington, D.C. 20549

Form 10-K

(Mark One)

  x ANNUAL REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934

For the fiscal year ended December 31, 2011

OR

  ¨ TRANSITION REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934

Commission file number 000-12477

Amgen Inc.

(Exact name of registrant as specified in its charter)

 

Delaware   95-3540776

(State or other jurisdiction of

incorporation or organization)

 

(I.R.S. Employer

Identification No.)

One Amgen Center Drive,   91320-1799
Thousand Oaks, California   (Zip Code)
(Address of principal executive offices)  

(805) 447-1000

(Registrant’s telephone number, including area code)

Securities registered pursuant to Section 12(b) of the Act:

 

Title of Each Class

 

Name of Each Exchange on Which Registered

Common stock, $0.0001 par value   The NASDAQ Global Select Market

Securities registered pursuant to Section 12(g) of the Act: None

Indicate by check mark if the registrant is a well-known seasoned issuer, as defined in Rule 405 of the Securities Act.    Yes  x    No  ¨

Indicate by check mark if the registrant is not required to file reports pursuant to Section 13 or Section 15(d) of the Act.    Yes  ¨    No  x

Indicate by check mark whether the registrant (1) has filed all reports required to be filed by Section 13 or Section 15(d) of the Securities Exchange Act of 1934 during the preceding 12 months (or for such shorter period that the registrant was required to file such reports), and (2) has been subject to such filing requirements for the past 90 days.    Yes  x    No  ¨

Indicate by check mark whether the registrant has submitted electronically and posted on its corporate Web site, if any, every Interactive Data File required to be submitted and posted pursuant to Rule 405 of Regulation S-T (§ 232.405 of this chapter) during the preceding 12 months (or for such shorter period that the registrant was required to submit and post such files).    Yes  x    No  ¨

Indicate by check mark if disclosure of delinquent filers pursuant to Item 405 of Regulation S-K is not contained herein, and will not be contained, to the best of registrant’s knowledge, in definitive proxy or information statements incorporated by reference in Part III of this Form 10-K or any amendment to this Form 10-K.  ¨

Indicate by check mark whether the registrant is a large accelerated filer, an accelerated filer, a non-accelerated filer, or a smaller reporting company. See definitions of “large accelerated filer,” “accelerated filer” and “smaller reporting company” in Rule 12b-2 of the Exchange Act. (Check one):

Large accelerated filer  x    Accelerated filer  ¨    Non-accelerated filer  ¨    Smaller reporting company ¨

(Do not check if a smaller reporting company)        

Indicate by check mark whether the registrant is a shell company (as defined in Rule 12b-2 of the Act)    Yes  ¨    No  x

The approximate aggregate market value of voting and non-voting stock held by non-affiliates of the registrant was $53,861,879,805 as of June 30, 2011(A)

 

(A) Excludes 966,638 shares of common stock held by directors and executive officers at June 30, 2011. Exclusion of shares held by any person should not be construed to indicate that such person possesses the power, directly or indirectly, to direct or cause the direction of the management or policies of the registrant, or that such person is controlled by or under common control with the registrant.

791,432,134

(Number of shares of common stock outstanding as of February 10, 2012)

DOCUMENTS INCORPORATED BY REFERENCE

Specified portions of the registrant’s Proxy Statement with respect to the 2012 Annual Meeting of stockholders to be held May 23, 2012, are incorporated by reference into Part III of this annual report.

 

 

 


Table of Contents

INDEX

 

           Page No.  
PART I     1   
Item 1.     

BUSINESS

    1   
    

Overview

    1   
    

Significant Developments

    2   
    

Marketed Products

    3   
    

Marketing and Distribution

    17   
    

Reimbursement

    18   
    

Manufacturing, Distribution and Raw Materials

    24   
    

Government Regulation

    26   
    

Research and Development and Selected Product Candidates

    30   
    

Business Relationships

    36   
    

Human Resources

    39   
    

Executive Officers of the Registrant

    39   
    

Geographic Area Financial Information

    40   
    

Investor Information

    40   
Item 1A.     

RISK FACTORS

    41   
Item 1B.     

UNRESOLVED STAFF COMMENTS

    61   
Item 2.     

PROPERTIES

    62   
Item 3.     

LEGAL PROCEEDINGS

    63   
Item 4.     

MINE SAFETY DISCLOSURES

    63   
PART II     64   
Item 5.     

MARKET FOR REGISTRANT’S COMMON EQUITY, RELATED STOCKHOLDER MATTERS AND ISSUER PURCHASES OF EQUITY SECURITIES

    64   
Item 6.     

SELECTED FINANCIAL DATA

    67   
Item 7.     

MANAGEMENT’S DISCUSSION AND ANALYSIS OF FINANCIAL CONDITION AND RESULTS OF OPERATIONS

    69   
Item 7A.     

QUANTITATIVE AND QUALITATIVE DISCLOSURES ABOUT MARKET RISK

    87   
Item 8.     

FINANCIAL STATEMENTS AND SUPPLEMENTARY DATA

    90   
Item 9.     

CHANGES IN AND DISAGREEMENTS WITH ACCOUNTANTS ON ACCOUNTING AND FINANCIAL DISCLOSURES

    90   
Item 9A.     

CONTROLS AND PROCEDURES

    90   
Item 9B.     

OTHER INFORMATION

    92   
PART III     92   
Item 10.     

DIRECTORS, EXECUTIVE OFFICERS AND CORPORATE GOVERNANCE OF THE REGISTRANT

    92   
Item 11.     

EXECUTIVE COMPENSATION

    92   
Item 12.     

SECURITY OWNERSHIP OF CERTAIN BENEFICIAL OWNERS AND MANAGEMENT AND RELATED STOCKHOLDER MATTERS

    93   
Item 13.     

CERTAIN RELATIONSHIPS AND RELATED TRANSACTIONS AND DIRECTOR INDEPENDENCE

    95   
Item 14.     

PRINCIPAL ACCOUNTING FEES AND SERVICES

    95   
PART IV     96   
Item 15.     

EXHIBITS AND FINANCIAL STATEMENT SCHEDULES

    96   

SIGNATURES

    104   

 

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PART I

 

Item 1. BUSINESS

Overview

Amgen Inc. (including its subsidiaries, referred to as “Amgen,” “the Company,” “we,” “our” or “us”) is the world’s largest independent biotechnology medicines company. We discover, develop, manufacture and market medicines for grievous illnesses. We focus solely on human therapeutics and concentrate on innovating novel medicines based on advances in cellular and molecular biology. Our mission is to serve patients.

We were incorporated in 1980 and organized as a Delaware corporation in 1987. Our public website is www.amgen.com. On our website, investors can find press releases, financial filings and other information about the Company. The U.S. Securities and Exchange Commission (SEC) website, www.sec.gov, also offers access to reports and documents we have electronically filed with or furnished to the SEC. These website addresses are not intended to function as hyperlinks, and the information contained in our website and in the SEC’s website is not intended to be a part of this filing.

As of December 31, 2011, we had 17,800 staff members worldwide. Approximately 6,500 of our staff members work in our research and development (R&D) function, approximately 4,900 work in manufacturing, approximately 4,400 work in our commercial operations and the rest are in general and administrative functions.

Currently, we market primarily recombinant protein therapeutics in supportive cancer care, inflammation and nephrology. Our principal products are Neulasta® (pegfilgrastim), a pegylated protein, based on the Filgrastim molecule, and NEUPOGEN® (Filgrastim), a recombinant-methionyl human granulocyte colony-stimulating factor (G-CSF), both of which selectively stimulate the production of neutrophils (a type of white blood cell that helps the body fight infection); Enbrel® (etanercept), an inhibitor of tumor necrosis factor (TNF), a substance that plays a role in the body’s response to inflammatory diseases; and Aranesp® (darbepoetin alfa) and EPOGEN® (epoetin alfa), erythropoiesis-stimulating agents (ESAs) that stimulate the production of red blood cells. Our principal products represented 87%, 91% and 93% of our sales in 2011, 2010 and 2009, respectively. Our other marketed products include Sensipar®/Mimpara® (cinacalcet), a small molecule calcimimetic that lowers serum calcium levels; Vectibix® (panitumumab), a monoclonal antibody that binds specifically to the epidermal growth factor receptor (EGFr); Nplate® (romiplostim), a thrombopoietin (TPO) receptor agonist that mimics endogenous TPO, the primary driver of platelet production; and Prolia® (denosumab) and XGEVA® (denosumab), which both contain the same active ingredient but are approved for different indications, patient populations, doses and frequencies of administration. Denosumab is a fully human monoclonal antibody that specifically targets RANKL, an essential regulator of osteoclasts (the cells that break down bone).

We maintain sales and marketing forces primarily in the United States, Europe and Canada. We have also entered into agreements with third parties to assist in the commercialization and marketing of certain of our products in specified geographic areas. (See Business Relationships.) Together with our partners, we market our products to healthcare providers, including physicians or their clinics, dialysis centers, hospitals and pharmacies. Most patients receiving our principal products for approved indications are covered by either government or private payer healthcare programs, which influence demand. The reimbursement environment continues to evolve with greater emphasis on both cost containment and demonstration of the economic value of products.

In addition to our marketed products, we have various product candidates in mid- to late-stage development in a variety of therapeutic areas, including oncology, hematology, inflammation, bone health, nephrology, cardiovascular and general medicine, which includes neuroscience. Our R&D organization has expertise in multiple treatment modalities, including large molecules (such as proteins, antibodies and peptibodies) and small molecules.

Our manufacturing operations consist of bulk manufacturing, formulation, fill and finish and distribution activities for all of our principal products as well as most of our product candidates. We operate a number of commercial and/or clinical manufacturing facilities, and our primary facilities are located in the United States, Puerto Rico and the Netherlands. (See Item 2. Properties.)

 

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Drug development in our industry is complex, challenging and risky, and failure rates are high. Product development cycles are very long — approximately 10 to 15 years from discovery to market. A potential new medicine must undergo many years of preclinical and clinical testing to establish its safety and efficacy for use in humans at appropriate dosing levels and with an acceptable benefit-risk profile. Biological products, which are produced in living systems, are inherently complex due to naturally occurring molecular variations. Highly specialized knowledge and extensive process and product characterization are required to transform laboratory-scale processes into reproducible commercial manufacturing processes. Upon approval, marketed products in our industry generally face substantial competition.

Our industry is highly regulated, and various U.S. and foreign regulatory bodies have substantial authority over how we conduct our business. Government authorities in the United States and other countries regulate the manufacturing and marketing of our products as well as our ongoing R&D activities. In recent years, regulators have placed a greater scrutiny on drug safety. This has led to, and may in the future lead to: fewer products being approved by the U.S. Food and Drug Administration (FDA) or other regulatory bodies; delays in receiving approvals; additional safety-related requirements; restrictions on the use of products, including expanded safety labeling, or required risk management activities.

Significant Developments

Following is a summary of significant developments that occurred in 2011 and early 2012 affecting our business. A more detailed discussion of each development follows in the appropriate section.

ESAs

 

   

The Centers for Medicare & Medicaid Services’ (CMS) Final Rule on Bundling in Dialysis became effective on January 1, 2011, and provides a single payment for all dialysis services, including drugs that were previously reimbursed separately.

 

   

On June 24, 2011, we announced that the FDA approved changes to the labels for the use of ESAs, including Aranesp® and EPOGEN®, in patients with chronic kidney disease (CKD) (June 2011 ESA label changes).

 

   

CMS finalized a rule to update various provisions of its bundled payment system for dialysis services and the related end stage renal disease (ESRD) Quality Incentive Program (QIP). The final rule eliminated for payment year 2013 and beyond the QIP’s measure that tracks the percent of a provider’s Medicare patients with a hemoglobin (Hb) level below 10 grams per deciliter (g/dL).

 

   

We entered into a seven-year supply agreement with DaVita Inc. (DaVita), commencing January 1, 2012, to supply EPOGEN® in amounts necessary to meet no less than 90% of DaVita’s and its affiliates’ requirements for ESAs used in providing dialysis services in the United States and Puerto Rico.

XGEVA®

 

   

On July 15, 2011, we announced that the European Commission (EC) granted marketing authorization for XGEVA® for the prevention of skeletal-related events (SREs) in adults with bone metastases from solid tumors.

Vectibix®

 

   

On November 10, 2011, the EC approved a variation to the marketing authorization for the use of Vectibix® in first- and second-line treatment of metastatic colorectal cancer (mCRC) in patients whose tumors contain wild-type KRAS genes.

 

   

We announced on July 29, 2011, that we received Complete Response Letters from the FDA on the first- and second-line mCRC supplemental Biologics License Applications (sBLA) for Vectibix® that we filed in late 2010. We are currently working to address their requests.

 

 

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Motesanib

 

   

We along with our partner Takeda Pharmaceutical Company Limited (Takeda) announced that the motesanib pivotal phase 3 trial (MONET1) did not meet its primary objective of demonstrating an improvement in overall survival in patients with advanced non-squamous non small cell lung cancer (NSCLC).

Business combinations

 

   

On March 4, 2011, we acquired BioVex Group, Inc. (BioVex), a privately held biotechnology company developing treatments for cancers and for the prevention of infectious disease, including talimogene laherparepvec (formerly referred to as OncoVEXGM-CSF), a novel oncolytic vaccine in phase 3 clinical development for the treatment of malignant melanoma.

   

On April 7, 2011, we acquired Laboratório Químico Farmacêutico Bérgamo Ltda (Bergamo), a privately held Brazilian pharmaceutical company that is a leading supplier of medicines to the hospital sector in Brazil with capabilities in oncology medicines.

   

On January 26, 2012, we announced that we entered into an agreement to acquire Micromet, Inc. (Micromet), a publicly held biotechnology company focused on the discovery, development and commercialization of innovative antibody-based therapies for the treatment of cancer. The acquisition, which is subject to customary closing conditions, is expected to close in the first quarter of 2012.

Return of capital to shareholders

 

   

In the third quarter of 2011, we began paying quarterly cash dividends of $0.28 per share of common stock, aggregating $500 million paid in 2011. In December 2011, we increased our quarterly declared dividend by 29% to $0.36 per share of common stock, payable in March 2012.

   

During 2011, we repurchased approximately 15% of our stock outstanding as of December 31, 2010, for a total cost of $8.3 billion.

Proposed legal settlement

 

   

We recorded a $780 million charge (the legal settlement charge) in connection with an agreement in principle to settle allegations relating to our sales and marketing practices.

Marketed Products

We market our principal products, Neulasta®, NEUPOGEN®, ENBREL, Aranesp® and EPOGEN®, in supportive cancer care, inflammation and nephrology. Certain of our marketed products face, and our product candidates, if approved, are also expected to face, substantial competition, including from products marketed by large pharmaceutical corporations, which may have greater clinical, research, regulatory, manufacturing, marketing, financial and human resources than we do. Our products’ competitive position among other biological and pharmaceutical products may be based on, among other things, safety, efficacy, reliability, availability, patient convenience/delivery devices, price, reimbursement and patent position and expirations.

Over the next several years, many of the existing patents on our principal products will expire, and we expect to face increasing competition thereafter, including from biosimilar products. A “biosimilar” product is a follow-on version of another biological product for which marketing approval is sought or has been obtained based on a demonstration that it is “biosimilar” to the original reference product. This demonstration will typically consist of comparative analytical, preclinical and clinical data from the biosimilar product to show that it has similar safety and efficacy as the reference product. The 2010 U.S. healthcare reform legislation authorized the FDA to approve biosimilar products under a new, abbreviated pathway. On February 9, 2012, the FDA released three draft guidance documents that provide insight into the FDA’s current thinking on the development of biosimilar products and broad parameters for the scientific assessment of biosimilar applications. The FDA guidance documents leave room for the FDA to consider, on a case-by-case basis, the specifics of what evidence would be required for a biosimilar product to gain approval (see Government Regulation). In the European Union

 

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(EU), there is already an established regulatory pathway for biosimilars and we are facing increasing competition from biosimilars. In the United States after patent expiration, we expect to face greater competition, including from manufacturers with biosimilar products approved in Europe that may seek to quickly obtain U.S. approval. Upon patent expiration for small molecule products, there is typically intense competition from generics manufacturers, which generally leads to significant and rapid declines in sales of the branded product. Given that our principal products are biologics, we do not believe the impact of biosimilar competition will be as significant as with small molecule products in part because successful competitors must have a broad range of specialized skills and capabilities unique to biologics, including significant regulatory, clinical and manufacturing expertise, and since the products are similar, but not identical, the biosimilars will have to compete against a product with an established efficacy and safety record. In some cases we may experience additional competition prior to the expiration of our patents as a result of agreements we have made in connection with the settlement of patent litigation with companies developing potentially competing products. (See, e.g., the discussions of Neulasta®/NEUPOGEN® and Aranesp® later in this section).

Further, the introduction of new products or the development of new processes or technologies by competitors or new information about existing products may result in increased competition for our marketed products, even for those protected by patents, or in a reduction of price that we receive from selling our products. In addition, the development of new treatment options or standards of care may reduce the use of our products or may limit the utility and application of ongoing clinical trials for our product candidates.

In addition to the challenges presented by competition, our existing products and product candidates are also subject to increasing regulatory compliance requirements that could be imposed as conditions of approval or after a product has been approved. This is increasingly true of new therapies with novel mechanisms of action. While such therapies may offer important benefits and/or better treatment alternatives, they may also involve relatively new or higher levels of scientific complexity and may therefore generate increased safety concerns. We design and implement comprehensive proactive pharmacovigilance programs for all of our products to help ensure the detection, assessment and communication of adverse effects. When deemed necessary and appropriate, additional measures for risk communication and mitigation are designed and implemented in consultation with regulatory agencies. As a condition of approval or due to safety concerns after a product has been approved, we may be required to perform additional clinical trials or studies, including postmarketing requirements (PMRs) and postmarketing commitments (PMCs). A PMR is a trial or study that a sponsor company is required by statute or regulation to conduct. A PMC is a trial or study that a sponsor company agrees to in writing, but is not required by law, to conduct. In addition, we may be required to implement risk management plans for our products in the various regions in which they are approved. For example, in 2008 the FDA began requiring risk evaluation and mitigation strategies (REMS) for various approved products to ensure that the benefits of the drugs outweigh the risks. A REMS may also be imposed as a condition of approval or after a product has been on the market. A REMS may include a medication guide or a patient package insert, a healthcare provider communication plan or elements to assure safe use that the FDA deems necessary. While the elements of REMS may vary, all REMS require the sponsor company to submit periodic assessment reports to the FDA to demonstrate that the goals of the REMS are being met. The FDA evaluates such assessments and may require additional modifications to the REMS elements. REMS may also be modified as the FDA and companies gain more experience with REMS and how they are implemented, operated and monitored. We currently have REMS for a number of our marketed products. (See discussion on PMRs, PMCs and REMS in Government Regulation.)

Most patients receiving our principal products for approved indications are covered by either government or private payer healthcare programs, which influence demand. The reimbursement environment continues to evolve with greater emphasis on both cost containment and demonstration of the economic value of products. In addition, the current worldwide economic conditions have also contributed to increasing pressures on cost containment.

Neulasta® (pegfilgrastim)/NEUPOGEN® (Filgrastim)

We were granted an exclusive license to manufacture and market Neulasta® and NEUPOGEN® in the United States, Europe, Canada, Australia and New Zealand under a licensing agreement with Kirin-Amgen, Inc.

 

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(K-A), a joint venture between Kirin Holdings Company, Limited (Kirin) and Amgen (see Business Relationships — Kirin-Amgen, Inc.) (See Business Relationships — Kirin-Amgen, Inc.)

Neulasta® and NEUPOGEN® stimulate production of neutrophils, a type of white blood cell important in the body’s fight against infection. Treatments for various diseases and diseases themselves can result in extremely low numbers of neutrophils, a condition called neutropenia. Myelosuppressive chemotherapy, one treatment option for individuals with certain types of cancers, targets cell types that grow rapidly, such as tumor cells. Normal cells that divide rapidly, such as those in the bone marrow that become neutrophils, are also vulnerable to the cytotoxic effects of myelosuppressive chemotherapy, resulting in neutropenia with an increased risk of severe infection. NEUPOGEN® is our registered trademark for Filgrastim, our recombinant-methionyl human G-CSF. Neulasta® is our registered trademark for pegfilgrastim, a pegylated protein based on the Filgrastim molecule. A polyethylene glycol molecule is added to the Filgrastim molecule. Because pegfilgrastim is eliminated through binding to its receptor on neutrophils and neutrophil precursor cells, pegfilgrastim remains in the circulation until neutrophil recovery has occurred. This neutrophil-mediated clearance allows for administration as a single dose per chemotherapy cycle, compared with NEUPOGEN®, which requires more frequent dosing.

We market Neulasta® and NEUPOGEN® primarily in the United States and Europe. Filgrastim is also marketed under the brand name GRANULOKINE® in Italy. Neulasta® was launched in the United States and Europe in 2002 and is indicated to decrease the incidence of infection associated with chemotherapy-induced febrile neutropenia in cancer patients with non-myeloid malignancies. Administration of Neulasta® in all cycles of chemotherapy is approved for patients receiving myelosuppressive chemotherapy associated with a clinically significant risk of febrile neutropenia. NEUPOGEN® was launched in the United States and Europe in 1991. NEUPOGEN® is indicated for reducing the incidence of infection as manifested by febrile neutropenia for patients with non-myeloid malignancies undergoing myelosuppressive chemotherapy; reducing the duration of neutropenia and neutropenia-related consequences for patients with non-myeloid malignancies undergoing myeloablative chemotherapy followed by bone marrow transplantation; reducing the incidence and duration of neutropenia-related consequences in symptomatic patients with congenital neutropenia, cyclic neutropenia or idiopathic neutropenia (collectively, severe chronic neutropenia); mobilizing peripheral blood progenitor cells (PBPC) in cancer patients who have undergone myeloablative chemotherapy for stem cell transplantation; and reducing the recovery time of neutrophils and the duration of fever following induction or consolidation chemotherapy treatment in adult patients with acute myeloid leukemia (AML).

Worldwide Neulasta®/NEUPOGEN® sales for the years ended December 31, 2011, 2010 and 2009, were $5.2 billion, $4.8 billion and $4.6 billion, respectively. U.S. Neulasta®/NEUPOGEN® sales for the years ended December 31, 2011, 2010 and 2009, were $4.0 billion, $3.6 billion and $3.4 billion, respectively. International Neulasta®/NEUPOGEN® sales for each of the three years ended December 31, 2011, 2010 and 2009, were $1.2 billion.

Our outstanding material patents for pegfilgrastim are described in the following table.

 

Territory

  

General Subject Matter

   Expiration  

U.S.

  

Pegylated G-CSF

     10/20/2015   

Europe(1)

  

Pegylated G-CSF

     2/8/2015   

 

 

(1) 

In some cases, this European patent may also be entitled to supplemental protection in one or more countries in Europe and the length of any such extension will vary by country.

Our outstanding material patents for Filgrastim are described in the following table.

 

Territory

  

General Subject Matter

   Expiration

U.S.

  

G-CSF polypeptides

   12/3/2013

U.S.

  

Methods of treatment using G-CSF polypeptides

   12/10/2013

 

 

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Our principal European patent relating to G-CSF expired in August 2006. Upon expiration of that patent, some companies received approval to market products, including biosimilars, that compete with NEUPOGEN® and Neulasta® in Europe, as further discussed below.

Any products or technologies that are directly or indirectly successful in treating neutropenia associated with chemotherapy, for bone marrow and PBPC transplant patients, severe chronic neutropenia and AML could negatively impact Neulasta® and/or NEUPOGEN® sales. Further, NEUPOGEN® competes with Neulasta® in the United States and Europe, and NEUPOGEN® sales have been adversely impacted by conversion to Neulasta®. However, we believe the conversion in the United States is substantially complete and that a significant amount of the conversion in Europe has already occurred.

The following table reflects companies and their currently marketed products that compete with Neulasta® and/or NEUPOGEN® in the United States and Europe in the supportive cancer care setting. The table below and the following discussion of competitor marketed products and products in development may not be exhaustive.

 

Territory

  

Competitor Marketed Product

  

Competitor

U.S.

   Leukine®   

Bayer HealthCare Pharmaceuticals (Bayer)

Europe

   Granocyte®   

Chugai Pharmaceuticals Co., Ltd./Sanofi-Aventis (Sanofi)

Europe

   Ratiograstim®(1)/Biograstim®(1)   

ratiopharm GmbH (ratiopharm)(2)/CT Arzneimittel GmbH (CT Arzneimittel)

Europe

   Tevagrastim®(1)   

Teva Pharmaceutical Industries Ltd. (Teva Pharmaceutical)

Europe

  

Zarzio®(1)/Filgrastim Hexal®(1)

  

Sandoz GmbH (Sandoz)/Hexal Biotech Forschungs GmbH (Hexal)

Europe

  

Nivestim®(1)

  

Hospira Inc. (Hospira)

 

(1) 

Approved via the EU biosimilar regulatory pathway.

(2) 

A subsidiary of Teva Pharmaceutical.

Several companies have short-acting filgrastim product candidates in phase 3 clinical development, including:

 

   

Merck & Company, Inc. (Merck) (MK-4214)

 

   

Intas/Apotex Inc. (Neukine)

 

   

Reliance Life Sciences Pvt. Ltd. (Religrast)

 

   

Biocon Ltd./Celgene Corporation (Celgene) (Nufil)

In addition, the following companies have long-acting filgrastim product candidates in phase 3 clinical development:

 

   

Teva Pharmaceutical (Neugranin™ and XM-22)

 

   

Sandoz (Peg G-CSF).

In February 2010, Teva Pharmaceutical announced that the FDA had accepted for review its Biologics License Applications (BLA) seeking U.S. approval to market XM02 (its filgrastim product currently sold under the brand name Tevagrastim® in several European countries) to stimulate the production of neutrophils under the brand name Neutroval™. On September 30, 2010, the FDA issued a Complete Response Letter requesting additional information from Teva Pharmaceutical to complete the review of its applications for approval of

 

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Neutroval™. If approved in the United States, this drug would compete with NEUPOGEN® and Neulasta® subject to the terms of the injunction and settlement agreement discussed below.

On November 30, 2009, Teva Pharmaceutical filed a declaratory judgment action against us alleging that certain of our NEUPOGEN® patents are invalid and not infringed by Neutroval™, and on January 15, 2010, we filed an answer and counterclaims seeking a declaratory judgment that our patents are valid and infringed. On July 15, 2011, we announced that the U.S. District Court in Pennsylvania entered final judgment and a permanent injunction against Teva Pharmaceutical and Teva Pharmaceuticals USA, Inc. (together defined as Teva) prohibiting them from infringing our patents relating to human G-CSF polypeptides and methods of treatment. The Court’s injunction extends until November 10, 2013, after which date Teva will no longer be prohibited by the injunction from selling Neutroval™ in the United States, subject to receiving FDA approval for human therapeutic use. Teva also agreed not to sell Neugranin™ in the United States before November 10, 2013, unless it first obtains a final court decision that our patents are not infringed by Neugranin™. Pursuant to the parties’ settlement, the launch date for either product could be sooner if certain unexpected events occur: a third party launches a similar G-CSF polypeptide product and we fail to sue that third party, or the patents are held invalid or unenforceable in a final court decision in an action brought by a third party.

Enbrel® (etanercept)

ENBREL is our registered trademark for etanercept, our TNF receptor fusion protein that inhibits the binding of TNF to its receptors, which can result in a significant reduction in inflammatory activity. TNF is one of the chemical messengers that help regulate the inflammatory process. When the body produces too much TNF, it overwhelms the immune system’s ability to control inflammation of the joints or of psoriasis-affected skin areas. ENBREL binds certain TNF molecules before they can trigger inflammation.

We acquired the rights to ENBREL in July 2002 with our acquisition of Immunex Corporation (Immunex). ENBREL was launched in the United States in November 1998 and in Canada in March 2001 for the treatment of rheumatoid arthritis (RA). In addition, ENBREL is now indicated for the treatment of adult patients with the following conditions: moderate to severe active RA; chronic moderate to severe plaque psoriasis patients who are candidates for systemic therapy or phototherapy; active psoriatic arthritis; and active ankylosing spondylitis.

We market ENBREL under a collaboration agreement with Pfizer Inc. (Pfizer) in the United States and Canada, which expires in the fourth quarter of 2013. (See Business Relationships — Pfizer Inc.) The rights to market and sell ENBREL outside the United States and Canada are reserved to Pfizer.

ENBREL sales for the years ended December 31, 2011, 2010 and 2009, were $3.7 billion, $3.5 billion and $3.5 billion, respectively.

In November 2011, we announced the issuance of U.S. Patent No. 8,063,182 related to ENBREL, which is owned by F. Hoffmann-La Roche Ltd. (Roche) and exclusively licensed to Amgen. This patent, which has a term of 17 years from issuance, is reflected in the following table along with our other outstanding material patents for etanercept.

 

Territory

  

General Subject Matter

   Expiration  

U.S.

  

TNFR DNA vectors, cells and processes for making proteins

     10/23/2012   

U.S.

  

Aqueous Formulation(1)

     2/27/2023   

U.S.

  

Fusion protein, and pharmaceutical compositions

     11/22/2028   

 

(1) 

This formulation patent relates to the currently approved liquid formulation of ENBREL, which formulation accounts for the majority of ENBREL sales in the United States. However, ENBREL is also sold as an alternative lyophilized formulation that requires reconstituting before it can be administered to the patient.

Any products or technologies that are directly or indirectly successful in treating rheumatologic conditions, which includes moderate to severe RA; moderate to severe polyarticular juvenile idiopathic arthritis; ankylosing spondylitis and psoriatic arthritis; and dermatologic conditions, which includes moderate to severe plaque

 

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psoriasis, could negatively impact ENBREL sales. Certain of the treatments for these indications include generic methotrexate and other products.

The following table reflects companies and their currently marketed products that compete with ENBREL in the United States and Canada in the inflammatory disease setting. The table below and the following discussion of competitor marketed products and products in development may not be exhaustive.

 

Territory

  

Therapeutic Area

  

Competitor
Marketed
Product

  

Competitor

U.S. & Canada

   Rheumatology & Dermatology    REMICADE®    Janssen Biotech, Inc. (Janssen)(1)/Merck

U.S. & Canada

   Rheumatology & Dermatology    HUMIRA®    Abbott Laboratories (Abbott)

U.S. & Canada

   Rheumatology & Dermatology    Simponi®    Janssen (1)

U.S. & Canada

   Rheumatology    Cimzia®    UCB/Nektar Therapeutics (Nektar)

U.S. & Canada

   Rheumatology    Orencia®    Bristol-Myers Squibb Company (BMS)

U.S. & Canada

   Rheumatology    Rituxan®    Roche

U.S.

   Rheumatology    Actemra®    Roche

U.S. & Canada

   Dermatology    Stelara®    Janssen (1)

 

(1) 

A subsidiary of Johnson & Johnson (J&J) formerly known as Centocor Ortho Biotech Products, L.P.

In December 2011, the FDA accepted a new drug application (NDA) from Pfizer for approval of tofacitinib in RA. In addition, several competitors have product candidates in phase 3 clinical development that may compete with ENBREL in the future:

 

   

Celgene (apremilast), in both psoriasis and psoriatic arthritis.

 

   

AstraZeneca PLC and Rigel Pharmaceuticals Inc. (fostamatinib) in RA.

 

   

Eli Lilly and Company (Eli Lilly) (LY 2439821) for moderate to severe plaque psoriasis.

 

   

UCB/Nektar’s Cimzia® in psoriatic arthritis,

 

   

Janssen’s Simponi® IV in RA and Stelara® in psoriatic arthritis.

 

   

Roche’s Actemra® SC in RA.

ESAs

Aranesp® and EPOGEN® are our registered trademarks for darbepoetin alfa and epoetin alfa, respectively, both of which are proteins that stimulate red blood cell production in a process known as erythropoiesis. Red blood cells transport oxygen to all cells of the body. Without adequate amounts of a protein called erythropoietin, the red blood cell count is reduced. A deficient red blood cell count can result in anemia, a condition in which insufficient oxygen is delivered to the body’s organs and tissues. Anemia can be associated with CKD in patients either on or not on dialysis. Individuals with CKD may suffer from anemia because they do not produce sufficient amounts of erythropoietin, which is normally produced in healthy kidneys and stimulates erythropoiesis. Anemia can also result from chemotherapy treatments for patients with non-myeloid malignancies.

ESAs, including ours, have faced and continue to face challenges. For example, based on adverse safety results observed beginning in late 2006 in various studies, performed by us and by others, that explored the use of ESAs in settings different from those outlined in the FDA approved label, the product labeling of our ESAs in the United States and the EU has been updated several times to reflect those safety concerns. In addition, due in part to certain of these developments, reimbursement of our ESAs in the United States was also revised resulting in changes in the way ESAs are used in clinical practice, including by decreasing the number of treated patients, average dose and duration of ESA therapy.

 

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Further, the following developments occurred with respect to ESAs in 2011:

 

   

CMS’s Final Rule on Bundling in Dialysis became effective on January 1, 2011, and provides a single payment for all dialysis services, including drugs that were previously reimbursed separately (except for oral drugs without intravenous equivalents, such as Sensipar®, which will be included in the bundle beginning in 2014). Substantially all dialysis providers in the United States opted into the bundled payment system in its entirety on January 1, 2011.

 

   

On June 24, 2011, we announced that the FDA had approved the June 2011 ESA label changes. While the previous label language specified a Hb target range of 10-12 g/dL for chronic renal failure (CRF) patients on dialysis as well as those not on dialysis, the modified labeling provides separate treatment guidance for these two populations. For patients on dialysis, who constitute the majority of CKD (or CRF) patients receiving ESA treatment, the new label advises physicians to initiate ESA therapy when the Hb level is less than 10 g/dL and to reduce or interrupt the dose when the Hb approaches or exceeds 11 g/dL. For CKD patients not on dialysis receiving ESA treatment, the new label advises physicians to initiate ESA therapy when the Hb level is less than 10 g/dL and to reduce or interrupt the dose when the Hb exceeds 10 g/dL. (With the June 2011 label changes, the FDA changed the term CRF to CKD in the ESA labels. We use CRF when referring to labels prior to June 2011 for historical accuracy.)

 

   

On November 1, 2011, CMS finalized a rule to update various provisions of its bundled payment system for dialysis services and the related ESRD QIP. The final rule eliminated for payment year 2013 and beyond the QIP’s measure that tracks the percent of a provider’s Medicare patients with a Hb level below 10 g/dL. CMS indicated that removal of this measure from the QIP was being done in response to the June 2011 ESA label changes.

 

   

On June 16, 2010, CMS opened a National Coverage Analysis (NCA) to examine the use of ESAs to manage anemia in patients with CKD and dialysis-related anemia. Following further analysis, on June 16, 2011, CMS issued a Final Decision Memorandum (FDM) in which it determined that it would not issue a National Coverage Determination (NCD) at that time for ESAs for treatment of anemia in adults with CKD, and that it would instead monitor the use of ESAs through its bundled payment system and its other policy avenues. In the absence of an NCD, Local Coverage Determinations (LCDs) may be made by 11 regional contractors called Medicare Administrative Contractors (MACs), which CMS contracts with to process Medicare claims. LCDs are binding on providers within their respective jurisdictions. Since CMS issued their FDM, one MAC has issued a final LCD relating to anemia in patients with CKD not on dialysis, and two more MACs have issued draft LCDs, all of which would restrict reimbursement to use in accordance with the revised label. Nonetheless, physician behavior may change at any time to be consistent with the label even before formal LCDs are implemented.

Certain of these developments have had a material adverse impact on sales of our ESAs.

In addition, in November 2011, we entered into a seven-year supply agreement with DaVita, commencing January 1, 2012, to supply EPOGEN® in amounts necessary to meet no less than 90% of DaVita’s and its affiliates’ requirements for ESAs used in providing dialysis services in the United States and Puerto Rico. Effective January 1, 2012, we also entered into a three-year non-exclusive supply agreement to supply EPOGEN® to Fresenius Medical Care North America, a subsidiary of Fresenius Medical Care AG & Co. KGaA (Fresenius Medical Care), following the 2011 expiration of our five-year ESA supply agreement with them.

We have an ongoing oncology pharmacovigilance program in place for Aranesp®. Of the clinical trials included in the program, five explore the use of ESAs in settings different from those outlined in the FDA approved label and are designated by the FDA as PMCs. Of the five studies, one was sponsored by Amgen while the other four were investigator-sponsored. Results of certain of those studies contributed to safety-related product labeling changes for our ESAs and changes in reimbursement, as noted above. Of the five studies, four are complete with final results of the remaining study expected in 2012. In addition, Janssen Research & Development, LLC (JRD), a subsidiary of J&J, and/or its investigators have conducted numerous studies that contribute to the understanding of ESA safety. Results of the JRD studies were submitted to the FDA.

 

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Additionally, based on discussions with the FDA, we and JRD have carefully considered potential new study designs to determine the effects of ESAs on survival and tumor outcomes in anemic patients with metastatic cancer receiving concomitant myelosuppressive chemotherapy. Based on those discussions, we are conducting a randomized, double-blind, placebo-controlled, phase 3 non-inferiority study evaluating overall survival when comparing advanced NSCLC patients on Aranesp® to patients receiving placebo (Study ‘782) as part of our Aranesp® pharmacovigilance program. In addition, JRD’s EPO-ANE-3010 study in breast cancer is ongoing. Both studies are designated by the FDA as PMR clinical trials. For the nephrology setting, we are in ongoing discussions with the FDA regarding additional PMRs to explore alternative ESA dosing strategies in CKD patients on dialysis and not on dialysis.

Adverse events or results of any of these studies could further affect product labeling, healthcare provider prescribing behavior, regulatory or private healthcare organization medical guidelines and/or reimbursement practices related to Aranesp® or EPOGEN®.

Aranesp® (darbepoetin alfa)

We were granted an exclusive license by K-A to manufacture and market Aranesp® in the United States, all European countries, Canada, Australia, New Zealand, Mexico, all Central and South American countries and certain countries in Central Asia, Africa and the Middle East.

We market Aranesp® primarily in the United States and Europe. Aranesp® was launched in 2001 in the United States and Europe for the treatment of anemia associated with CRF (both in patients on dialysis and patients not on dialysis) and is also indicated for the treatment of anemia due to concomitant chemotherapy in patients with non-myeloid malignancies.

Worldwide Aranesp® sales for the years ended December 31, 2011, 2010 and 2009, were $2.3 billion, $2.5 billion and $2.7 billion, respectively. For the years ended December 31, 2011, 2010 and 2009, U.S. Aranesp® sales were $1.0 billion, $1.1 billion and $1.3 billion, respectively, and international Aranesp® sales were $1.3 billion, $1.4 billion and $1.4 billion, respectively.

Our outstanding material patents for darbepoetin alfa are described in the following table.

 

Territory

  

General Subject Matter

   Expiration  

U.S.

  

Glycosylation analogs of erythropoietin proteins

     5/15/2024   

Europe(1)

  

Glycosylation analogs of erythropoietin proteins

     8/16/2014   

 

(1) 

In some cases, this European patent may also be entitled to supplemental protection in one or more countries in Europe and the length of any such extension will vary by country.

Our principal European patent relating to epoetin alfa expired in December 2004. Although we do not market EPOGEN® in Europe, upon expiration of this patent, some companies received approval to market products, including biosimilars, that compete with Aranesp® in Europe, as further discussed below.

Any products or technologies that are directly or indirectly successful in addressing anemia associated with chemotherapy and/or renal failure could negatively impact Aranesp® sales. In the United States, Aranesp® competes with EPOGEN®, primarily in the U.S. hospital dialysis clinic setting.

 

 

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The following table reflects companies and their currently marketed products that compete with Aranesp® in the United States and Europe in the supportive cancer care and nephrology segments, unless otherwise indicated. The table below and the following discussion of competitor marketed products and products in development may not be exhaustive.

 

Territory

  

Competitor Marketed Product

  

Competitor

U.S.

   PROCRIT®(1)    Janssen(2)

Europe

   EPREX®/ERYPO®    Janssen-Cilag(2)

Europe

   NeoRecormon®    Roche

Europe

   Retacrit™(3)/Silapo®(3)    Hospira/Stada Arzneimittel AG

Europe

   Binocrit®(3)/epoetin alfa Hexal®(3)/Abseamed®(3)   

Sandoz/Hexal/Medice Arzneimittel Pütter GmbH & Co. KG

Europe

   MIRCERA®(4)    Roche

Europe

   Eporatio®/Biopoin®    ratiopharm (5)/CT Arzneimittel

 

(1) 

PROCRIT® competes with Aranesp® in the supportive cancer care and pre-dialysis settings.

 

(2) 

A subsidiary of J&J.

 

(3) 

Approved via the EU biosimilar regulatory pathway.

 

(4) 

Competes with Aranesp® in the nephrology segment only. Pursuant to a December 2009 settlement agreement between Amgen and Roche, Roche is allowed to begin selling MIRCERA® in the United States in mid-2014 under terms of a limited license agreement. MIRCERA® has been approved by the FDA for the treatment of anemia associated with CRF.

 

(5) 

A subsidiary of Teva Pharmaceutical.

In addition to competition from these marketed products, Affymax, Inc. (Affymax) and Takeda are co-developing peginesatide, a synthetic, PEGylated peptidic compound that binds to and stimulates the erythropoietin receptor and thus acts as an ESA, for the treatment of anemia in CRF patients on dialysis and have submitted an NDA to the FDA. On December 7, 2011, Affymax and Takeda announced that the Oncology Drug Advisory Committee (ODAC) panel voted 15 to 1, with 1 abstention, that peginesatide demonstrated a favorable risk-benefit profile for use in the treatment of dialysis patients with anemia due to CKD. The FDA has targeted a Prescription Drug User Fee Act (PDUFA) action date of March 27, 2012.

EPOGEN® (epoetin alfa)

We were granted an exclusive license to manufacture and market EPOGEN® in the United States under a licensing agreement with K-A. We have retained exclusive rights to market EPOGEN® in the United States for dialysis patients. We granted Ortho Pharmaceutical Corporation, a subsidiary of J&J (which has assigned its rights under the Product License Agreement to Janssen), a license to commercialize recombinant human erythropoietin as a human therapeutic in the United States in all indications other than dialysis.

We launched EPOGEN® in the United States in 1989 for the treatment of anemia associated with CRF in patients who are on dialysis. We market EPOGEN® in the United States for the treatment of anemic adult and pediatric patients with CRF who are on dialysis. EPOGEN® is indicated for elevating or maintaining the red blood cell level (as determined by hematocrit or Hb measurements) and decreasing the need for blood transfusions in these patients.

EPOGEN® sales in the United States for the years ended December 31, 2011, 2010 and 2009, were $2.0 billion, $2.5 billion and $2.6 billion, respectively.

Our outstanding material patents for epoetin alfa are described in the following table.

 

Territory

  

General Subject Matter

   Expiration  

U.S.

  

Process of making erythropoietin

     8/15/2012   

U.S.

  

Product claims to erythropoietin

     8/20/2013   

U.S.

  

Pharmaceutical compositions of erythropoietin

     8/20/2013   

U.S.

  

Cells that make certain levels of erythropoietin

     5/26/2015   

 

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Any products or technologies that are directly or indirectly successful in addressing anemia associated with renal failure could negatively impact EPOGEN® sales. In the United States, as noted above, EPOGEN® and Aranesp® compete with each other, primarily in the U.S. hospital dialysis clinic setting. In addition, EPOGEN® could face additional competition from those products noted in the Aranesp® section above that may be used in dialysis in the United States.

Other Marketed Products

Our other marketed products include Sensipar®/Mimpara® (cinacalcet), Vectibix® (panitumumab), Nplate® (romiplostim), Prolia® (denosumab) and XGEVA® (denosumab).

Sensipar®/Mimpara® (cinacalcet)

Sensipar® is our registered trademark in the United States and Mimpara® is our registered trademark in Europe for cinacalcet, our small molecule medicine used in treating CKD patients on dialysis who produce too much parathyroid hormone (PTH), a condition known as secondary hyperparathyroidism. In 2004, Sensipar®/Mimpara® was approved in the United States and Europe for the treatment of secondary hyperparathyroidism in CKD patients on dialysis and for the treatment of hypercalcemia in patients with parathyroid carcinoma. In 2008, Mimpara® was approved in Europe for the reduction of hypercalcemia in patients with primary hyperparathyroidism (PHPT) where a parathyroidectomy is not clinically appropriate or is contraindicated. In 2011, Sensipar® was approved in the United States for the treatment of severe hypercalcemia in patients with PHPT who are unable to undergo parathyroidectomy. We market Sensipar® primarily in the United States and Mimpara® primarily in Europe.

As previously discussed, CMS’s Final Rule on Bundling in Dialysis became effective on January 1, 2011 and provides a single payment for all dialysis services. Oral drugs without intravenous equivalents, such as Sensipar® and phosphate binders, will continue to be reimbursed separately under the Medicare Part D benefit until 2014 when they will be reimbursed under the bundled payment system. Inclusion in the bundled payment system may reduce utilization of these oral drugs and have a material adverse impact on Sensipar® sales. (See Reimbursement.)

The phase 3 EValuation Of Cinacalcet HCl Therapy to Lower CardioVascular Events (E.V.O.L.V.E™) trial, initiated in 2006, is a large (3,800 patient), multi-center, international, randomized, double-blind study to assess the effects of Sensipar®/Mimpara® on mortality and cardiovascular morbidity in patients with CKD undergoing maintenance dialysis. The E.V.O.L.V.E™ study completed enrollment in January 2008 and we anticipate data from the study in 2012.

Worldwide Sensipar®/Mimpara® sales for the years ended December 31, 2011, 2010 and 2009, were $808 million, $714 million and $651 million, respectively.

Our outstanding material patents for cinacalcet are described in the following table.

 

Territory

  

General Subject Matter

   Expiration  

U.S.

  

Calcium receptor-active molecules including species

     10/23/2015   

U.S.

  

Calcium receptor-active molecules

     3/8/2018   

U.S.

  

Methods of treatment

     12/14/2016   

Europe(1)

  

Calcium receptor-active molecules

     10/23/2015   

 

(1) 

In some cases, this European patent may also be entitled to supplemental protection in one or more countries in Europe and the length of any such extension will vary by country.

Any products or technologies that are directly or indirectly successful in treating secondary hyperparathyroidism in patients with CKD on dialysis and/or hypercalcemia in patients with parathyroid carcinoma could negatively impact Sensipar®/Mimpara® sales.

 

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The following table reflects companies and their currently marketed products that compete with Sensipar® in the United States and with Mimpara® in Europe in the nephrology segment for patients with CKD on dialysis. The table below and the following discussion of competitor marketed products and products in development may not be exhaustive.

 

Territory

  

Competitor Marketed Product

  

Competitor

U.S.

   Hectorol®    Genzyme Corporation (Genzyme)

U.S.

   Rocaltrol®    Roche

U.S.

   Calcijex®    Abbott

U.S.

   Calcium Acetate®    Roxane Laboratories/Sandoz

U.S. & Europe

   Zemplar®    Abbott

U.S. & Europe

   Renagel®    Genzyme

U.S. & Europe

   Renvela®    Genzyme

U.S. & Europe

   PhosLo®/Rephoren®    Fresenius Medical Care

U.S. & Europe

   OsvaRen®    Fresenius Medical Care

U.S. & Europe

   Fosrenol®    Shire Pharmaceuticals Group Plc

On July 25, 2008, we filed a lawsuit against Teva and Barr Pharmaceuticals Inc. (Barr) for infringement of four Sensipar® patents. The lawsuit was based on Abbreviated New Drug Applications filed by Teva and Barr that sought approval to market generic versions of Sensipar®. Following trial, on January 7, 2011, the U.S. District Court for the District of Delaware granted an injunction prohibiting Teva and Barr from commercializing generic versions of Sensipar® in the United States until expiration of three of those patents. These generic versions could compete with Sensipar® in the future.

Vectibix® (panitumumab)

Vectibix® is our registered trademark for panitumumab, our monoclonal antibody for the treatment of patients with EGFr expressing mCRC after disease progression on, or following fluoropyrimidine-, oxaliplatin- and irinotecan- containing chemotherapy regimens. EGFr is a protein that plays an important role in cancer cell signaling and is over-expressed in many human cancers. Vectibix® binds with high affinity to EGFrs and interferes with signals that might otherwise stimulate growth and survival of the cancer cell. We acquired full ownership of Vectibix® with our acquisition of Abgenix, Inc. (Abgenix) in April 2006. In September 2006, Vectibix® received FDA accelerated approval in the United States, based upon clinical trial data from a study demonstrating a statistically significant improvement in progression-free survival and with the condition that Amgen conduct a confirmatory trial to verify the clinical benefit of panitumumab through demonstration of an improvement in overall survival. (See discussion of the ‘181 trial below.) In the EU, the conditional approval of Vectibix® as monotherapy, for the treatment of patients with EGFr expressing metastatic colorectal carcinoma with non-mutated (wild-type) KRAS genes after failure of fluoropyrimidine-, oxaliplatin-, and irinotecan-containing chemotherapy regimens, was received in December 2007 and is reviewed annually by the Committee for Medicinal Products for Human Use (CHMP). Each year thereafter, the EU conditional marketing authorization was renewed with an additional specific obligation to conduct a clinical trial in the approved monotherapy indication. In 2010, we began enrollment for this additional clinical trial which compares the effect of Vectibix® versus Erbitux® (cetuximab) on overall survival for chemorefractory mCRC patients with wild-type KRAS genes. KRAS is a protein found in all human cells. Some colorectal cancers have mutations in the KRAS gene. Vectibix® has been shown to be ineffective in people whose tumors had KRAS mutations in codon 12 or 13.

In 2009, we announced results from the ‘203 and ‘181 pivotal phase 3 trials evaluating Vectibix® in combination with chemotherapy (FOLFOX or FOLFIRI) as a first- and second-line treatment for mCRC, respectively. Both studies demonstrated that Vectibix® administered with chemotherapy significantly improved progression-free survival in patients with wild-type KRAS mCRC. Additionally, both studies showed numeric improvements in median overall survival in the same patient population. The numeric improvements in median overall survival failed to achieve statistical significance. It was previously agreed with the FDA that the ‘181 study would serve as the confirmatory trial for establishing full approval for the mCRC indication.

 

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On February 8, 2011, we and four other sponsor companies met with the FDA and the ODAC to discuss the status of our respective PMCs for product indications that had been granted accelerated approval by the FDA prior to 2009, including Vectibix®. At that meeting, we updated the Committee on the completion and submission of the main PMC for Vectibix® and on the confirmatory ’181 study; and we participated in an open discussion with the ODAC on the accelerated approval process.

On July 29, 2011, we announced that we received Complete Response Letters from the FDA on the first- and second-line mCRC sBLAs that we filed in late 2010. The FDA did not ask for new clinical studies but did request an updated safety analysis and additional analyses of the overall survival data in the ’181 and ’203 studies using more mature data sets. The FDA has also informed us that approval for the first- and second-line mCRC indications will be contingent upon approval of the companion diagnostic device being developed in collaboration with QIAGEN N.V., which identifies a patient’s KRAS gene status. We are currently working on addressing the FDA’s requests in the Complete Response Letters.

On November 10, 2011, the EC approved a variation to the marketing authorization for Vectibix® to include indications for the treatment of patients with wild-type KRAS mCRC in first- and second-line in combination with chemotherapy.

Worldwide Vectibix® sales for the years ended December 31, 2011, 2010 and 2009, were $322 million, $288 million and $233 million, respectively.

Our outstanding material patents for panitumumab are described in the following table.

 

Territory

  

General Subject Matter

   Expiration

U.S.

  

Human monoclonal antibodies to EGFr

   4/8/2020

U.S.

  

Human monoclonal antibodies to EGFr

   5/5/2017

Europe

  

Fully human antibodies that bind EGFr

   12/3/2017

Europe(1)

  

Human monoclonal antibodies to EGFr

   5/5/2018

 

 

(1) 

In some cases, this European patent may also be entitled to supplemental protection in one or more countries in Europe and the length of any such extension will vary by country.

Any products or technologies that are directly or indirectly successful in treating mCRC after disease progression on, or following fluoropyrimidine-, oxaliplatin- and irinotecan- containing chemotherapy regimens could negatively impact Vectibix® sales. The following table reflects the companies that currently market Erbitux®, which competes with Vectibix® in the United States and Europe. The table below and the following discussion of products in development may not be exhaustive.

 

Territory

  

Competitor Marketed Product

  

Competitor

U.S.

   Erbitux®    Eli Lilly/BMS

Europe

   Erbitux®    Merck KGaA

In addition to competition from Erbitux®, the following products in development could compete with Vectibix® in the future:

 

   

Sanofi filed a BLA with the FDA for approval of ZALTRAP™ for second-line mCRC in early 2012.

 

   

Bayer announced results from its phase 3 trial for regorafenib in patients with mCRC. Bayer is in discussions with health authorities worldwide regarding next steps in filing for approval.

Nplate® (romiplostim)

In August 2008, the FDA approved Nplate® for the treatment of thrombocytopenia in splenectomized (spleen removed) and non-splenectomized adults with chronic immune thrombocytopenic purpura (ITP). Nplate® works by raising and sustaining platelet counts. We were granted an exclusive license by K-A to manufacture and market Nplate® in the United States, all European countries, Canada, Australia, New Zealand, Mexico, all Central and South American countries and certain countries in Central Asia, Africa and the Middle East. In

 

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February 2009, we announced that the EC had granted marketing authorization for Nplate® for the treatment of splenectomized adult chronic ITP patients who are refractory to other treatments (e.g., corticosteroids, immunoglobulins). In the EU, Nplate® may also be considered as second-line treatment for adult non-splenectomized ITP patients where surgery is contraindicated.

Worldwide Nplate® sales for the years ended December 31, 2011, 2010 and 2009, were $297 million, $229 million and $110 million, respectively.

Our outstanding material patents for romiplostim are described in the following table.

 

Territory

  

General Subject Matter

   Expiration

U.S.

  

Thrombopoietic compounds

   1/19/2022

U.S.

  

Thrombopoietic compounds

   10/22/2019

Europe(1)

  

Thrombopoietic compounds

   10/22/2019

 

(1) 

In some cases, this European patent may also be entitled to supplemental protection in one or more countries in Europe and the length of any such extension will vary by country.

Any products or technologies that are directly or indirectly successful in treating thrombocytopenia in splenectomized and non-splenectomized adults with chronic ITP could negatively impact Nplate® sales. The following table reflects companies and their currently marketed products that compete with Nplate® in the United States and Europe and may not be exhaustive.

 

Territory

  

Competitor Marketed Product

  

Competitor

U.S.

   Promacta®    GlaxoSmithKline plc (GSK)

Europe

   Revolade®    GSK

Prolia®/XGEVA® (denosumab)

In 2010, we launched Prolia® and XGEVA®, both of which contain the same active ingredient but which are approved for different indications, patient populations, doses and frequencies of administration. We have a collaboration agreement with Glaxo Group Limited (Glaxo), a wholly owned subsidiary of GSK, for the commercialization of denosumab in certain countries. (See Business Relationships — Glaxo Group Limited.)

Prolia®

On June 1, 2010, the FDA approved Prolia® for the treatment of postmenopausal women with osteoporosis at high risk for fracture, defined as a history of osteoporotic fracture, or multiple risk factors for fracture, or patients who have failed or are intolerant to other available osteoporosis therapy. On September 19, 2011, we announced that the FDA approved two additional indications for Prolia® as a treatment to increase bone mass in women at high risk for fracture receiving adjuvant aromatase inhibitor therapy for breast cancer and as a treatment to increase bone mass in men at high risk for fracture receiving androgen deprivation therapy for non-metastatic prostate cancer.

We estimate that the large majority of Prolia® usage to date in the United States has been under Medicare Part B. Additionally, most potential U.S. Prolia® patients now also have coverage for Prolia® under Medicare Part D. Future U.S. product sales for Prolia® will depend primarily on postmenopausal osteoporosis disease state awareness, the willingness of primary care physicians to prescribe the product and the availability of reimbursement for and patient acceptance of the product.

On May 25, 2010, the EC granted marketing authorization for Prolia® for the treatment of osteoporosis in postmenopausal women at increased risk of fractures and for the treatment of bone loss associated with hormone ablation in men with prostate cancer at increased risk of fractures. Since the first reimbursement authority was received in Germany in July 2010, reimbursement authority approval has been granted in most EU countries.

Worldwide Prolia® sales for the years ended December 31, 2011 and 2010, were $203 million and $33 million, respectively.

 

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Any products or technologies that are directly or indirectly successful in treating postmenopausal osteoporosis (PMO) in women at high risk for fracture could negatively impact Prolia® sales.

The following table and discussion reflect other companies and their currently marketed products that compete with Prolia®. The table below and the following discussion of competitor marketed products and products in development may not be exhaustive.

 

Territory

  

Competitor Marketed Product

  

Competitor

U.S. & Europe

   FOSAMAX®(1)    Merck

U.S. & Europe

   Actonel®AtelviaTM    Warner Chilcott PLC

U.S. & Europe

   Boniva®/Bonviva®    Roche

U.S. & Europe

   Evista®    Eli Lilly

U.S. & Europe

   Forteo®/Forsteo™    Eli Lilly

U.S. & Europe

   Miacalcin®    Novartis AG (Novartis)

U.S. & Europe

   Aclasta®/Reclast®    Novartis

Europe

   Conbriza®    Pfizer

Europe

   Fablyn®    Pfizer

 

(1) 

Merck’s patent covering the use of FOSAMAX® to treat bone loss expired in the United States in February 2008. Following the patent expiry, generic alendronate, which competes with FOSAMAX® and Prolia®, became available.

We expect several additional marketed products noted above to lose patent protection over the next several years, including Boniva® in 2012, at which time we expect generic versions of these products would become commercially available and compete with Prolia®.

The following companies have product candidates in phase 3 clinical development that may compete with Prolia® in the future:

 

   

Merck (odanacatib), for PMO.

 

   

Radius Health, Inc. (BA058) for PMO.

XGEVA®

On November 18, 2010, the FDA approved XGEVA® for the prevention of SREs in patients with bone metastases from solid tumors. XGEVA® is not indicated for the prevention of SREs in patients with multiple myeloma.

On May 17, 2011, we announced results of a pivotal phase 3 trial (Study ‘147) in 1,432 men with castration-resistant prostate cancer that has not yet spread to bone. The trial demonstrated that XGEVA® significantly improved median bone metastasis-free survival by 4.2 months compared to placebo (primary endpoint) and significantly improved time to first occurrence of bone metastases (secondary endpoint). Overall survival was similar between the XGEVA® and placebo arms (secondary endpoint), and adverse events and serious adverse events were relatively similar. Hypocalcemia and osteonecrosis of the jaw (ONJ) were reported with increased frequencies in the XGEVA® treated patients compared to placebo. The yearly rate of ONJ in the XGEVA® arm was similar to prior XGEVA® trial results. Back pain was the most common adverse event reported in the XGEVA® arm of the trial. On June 27, 2011, we announced the submission of an sBLA to the FDA to expand the indication to treat men with castration-resistant prostate cancer to reduce the risk of developing bone metastases. On February 8, 2012, the FDA convened the ODAC to discuss the sBLA filing. The ODAC panel voted 12 to 1 that the overall magnitude of benefit demonstrated with early treatment with XGEVA® to delay bone metastases was not sufficient to conclude a positive risk-benefit ratio in the absence of additional measures impacting quality of life or other disease outcomes. The FDA often seeks the advice of an advisory committee such as ODAC when evaluating a potential new treatment. The FDA has targeted a PDUFA action date of April 26, 2012.

 

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On July 15, 2011, we announced that the EC granted marketing authorization for XGEVA® for the prevention of SREs (pathological fracture, radiation to bone, spinal cord compression or surgery to bone) in adults with bone metastases from solid tumors. The timing of reimbursement authority approval of pricing in individual EU countries will vary by country, which could follow the EC approval by many months. For example, in August 2011, XGEVA® received reimbursement authority in Germany. The EC also granted XGEVA® an additional year of data and market exclusivity in the EU since the indication was considered new for denosumab and based on the significant clinical benefit of XGEVA® in comparison with existing therapies.

U.S. XGEVA® sales for the years ended December 31, 2011 and 2010, were $351 million and $8 million, respectively.

Any products or technologies that are directly or indirectly successful in treating for the prevention of SREs in patients with bone metastases from solid tumors could negatively impact XGEVA® sales.

The following table reflects currently marketed products that compete with XGEVA®. The table below and the following discussion of competitor marketed products may not be exhaustive.

 

Territory

  

Competitor Marketed Product

  

Competitor

U.S. & Europe

   Zometa®(1)    Novartis

U.S. & Europe

   Aredia®(2)    Novartis

 

(1) 

Novartis has indicated that patent protection on the active ingredient for Zometa® will expire in 2013 in the United States and 2012 in other major markets. At such time, we expect that generic forms of zoledronic acid may become commercially available and compete with Zometa® and XGEVA®.

 

(2) 

Novartis’s patent covering the use of Aredia® to treat tumor-induced hypercalcemia, osteolysis from multiple myeloma and bone metastases from breast cancer expired in the United States in 2001. Following the patent expiry, generic pamidronate, which competes with Aredia® and XGEVA®, became available from other companies.

In addition, Bayer has a product candidate, alpharadin, in phase 3 clinical development for SREs in patients with prostate cancer, that may compete with XGEVA® in the future.

Our outstanding material patents for denosumab are described in the following table.

 

Territory

  

General Subject Matter

  

Expiration(1)

U.S.

   RANKL antibodies; methods of interfering with RANK signaling    12/22/2017

U.S.

   Methods of treatment    11/11/2018

U.S.

   RANKL antibodies including sequences    2/19/2025

U.S.

   Nucleic acids encoding RANKL antibodies, and methods of producing the same    11/11/2023

Europe

   RANKL antibodies    12/22/2017

Europe

   Medical use of RANKL antibodies    4/15/2018

Europe

   RANKL antibodies including epitope binding    2/23/2021

Europe

   RANKL antibodies including sequences    6/25/2022

 

(1)

In some cases, these patents may be entitled to patent term extension in the United States or supplemental protection in one or more countries in Europe and the length of any such extension will vary by country.

Marketing and Distribution

We maintain sales and marketing forces primarily in the United States, Europe and Canada to support our currently marketed products. We have also entered into agreements with third parties to assist in the commercialization and marketing of certain of our products in specified geographic areas. (See Business Relationships.) Together with our partners, we market our products to healthcare providers, including physicians or their clinics, dialysis centers, hospitals and pharmacies. We also market certain products directly to consumers

 

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through direct-to-consumer print and television advertising, and also through the Internet. In addition, for certain of our products, we promote programs to increase public awareness of the health risks associated with the diseases these products treat, as well as provide support to various patient education and support programs in the related therapeutic areas. (See Government Regulation — FDA Regulation of Product Marketing and Promotion for a discussion of the government regulation over product marketing and promotion.)

In the United States, we sell primarily to pharmaceutical wholesale distributors. We utilize those wholesale distributors as the principal means of distributing our products to healthcare providers. In Europe, we sell principally to healthcare providers and/or pharmaceutical wholesale distributors depending on the distribution practice in each country. We monitor the financial condition of our larger customers, and we limit our credit exposure by setting credit limits and, for certain customers, by requiring letters of credit.

We had product sales to three customers each accounting for more than 10% of total revenues for the years ended December 31, 2011, 2010 and 2009. For 2011, on a combined basis, these customers accounted for 72% and 90% of worldwide gross revenues and U.S. gross product sales, respectively, as noted in the following table. Certain information with respect to these customers for the years ended December 31, 2011, 2010 and 2009, was as follows (dollar amounts in millions):

 

     2011      2010      2009  

AmerisourceBergen Corporation:

        

Gross product sales

   $ 7,574       $ 7,678       $ 7,179   

% of total gross revenues

     36%         38%         37%   

% of U.S. gross product sales

     45%         47%         46%   

McKesson Corporation:

        

Gross product sales

   $ 4,591       $ 3,913       $ 3,694   

% of total gross revenues.

     22%         19%         19%   

% of U.S. gross product sales

     27%         24%         24%   

Cardinal Health, Inc:

        

Gross product sales

   $ 3,021       $ 2,813       $ 2,841   

% of total gross revenues.

     14%         14%         15%   

% of U.S. gross product sales

     18%         17%         18%   

Reimbursement

Sales of all of our principal products are dependent in large part on the availability and extent of coverage and reimbursement from third-party payers, including government and private insurance plans. Most patients receiving our products are covered by government healthcare programs or private insurers. Governments may regulate coverage, reimbursement and/or pricing of our products to control costs or to affect levels of use of our products, and private insurers may adopt or be influenced by government coverage and reimbursement methodologies. Worldwide use of our products may be affected by cost containment pressures and cost shifting from governments and private insurers to healthcare providers or patients in response to ongoing initiatives to reduce or reallocate healthcare expenditures. An increasing worldwide focus on patient access controls and cost containment by public and private insurers has resulted, and may continue to result, in reduced reimbursement rates for our products. In addition, recent healthcare reform efforts enacted in the United States have made substantial long-term changes to the reimbursement of our products, and those changes have had, and are expected to continue to have, a significant impact on our business.

U.S. Reimbursement System

Our principal products are sold primarily in the United States and healthcare providers, including doctors, hospitals and other healthcare professionals and providers, are reimbursed for covered services and products they use by the government through Medicare, Medicaid and other government healthcare programs as well as through private payers. Government healthcare programs are funded primarily through the payment of taxes by individuals and businesses. The public and private components of this multi-payer system are described below.

 

 

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Medicare and Other Forms of Public Health Insurance

Medicare is a federal program administered by the federal government that covers individuals age 65 and over as well as those with certain disabilities or ESRD, regardless of their age. The primary Medicare programs that affect reimbursement for our products are Medicare Part B, which covers physician services and outpatient care, and Medicare Part D, which provides a voluntary outpatient prescription drug benefit. CMS is the federal agency responsible for administering Medicare (as well as Medicaid, described below) and, among its responsibilities, has authority to promulgate regulations and policies, as well as issue reimbursement codes for drugs, all of which can determine how medical items and services are covered and reimbursed by Medicare. CMS can also issue Medicare NCDs which are national policy statements granting, limiting or excluding Medicare coverage for specific medical items or services applicable throughout the United States. In the absence of a relevant NCD, Medicare coverage determinations for a particular medical item or service are left to MACs, whose LCD’s are binding on providers within their respective jurisdictions. CMS sometimes uses advisory committees of external experts in order to obtain independent expert advice on scientific, technical and policy matters. For example, the Medicare Evidence Development and Coverage Advisory Committee (MEDCAC) was established to provide independent guidance and expert advice to CMS on specific clinical topics. The MEDCAC reviews and evaluates medical literature, technology assessments, and examines data and information on the effectiveness and appropriateness of medical items and services that are covered under Medicare, or that may be eligible for coverage under Medicare.

Medicare Part B Coverage of Drugs and ESRD. Medicare Part B provides limited coverage of outpatient drugs and biologicals that are reasonable and necessary for a medically accepted diagnosis or treatment of an illness or injury and that fall into a statutory benefit category. One such category relevant to our products is for drugs and biologicals furnished “incident to” a physician’s services. Generally, “incident to” drugs and biologicals are covered if they satisfy certain criteria, including that they are of the type that are not usually self-administered by the patient. Medicare Part B also covers certain drugs pursuant to specific statutory benefit categories, such as blood-clotting factors and certain immunosuppressive drugs, erythropoietin and certain oral cancer drugs. Many of our principal products are currently covered under Medicare Part B (as well as other government healthcare programs). In addition, most patients with ESRD, regardless of age, are eligible for coverage of dialysis treatment through the ESRD Program under Medicare Part B. Because Medicare Part B is the primary payer for dialysis treatment, reimbursement for products, such as EPOGEN®, that are typically administered in dialysis centers and other settings is particularly sensitive to changes in Medicare coverage and reimbursement policy. Since January 1, 2011, dialysis treatment has been reimbursed by Medicare under a bundled payment system described in more detail below. (See Dialysis Reimbursement.)

Medicare Part D. Medicare Part D provides a voluntary prescription drug benefit for Medicare eligible beneficiaries. The coverage is available through various private plans that provide insurance coverage for prescription drugs for a monthly premium and with patient cost sharing. The list of prescription drugs covered by Medicare Part D plans varies by plan, but drug lists maintained by individual plans must cover certain classes of drugs and biologicals; specifically the statute stipulates that Medicare Part D plans have at least two drugs in each unique therapeutic category or class, subject to certain exceptions.

Medicaid. Medicaid is a joint federal and state program administered by individual states for low-income and disabled eligible beneficiaries. CMS also has responsibility for federal administration of the Medicaid program. Under federal law, states must cover low-income adults and children, pregnant women, disabled individuals and seniors, and states have the option of expanding eligibility beyond those groups of beneficiaries. Medicaid is financed jointly by the states and federal government through taxes. Medicaid offers a broad set of benefits, including prescription drugs. Medicaid includes the Drug Rebate Program which requires manufacturers to provide rebates to the states for products covered and reimbursed by state Medicaid programs.

See Item 1A. Risk Factors — Our sales depend on coverage and reimbursement from third-party payers.

Private Health Insurance

Employer-sponsored insurance. Employer-sponsored insurance currently represents the main pathway by which Americans receive private health insurance. Many employers provide health insurance as part of

 

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employees’ benefit packages. Insurance plans are administered by private companies, both for-profit and not-for-profit, and some companies are “self-insured” (i.e., they pay for all healthcare costs incurred by employees directly through a plan administered by a third party). Generally, employer-sponsored insurance premiums are paid primarily by employers and secondarily by employees.

Individual market. The individual market covers part of the population that is self-employed or retired. In addition, it covers some people who are unable to obtain insurance through their employers. The plans are administered by private insurance companies. Individuals pay out-of-pocket insurance premiums for coverage, and the benefits vary widely according to plan specifications.

Reimbursement of Our Principal Products

Neulasta®, NEUPOGEN® and Aranesp®. Medicare and Medicaid payment policies for drugs and biologicals are subject to various laws and regulations. The Medicare program covers our principal products Neulasta®, NEUPOGEN® and Aranesp® (as well as certain of our other products including Vectibix®, Nplate®, Prolia® and XGEVA®) under Part B, when administered in the physician clinic setting and the hospital outpatient settings. Healthcare providers are reimbursed for these products under a “buy and bill” process where providers purchase the product in advance of treatment and then submit a reimbursement claim to Medicare following administration of the product. Medicare reimburses providers using a payment methodology based on a fixed percentage of each product’s average sales price (ASP). ASP is calculated by the manufacturer based on a statutorily defined formula and submitted to CMS. A product’s ASP is calculated and reported to CMS on a quarterly basis and therefore may change each quarter. The ASP in effect for a given quarter (the Current Period) is based upon certain historical sales and sales incentive data covering a defined period of time preceding the Current Period. CMS publishes the ASPs for products in advance of the quarter in which they go into effect so healthcare providers will know the applicable reimbursement rates. In the calculation of ASP, CMS currently allows manufacturers to make reasonable assumptions consistent with the general requirements and the intent of the Medicare statute and regulations and their customary business practices and in the future CMS may provide more specific guidance. Any changes to the ASP calculations directly affect the Medicare reimbursement for our products administered in the physician clinic setting, hospital outpatient setting and, to a lesser extent, the dialysis facility setting. (See EPOGEN® and Dialysis Reimbursement.) Our ASP calculations are reviewed quarterly for completeness and based on such review, we have on occasion restated our reported ASPs to reflect calculation changes both prospectively and retroactively. (See Items 1A. Risk Factors — Our sales depend on coverage and reimbursement from third-party payers.)

Since 2005, products provided in the physician office setting under Medicare Part B have been reimbursed at 106% of their ASP (sometimes referred to as “ASP+6%”), and in 2012 will continue to be reimbursed at this rate pursuant to the 2012 Medicare Physician Fee Schedule Final Rule. In the hospital outpatient setting, from 2006 to 2010 Medicare reimbursement rates fell incrementally from ASP+6% to ASP+4%, then rose in 2011 to ASP+5%. Pursuant to the 2012 Hospital Outpatient Prospective Payment Final Rule, the rate will fall again to ASP+4% in 2012. CMS has the regulatory authority to further adjust formulas in future years. The extent to which commercial payers adopt the use of ASP as a payment methodology is often based on the contractual relationship between the provider and the insurer.

Dialysis Reimbursement. Currently, dialysis providers in the United States are reimbursed for EPOGEN® primarily by Medicare through the ESRD Program, which is established by federal law and implemented by CMS. Historically, the ESRD Program reimbursed Medicare providers for 80% of allowed dialysis costs; the remainder was paid by other sources, including patients, state Medicaid programs, private insurance, and to a lesser extent, state kidney patient programs. Until January 1, 2011, Medicare reimbursed for separately billable dialysis drugs (including Aranesp® and EPOGEN®) administered in both freestanding and hospital-based dialysis centers, at ASP+6%, using the same payment amount methodology used in the physician clinic setting under Part B. On January 1, 2011, CMS’s bundled payment system went into effect for dialysis providers which provides a single payment for all dialysis services including drugs, supplies and non-routine laboratory tests that were previously reimbursed separately. ESRD providers receive a designated payment for each dialysis treatment and can be paid for up to three treatments per week, unless medical necessity justifies more frequent treatments. Oral

 

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drugs without intravenous equivalents, including Sensipar® and phosphate binders, will remain under the Medicare Part D benefit until 2014 when they will be reimbursed under the bundled payment system.

To encourage dialysis providers to continue to provide quality dialysis treatment under the new bundled payment system, CMS also implemented the ESRD QIP. Under the QIP, beginning in 2012, ESRD facilities will be subject to a payment penalty of up to 2% of amounts reimbursed for failure to meet or exceed CMS’ quality performance standards, including performance standards related to anemia management and dialysis adequacy. Under the QIP as originally implemented, a provider’s penalty in 2012 will be based on the provider’s composite score for the following performance measures achieved during 2010:

 

   

the percent of Medicare patients with Hb levels below 10 g/dL constitutes 50% of the weighting;

 

   

the percent of Medicare patients with Hb levels above 12 g/dL represents 25% of the weighting; and

 

   

the percent of Medicare patients with an average Urea Reduction Ratio of greater than or equal to 65% constitutes 25% of the weighting.

On November 1, 2011, CMS finalized a rule to update the QIP, eliminating for payment year 2013 and beyond the QIP’s measure that tracks the percent of a provider’s Medicare patients with a Hb level below 10 g/dL. Beginning in payment year 2013, the remaining two metrics will each constitute 50% of the weighting. CMS indicated that removal of this measure from the QIP was being done in response to the June 2011 ESA label changes.

ENBREL Reimbursement. The majority of prescription claims for ENBREL are paid through private insurance companies. Under Medicare, ENBREL is reimbursed through the Part D program, although less than 10% of all ENBREL U.S. prescriptions are reimbursed by Medicare.

Medicaid Reimbursement

Since 1991, we have participated in the Medicaid drug rebate program established in Section 1927 of the Social Security Act by the Omnibus Budget Reconciliation Act of 1990 and subsequent amendments of that law. Under the Medicaid drug rebate program, we pay a rebate to the states for each unit of our product reimbursed by state Medicaid programs. As more fully described below, the healthcare reform law enacted in the United States in March 2010 made certain changes in how those rebates are calculated and to whom they must be extended. (See U.S. Healthcare Reform.) The amount of the rebate for each of our products is currently set by law as a minimum of 23.1% of the Average Manufacturer Price (AMP) of that product, or if it is greater, the difference between AMP and the best price available from us to any non-government customer. The rebate amount is determined for each quarter based on our reports to CMS of the quarter’s AMP and best price for each of our products. The rebate amount also includes an inflation adjustment if AMP increases faster than inflation. As described below, the statutory definition of AMP changed in 2010 as a result of the U.S. healthcare reform law, and in January 2012, CMS issued a proposed rule further defining the new AMP definition. Until that rule is finalized, we are required to make reasonable assumptions when calculating AMP. Once CMS’s proposed rule is finalized, we will have to determine whether our calculations should be amended and whether we will need to restate our prior AMPs.The terms of our participation in the Medicaid drug rebate program impose an obligation to correct the prices reported in previous quarters, as may be necessary. Any such corrections could result in an overage or underage in our rebate liability for past quarters, depending on the direction of the correction. In addition to retroactive rebates, if we were found to have knowingly submitted false information to the government, in addition to other penalties available to the government, the statute provides for civil monetary penalties in the amount of $100,000 per item of false information.

Related to our participation in the Medicaid drug rebate program is a requirement that we extend comparable discounts under the Public Health Service (PHS) drug pricing program to a variety of community health clinics and other entities that receive health services grants from the PHS, as well as hospitals that serve a disproportionate share of Medicare and Medicaid beneficiaries. As more fully described below, the list of entities to which we are required to extend these discounts also expanded as a result of the U.S. healthcare reform law.

 

 

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We also make our products available to authorized users of the Federal Supply Schedule (FSS) of the General Services Administration. Since 1993, as a result of the Veterans Health Care Act of 1992 (the VHC Act), federal law has required that we offer deeply discounted FSS contract pricing for purchases by the Department of Veterans Affairs, the Department of Defense, the Coast Guard and the PHS (including the Indian Health Service) in order for federal funding to be available for reimbursement of our products under the Medicaid program or purchase of our products by those four federal agencies and certain federal grantees. FSS pricing to those four federal agencies must be equal to or less than the Federal Ceiling Price (FCP), which is 24% below the Non-Federal Average Manufacturer Price (Non-FAMP) for the prior fiscal year. The accuracy of our reported Non-FAMPs, FCPs and our FSS contract prices may be audited by the government under applicable federal procurement laws and the terms of our FSS contract. Among the remedies available to the government for inaccuracies in calculation of Non-FAMPs and FCPs is recoupment of any overcharges to the four specified Federal agencies based on those inaccuracies. Also, if we were found to have knowingly reported a false Non-FAMP, in addition to other penalties available to the government, the VHC Act provides for civil monetary penalties of $100,000 per item that is incorrect. Finally, we are required to disclose in our FSS contract proposal all commercial pricing that is equal to or less than our proposed FSS pricing, and subsequent to award of an FSS contract, we are required to monitor certain commercial price reductions and extend commensurate price reductions to the government, under the terms of the FSS contract Price Reductions Clause. Among the remedies available to the government for any failure to properly disclose commercial pricing and/or to extend FSS contract price reductions is recoupment of any FSS overcharges that may result from such omissions.

U.S. Healthcare Reform. In March 2010, the Patient Protection and Affordable Care Act (the PPACA) and the companion Health Care and Education Reconciliation Act, which made certain changes and adjustments to the PPACA, primarily with respect to the PPACA’s financial and budgetary impacts, were signed into law. We refer to those two laws collectively as the “U.S. healthcare reform law.” The U.S. healthcare reform law imposes additional costs on and reduces the revenue of companies in the biotechnology and pharmaceutical industries. The following paragraphs describe certain provisions of the new healthcare reform law that are affecting and will affect the reimbursement of our products.

The U.S. healthcare reform law increased the rebates we pay to the states for our products that are covered and reimbursed by state Medicaid programs. The healthcare reform law increased the minimum base Medicaid rebate rate payable on our products reimbursed by Medicaid from 15.1% to 23.1% of the AMP of the product, or if it is greater, the difference between the AMP and the best price available from us to any non-government customer. The change in the minimum rebate percentage was effective on January 1, 2010. The healthcare reform law also extended the Medicaid drug rebate program to patients in Medicaid managed care insurance plans for whom rebates were not previously required. The extension of rebates to patients in Medicaid managed care plans was effective on March 23, 2010.

As mentioned above, the U.S. healthcare reform law also expanded the list of provider institutions to which we must extend discounts under the PHS 340B drug pricing program. The U.S. healthcare reform law added certain cancer centers, children’s hospitals, critical access hospitals and rural referral centers to the list of entities to which these discounts must be extended. This change to the list of eligible entities was effective on January 1, 2010. The U.S. healthcare reform law also imposed a new fee (the U.S. healthcare reform federal excise fee) on manufacturers and importers of “branded prescription drugs,” which includes drugs approved under section 505(b) of the Federal Food, Drug, and Cosmetic Act or biologicals licensed under section 351(a) of the Public Health Service Act. Beginning in 2011, the U.S. healthcare reform law sets an aggregate annual fee, to be paid by these manufacturers and importers, totaling $28 billion over 10 years, of which $2.5 billion was payable in 2011. This annual fee is apportioned among the participating companies, including us, based on each company’s sales of qualifying products to, and utilization by, certain U.S. government programs during the preceding calendar year. The additional fee became effective January 1, 2011, and is not deductible for U.S. federal income tax purposes. Manufacturers and importers of generic or biosimilar drugs are not subject to the fee.

Since the Medicare Part D drug benefit took effect in 2006, beneficiaries enrolled in Part D plans have been required to pay 100% of their prescription drug costs after their total drug spending exceeds an initial coverage limit until they qualify for catastrophic coverage. This coverage gap is sometimes referred to as the Part D

 

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“doughnut hole.” The U.S. healthcare reform law reduces the “doughnut hole” by requiring manufacturers like us to provide a 50% discount to Medicare Part D patients whose prescription expenses exceed the Part D prescription drug coverage limit but have not yet reached the catastrophic coverage threshold. This provision became effective January 1, 2011.

The U.S. healthcare reform law also expands the Medicaid eligibility to include those with incomes up to 133% of the federal poverty level (FPL), from 100% of the FPL. This provision becomes effective January 1, 2014.

Impact of Budget Control Act on U.S. Reimbursement

The Budget Control Act of 2011, signed into law in the United States in August 2011, mandated a two percent reduction in government payments for all Medicare services (including the administration of separately-billable drugs and payment for drugs in all Medicare programs) for federal fiscal years 2013 through 2021, unless a subsequent deficit reduction law was passed before January 2012. As no additional deficit reduction law was enacted by January 2012, the payment reduction (or “sequestration”) will likely start in January 2013 and continue until December 2021, subject to administrative implementation of the Budget Control Act or future statutory revision. A reduction in the availability or extent of reimbursement from U.S. government programs as a result of the sequestration or from other changes designed to achieve similar federal budget savings could have a material adverse effect on the sales of our products, our business and results of operations.

Reimbursement Outside the United States

Generally, in Europe and other countries outside the United States, government-sponsored healthcare systems have traditionally been the primary payers of all healthcare costs, including payment for drugs and biologicals. Over the past several years, the reimbursement environment in Europe has become very challenging, including as a result of the proliferation of Health Technology Assessment (HTA) organizations (e.g., National Institute for Health and Clinical Excellence (NICE) in the UK) that make recommendations and/or determinations of coverage and reimbursement based on both the clinical as well as the economic value of a product. Although the methods employed by different HTA agencies vary from country to country, the use of formal economic metrics has been increasing across Europe as well as in several emerging markets throughout the world. In addition to determining whether or not a new product will be reimbursed, these agencies are becoming increasingly involved in setting the maximum price at which the product will be reimbursed — the “value-based” price for a product.

With increased budgetary constraints, payers in many countries employ a variety of measures to exert downward price pressure. In some countries, international price referencing is the primary mechanism for price control whereby the ceiling price of a pharmaceutical or biological product is set based on the prices in particular benchmark countries. These price referencing rules are increasing in complexity as payers seek lower-price benchmarks against which to compare themselves. Trends across Europe are also leading toward increased price transparency, with the development of databases to include prices across Europe and requests from specific national payers to provide commercially confidential net price information. Additional cost-containment measures can include therapeutic reference pricing (e.g., setting the reimbursement rate for a given class of agents at the lowest price within the class), increasing mandates or incentives for generic substitution and government-mandated price cuts. In addition, healthcare reform in France, Germany and Spain, as well as austerity plans in a number of countries, including Greece, Italy and Portugal, have targeted the pharmaceutical sector with multiple mechanisms to reduce government healthcare expenditures. Other countries may follow and/or take similar or more extensive actions to reduce expenditures on drugs and biologics, including implementing mandatory price reductions, initiating clawbacks of payments made to companies when national hospital drug spending thresholds are exceeded, establishing preferences for biosimilar products, or reducing the amount of reimbursement. Similarly, fiscal constraints may also impact the extent to which countries are willing to reward new innovative therapies and/or allow access to new technologies.

 

 

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In many countries, the influence of regional and hospital payers also contributes to whether patients have access to certain products. For example, a product may be successfully listed on a national formulary, but may also be subject to further evaluations or competitive bidding by payers at a regional or hospital level. The impact of multiple layers of assessment can result in delay or failure to secure access and/or net price pressure.

Payers in some countries are using and others are beginning to experiment with alternative payment mechanisms (e.g., payment caps, risk sharing) as a means to maintain access to innovative therapies while increasing their budget certainty. Requirements for such payment mechanisms can impact Amgen’s business through increased net price concessions and added administrative burden.

Fraud and Abuse Regulations Related to Reimbursement

As participants in government reimbursement programs, we are subject to various U.S. federal and state laws, as well as foreign laws, pertaining to healthcare “fraud and abuse,” including anti-kickback laws and false claims laws. (See Government Regulation — Other.) Violations of fraud and abuse laws can result in stringent enforcement penalties up to and including complete exclusion from federal healthcare programs (including Medicare and Medicaid).

Manufacturing, Distribution and Raw Materials

Manufacturing

Biological products, which are produced in living systems, are inherently complex due to naturally-occurring molecular variations. Highly specialized knowledge and extensive process and product characterization are required to transform laboratory scale processes into reproducible commercial manufacturing processes. Our manufacturing operations consist of bulk manufacturing, formulation, fill and finish and distribution activities. Bulk manufacturing includes fermentation and/or cell culture, processes by which our proteins are produced, and also includes purification of the proteins to a high quality. The proteins are then formulated into a stable form. The fill process dispenses the formulated bulk protein into vials or syringes. Finally, in the finish process, our products are packaged for distribution.

We operate a number of commercial and/or clinical manufacturing facilities, and our primary facilities are located in the United States, Puerto Rico and the Netherlands. (See Item 2. Properties.) We also use and expect to continue to use third-party contract manufacturers to produce or assist in the production of certain of our large molecule marketed products as well as a number of our clinical product candidates. Manufacturing of Sensipar®/Mimpara®, our small molecule product, is currently performed by third-party contract manufacturers, except for certain finish activities performed by us in Puerto Rico.

The global supply of our products depends on actively managing the inventory produced at our facilities and by third-party contract manufacturers and the uninterrupted and efficient operation of these facilities. During the manufacturing scale-up process, and even after achieving sustainable commercial manufacturing, we may encounter difficulties or disruptions due to defects in raw materials or equipment, contamination or other factors that could impact product availability. (See Item 1A. Risk Factors — Manufacturing difficulties, disruptions or delays could limit supply of our products and limit our product sales and — We rely on third-party suppliers for certain of our raw materials, medical devices and components.)

Commercial Bulk Manufacturing

We operate commercial bulk manufacturing facilities in Puerto Rico and in several locations throughout the United States. (See Item 2. Properties.) We perform commercial bulk manufacturing for our proteins except Vectibix®, which is performed by a third-party contract manufacturer. We also supplement commercial bulk manufacturing for ENBREL, Prolia® and XGEVA® with a third-party contract manufacturer.

Commercial Formulation, Fill and Finish Manufacturing

We perform most of our commercial protein formulation, fill and finish manufacturing in our Puerto Rico facility. Formulation, fill and finish manufacturing for Nplate® and Vectibix® is performed by third-party

 

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contract manufacturers. In addition to the formulation, fill and finish of ENBREL performed by us in Puerto Rico, fill and finish of a certain portion of ENBREL is also performed by third-party contract manufacturers. We also conduct certain finish activities in the Netherlands. (See Item 2. Properties.)

Clinical Manufacturing

Clinical bulk, formulation, fill and finish manufacturing facilities are operated primarily in our Thousand Oaks, California location. (See Item 2. Properties.) Clinical bulk and fill manufacturing activities for our clinical product candidate, talimogene laherparepvec, are performed at our Woburn, Massachusetts facility. Certain finish activities for our clinical products are also performed in the Netherlands. In addition, we also utilize third-party contract manufacturers for certain of our clinical products.

See Item 1A. Risk Factors — We perform a substantial amount of our commercial manufacturing activities at our Puerto Rico manufacturing facility and a substantial amount of our clinical manufacturing activities at our Thousand Oaks, California manufacturing facility; if significant natural disasters or production failures occur at the Puerto Rico facility, we may not be able to supply these products or, at the Thousand Oaks facility, we may not be able to continue our clinical trials.

Distribution

We operate distribution centers in the United States, principally in Kentucky and California, and in the Netherlands for worldwide distribution of the majority of our commercial and clinical products. In addition, we also use third-party distributors to supplement distribution of our commercial and clinical products in certain areas of the world.

Other

In addition to the manufacturing and distribution activities noted above, our operations in the United States, Puerto Rico and the Netherlands perform key manufacturing support functions, including quality control, process development, procurement, distribution and production scheduling. Certain of those manufacturing and distribution activities are highly regulated by the FDA as well as other international regulatory agencies. (See Government Regulation — FDA Regulation of Manufacturing Standards.)

Manufacturing Initiatives

We have multiple ongoing initiatives that are designed to optimize our manufacturing network and/or mitigate risks while continuing to ensure adequate supply of our commercial products. The facilities impacted by each of these initiatives will require qualification and licensure by various regulatory authorities. These initiatives include:

 

   

Construction of a new formulation and fill facility at our Puerto Rico site;

 

   

Expansion of our bulk protein facilities at our Puerto Rico site;

 

   

Modification and expansion of our recently acquired formulation, fill and finish site in Ireland; and

 

   

Expansion of our Colorado and Rhode Island facilities to enable manufacturing of certain clinical products as well as to provide alternative bulk manufacturing sources for certain marketed products.

In addition to these initiatives, we have projects designed to operate our facilities at appropriate production capacity over the next few years, further optimize manufacturing asset utilization, continue our use of third-party contract manufacturers and maintain a state of regulatory compliance. (See Item 1A. Risk Factors — Manufacturing difficulties, disruptions or delays could limit supply of our products and limit our product sales.)

Raw Materials and Medical Devices

Certain raw materials necessary for the commercial and clinical bulk manufacturing of our products are provided by unaffiliated third-party suppliers, certain of which may be our only source for such materials. Also,

 

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certain medical devices and components necessary for the formulation, fill and finish of our products are provided by unaffiliated third-party suppliers, certain of which may be the sole source. Certain of the raw materials, medical devices and components are the proprietary products of those unaffiliated third-party suppliers and are specifically cited in our drug application with regulatory agencies so that they must be obtained from the specific sole source or sources and could not be obtained from another supplier unless and until the regulatory agency approved such supplier. We currently attempt to manage the risk associated with such suppliers by inventory management, relationship management and evaluation of alternative sources when feasible. We also monitor the financial condition of certain suppliers and their ability to supply our needs.

Certain of the raw materials required in the commercial and clinical manufacturing of our products are sourced from other countries and/or derived from biological sources, including mammalian tissues. In addition, one of our marketed products also uses bovine serum and human serum albumin. Some countries in which we market our products may restrict the use of certain biologically derived substances in the manufacture of drugs. We continue to investigate alternatives to certain biological sources and alternative manufacturing processes that do not require the use of certain biologically derived substances because such raw materials may be subject to contamination and/or recall. A material shortage, contamination, recall and/or restriction of the use of certain biologically derived substances or other raw materials, which may be sourced from other countries and that are used in the manufacture of our products could adversely impact or disrupt the commercial manufacturing of our products or could result in a mandated withdrawal of our products from the market. (See Item 1A. Risk Factors — We rely on third-party suppliers for certain of our raw materials, medical devices and components.)

We perform various procedures to assist in authenticating the source of raw materials, including intermediary materials used in the manufacture of our products, which include verification of the country of origin. These procedures are incorporated into the manufacturing processes we and our third-party contract manufacturers perform.

Government Regulation

Regulation by government authorities in the United States and other countries is a significant factor in the production and marketing of our products and our ongoing R&D activities.

In order to clinically test, manufacture and market products for therapeutic use, we must satisfy mandatory procedures and safety and effectiveness standards established by various regulatory bodies. In the United States, the Public Health Service Act, the Federal Food, Drug and Cosmetic Act (FDCA) and the regulations promulgated thereunder, as well as other federal and state statutes and regulations govern, among other things, the raw materials and components used in the production, research, development, testing, manufacture, quality control, labeling, storage, record keeping, approval, advertising and promotion, and distribution of our products. Failure to comply with the applicable regulatory requirements may subject us to a variety of administrative and/or judicially imposed sanctions. The sanctions could include the FDA’s refusal to approve pending applications, withdrawals of approvals, delay or suspension of clinical trials, warning letters, product recalls, product seizures, total or partial suspension of our operations, injunctions, fines, civil penalties and/or criminal prosecution.

Clinical Development. We must conduct extensive clinical trials designed to establish the safety and efficacy of product candidates in order to file for regulatory approval to market a product. Product development and approval within that regulatory framework takes a number of years and involves our expenditure of substantial resources, and any approval we obtain remains costly for us to maintain. After laboratory analysis and preclinical testing in animals, we file an investigational new drug application (IND) with the FDA to begin human testing. The IND automatically becomes effective 30 days after receipt by the FDA, unless the FDA raises concerns or questions. In such a case, we and the FDA must resolve any outstanding concerns before the clinical trial can begin.

Typically, we undertake a three-phase human clinical testing program. In phase 1, we conduct small clinical trials to investigate the safety and proper dose ranges of our product candidates in a small number of human subjects. In phase 2, we conduct clinical trials to investigate side effect profiles and the efficacy of our product candidates in a larger number of patients who have the disease or condition under study. In phase 3, we conduct

 

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clinical trials to investigate the safety and efficacy of our product candidates in a large number of patients who have the disease or condition under study. The time and expense required for us to perform this clinical testing is substantial and may vary by product. For example, the clinical trials for the BLA for Prolia®/XGEVA® were large and required substantial time and resources to recruit patients and significant expense to execute. Historically, our products have required smaller, shorter trials. Foreign studies performed under an IND must meet the same requirements that apply to U.S. studies. The FDA will accept a foreign clinical study not conducted under an IND only if the study is well-designed, well-conducted, performed by qualified investigators, and conforms to good clinical practice. Phase 1, 2 and 3 testing may not be completed successfully within any specified time period, if at all. (See Item 1A. Risk Factors — We may not be able to develop commercial products.) The FDA monitors the progress of each trial conducted under an IND and may, at its discretion, re-evaluate, alter, suspend, or terminate the testing based on the data accumulated to that point and the FDA’s risk/benefit assessment with regard to the patients enrolled in the trial. (See Item 1A. Risk Factors — We must conduct clinical trials in humans before we can commercialize and sell any of our product candidates or existing products for new indications.)

Applications. The results of preclinical and clinical trials are submitted to the FDA in the form of a BLA for biologic products subject to the Public Health Service Act or an NDA for drugs subject to the approval provisions of the FDCA. The submission of the application is no guarantee that the FDA will find it complete and accept it for filing. If an application is accepted for filing, following the FDA’s review, the FDA may grant marketing approval, request additional information, or deny the application if it determines that the application does not provide an adequate basis for approval. We cannot take any action to market any new drug or biologic product in the United States until our appropriate marketing application has been approved by the FDA.

Post-approval Phase. After we have obtained approval to market our products, we monitor adverse events from the use of our products and report such events to regulatory agencies, along with information from post marketing surveillance or studies. We may utilize other research approaches to learn or confirm information about our marketed products, including observational studies and patient registries, and may engage in risk management activities such as physician education initiatives and patient advocacy group initiatives. We may also conduct, or be required by regulatory agencies to conduct, further clinical trials to provide additional information on our marketed products’ safety and efficacy. Those additional trials may include studying different doses or schedules of administration that were used in previous studies, use in other patient populations or other stages of the disease or use over a longer period of time. Additional trials of this nature are sometimes required by regulatory agencies as a condition of their approval to market our products and they might also request or require that we conduct specific studies, including observational epidemiological studies, in order to identify or assess possible safety risks of our marketed products that are observed or suggested by available scientific data and such trials are sometimes referred to as PMCs or PMRs. In the United States, under the Food and Drug Administration Amendments Act of 2007 (the FDAAA), if the FDA becomes aware of new safety information after approval of a product, it may require us to conduct further clinical trials to assess a known or potential serious risk. If we are required to conduct such a post-approval study, periodic status reports must be submitted to the FDA. Failure to conduct such post-approval studies in a timely manner may result in substantial civil or criminal penalties. Data resulting from these clinical trials may result in expansions or restrictions to the labeled indications for which our products have already been approved and to the reimbursement provided by government and commercial payers for our products.

The FDAAA also gave the FDA authority to require companies to implement a REMS for a product to ensure that the benefits of the drugs outweigh the risks. While risk management activities and programs are not new, with FDAAA the FDA gained new authority to implement specific risk management requirements and new enforcement power to ensure that the goals of the REMS are being met. The FDA began to implement REMS in 2008. The FDA may require the submission of a REMS before a product is approved or after approval based on new safety information, including new analyses of existing safety information. In determining whether a product will require a REMS before the product is approved, the FDA may consider a number of factors including:

 

   

estimated size of the population likely to use the product;

 

   

seriousness of the condition treated and expected benefits of the product;

 

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duration of treatment with the product;

 

   

seriousness of known or potential adverse events associated with the product; and

 

   

whether the product is a new molecular entity.

All REMS are required to have a timetable for assessment and may have one or more of the following:

 

   

distribution of a medication guide or a patient package insert to patients;

 

   

communication plan for the healthcare provider or institution, such as a Dear Healthcare Professional Letter;

 

   

elements to assure safe use including, but not limited to:

 

  ¡    

specific training, experience or certification for prescribers;

 

  ¡    

certification of medication dispensing sites and dispensing in limited settings;

 

  ¡    

monitoring of specific patients; and

 

  ¡    

enrollment of patients in a registry.

Each REMS is unique and varies depending on the specific factors required. While the elements of REMS may vary, all REMS require the sponsor to submit periodic assessment reports to the FDA to demonstrate that the goals of the REMS are being met. Failure to comply with a REMS, including submission of a required assessment or any modification to a REMS, may result in substantial civil or criminal penalties and can result in additional limitations being placed on a product’s use and, potentially, withdrawal of the product from the market. We currently have approved REMS for our ESAs, Prolia® and Nplate®. As REMS are relatively new, the FDA and sponsor companies continue to learn how best to implement, operate and monitor the effectiveness of REMS, and the requirements of our REMS and those of other companies may change over time.

Adverse events that are reported after marketing approval also can result in additional limitations being placed on a product’s use and, potentially, withdrawal of the product from the market. The FDA has authority to mandate labeling changes to products at any point in a product’s lifecycle based on new safety information or as part of an evolving label change to a particular class of products.

The FDA also uses various advisory committees of external experts to assist in its mission to protect and promote the public health, to obtain independent expert advice on scientific, technical and policy matters. The committees are generally advisory only and FDA officials are not bound to or limited by their recommendations. We have participated in meetings of the ODAC, the Cardiovascular and Renal Drug Advisory Committee and the Advisory Committee for Reproductive Health Drugs, among others, to address certain issues related to our products, including Aranesp®, EPOGEN®, Prolia® and XGEVA®.

FDA Approval of Biosimilar Products. The U.S. healthcare reform law authorizes the FDA to approve biosimilar products under a separate, abbreviated pathway. The new law establishes a period of 12 years of data exclusivity for reference products in order to preserve incentives for future innovation and outlines statutory criteria for science-based biosimilar approval standards that take into account patient safety considerations. Under this framework, data exclusivity protects the data in the innovator’s regulatory application by prohibiting others, for a period of 12 years, from gaining FDA approval based in part on reliance or reference to the innovator’s data in their application to the FDA. The new law does not change the duration of patents granted on biologic products. On February 9, 2012, the FDA released three draft guidance documents as part of the implementation of the abbreviated approval pathway for biosimilar products. While FDA guidance documents are not legally binding on the public or on the FDA, they indicate the FDA’s views on a subject. The draft guidance documents provide insight to the FDA’s current thinking on the development of biosimilar products and address a range of technical, scientific and regulatory issues. The guidance documents generally provide that, for approval, a sponsor must demonstrate that the proposed product is “biosimilar” to a single reference product already licensed by the FDA. In assessing biosimilarity, the FDA indicated that it intends to use a risk-based “totality of the evidence” approach to evaluate all available data submitted by the applicant. Generally, a

 

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biosimilar application must include a clinical study or studies sufficient to demonstrate safety, purity and potency in one or more indications for which the reference product is licensed and the biosimilar applicant seeks approval. The scope and magnitude of clinical data needed will depend on the extent of uncertainty about the biosimilarity of the product as well as the frequency and severity of safety risks associated with the reference product. The FDA indicated that it is still evaluating a number of relevant issues, including criteria for interchangeability (which FDA indicated would be “higher standard” than biosimilarity). The FDA will accept public comments on the guidance documents for 60 days, following which it may issue final guidance. The FDA has also stated publicly that it intends to hold a follow-up public meeting in the near future to obtain feedback on what additional clarification on the biosimilars approval process is needed.

FDA Regulation of Product Marketing and Promotion. The FDA closely reviews and regulates the marketing and promotion of products. We are required to obtain FDA approval before marketing or promoting a product as a treatment for a particular indication. Our product promotion for approved product indications must comply with the statutory standards of the FDCA, and the FDA’s implementing regulations and standards. The FDA’s review of marketing and promotional activities encompasses, but is not limited to, direct-to-consumer advertising, healthcare provider-directed advertising and promotion, sales representative communications to healthcare professionals, promotional programming and promotional activities involving the Internet. The FDA may also review industry-sponsored scientific and educational activities. The FDA may take enforcement action against a company for promoting unapproved uses of a product or for other violations of its advertising and labeling laws and regulations. Enforcement action may include product seizures, injunctions, civil or criminal penalties or regulatory letters, which may require corrective advertising or other corrective communications to healthcare professionals. Failure to comply with the FDA’s regulations also can result in adverse publicity or increased scrutiny of company activities by the U.S. Congress or other legislators.

FDA Regulation of Manufacturing Standards. The FDA regulates and inspects equipment, facilities, laboratories and processes used in the manufacturing and testing of products prior to providing approval to market a product. If after receiving approval from the FDA, we make a material change in manufacturing equipment, location or process, additional regulatory review may be required. We also must adhere to current Good Manufacturing Practice regulations and product-specific regulations enforced by the FDA through its facilities inspection program. The FDA also conducts regular, periodic visits to re-inspect our equipment, facilities, laboratories and processes following an initial approval. If, as a result of those inspections, the FDA determines that our equipment, facilities, laboratories or processes do not comply with applicable FDA regulations and conditions of product approval, the FDA may seek civil, criminal or administrative sanctions and/or remedies against us, including suspension of our manufacturing operations. Such issues may also delay the approval of new products undergoing FDA review.

Approval and Post-Approval Regulation Outside the United States. In the EU countries, Switzerland, Canada and Australia, regulatory requirements and approval processes are similar in principle to those in the United States. Additionally, depending on the type of drug for which approval is sought, there are currently two potential tracks for marketing approval in the EU, including a centralized procedure. In the centralized procedure, which is required of all products derived from biotechnology, a company submits a single marketing authorization application to the European Medicines Agency (EMA) who conducts a thorough evaluation, drawing from its scientific resources across Europe. If the drug product is proven to fulfill the requirements for quality, safety and efficacy, the CHMP adopts a positive opinion, which is transmitted to the EC for final approval of the marketing authorization. While the EC generally follows the CHMP’s opinion, it is not bound to do so. In the EU, biosimilar products have been approved under a sub-pathway of the centralized procedure since 2006. The pathway allows sponsors of a biosimilar product to seek and obtain regulatory approval based in part on the clinical trial data of an originator product to which the biosimilar product has been demonstrated to be “similar.” In many cases, this allows biosimilar products to be brought to market without conducting the full suite of clinical trials typically required of originators. After evaluation and marketing authorization, various parties, including the national competent authorities, the EMA, the EC and the marketing authorization holders share responsibilities for the detection, assessment and prevention of adverse effects and other medicine-related problems in a process known as pharmacovigilance. Healthcare professionals and patients are also encouraged to

 

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report adverse effects and other medicine-related problems. This process includes the collection of adverse drug reaction reports as part of the follow-up on any side effects of a product, and upon assessment, the authorities can decide to demand that product labels be updated with safety data or warnings, that safety data or warnings be provided to healthcare professionals, or recommend the temporary suspension or complete withdrawal of a product from the market.

Other. We are also subject to various federal and state laws, as well as foreign laws, pertaining to healthcare “fraud and abuse,” including anti-kickback laws and false claims laws. Anti-kickback laws make it illegal to solicit, offer, receive or pay any remuneration in exchange for, or to induce, the referral of business, including the purchase or prescription of a particular drug that is reimbursed by a state or federal program. The federal government and the states have published regulations that identify “safe harbors” or exemptions for certain arrangements that do not violate the anti-kickback statute. We seek to comply with the safe harbors wherever possible. Due to the breadth of the statutory provisions and the absence of guidance in the form of regulations or court decisions addressing some of our practices, it is possible that our practices might be challenged under anti-kickback or similar laws. False claims laws prohibit knowingly and willingly presenting, or causing to be presented for payment to third-party payers (including Medicare and Medicaid), claims for reimbursed drugs or services that are false or fraudulent, claims for items or services not provided as claimed or claims for medically unnecessary items or services. Our activities related to the sale and marketing of our products may be subject to scrutiny under these laws. Violations of fraud and abuse laws may be punishable by criminal and/or civil sanctions, including fines and civil monetary penalties, as well as the possibility of exclusion from federal healthcare programs (including Medicare and Medicaid). If the government were to allege against or convict us of violating those laws or if we entered into a settlement with the government, there could be a material adverse effect on our business, including our stock price. Our activities could be subject to challenge for the reasons discussed above and due to the broad scope of those laws and the increasing attention being given to them by law enforcement authorities.

We are also subject to regulation under the Occupational Safety and Health Act, the Toxic Substances Control Act, the Resource Conservation and Recovery Act and other current and potential future federal, state or local laws, rules and/or regulations. Our R&D activities involve the controlled use of hazardous materials, chemicals, biological materials and various radioactive compounds. We believe our procedures comply with the standards prescribed by federal, state or local laws, rules and/or regulations; however, the risk of injury or accidental contamination cannot be completely eliminated. While we are not required to do so, we strive to conduct our research and manufacturing activities in a manner that meets the intents and purposes of the National Institutes of Health Guidelines for Recombinant DNA Research.

Additionally, the U.S. Foreign Corrupt Practices Act (FCPA) prohibits U.S. corporations and their representatives from offering, promising, authorizing or making payments to any foreign government official, government staff member, political party or political candidate in an attempt to obtain or retain business abroad. The scope of the FCPA includes interactions with certain healthcare professionals in many countries. Other countries have enacted similar anti-corruption laws and/or regulations.

Our present and future business has been and will continue to be subject to various other U.S. and foreign laws, rules and/or regulations.

Research and Development and Selected Product Candidates

Our vision is to deliver therapeutics that can make a meaningful difference in patients’ lives. Therefore, we focus our R&D on novel human therapeutics for the treatment of grievous illness in the areas of oncology, hematology, inflammation, bone health, nephrology, cardiovascular and general medicine, which includes neuroscience. We take a modality-independent approach to R&D — that is, we identify targets, and then choose the modality best suited to address a specific target. As such, our discovery research programs may yield targets that lead to the development of human therapeutics delivered as large molecules (such as proteins, antibodies and peptibodies) or small molecules.

 

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We have major R&D centers in several locations throughout the United States and in the United Kingdom, as well as smaller research centers and development facilities globally. (See Item 2. Properties.)

We conduct clinical trial activities using both our internal staff and third-party contract clinical trial service providers. In order to increase the number of patients available for enrollment for our clinical trials, we have and will continue to open clinical sites and enroll patients in a number of geographic locations. (See Item 1A. Risk Factors — We must conduct clinical trials in humans before we can commercialize and sell any of our product candidates or existing products for new indications.)

Some of our competitors are actively engaged in R&D in areas where we have products or where we are developing product candidates or new indications for existing products. For example, we compete with other clinical trials for eligible patients, which may limit the number of available patients who meet the criteria for certain clinical trials. The competitive marketplace for our product candidates is significantly dependent upon the timing of entry into the market. Early entry may have important advantages in gaining product acceptance, contributing to the product’s eventual success and profitability. Accordingly, we expect that in some cases, the relative speed with which we can develop products, complete clinical testing, receive regulatory approval and supply commercial quantities of the product to the market is expected to be important to our competitive position.

In addition to product candidates and marketed products generated from our internal R&D efforts, we acquire companies, acquire and license certain product and R&D technology rights and establish R&D arrangements with third parties to enhance our strategic position within our industry by strengthening and diversifying our R&D capabilities, product pipeline and marketed product base. These licenses and arrangements generally provide for non-refundable upfront license fees, R&D and commercial performance milestone payments, cost sharing, royalty payments and/or profit sharing.

Various public and privately owned companies, research organizations, academic institutions and governmental agencies conduct a significant amount of R&D in the biotechnology industry. We face competition in pursuing R&D arrangements and licensing or acquisition activities from other pharmaceutical and biotechnology companies that also seek to license or acquire technologies, product candidates or marketed products from these entities. Accordingly, we may have difficulty entering into R&D arrangements and licensing or acquiring technologies, product candidates and marketed products on acceptable terms.

See Government Regulation — Clinical Development for a discussion of the government regulation over clinical development.

 

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The following table is a selection of certain of our product candidates by phase of development in our therapeutic areas of focus as of February 10, 2012, unless otherwise indicated. Each target indication for product candidates in phase 3 is listed separately. Additional product candidate (pipeline) information can be found on our website at http://www.amgen.com. (This website address is not intended to function as a hyperlink, and the information contained on our website is not intended to be a part of this filing.)

 

Molecule

  

Disease/Condition

   Therapeutic Area

Phase 3 Programs

     

AMG 386

   Ovarian cancer    Hematology/Oncology

Aranesp® (darbepoetin alfa)

   Myelodysplastic syndromes    Hematology/Oncology

Aranesp® (darbepoetin alfa)

   Anemia in heart failure    Nephrology

Ganitumab

   Pancreatic cancer    Hematology/Oncology

Motesanib

   First-line non-small cell lung cancer    Hematology/Oncology

Prolia® (denosumab)

   Male osteoporosis    Bone Health

Sensipar®/Mimpara® (cinacalcet)

  

Cardiovascular disease in patients with secondary hyperparathyroidism and chronic kidney disease undergoing maintenance dialysis

   Nephrology

Sensipar®/Mimpara® (cinacalcet)

   Post renal transplant    Nephrology

Talimogene laherparepvec

   Malignant melanoma    Hematology/
Oncology

Vectibix® (panitumumab) — US Only

   First- and second-line colorectal cancer    Hematology/Oncology

XGEVA® (denosumab)

   Delay or prevention of bone metastases in prostate cancer    Hematology/Oncology

XGEVA® (denosumab)

   Delay or prevention of bone metastases in breast cancer    Hematology/Oncology

Phase 2 Programs

     

AMG 145

   Hypercholesterolemia    Cardiovascular

AMG 151

   Type 2 diabetes    General Medicine

AMG 386

   Various cancer types    Hematology/Oncology

AMG 785

   Bone-related conditions, including postmenopausal osteoporosis and fracture healing    Bone Health

AMG 827

   Inflammatory diseases    Inflammation

AMG 888

   Various cancer types    Hematology/Oncology

Prolia® (denosumab)

   Rheumatoid arthritis    Inflammation

Ganitumab

   Various cancer types    Hematology/Oncology

Nplate® (romiplostim)

   Chemotherapy-induced thrombocytopenia    Hematology/Oncology

Omecamtiv mecarbil

   Heart failure    Cardiovascular

Rilotumumab

   Various cancer types    Hematology/Oncology

Vectibix® (panitumumab)

   Locally advanced head and neck cancer    Hematology/Oncology

XGEVA® (denosumab)

   Giant cell tumor of the bone    Hematology/Oncology

Phase 1 Programs

     

AMG 139

   Inflammatory diseases    Inflammation

AMG 157

   Asthma    Inflammation

AMG 167

   Bone-related conditions    Bone Health

AMG 181

   Inflammatory diseases    Inflammation

AMG 208

   Various cancer types    Hematology/Oncology

AMG 319

   Hematologic malignancies    Hematology/Oncology

AMG 337

   Various cancer types    Hematology/Oncology

AMG 557

   Systemic lupus erythematosus    Inflammation

AMG 579

   Neuroscience    General Medicine

AMG 729

   Autoimmune diseases    Inflammation

AMG 745

   Muscle-wasting disorders    General Medicine

AMG 747

   Neuroscience    General Medicine

AMG 761

   Asthma    Inflammation

AMG 780

   Various cancer types    Hematology/Oncology

AMG 811

   Systemic lupus erythematosus    Inflammation

AMG 820

   Various cancer types    Hematology/Oncology

AMG 876

   Type 2 diabetes    General Medicine

AMG 900

   Various cancer types    Hematology/Oncology

 

Phase 1

clinical trials investigate safety and proper dose ranges of a product candidate in a small number of human subjects.

 

Phase 2

clinical trials investigate side effect profiles and efficacy of a product candidate in a large number of patients who have the disease or condition under study.

 

Phase 3

clinical trials investigate the safety and efficacy of a product candidate in a large number of patients who have the disease or condition under study.

 

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The following text provides additional information about selected product candidates that have advanced into human clinical trials.

AMG 386

AMG 386 is a peptibody that inhibits the interaction between the endothelial cell-selective Tie2 receptor and its ligands Ang1and Ang2. It is being investigated as a cancer treatment.

In 2011, we announced that enrollment was suspended in the phase 3 study in recurrent ovarian cancer due to DOXIL® (doxorubicin HCl liposome injection) supply issues. We initiated a second phase 3 study in recurrent ovarian cancer in 2011. We initiated a phase 3 study for the treatment of first-line ovarian cancer and plan to initiate other phase 2 studies for the treatment of NSCLC and breast cancer in 2012. Phase 2 studies of AMG 386 for treatment of renal cell carcicoma and hepatocellular carcinoma are ongoing.

Aranesp® (darbepoetin alfa)

Aranesp® is a recombinant human protein agonist of the erythropoietin receptor.

The RED-HF® trial phase 3 study, initiated in 2006, is a large (2,600 subjects planned), global, randomized, double-blind, placebo-controlled study to evaluate the effect of treatment of anemia with darbepoetin alfa on morbidity and mortality in patients with symptomatic left ventricular heart failure. The RED-HF® trial continues to enroll subjects and we anticipate data from the study in 2013. In 2011, we initiated a phase 3 study of Aranesp® for the treatment of low risk myelodysplastic syndromes.

Ganitumab (AMG 479)

Ganitumab is a fully human monoclonal antibody antagonist of IGF-1 receptor. It is being investigated as a cancer treatment.

In 2011, we initiated a phase 3 study for the treatment of first-line metastatic pancreatic cancer.

A phase 2 study for the treatment of small cell lung cancer is ongoing.

Motesanib

Motesanib is an orally-administered small molecule antagonist of vascular endothelial growth factor receptors 1, 2 and 3, platelet-derived growth factor receptors and stem cell factor receptor. It is being investigated as a cancer treatment. We are developing this product in collaboration with Takeda and Millennium Pharmaceuticals: The Takeda Oncology Company (Millennium).

In March 2011, we along with Takeda and Millennium announced top-line results from the MONET1 pivotal phase 3 trial evaluating motesanib administered in combination with paclitaxel and carboplatin in 1,090 patients with advanced non-squamous NSCLC. The trial did not meet its primary objective of demonstrating an improvement in overall survival (hazard ratio 0.90, 95% confidence interval 0.78 — 1.04, p=0.14). Detailed results were also presented at a medical meeting in May 2011. The parties continue to further analyze the data to explore potential opportunities for additional development in first-line NSCLC.

Denosumab

Denosumab is a fully human monoclonal antibody that specifically targets a ligand known as RANKL (that binds to a receptor known as RANK) which is a key mediator of osteoclast formation, function, and survival. Denosumab is being studied across a range of conditions including osteoporosis, treatment-induced bone loss, rheumatoid arthritis and numerous tumor types across the spectrum of cancer-related bone diseases.

Prolia® (denosumab)

The phase 3 study evaluating Prolia® patients with male osteoporosis was completed and based on the results we announced on November 21, 2011, an sBLA was filed with the FDA for the indication to increase

 

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bone mass in men with osteoporosis at high risk for fracture. We also plan to initiate a phase 3 study of Prolia® for the treatment of Glucocorticoid-Induced Osteoporosis in 2012.

XGEVA® (denosumab)

In April 2011, we announced that we plan to file for the treatment of giant cell tumor of the bone. On June 27, 2011, we announced the submission of an sBLA to the FDA to expand the indication for XGEVA® to treat men with castration-resistant prostate cancer to reduce the risk of developing bone metastases. On February 8, 2012, the FDA convened the ODAC to discuss the sBLA filing. The ODAC panel voted 12 to 1 that the overall magnitude of benefit demonstrated with early treatment with XGEVA® to delay bone metastases was not sufficient to conclude a positive risk-benefit ratio in the absence of additional measures impacting quality of life or other disease outcomes. The FDA has targeted a PDUFA action date of April 26, 2012. A phase 3 study for the delay or prevention of bone metastases in patients with adjuvant breast cancer is ongoing. We are planning an additional phase 3 SRE study in patients with multiple myeloma.

Sensipar®/Mimpara® (cinacalcet)

Sensipar®/Mimpara® is an orally-administered small molecule that lowers PTH levels in blood by signaling through the calcium-sensing receptor in parathyroid tissue to inhibit PTH secretion. It also lowers blood calcium and phosphorous levels.

The phase 3 E.V.O.L.V.E™ trial, initiated in 2006, is a large (3,800 patient), multi-center, international, randomized, double-blind study to assess the effects of Sensipar®/Mimpara® on mortality and cardiovascular morbidity in patients with CKD undergoing maintenance dialysis. The E.V.O.L.V.E™ study completed enrollment in January 2008 and we anticipate data from the study in 2012.

Sensipar®/Mimpara ® is also being evaluated in post renal transplant patients.

Talimogene laherparepvec (formerly known as OncoVEXGM-CSF)

Talimogene laherparepvec is an oncolytic immunotherapy derived from HSV-1. It is being investigated as a cancer treatment.

On March 4, 2011, we acquired BioVex, a privately held biotechnology company developing treatments for cancer and the prevention of infectious disease, including talimogene laherparepvec, then in phase 3 clinical development for the treatment of malignant melanoma and head and neck cancer. On July 29, 2011, we announced our decision to terminate the phase 3 trial in patients with head and neck cancer. The phase 3 study for the treatment of malignant melanoma is ongoing.

Vectibix® (panitumumab)

Vectibix® is a monoclonal antibody antagonist of the EGFr pathway. It is being investigated as a cancer treatment.

In July 2011, we announced that we received Complete Response Letters from the FDA on the first- and second-line line mCRC sBLAs requesting additional information from the ‘181 and ‘203 studies. A phase 2 study for the treatment of locally advanced head and neck cancer is ongoing.

AMG 145

AMG 145 is a fully human monoclonal antibody to Proprotein Convertase Subtilisin/Kexin Type 9 (PCSK9), a negative regulator of low-density lipoprotein receptor. AMG 145 is being investigated for the treatment of hypercholesterolemia.

Phase 1 single and multiple ascending dose studies have been completed. Results of the phase 1 single dose study were presented at a medical conference in November 2011. In 2011, phase 2 studies of AMG 145 for the treatment of hypercholesterolemia were initiated.

 

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AMG 151

AMG 151 is an orally-administered small molecule glucokinase activator. It reduces glucose levels via a dual mechanism of action — working in both the pancreas and the liver. It is being investigated as a treatment of type 2 diabetes.

In 2011 we initiated a phase 2 study of AMG 151 for the treatment of type 2 diabetes.

AMG 785

AMG 785 is a humanized monoclonal antibody that targets sclerostin, a protein secreted by bone cells that inhibits bone formation. AMG 785 (also known as CDP7851) is being developed in collaboration with UCB for bone-related conditions, including postmenopausal osteoporosis and fracture healing.

In April 2011, we announced top-line results from the phase 2 clinical study comparing sclerostin-antibody AMG 785 to placebo in postmenopausal women with low bone mineral density BMD for the treatment of PMO. We plan to initiate phase 3 studies for the treatment of PMO in 2012. Phase 2 studies of AMG 785 for the treatment of fracture healing are ongoing.

AMG 827

AMG 827 is a human monoclonal antibody that binds to and blocks signaling via the interleukin-17 receptor. It is being investigated as a treatment for a variety of inflammatory diseases.

We reported the results from the phase 2 psoriasis study at a medical meeting in May 2011. Based on the study results, we plan to initiate phase 3 studies for the treatment of psoriasis in 2012. In 2011, we announced that following the review of the results, we have elected to discontinue our phase 2 studies for the treatment of RA and Crohn’s disease. In October 2011, we initiated a phase 2 study for the treatment for psoriatic arthritis. A phase 2 study of AMG 827 for the treatment of asthma is ongoing.

AMG 888

AMG 888 is a fully human monoclonal antibody that inhibits human epidermal growth factor receptor 3 (HER3) oncogenic signaling. AMG 888 is being investigated as a cancer treatment. Amgen is developing this product in collaboration with Daiichi Sankyo.

Daiichi Sankyo initiated a phase 1b/2 study of AMG 888 (U3-1287) in advanced NSCLC in 2010, a phase 1b study in Japan in 2nd line NSCLC in 2011, and a phase 1b/2 study in metastatic breast cancer in 2012.

Nplate® (romiplostim)

Nplate® is a peptibody agonist of the TPO receptor.

Nplate® is being evaluated in chemotherapy-induced thrombocytopenia.

Omecamtiv mecarbil

Omecamtiv mecarbil is a small molecule activator of cardiac myosin. Omecamtiv mecarbil is being investigated to improve cardiac contractility in subjects with heart failure. We are developing this product in collaboration with Cytokinetics, Inc.

In 2011, we initiated a phase 2 study for the treatment of heart failure in patients with left ventricular systolic dysfunction who are hospitalized for acute heart failure.

Rilotumumab (AMG 102)

Rilotumumab is a fully human monoclonal antibody that blocks the action of hepatocyte growth factor/scatter factor. It is being investigated as a cancer treatment.

 

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Results from a phase 2 study in gastric cancer in combination with chemotherapy were reported at a meeting in September 2011. Phase 2 combination studies in the prostate and small cell lung cancer settings continue.

As of February 9, 2011, we had nine phase 3 programs. As of February 10, 2012, we had twelve phase 3 programs, as one was added as the result of our BioVex acquisition and two programs had advanced into phase 3 trials. These changes are set forth in the following table:

 

Molecule

  

Disease / Condition

  

Program Change

Talimogene laherparepvec

   Malignant melanoma    Added through acquisition of BioVex

Sensipar®/ Mimpara® (cinacalcet)

   Post Renal Transplant    Advanced to Phase 3

Aranesp® (darbepoetin alfa)

   Myelodysplastic syndromes    Advanced to Phase 3

Phase 3 Product Candidate Patent Information

Our outstanding patents for each of our product candidates in phase 3 development that have yet to be approved for any indication are described in the following table. Patents for products already approved for one or more indications but currently undergoing phase 3 clinical trials for additional indications are previously described. (See Marketed Products.)

 

Molecule

   Territory   

General Subject Matter

   Estimated Expiration*

AMG 386

   U.S.

 

Europe

  

DNA, polypeptides and compositions

 

DNA, polypeptides, compositions and method of treatment

   2025

 

2019-2022

Ganitumab

   U.S.   

Antibodies and compositions

   2029

Motesanib

   U.S.

 

Europe

  

Motesanib and compositions

 

Motesanib, compositions and use for treatment of cancer

   2022

 

2022

Talimogene laherparepvec

   U.S.   

Modified HSV1 compounds and strains and methods of treatment using modified HSV1 strains

   2021
   Europe   

Modified HSV1 compounds and strains and methods of treatment using modified HSV1 strains

   2021

 

*

Patent expiration ranges for each region are based on one or more issued patents, some of which may be or become eligible for term adjustments, extensions or supplemental protection certificates not captured in this estimate. In addition, new patents may be issued in the future, and existing patents may be challenged, invalidated or circumvented by third parties.

Business Relationships

From time to time, we enter into business relationships, including joint ventures and collaborative arrangements, for the R&D, manufacture and/or commercialization of products and/or product candidates. In addition, we also acquire product and R&D technology rights and establish R&D collaborations with third parties to enhance our strategic position within our industry by strengthening and diversifying our R&D capabilities, product pipeline and marketed product base. These arrangements generally provide for non-refundable upfront license fees, regulatory and commercial performance milestone payments, cost sharing, royalty payments and/or profit sharing. The activities under our collaboration agreements are performed with no guarantee of either technological or commercial success, and each is unique in nature.

 

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Trade secret protection for our unpatented confidential and proprietary information is important to us. To protect our trade secrets, we generally require counterparties to execute confidentiality agreements upon the commencement of the business relationship with us. However, others could either develop independently the same or similar information or obtain access to our information.

Kirin-Amgen, Inc.

K-A is a 50-50 joint venture with Kirin. K-A develops and then out licenses to third parties certain product rights which have been transferred to this joint venture from Kirin and Amgen.

K-A has given us exclusive licenses to manufacture and market: (i) G-CSF and pegfilgrastim in the United States, Europe, Canada, Australia and New Zealand, (ii) darbepoetin alfa, romiplostim and AMG 827 in the United States, Europe, Canada, Australia, New Zealand, Mexico, all Central and South American countries and certain countries in Central Asia, Africa and the Middle East, and (iii) recombinant human erythropoietin in the United States. We currently market pegfilgrastim, G-CSF, darbepoetin alfa, recombinant human erythropoietin and romiplostim under the brand names Neulasta®, NEUPOGEN®/GRANULOKINE®, Aranesp®, EPOGEN® and Nplate®, respectively. AMG 827 is currently in phase 2 development. Under these agreements, we pay K-A royalties based on product sales. In addition, we also receive payments from K-A for milestones earned and for conducting certain R&D activities on its behalf. (See Note 7, Related party transactions, to the Consolidated Financial Statements.)

K-A has also given Kirin exclusive licenses to manufacture and market: (i) G-CSF and pegfilgrastim in Japan, Taiwan and South Korea, (ii) darbepoetin alfa, romiplostim and AMG 827 in Japan, China, Taiwan, South Korea and in certain other countries in Asia, and (iii) recombinant human erythropoietin in Japan. K-A also gave Kirin and Amgen co-exclusive licenses to manufacture and market G-CSF, pegfilgrastim and recombinant human erythropoietin in China, which Amgen subsequently assigned to Kirin, and as a result, Kirin now exclusively manufactures and markets G-CSF and recombinant human erythropoietin in China. Kirin markets G-CSF, darbepoetin alfa, romiplostim and recombinant human erythropoietin under the brand names GRAN®/Grasin®/Filgrastim®, NESP®, ROMIPLATE® and ESPO®, respectively. Kirin received approval for pegfilgrastim in Taiwan in September 2011 under the brand name Neulasta®. Kirin is currently in the process of seeking marketing approval for pegfilgrastim in South Korea. Under these agreements, Kirin pays K-A royalties based on product sales. In addition, Kirin also receives payments from K-A for conducting certain R&D activities on its behalf.

K-A has also given J&J exclusive licenses to manufacture and market recombinant human erythropoietin for all geographic areas of the world outside the United States, China and Japan. K-A has also given Roche exclusive licenses to market pegfilgrastim and G-CSF in all territories not licensed to Amgen and Kirin. Under these agreements, J&J and Roche pay royalties to K-A based on product sales.

Pfizer Inc.

We are in a collaboration with Pfizer to co-promote ENBREL in the United States and Canada. The rights to market ENBREL outside of the United States and Canada are reserved to Pfizer. Under the agreement, a management committee comprised of equal representation from Amgen and Pfizer is responsible for overseeing the marketing and sales of ENBREL, including strategic planning, the approval of an annual marketing plan, product pricing and the establishment of a brand team. Amgen and Pfizer share in the agreed-upon selling and marketing expenses approved by the joint management committee. We currently pay Pfizer a percentage of annual gross profits on our ENBREL sales in the United States and Canada attributable to all approved indications on a scale that increases as gross profits increase; however, we maintain a majority share of ENBREL profits. After expiration of the agreement in the fourth quarter of 2013, we will be required to pay Pfizer a declining percentage of annual net ENBREL sales in the United States and Canada for three years, ranging from 12% to 10%. The amounts of such payments are anticipated to be significantly less than what would be owed based on the terms of the current ENBREL profit share.

 

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Glaxo Group Limited

We are in a collaboration with Glaxo for the commercialization of denosumab for osteoporosis indications in Europe, Australia, New Zealand and Mexico (the Primary Territories). We have retained the rights to commercialize denosumab for all indications in the United States and Canada and for oncology indications in the Primary Territories. Under a related agreement, Glaxo will commercialize denosumab for all indications in countries, excluding Japan, where we did not have a commercial presence at the commencement of the agreement, including China, Brazil, India, Taiwan and South Korea (the Expansion Territories). In the Expansion Territories, Glaxo is responsible for all development and commercialization costs and will purchase denosumab from us to meet demand. In the future, we have the option of expanding our role in the commercialization of denosumab in the Primary Territories and certain of the Expansion Territories. In the Primary Territories, we share equally in the commercialization profits and losses related to the collaboration after accounting for expenses, including an amount payable to us in recognition of our discovery and development of denosumab. Glaxo is also responsible for bearing a portion of the cost of certain specified development activities in the Primary Territories.

Takeda Pharmaceutical Company Limited

We are in a collaboration with Takeda, which provides Takeda the exclusive rights to develop and commercialize for the Japanese market up to 12 molecules from our portfolio across a range of therapeutic areas, including oncology and inflammation (collectively the “Japanese market products”) and for the worldwide development and commercialization of our product candidate, motesanib, in the oncology area. The Japanese market products include: (i) Vectibix®, which received regulatory approval in Japan, in 2010, for unresectable, advanced or recurrent colorectal cancer with wild-type KRAS, (ii) AMG 386, which is in a phase 3 trial for recurrent ovarian cancer, and (iii) ganitumab (AMG 479), which is in a phase 3 trial for first-line metastatic pancreatic cancer. Through collaboration committees, the parties jointly coordinate and oversee Takeda’s development and commercialization of the Japanese market products in Japan. The parties share responsibility for the development of motesanib outside Japan and Takeda is responsible for development in Japan. Additionally, Amgen shall be responsible for commercialization of motesanib in North America and Takeda shall be responsible for commercialization outside of North America. Each party has the right to participate in the commercialization of motesanib in the other party’s territory. In addition, under the collaboration Amgen will manufacture and supply Takeda motesanib and the Japanese market products for both clinical and commercial purposes. In 2011, we announced that the motesanib pivotal phase 3 trial (MONET1) did not meet its primary objective of demonstrating an improvement in overall survival.

Daiichi Sankyo Company, Limited

We are in a collaboration with Daiichi Sankyo, which provides Daiichi Sankyo the exclusive rights to develop and commercialize denosumab in Japan for osteoporosis, oncology and certain other indications. As part of the agreement, Amgen received exclusive worldwide rights to certain Daiichi Sankyo intellectual property to the extent applicable to denosumab. Through collaboration committees, the parties jointly coordinate and oversee Daiichi Sankyo’s development and commercialization of denosumab in Japan.

DaVita Inc.

In November 2011, we entered into a seven-year supply agreement with DaVita, commencing January 1, 2012. Pursuant to this agreement, we will supply EPOGEN in amounts necessary to meet no less than 90% of DaVita’s and its affiliates’ requirements for ESAs used in providing dialysis services in the United States and Puerto Rico. The agreement may be terminated by either party before expiration of its term in the event of certain breaches of the agreement by the other party.

Fresenius Medical Care North America

In October 2011, the five-year supply agreement for ESAs with Fresenius Medical Care North America expired. Effective January 1, 2012, we entered into a three-year non-exclusive supply agreement with them to supply EPOGEN®.

 

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Human Resources

As of December 31, 2011, Amgen had approximately 17,800 staff members, which includes approximately 300 part-time staff members. There can be no assurance that we will be able to continue attracting and retaining qualified personnel in sufficient numbers to meet our needs. None of our staff members are covered by a collective bargaining agreement, and we have experienced no work stoppages. We consider our staff relations to be good.

Trade secret protection for our unpatented confidential and proprietary information is important to us. To protect our trade secrets, we generally require our staff members, material consultants and scientific advisors to execute confidentiality agreements upon commencement of employment or a consulting relationship with us. However, others could either develop independently the same or similar information or obtain access to our information.

Executive Officers of the Registrant

The executive officers of the Company as of February 13, 2012, are as follows:

Mr. Kevin W. Sharer, age 63, has served as a director of the Company since November 1992. Mr. Sharer has been the Company’s Chief Executive Officer since May 2000 and has also been Chairman of the Board of Directors since January 2001. Effective as of May 23, 2012, Mr. Sharer will step down as CEO of the Company. Mr. Sharer will remain as Chairman of the Board of Directors until December 31, 2012, at which time he will retire from the Board and the Company. From May 2000 to May 2010, Mr. Sharer served as the Company’s President and Chief Operating Officer. From October 1992 to May 2000, Mr. Sharer served as President and Chief Operating Officer of the Company. From April 1989 to October 1992, Mr. Sharer was President of the Business Markets Division of MCI Communications Corporation. From February 1984 to March 1989, Mr. Sharer held numerous executive capacities at General Electric Company (GE). Mr. Sharer is a director of Chevron Corporation and Northrop Grumman Corporation. He is Chairman of the Board of the Los Angeles County Museum of Natural History.

Mr. David W. Beier, age 63, became Senior Vice President, Global Government and Corporate Affairs in March 2008. He joined the Company in 2003 as Senior Vice President, Global Government Affairs. Previously, Mr. Beier was a partner with the law firm of Hogan and Hartson in Washington, D.C. From 1998 to early 2001, Mr. Beier served as Chief Domestic Policy Advisor to the Vice President of the United States. He also held positions as Vice President of Government Affairs and Public Policy for Genentech and staff counsel in the U.S. House of Representatives.

Dr. Fabrizio Bonanni, age 65, became Executive Vice President, Operations in August 2007. He served as Senior Vice President, Manufacturing of the Company from 2004 to August 2007. Dr. Bonanni joined the Company in 1999 as Senior Vice President, Quality and Compliance, and in June 2001, he also became the Corporate Compliance Officer. Previously, Dr. Bonanni held various management positions at Baxter International, Inc. from 1974 to 1999, including positions as Corporate Vice President, Regulatory and Clinical Affairs and Corporate Vice President, Quality System.

Mr. Robert A. Bradway, age 49, has served as a director of the Company since October 2011. Mr. Bradway has been the Company’s President and Chief Operating Officer since May 2010 and will succeed to the role of Chief Executive Officer in May 2012. Mr. Bradway joined the Company in 2006 as Vice President, Operations Strategy and served as Executive Vice President and Chief Financial Officer from April 2007 to May 2010. Prior to joining the Company, he was a Managing Director at Morgan Stanley in London where he had responsibility for the firm’s banking department and corporate finance activities in Europe and focused on healthcare.

Dr. Sean E. Harper, age 49, became Executive Vice President, Research and Development in February 2012. Dr. Harper joined the Company in 2002, and has held leadership roles in early development, medical sciences and global regulatory and safety. Dr. Harper served as Senior Vice President, Global Development and

 

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Corporate Chief Medical Officer from March 2007 to February 2012. Prior to joining the Company, Dr. Harper worked for five years at Merck Research Laboratories.

Mr. Anthony C. Hooper, age 57, became Executive Vice President, Global Commercial Operations in October 2011. From March 2010 to October 2011, Mr. Hooper was Senior Vice President, Commercial Operations and President, U.S., Japan and Intercontinental of BMS, a pharmaceutical company. From January 2009 to March 2010, Mr. Hooper was President, Americas of BMS. From January 2004 to January 2009, Mr. Hooper was President, U.S. Pharmaceuticals, Worldwide Pharmaceuticals Group, a division of BMS. Prior to this, Mr. Hooper held various senior leadership positions at BMS. In his roles at BMS, Mr. Hooper led commercial operations in mature and emerging markets. Prior to joining BMS, Mr. Hooper was Assistant Vice President of Global Marketing for Wyeth Laboratories.

Mr. Brian McNamee, age 55, became Senior Vice President, Human Resources in June 2001. From November 1999 to June 2001, Mr. McNamee served as Vice President of Human Resources at Dell Computer Corp. From 1998 to 1999, Mr. McNamee served as Senior Vice President, Human Resources for the National Broadcasting Corporation, a division of GE. From July 1988 to November 1999, Mr. McNamee held human resources positions at GE.

Mr. Jonathan M. Peacock, age 53, became Executive Vice President and Chief Financial Officer in September 2010. Prior to joining Amgen, Mr. Peacock served as Chief Financial and Administration Officer of Novartis Pharmaceuticals AG, a healthcare company based in Switzerland, beginning in 2005. From 1998 to 2005, Mr. Peacock was a partner at McKinsey and Co., where he co-led the European Corporate Finance Practice. Mr. Peacock was also a partner at Price Waterhouse in London and New York from 1993 to 1998.

Ms. Anna S. Richo, age 51, became Senior Vice President and Chief Compliance Officer in June 2008. From December 2003 to June 2008, Ms. Richo served as Vice President, Law. Prior to Amgen, she spent 12 years at Baxter Healthcare Corporation in roles of increasing responsibility in law, including Vice President, Law, for Baxter’s BioScience Division. Also, for more than five years, Ms. Richo served on the Board of Directors of Cytyc Corporation and was a member of the Audit and Finance Committees.

Mr. David J. Scott, age 59, became Senior Vice President, General Counsel and Secretary in March 2004. From May 1999 to February 2004, Mr. Scott served as Senior Vice President and General Counsel of Medtronic, Inc. and also as Secretary from January 2000. From December 1997 to April 1999, Mr. Scott served as General Counsel of London-based United Distillers & Vintners. Mr. Scott also served in executive roles at Grand Metropolitan plc and RJR Nabisco, Inc., and was an attorney in private practice.

Geographic Area Financial Information

For financial information concerning the geographic areas in which we operate, see Note 19, Segment information — Geographic information, to the Consolidated Financial Statements.

Investor Information

Financial and other information about us is available on our website (http://www.amgen.com) (This website address is not intended to function as a hyperlink, and the information contained in our website is not intended to be a part of this filing). We make available on our website, free of charge, copies of our Annual Report on Form 10-K, Quarterly Reports on Form 10-Q, current reports on Form 8-K and amendments to those reports filed or furnished pursuant to Section 13(a) or 15(d) of the Exchange Act as soon as reasonably practicable after filing or submitting such material electronically or otherwise furnishing it to the SEC. In addition, we have previously filed registration statements and other documents with the SEC. Any document we file may be inspected, without charge, at the SEC’s public reference room at 100 F Street NE, Washington, D.C. 20549 or at the SEC’s internet address at http://www.sec.gov (This website address is not intended to function as a hyperlink, and the information contained in the SEC’s website is not intended to be a part of this filing). Information related to the operation of the SEC’s public reference room may be obtained by calling the SEC at 1-800-SEC-0330.

 

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Item 1A. RISK FACTORS

This report and other documents we file with the SEC contain forward-looking statements that are based on current expectations, estimates, forecasts and projections about us, our future performance, our business or others on our behalf, our beliefs and our management’s assumptions. These statements are not guarantees of future performance and involve certain risks, uncertainties and assumptions that are difficult to predict. You should carefully consider the risks and uncertainties facing our business. The risks described below are not the only ones facing us. Our business is also subject to the risks that affect many other companies, such as employment relations, general economic conditions, geopolitical events and international operations. Further, additional risks not currently known to us or that we currently believe are immaterial may in the future materially and adversely affect our business, operations, liquidity and stock price.

Our sales depend on coverage and reimbursement from third-party payers.

Sales of all of our principal products are dependent on the availability and extent of coverage and reimbursement from third-party payers, including government healthcare programs and private insurance plans. Governments and private payers may regulate prices, reimbursement levels and/or access to our products to control costs or to affect levels of use of our products. We rely in large part on the reimbursement of our principal products through government programs such as Medicare and Medicaid in the United States and similar programs in foreign countries and a reduction in the coverage and/or reimbursement for our products could have a material adverse effect on our product sales, business and results of operations.

In the United States, there is an increased focus by the federal government and others on analyzing the impact of various regulatory programs on the federal deficit, which could result in increased pressure on federal programs to reduce costs. For example, the Budget Control Act of 2011, signed into law in the United States in August 2011, mandated a two percent reduction in government payments for all Medicare services (including the administration of separately-billable drugs and payment for drugs in all Medicare programs) for federal fiscal years 2013 through 2021, unless a subsequent deficit reduction law was passed before January 2012. As no additional deficit reduction law was enacted by January 2012, the payment “sequestration” will likely start in January 2013 and continue until December 2021. The sequestration remains subject to administrative implementation of the Budget Control Act or future statutory revision by Congress, who could block, limit or otherwise modify the automatic spending cuts. Several alternative deficit reduction proposals have been put forth by President Obama and/or Congressional committees, including proposals designed to further limit federal healthcare expenditures. While we cannot predict whether any deficit reduction actions will be approved by Congress and/or whether a budget sequestration will ultimately occur for Medicare services, a reduction in the availability or extent of reimbursement from U.S. government programs as a result of changes such as those that have been proposed or from other changes designed to achieve similar federal budget savings could have a material adverse effect on the sales of our products, our business and results of operations.

In March 2010 the United States adopted significant healthcare reform through the enactment of the PPACA and the Healthcare and Education Reconciliation Act (See Item 1. Business — Reimbursement — U.S. Healthcare Reform.) A major goal of the healthcare reform law is to provide greater access to healthcare coverage for more Americans. Accordingly, the healthcare reform law requires individual U.S. citizens and legal residents to maintain qualifying health coverage, imposes certain requirements on employers with respect to offering health coverage to employees, amends insurance regulations regarding when coverage can be provided and denied to individuals, and expands existing government healthcare coverage programs to more individuals in more situations, with most of these changes going into effect by January 2014. We do not expect a significant increase in sales of our products as a result of the 2014 expansions in healthcare coverage. While we cannot fully predict the ultimate impact the healthcare reform law will have on us, or how the law may change due to statutory revision or judicial review, we expect that the new law will continue to have a material adverse effect on our business and results of operations.

Public and private insurers have pursued, and continue to pursue, aggressive cost containment initiatives, including increased focus on comparing the effectiveness, benefits and costs of similar treatments, which could result in lower reimbursement rates for our products. A substantial portion of our U.S. business relies on

 

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reimbursement under Medicare Part B coverage. Any deterioration in the timeliness or certainty of payment by Medicare to physicians, including as a result of changes in policy or regulations, or as a result of operational difficulties, could negatively impact the willingness of physicians to prescribe our products for patients relying on Medicare for their medical coverage. Most of our products furnished to Medicare beneficiaries in both a physician office setting and hospital outpatient setting are reimbursed under the Medicare Part B ASP payment methodology. (See Item1. Business — Reimbursement — Reimbursement of Our Principal Products.) ASP-based reimbursements of products under Medicare may be below or could fall below the cost that some medical providers pay for such products, which could materially and adversely affect sales of our products. We also face certain risks relating to the calculation of ASP. ASP is calculated by the manufacturer based on a statutorily defined formula and submitted to CMS. However, the statute, regulations and CMS guidance do not define specific methodologies for all aspects of the calculation of ASP. For example, in the Medicare Physician Fee Schedule Final Rule for 2012, CMS did not address a proposed methodology for treatment of bundled price concessions. Consequently, the current CMS guidance is that manufacturers may make “reasonable assumptions” in their calculation of ASP consistent with the general requirements and the intent of the Medicare statute, federal regulations and their customary business practices. As a result, we are required to apply our judgment in certain aspects of calculating ASP which are disclosed to CMS and also are subject to further CMS review. If our calculation of ASP is incorrect, we could be subject to substantial fines and penalties which could have a material adverse impact on our business and results of operations. Additionally, we are required to pay rebates to the federal government on products reimbursed by Medicaid at a rate of 23.1% of the AMP of a product, or if it is greater, the difference between the AMP and the best price available to any non-government customer. The PPACA changed the definition of AMP, and in January 2012 CMS issued a proposed rule further defining the new AMP definition. Until that rule is final, we will be required to apply our reasonable judgment in certain aspects of the AMP calculation. Once this CMS rule has been finalized, we will have to determine whether our interpretation of AMP follows the rule or if our calculations will need to be amended and this could have a material adverse impact on our business and results of operations.

Other initiatives reviewing the coverage or reimbursement of our products could result in less extensive coverage or lower reimbursement rates. For example, in July 2007, CMS issued an NCD where it determined that ESA treatment was not reasonable and necessary for certain clinical conditions and established Medicare coverage parameters for FDA-approved ESA use in oncology. Generally, an NCD is a national policy statement granting, limiting or excluding Medicare coverage or reimbursement for a specific medical item or service. We believe the restrictions in the 2007 NCD changed the way ESAs are used in clinical practice, for example, by decreasing the number of treated patients, the average ESA dose and the duration of ESA therapy in the oncology setting. As a result, we believe these restrictions have had a material adverse effect on the use, reimbursement and sales of Aranesp®, which in turn had a material adverse effect on our business and results of operations. The reimbursement of ESAs in the nephrology setting has also been reviewed by CMS. On June 16, 2010, CMS opened an NCA to examine the use of ESAs to manage anemia in patients with CKD and dialysis-related anemia. Following further analysis, on June 16, 2011, CMS issued a FDM in which it determined that it would not issue an NCD at that time for ESAs for treatment of anemia in adults with CKD, and that it would instead monitor the use of ESAs through the ESRD bundled payment system and its other policy avenues. In the absence of an NCD, Medicare determinations are made by the eleven regional MACs, one of which has already issued a final LCD relating to anemia in patients with CKD not on dialysis, and two more MACs have issued draft LCDs in this setting. All three final or draft LCDs would restrict reimbursement of ESAs to use in accordance with the revised FDA label. Other MACs could also issue LCDs that similarly or further restrict reimbursement for ESAs in this setting, and physician behavior may change to be consistent with the revised label even before formal LCDs are implemented, all of which could have a further material adverse effect on the reimbursement, use and sales of Aranesp®. Additionally, CMS could still propose an NCD and/or further review or change the reimbursement of ESAs in the nephrology setting at some point in the future. CMS has also previously identified a list of potential future NCDs that includes the category of thrombopoiesis stimulating agents (platelet growth factors), the category of drugs that includes Nplate®, and a discussion on bisphosphonates used to treat osteoporosis. CMS has not announced whether it will proceed with an NCA related to thrombopoiesis stimulating agents and, while

 

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Prolia® and XGEVA® are not bisphosphonates, there is the possibility that CMS might evaluate other agents, including RANK Ligand inhibitors such as Prolia® and XGEVA®.

In the dialysis setting, the reimbursement rates for our products are also subject to downward pressure. In the United States, dialysis providers are reimbursed for EPOGEN® primarily by the federal government through Medicare’s ESRD Program. (See Item 1. Business — Reimbursement — Reimbursement of Our Principal Products — Dialysis Reimbursement.) Until January 1, 2011, Medicare reimbursed for separately billable dialysis drugs (including Aranesp® and EPOGEN®) administered in both freestanding and hospital-based dialysis centers at ASP+6%, using the same ASP payment amount methodology used in the physician clinic setting under Part B. On January 1, 2011, CMS’s bundled payment system went into effect for dialysis providers which provides a single payment for all dialysis services including drugs, supplies, and non-routine laboratory tests that were previously reimbursed separately. On November 1, 2011, following our June 2011 announcement of changes to the labels for the use of ESAs in patients with CKD (See Item 1. Business — Marketed Products — ESAs), CMS finalized a rule to update various provisions of its bundled payment system for dialysis services and the related ESRD QIP. The final rule eliminated for payment year 2013 and beyond one of the QIP’s measures which tracks the percent of a provider’s Medicare patients with a Hb level below 10 g/dL. (See Item 1. Business — Reimbursement — Reimbursement of Our Principal Products — Dialysis Reimbursement.) CMS indicated that removal of this quality measure from the QIP was being done in response to the June 2011 ESA label changes. We believe that the implementation of these various changes in the dialysis setting has resulted and may continue to result in a material adverse impact on the reimbursement, use and sales of EPOGEN® and on our business and results of operations.

The government-sponsored healthcare systems in Europe and many other foreign countries are the primary payers for healthcare expenditures, including payment for drugs and biologics, in those regions. Mandatory price reductions continue to be a significant aspect of business for the pharmaceutical and biotechnology industries outside of the United States. Healthcare reform in France, Germany and Spain, as well as austerity plans in a number of countries, including Italy, Greece and Portugal, have targeted the pharmaceutical sector with multiple mechanisms to reduce government expenditures. We expect that countries will continue to take aggressive actions to reduce expenditures on drugs and biologics, including mandatory price reductions, clawbacks of payments made to companies when national hospital drug spending thresholds are exceeded, preferences for biosimilar products, changes in international price referencing and transparency to achieve prices similar to that in lower-priced countries, and reductions in the amount of reimbursement. Similarly, fiscal constraints may also impact the extent to which countries are willing to reward new innovative therapies and/or allow access to new technologies. The proliferation of HTA organizations (e.g., NICE in the UK) has led to determinations of coverage and reimbursement based on both the clinical as well as the economic value of a product; these agencies are also increasingly setting the maximum price at which products will be reimbursed. While we cannot fully predict the extent of further price reductions and/or reimbursement restrictions taken by governmental payers outside of the United States or the impact such actions will have on our business, such reductions in price and/or the coverage and reimbursement for our products could have a material adverse effect on the sales of our products, our business and results of operation.

Additional initiatives addressing the coverage or reimbursement of our products could result in less extensive coverage or lower reimbursement, which could negatively affect sales of our products. If, for any of these or other reasons, reimbursement rates are reduced, or if healthcare providers anticipate reimbursement being reduced, providers may narrow the circumstances in which they prescribe or administer our products, which could reduce the use and/or sales of our products. A reduction in the use and sales of our products could have a material adverse effect on our business and results of operations.

Our current products and products in development cannot be sold if we do not maintain or gain regulatory approval.

Our business is subject to extensive regulation by numerous state and federal governmental authorities in the United States, including the FDA, and by foreign regulatory authorities, including the EMA. We are required in the United States and in foreign countries to obtain approval from regulatory authorities before we can

 

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manufacture, market and sell our products. Once approved, the FDA and other U.S. and foreign regulatory agencies have substantial authority to require additional testing, change product labeling or mandate withdrawals of our products. Also, legislative bodies or regulatory agencies could enact new laws or regulations or change existing laws or regulations at any time, which could affect our ability to obtain or maintain approval of our products. For example, the 2007 creation of the FDAAA significantly added to the FDA’s authority, allowing the FDA to (i) require sponsors of marketed products to conduct post-approval clinical studies; (ii) mandate labeling changes to products and (iii) require sponsors to implement a REMS for a product. Failure to comply with FDAAA requirements could result in significant civil monetary penalties, reputational harm and increased product liability risk. Current policy discussions underway in the United States include debates about the implementation of the new, abbreviated pathway for biosimilars established under the healthcare reform law; renegotiation of the PDUFA, which governs the user fees pharmaceutical and biological companies pay to the FDA that provide a substantial portion of the FDA’s operating budget, in anticipation of re-authorization before September 30, 2012; and reforms to the regulations that govern diagnostics and medical devices which are sometimes used in conjunction with our products. We are unable to predict when and whether any changes to laws or regulatory policies affecting our business could occur, and such changes could have a material adverse effect on our business and results of operations.

Obtaining and maintaining regulatory approval has been and will continue to be increasingly difficult, time-consuming and costly. For example, in October 2009 we received Complete Response Letters from the FDA for the BLA for Prolia® in the treatment and prevention of PMO and in the treatment and prevention of bone loss due to hormone ablation therapy (HALT) in breast and prostate cancer patients. The Complete Response Letter related to the PMO indication requested several items, including further information on the design and background adverse event rates to inform the methodology of our previously submitted post-marketing surveillance program. The FDA also requested a new clinical program to support the approval of Prolia® for the prevention of PMO, updated safety data and stated that a REMS is necessary for Prolia®. The Complete Response Letter related to the HALT indication requested additional information regarding the safety of Prolia® in patients with breast cancer receiving aromatase inhibitor therapy and patients with prostate cancer receiving Androgen Deprivation Therapy. The FDA specifically requested results from additional adequate and well-controlled clinical trials demonstrating that Prolia® has no detrimental effects on either time to disease progression or overall survival. Following the submission of further information, including clinical trial data from a number of trials evaluating denosumab in various oncology indications, in September 2011 the FDA approved Prolia® as a treatment to increase bone mass in women at high risk for fracture receiving adjuvant aromatase inhibitor therapy for breast cancer and as a treatment to increase bone mass in men at high risk for fracture receiving androgen deprivation therapy for non-metastatic prostate cancer. In addition, there may be situations in which demonstrating the efficacy and safety of a product candidate may not be sufficient to gain regulatory approval unless superiority to comparative products can be shown.

Some of our products are approved by U.S. and foreign regulatory authorities on a conditional basis with full approval conditioned upon fulfilling the requirements of regulators. Regulatory authorities are placing greater focus on monitoring products originally approved on an accelerated or conditional basis and on whether the sponsors of such products have met the conditions of the accelerated or conditional approvals. Vectibix®, for example, received accelerated approval in the United States and conditional approval in the EU, with full approval conditioned on conducting additional clinical trials of the use of Vectibix® as a therapy in treating mCRC. (See Item 1. Business — Marketed Products — Other Marketed Products — Vectibix® (panitumumab).) If we are unable to fulfill the requirements of regulators that were conditions of our products’ accelerated or conditional approval, we may not receive full approval for these products or may be required to change the products’ labeled indications or even withdraw the products from the market.

Following recent FDA and FDA advisory committee discussions and actions with respect to other therapeutic oncology products previously granted accelerated approval by the FDA, questions remain about regulatory authorities’ views regarding the adequacy for approval of therapeutic oncology products that have demonstrated a statistically significant improvement in progression-free survival but have not shown a statistically significant improvement in overall survival. A number of our products and product candidates have

 

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used endpoints other than overall survival, such as progression-free survival and bone-metastasis-free survival (BMFS), in the clinical trial data submitted for agency review or in clinical trials now being conducted. The use of endpoints such as progression-free survival or BMFS, in the absence of other measures of clinical benefit, may not be sufficient for approval even when such results are statistically significant. For example, our pivotal phase 3 Study ’147 evaluated XGEVA® for its ability to improve BMFS in men with castration-resistant prostate cancer that has not yet spread to bone. On February 8, 2012, the FDA convened the ODAC to discuss our sBLA filing for XGEVA® to delay bone metastases in prostate cancer and the data from Study ’147 submitted to support the filing. During its presentation to the ODAC, the FDA questioned the magnitude of the improvement in BMFS demonstrated in Study ’147, and indicated that a further clinical trial might help address some of the remaining unresolved questions regarding the clinical significance of the benefit achieved by XGEVA® in this setting. The ODAC panel concluded that the magnitude of benefit demonstrated with early treatment with XGEVA® to delay bone metastases was not sufficient to conclude a positive risk-benefit ratio for XGEVA® in the absence of additional measures impacting quality of life or other disease outcomes. Further, some of our products or product candidates may be used with a companion diagnostic product, such as a test kit, or companion device, such as an injector or other delivery system. These product candidates or expanded indications of our products may not be approved if the companion diagnostic product or companion device does not gain or maintain regulatory approval. These companion diagnostics and devices may be provided by single-source unaffiliated third-party companies. We are dependent on the sustained cooperation and effort of those third-party companies in conducting the studies required for such approval by the applicable regulatory agencies. Delays in the studies or failure of the third-party company to obtain regulatory approval of the companion diagnostic or device could negatively impact the approval of our product candidate or the expanded indication of our product and we may incur increased development costs, delays in regulatory approval and/or associated delays in a product candidate reaching the market or the expansion of existing product labels for new indications.

In addition to the clinical trials that we choose to or are required to conduct, other organizations may also conduct clinical trials that use our products. Such clinical trials may evaluate our products in areas in which we do not have and are not seeking an approved indication. However, negative results or safety signals arising in other organizations’ clinical trials may nonetheless prompt regulatory agencies to take regulatory actions that affect our approved indications, including requiring the addition of relevant safety data to the approved labeling or even withdrawing approval for our products.

The occurrence of a number of high profile safety events has caused an increased public and governmental concern about potential safety issues relating to pharmaceutical and biological products and certain of our products and product candidates. (See Our ESAs continue to be under review and receive scrutiny by regulatory authorities.) As a result of this increased concern in recent years, the U.S. regulatory environment has evolved and safety signals and safety concerns resulting from pre-clinical data, clinical trials (including sub-analyses and meta-analyses), market use or other sources are receiving greater scrutiny. For example, a number of regulatory agencies around the world, including the FDA and the EMA, have initiated programs to directly monitor for safety issues rather than wait for patients, providers or manufacturers to report safety problems with products or medical devices. And at least one private, for-profit company has begun aggregating and analyzing FDA adverse event data on its website using its own independent methodology, which could highlight new perceived risks of our products and product candidates. Actual or perceived safety problems or signals could lead to revised or restrictive labeling of our approved products or a class of products, potentially including limitations on the use of approved products in certain patients because of:

 

   

the identification of actual or theoretical safety or efficacy concerns with respect to any of our products by regulatory agencies;

 

   

an increased rate or number of previously-identified safety-related events;

 

   

the discovery of significant problems or safety signals or trends with a similar product that implicates an entire class of products;

 

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subsequent concerns about the sufficiency of the data or studies underlying the label or changes to the underlying safety/efficacy analysis related to results from clinical trials, including sub-analyses, or meta-analysis (a meta-analysis is the review of studies using various statistical methods to combine results from previous separate but related studies) of clinical trials or clinical data performed by us or others; and

 

   

new legislation or rules by regulatory agencies.

For example, in December 2009, based on the Trial to Reduce Cardiovascular Events with Aranesp® Therapy (TREAT) results, we updated the boxed warning in the labeling information for ESAs, to reflect an increased risk of stroke when ESAs are administered to CRF patients to target Hb levels of 13 g/dL and above. In October 2010, we submitted additional proposed labeling changes regarding the use of ESAs in CRF patients not on dialysis that would limit treatment to patients who are most likely to benefit, specifically those with significant anemia (<10 g/dL), and who are at high risk for transfusion and for whom transfusion avoidance is considered clinically important, including those in whom it is important to preserve kidney transplant eligibility. In June 2011, we announced that the FDA had approved further changes to the labels for the use of ESAs, including Aranesp® and EPOGEN®, in patients with CKD. (See Our ESAs continue to be under review and receive scrutiny by regulatory authorities.)

In addition to revised labeling for our products, discovery of new safety information or previously unknown safety concerns and/or safety signals with our products or similar products could also lead to:

 

   

requirement of risk management activities (including a REMS) or other FDA compliance actions related to the promotion and sale of our products;

 

   

mandated PMCs/PMRs or pharmacovigilance programs for our approved products;

 

   

product recalls of our approved products;

 

   

revocation of approval for our products from the market completely, or within particular therapeutic areas, and/or;

 

   

increased timelines or delays in being approved by the FDA or other regulatory bodies; and

 

   

fewer treatments or product candidates being approved by regulatory bodies.

Product safety concerns could cause regulatory agencies to impose risk management activities upon us (including a REMS), which may require substantial costs and resources to negotiate, develop, implement and administer. The results of these risk management activities could:

 

   

impact the ability of healthcare providers to prescribe, dispense or use our products;

 

   

limit patient access to our products;

 

   

reduce patient willingness to use our products;

 

   

place administrative burdens on healthcare providers in prescribing our products; and

 

   

affect our ability to compete against products that do not have a REMS or similar risk management activities.

We currently have approved REMS for our ESAs, Prolia® and Nplate®, and we use third-party service providers to assist in the administration of our REMS that include elements to assure safe use. For example, our ESA REMS requires applicable healthcare providers and institutions to enroll in the program, receive education about the product and the REMS and document and report certain information to us over time. We are responsible for tracking and documenting certain elements of healthcare provider and institution compliance with the ESA REMS and providing the FDA with periodic assessment reports to demonstrate that the goals of the REMS are being met. If we or third-party service providers acting on our behalf fail to effectively implement and/or administer the REMS for our products, we may be required to modify such REMS, and we may be subject to FDA enforcement actions or to civil penalties.

 

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Further, if new medical data or product quality issues suggest an unacceptable safety risk or previously unidentified side-effects, we may withdraw some or all affected product — either voluntarily or by regulatory mandate — in certain therapeutic areas, or completely recall a product presentation from the market for some period or permanently. For example, in September 2009, we initiated a voluntary recall of a limited number of ENBREL SureClick® lots due to a defect in the glass syringe barrel which resulted in a small number of broken syringes following assembly of the autoinjector device. In October 2010, we initiated a voluntary recall of certain lots of ENBREL due to identification of cracks in a small number of the glass syringes which may have resulted in product leakage and syringe breakage. Further, beginning in September 2010, we initiated a voluntary recall of certain lots of EPOGEN® and J&J voluntarily recalled certain lots of PROCRIT®, manufactured by us, because a small number of vials in each lot were found to contain glass lamellae (extremely thin, barely visible glass flakes) which we believed was a result of the interaction of the product formulation with glass vials during the shelf life of the product. The recalls were executed in close cooperation with the FDA. We may experience the same or other problems in the future, resulting in broader product recalls, adverse event trends, delayed shipments, supply constraints, contract disputes and/or stock-outs of our products, which may materially and adversely affect the sales of our products, our business and results of operations. Additionally, if other parties (including our independent clinical trial investigators or our licensees, such as J&J, Pfizer, Glaxo, Takeda and Daiichi Sankyo) report or fail to effectively report to regulatory agencies side effects or other safety concerns that occur from their use of our products in clinical trials or studies or from marketed use, resulting regulatory action could materially and adversely affect the sales of our products, our business and results of operations.

Current global economic conditions may negatively affect us and may magnify certain risks that affect our business.

Our operations and performance have been, and may continue to be, affected by economic conditions in the United States and throughout the world. Sales of our principal products are dependent, in part, on the availability and extent of reimbursement from third-party payers, including government programs such as Medicare and Medicaid and private payer healthcare and insurance programs. (See Our sales depend on coverage and reimbursement from third-party payers.) As more fully explained below, financial pressures may cause government or other third-party payers to more aggressively seek cost containment through mandatory discounts on our products, policies requiring the automatic substitution of generic or biosimilar products, higher hurdles for initial reimbursement approval for new products or other similar measures. (See We expect to face increasing competition from biosimilar products which could impact our profitability.) Additionally, as a result of the current global economic downturn, our third-party payers may delay or be unable to satisfy their reimbursement obligations. A reduction in the availability or extent of reimbursement from government and/or private payer healthcare programs or increased competition from lower cost biosimilar products could have a material adverse effect on the sales of our products, our business and results of operations. In addition, as a result of the economic downturn, some employers may seek to reduce costs by reducing or eliminating employer group healthcare plans or transferring a greater portion of healthcare costs to their employees. Job losses or other economic hardships may also result in reduced levels of coverage for some individuals, potentially resulting in lower levels of healthcare coverage for themselves or their families. These economic conditions may affect patients’ ability to afford healthcare as a result of increased co-pay or deductible obligations, greater cost sensitivity to existing co-pay or deductible obligations, lost healthcare insurance coverage or for other reasons. We believe such conditions have led and could continue to lead to changes in patient behavior and spending patterns that negatively affect usage of certain of our products, including delaying treatment, rationing prescription medications, leaving prescriptions unfilled, reducing the frequency of visits to healthcare facilities, utilizing alternative therapies and/or foregoing healthcare insurance coverage. In addition to its effects on consumers, the economic downturn may have also increased cost sensitivities among medical providers in the United States, such as oncology clinics, particularly in circumstances where providers may experience challenges in the collection of patient co-pays or be forced to absorb treatment costs as a result of coverage decisions or reimbursement terms. Collectively, we believe these changes have resulted and may continue to result in reduced demand for our products, which could materially and adversely affect the sales of our products, our business and

 

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results of operations. Any resulting decrease in demand for our products could also cause us to experience excess inventory write-offs and/or excess capacity or impairment charges at certain of our manufacturing facilities.

In Europe, economic conditions across the region could potentially be impacted by countries of key concern like Greece, which is facing possible default of its sovereign debt obligations, and Spain, France and Italy, whose sovereign debt obligations were recently downgraded. Economic conditions continue to affect our operations and performance outside the United States as well, particularly in countries where government-sponsored healthcare systems are the primary payers for healthcare expenditures, including drugs and biologics. (See Our sales depend on coverage and reimbursement from third-party payers.)

We also rely upon third parties for certain parts of our business, including licensees and partners, wholesale distributors of our products, contract clinical trial providers, contract manufacturers and single third-party suppliers. Because of the recent volatility in the financial markets, there may be a disruption or delay in the performance or satisfaction of commitments to us by these third parties which could have a material adverse effect on the sales of our products, our business and results of operations. Current economic conditions may adversely affect the ability of our distributors, customers and suppliers to obtain liquidity required to buy inventory or raw materials and to perform their obligations under agreements with us, which could disrupt our operations. Further, economic conditions appear to have affected, and may continue to affect, the business practices of our wholesale distributors in a manner that contributes to lower sales of our products. Although we monitor our distributors’, customers’ and suppliers’ financial condition and their liquidity in order to mitigate our business risks, some of our distributors, customers and suppliers may become insolvent, which could have a material adverse effect on the sales of our products, our business and results of operations. These risks may be elevated with respect to our interactions with third parties with substantial operations in countries where current economic conditions are the most severe, particularly where such third parties are themselves exposed to sovereign risk from business interactions directly with fiscally-challenged government payers.

We maintain a significant portfolio of investments disclosed as cash equivalents and marketable securities on our Consolidated Balance Sheet. The value of our investments may be adversely affected by interest rate fluctuations, downgrades in credit ratings, illiquidity in the capital markets and other factors that may result in other than temporary declines in the value of our investments. Any of those events could cause us to record impairment charges with respect to our investment portfolio or to realize losses on the sale of investments.

Our ESAs continue to be under review and receive scrutiny by regulatory authorities.

Beginning in 2006, adverse safety results involving ESAs were observed and since that time our ESAs have been the subject of ongoing review and scrutiny by regulatory authorities and other agencies. In the United States, the FDA has reviewed and continues to review the benefit-risk profile of ESAs, which has resulted in and could result in future changes to ESA labeling and usage. For example, in August 2008, we revised the labeling for our ESAs as the FDA directed. In addition, in July 2007 CMS issued an NCD for non-renal ESAs that determined that ESA treatment was not reasonable and necessary for certain clinical conditions, and established Medicare coverage parameters for FDA-approved ESA use in oncology. Since these labeling and reimbursement changes, we experienced a substantial reduction in our ESA sales, in particular Aranesp sales in the U.S. supportive cancer care setting. U.S. regulators have also reviewed the use of ESAs in the nephrology setting. In October 2009, the results from TREAT, a phase 3 pivotal study of patients with CKD not on dialysis were published in the New England Journal of Medicine. The study failed to meet its primary objectives of demonstrating a reduction in all-cause mortality, cardiovascular morbidity, including heart failure, heart attack, stroke or hospitalization for myocardial ischemia, or time to ESRD. On December 16, 2009, based on the TREAT results, we updated the boxed warning in the labeling information for ESAs, to reflect an increased risk of stroke when ESAs are administered to CRF patients to target Hb levels of 13 g/dL and above. And in June 2011, we announced that the FDA approved further changes to the labels for the use of ESAs, including Aranesp® and EPOGEN®, in patients with CKD. Over the past several years, CMS has also reviewed the use of ESAs and has considered and incorporated significant changes in the ways ESAs are reimbursed in the nephrology setting, including the implementation of the ESRD bundled payment system, subsequent changes to

 

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the QIP and consideration of a possible NCD to manage anemia in patients with CKD and dialysis-related anemia. Further restrictions are possible as the regional MACs implement LCDs to address Medicare coverage for ESAs in CKD not on dialysis within their respective geographic areas, and such restrictions could have a material adverse effect on the reimbursement, use and sales of Aranesp®. (See Our sales depend on coverage and reimbursement from third-party payers.) Together, these labeling and reimbursement changes, along with the approved REMS for ESAs, have had and may continue to have a material adverse effect on sales of our ESAs, our business and results of operations. We do not know what effect, if any, the June 2011 ESA label changes will have on the final version of the Kidney Disease: Improving Global Outcomes group (KDIGO) global anemia clinical practice guidelines which KDIGO has indicated could be available by early 2012. (See Guidelines and recommendations published by various organizations can reduce the use of our products.)

We have also agreed with the FDA to conduct a number of PMCs for our ESAs. In 2004, we agreed with the FDA to a robust pharmacovigilance program to continue to study the safety surrounding the use of darbepoetin alfa in the oncology setting. Of the five studies originally part of that pharmacovigilance program, four are complete, and the results of certain of those studies contributed to safety-related product labeling changes for our ESAs and changes in reimbursement, as noted above. The remaining study, the LNH03-6B Study, is being conducted by the Groupe d’Etudes des Lymphomes de l’Adulte, which presented second interim analysis results at the annual meeting of the American Society of Clinical Oncology in June 2011, and is currently estimated to be completed in 2012. Other trials have subsequently been initiated to inform on the safety of ESAs. In 2009 we initiated Study ‘782, a phase 3 non-inferiority study evaluating overall survival when comparing NSCLC patients on Aranesp® to patients receiving placebo, as part of our Aranesp® pharmacovigilance program. In addition, JRD’s EPO-ANE-3010 study, which evaluates the use of epoetin alfa in patients with breast cancer, is ongoing. Both of these studies are designated by the FDA as PMRs and must be conducted to maintain regulatory approval and marketing authorization. For the nephrology setting, we are in ongoing discussions with the FDA regarding additional PMRs to explore alternative ESA dosing strategies in CKD patients on dialysis and not on dialysis. Although we cannot predict the results or the outcomes of ongoing clinical trials, or the extent to which regulatory authorities may require additional labeling changes as a result of these or other trials, we cannot exclude the possibility that unfavorable results from clinical trials, including PMCs, could have a material adverse effect on the reimbursement, use and sales of our ESAs and on our business and results of operations.

Regulatory authorities outside the United States have also reviewed and scrutinized the use of ESAs. In June 2008, the EMA recommended updating the product information for ESAs with a new warning for their use in cancer patients, which was approved by the EC in October 2008. The product information for all ESAs was updated to advise that, in some clinical situations, blood transfusions should be the preferred treatment for the management of anemia in patients with cancer and that the decision to administer ESAs should be based on a benefit-risk assessment with the participation of the individual patient. Following the October 2008 revision, we experienced a reduction of Aranesp® sales in the supportive cancer care setting in the EU. In addition, following the June 2011 ESA label changes in the United States, regulatory agencies outside the United States have sought additional information from us about the use and safety of ESAs in the CKD setting. Additional labeling or reimbursement changes by these regulatory authorities could materially and adversely affect the reimbursement, use and sales of our ESAs, our business and results of operations.

We continue to receive results from meta-analyses or previously initiated clinical trials using ESAs, including PMCs. For example, in May 2009, the Cochrane Collaboration published its independent meta-analysis of patient-level data from previously conducted, randomized, controlled, clinical studies evaluating ESAs in cancer patients which we submitted to the FDA and the EMA. This Cochrane meta-analysis of patient-level data from previous studies corroborates prior analyses indicating that the use of ESAs may increase the risk of death in cancer patients. The studies in the analysis all predate the current label, which advises using the least amount of ESA necessary to avoid transfusion, but they do not exclude the potential for adverse outcomes when ESAs are prescribed according to the current label. In addition, data from the RED-HF® trial evaluating the effect of treatment of anemia with darbepoetin alfa on morbidity and mortality in patients with symptomatic left ventricular heart failure is anticipated in 2012. Unfavorable results from these or similar trials or meta-analyses

 

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of previous clinical trials could materially and adversely affect the use and sales of our ESAs, our business and results of operations.

We must conduct clinical trials in humans before we can commercialize and sell any of our product candidates or existing products for new indications.

Before we can sell any products, we must conduct clinical trials to demonstrate that our product candidates are safe and effective for use in humans. The results of those clinical trials are used as the basis to obtain approval from regulatory authorities such as the FDA and EMA. (See Our current products and products in development cannot be sold if we do not maintain or gain regulatory approval.) We are required to conduct clinical trials using an appropriate number of trial sites and patients to support the product label claims. The length of time, number of trial sites and patients required for clinical trials vary substantially and therefore, we may spend several years and incur substantial expense in completing certain clinical trials. Delays in planned clinical trials can result in increased development costs, delays in regulatory approvals, associated delays in product candidates reaching the market and revisions to existing product labels.

In addition, in order to increase the number of patients available for enrollment for our clinical trials, we have and will continue to open clinical sites and enroll patients in a number of new geographic locations where our experience conducting clinical trials is more limited, including Russia, India, China, South Korea, the Philippines, Singapore and some Central and South American countries either through utilization of third-party contract clinical trial providers entirely or in combination with local staff. Conducting clinical trials in locations where we have limited experience requires substantial time and resources to identify and understand the unique regulatory environments of individual countries. Further, we must ensure the timely production, distribution and delivery of the clinical supply of our product candidates to the numerous and varied clinical trial sites. If we fail to adequately manage the design, execution and regulatory aspects of our large, complex and regulatorily diverse clinical trials or manage the production or distribution of our clinical supply, corresponding regulatory approvals may be delayed or we may fail to gain approval for our product candidates or could lose our ability to market existing products in certain therapeutic areas or altogether. If we are unable to market and sell our product candidates or are unable to obtain approvals in the timeframe needed to execute our product strategies, our business and results of operations could be materially and adversely affected. Additional information on our clinical trials can be found on our website at www.amgen.com. (This website address is not intended to function as a hyperlink, and the information contained on our website is not intended to be a part of this filing.)

We rely on independent third-party clinical investigators to recruit subjects and conduct clinical trials in accordance with the applicable study protocols and laws and regulations. We also may acquire companies that have ongoing clinical trials. These trials may not be conducted to the same standards as ours; however, once an acquisition has been completed we assume responsibility for the conduct of the trial, including any potential risks and liabilities associated with the past and prospective conduct of those trials. If regulatory authorities determine that we or others, including our licensees or the independent investigators selected by us or by a company we have acquired, have not complied with regulations in the research and development of a product candidate, a new indication for an existing product or information to support a current indication, they may refuse to accept trial data from the site, not approve the product candidate or new indication or maintain approval of the current indication in its current form or at all, and we would not be able to market and sell it. If we were unable to market and sell our products or product candidates, our business and results of operations could be materially and adversely affected.

Further, we rely on unaffiliated third-party vendors to perform certain aspects of our clinical trial operations. In addition, some of our clinical trials involve drugs manufactured and marketed by other pharmaceutical companies. These drugs may be administered in a clinical trial in combination with one of our product candidates or in a head-to-head study comparing the products’ relative efficacy and safety. In the event that any of these vendors or pharmaceutical companies have unforeseen issues that negatively impact the quality of their work or creates a shortage of supply, our ability to complete our applicable clinical trials and/or evaluate clinical results may also be negatively impacted. As a result, this could adversely affect our ability to file for, gain or maintain regulatory approvals worldwide on a timely basis, if at all.

 

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Patients may also suffer adverse medical events or side effects in the course of our, our licensees, partners or independent investigators’ clinical trials which could:

 

   

delay the clinical trial program;

 

   

require additional or longer trials to gain approval;

 

   

prohibit regulatory approval of our product candidates or new indications for existing products; and

 

   

render the product candidate commercially unfeasible or limit our ability to market existing products completely or in certain therapeutic areas.

Safety signals, trends, adverse events or results from clinical trials or studies performed by us or by others (including our licensees or independent investigators) or from the marketed use of our drugs or similar products that result in revised safety-related labeling or restrictions on the use of our approved products could negatively impact healthcare provider prescribing behavior, use and sales of our products, regulatory or private health organization medical guidelines and reimbursement for our products, all of which could have a material adverse effect on our business and results of operations.

Clinical trials must be designed based on the current standard of medical care. However in certain diseases, such as cancer, the standard of care is evolving rapidly. In these diseases, the duration of time needed to complete certain clinical trials may result in the design of such clinical trials being based on an out of date standard of medical care, limiting the utility and application of such trials. We may not obtain favorable clinical trial results and may not be able to obtain regulatory approval for new product candidates, new indications for existing products or maintenance of our current labels on this basis. Further, clinical trials conducted by others, including our licensees, partners or independent investigators, may result in unfavorable clinical trials results that may call into question the safety of our products in off-label or on label uses that may result in label restrictions and/or additional trials.

Even after a product is on the market, safety concerns may require additional or more extensive clinical trials as part of a pharmacovigilance program of our product or for approval of a new indication. For example, we have initiated Study ‘782 as part of our Aranesp® oncology pharmacovigilance program. (See Our ESAs continue to be under review and receive scrutiny by regulatory authorities.) In connection with the June 2011 ESA label changes, we also agreed to conduct additional clinical trials examining the use of ESAs in CKD. Additional clinical trials we initiate, including those required by the FDA, could result in substantial additional expense and the outcomes could result in additional label restrictions or the loss of regulatory approval for an approved indication, each of which could have a material adverse effect on the sales of our products, our business and results of operations. Additionally, any negative results from such trials could materially affect the extent of approvals, the use, reimbursement and sales of our products.

We expect to face increasing competition from biosimilar products.

We currently face competition in Europe from biosimilar products, and we expect to face increasing competition from biosimilars in the future. In 2010, lawmakers in the United States enacted healthcare reform legislation which included an abbreviated regulatory pathway for the approval of biosimilars. The EU has already created such a regulatory pathway. To the extent that governments adopt more permissive approval frameworks and competitors are able to obtain broader marketing approval for biosimilars, our products will become subject to increased competition. Expiration or successful challenge of applicable patent rights could trigger such competition, and we could face more litigation regarding the validity and/or scope of our patents.

In the EU, the EC has granted marketing authorizations for several biosimilars pursuant to a set of general and product class-specific guidelines for biosimilar approvals issued over the past few years. In 2006, the EMA developed and issued final regulatory guidelines related to the development and approval of biosimilar products. The final guidelines included clinical trial guidance for certain biosimilar products, including erythropoietins and G-CSFs, recommending that applicants seeking approval of such biosimilar products conduct pharmacodynamic, toxicological and clinical safety studies as well as a pharmacovigilance program. In late 2011, the EMA

 

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announced plans to issue in the first half of 2012 final guidelines on the approval process for biosimilar monoclonal antibodies and draft guidelines on the approval process for other biosimilar drugs. Some companies have received and other companies are seeking approval to market erythropoietin and G-CSF biosimilars in the EU, presenting additional competition for our products. (See Our marketed products face substantial competition.) For example, following the expiration of the principal European patent relating to recombinant G-CSF in August 2006, the EC issued marketing authorizations for the first G-CSF biosimilar products and the products were launched in certain EU countries in 2008 and 2009. There are now several G-CSF biosimilars available in the EU marketed by different companies and these G-CSF biosimilar products compete with NEUPOGEN® and Neulasta®. Further, as in an effort to reduce costs, countries in the EU may in the future permit the automatic substitution by pharmacists of biosimilars for the corresponding innovator products or adopt other biosimilar uptake measures. We cannot predict to what extent the entry of biosimilar products or other competing products will impact future sales of our products in the EU. Our inability to compete effectively could reduce sales, which could have a material adverse effect on our business and results of operations.

On March 23, 2010, President Obama signed into law the PPACA which authorized the FDA to approve biosimilar products under a separate, abbreviated pathway. The law established a period of 12 years of data exclusivity for reference products in order to preserve incentives for future innovation and outlined statutory criteria for science-based biosimilar approval standards that take into account patient safety considerations. Under this framework, data exclusivity protects the data in the innovator’s regulatory application by prohibiting, for a period of 12 years, others from gaining FDA approval based in part on reliance or reference to the innovator’s data in their application to the FDA. The law does not change the duration of patents granted on biologic products. On February 9, 2012, the FDA released three draft guidance documents that provide insight into the FDA’s current thinking on the development of biosimilar products and broad parameters for the scientific assessment of biosimilar applications. The documents provide guidance in the development of biosimilar versions of currently approved biological products and indicate that the clinical trials and other steps required for approval of each biosimilar product will depend on a variety of factors, including the complexity of the protein, the sophistication of the manufacturing required and the potential risks of the product. A growing number of companies have announced their intentions to develop biosimilar versions of existing biotechnology products, including a number of our products. Further, biosimilar manufacturers with approved products in Europe may seek to quickly obtain U.S. approval now that the regulatory pathway for biosimilars has been enacted. In addition, critics of the 12-year exclusivity period in the biosimilar pathway law will likely seek to shorten the data exclusivity period. President Obama’s proposed 2013 budget includes a proposal to lower the data exclusivity period to seven years, but this would require new legislation be passed by Congress. Critics may also encourage the FDA to interpret narrowly the law’s provisions regarding which new products receive data exclusivity. While we are unable to predict the precise impact of the pending introduction of biosimilars on our products, or the degree to which the FDA’s recent guidelines will contribute to that impact, we expect in the future to face greater competition in the United States as a result of biosimilar products and downward pressure on our product prices and sales, subject to our ability to enforce our patents. (See Item 7A. Management’s Discussion and Analysis of Financial Condition and Results of Operations — Financial Condition, Liquidity and Capital Resources.) This additional competition could have a material adverse effect on our business and results of operations.

We may not be able to develop commercial products.

Successful product development in the biotechnology industry is highly uncertain, and very few R&D projects produce a commercial product. We intend to continue to make significant R&D investments. Product candidates or new indications for existing products (collectively, “product candidates”) that appear promising in the early phases of development may fail to reach the market for a number of reasons, such as:

 

   

the product candidate did not demonstrate acceptable clinical trial results even though it demonstrated positive preclinical trial results, for reasons that could include changes in the standard of care of medicine;

 

   

the product candidate was not effective or more effective than currently available therapies in treating a specified condition or illness;

 

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the product candidate is not cost effective in light of existing therapeutics;

 

   

the product candidate had harmful side effects in humans or animals;

 

   

the necessary regulatory bodies, such as the FDA or EMA, did not approve our product candidate for an intended use;

 

   

the product candidate was not economical for us to manufacture and commercialize;

 

   

other parties have or may have proprietary rights relating to our product candidate, such as patent rights, and will not let us sell it on reasonable terms, or at all;

 

   

we and certain of our licensees, partners or independent investigators may fail to effectively conduct clinical development or clinical manufacturing activities; and

 

   

the regulatory pathway to approval for product candidates is uncertain or not well-defined.

Several of our product candidates have failed or been discontinued at various stages in the product development process. For example, in June 2004, we announced that the phase 2 study of Glial Cell Lined-Derived Neurotrophic Factor (GDNF) for the treatment of advanced Parkinson’s disease did not meet the primary study endpoint upon completion of nine months of the double-blind treatment phase of the study. The conclusion was reached even though a small phase 1 pilot investigator-initiated open-label study over a three-year period appeared to result in improvements for advanced Parkinson’s disease patients. Subsequently, we discontinued clinical development of GDNF in patients with advanced Parkinson’s disease.

Our marketed products face substantial competition.

We operate in a highly competitive environment. Our products compete with other products or treatments for diseases for which our products may be indicated. Our competitors market products or are actively engaged in R&D in areas where we have products, where we are developing product candidates or new indications for existing products. In the future, we expect that our products will compete with new drugs currently in development, drugs currently approved for other indications that may later be approved for the same indications as those of our products and drugs approved for other indications that are used off-label. Large pharmaceutical companies and generics manufacturers of pharmaceutical products are expanding into the biotechnology field with increasing frequency, and some pharmaceutical companies and generics manufacturers have formed partnerships to pursue biosimilar products. These companies may have greater resources than we do. In addition, some of our competitors may have technical or competitive advantages over us for the development of technologies and processes. These resources may make it difficult for us to compete with them to successfully discover, develop and market new products and for our current products to compete with new products or new product indications that these competitors may bring to market. As a result, our products may compete against products that have lower prices, equivalent or superior performance, better safety profile, are easier to administer or that are otherwise competitive with our products.

Concentration of sales at certain of our wholesaler distributors and consolidation of free-standing dialysis clinic businesses may negatively impact our bargaining power and profit margins.

The substantial majority of our U.S. product sales are made to three pharmaceutical product wholesaler distributors, AmerisourceBergen Corporation, Cardinal Health, Inc. and McKesson Corporation. These distributors, in turn, sell our products to their customers, which include physicians or their clinics, dialysis centers, hospitals and pharmacies. In addition, one of our products, EPOGEN®, is sold primarily to free-standing dialysis clinics, which have experienced significant consolidation. Two organizations, DaVita and Fresenius Medical Care North America, own or manage a large number of the outpatient dialysis facilities located in the United States and account for a substantial majority of all EPOGEN® sales in the free-standing dialysis clinic setting. Due to this concentration, these entities have substantial purchasing leverage, which may put pressure on

 

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our pricing by their potential ability to extract price discounts on our products or fees for other services, correspondingly negatively impacting our bargaining position and profit margins.

Our business may be affected by litigation and government investigations.

We and certain of our subsidiaries are involved in legal proceedings. (See Note 18, Contingencies and commitments, in the notes to our consolidated financial statements in our annual report.) Civil and criminal litigation is inherently unpredictable, and the outcome can result in excessive verdicts, fines, penalties, exclusion from the federal healthcare programs and/or injunctive relief that affect how we operate our business. Defense of litigation claims can be expensive, time-consuming and distracting and it is possible that we could incur judgments or enter into settlements of claims for monetary damages or change the way we operate our business, which could have a material adverse effect on our business and results of operations. In addition, product liability is a major risk in testing and marketing biotechnology and pharmaceutical products. We may face substantial product liability exposure in human clinical trials and for products that we sell after regulatory approval. Product liability claims, regardless of their merits, could be costly and divert management’s attention and adversely affect our reputation and the demand for our products. Amgen and Immunex have previously been named as defendants in product liability actions for certain of our products.

We are also involved in government investigations that arise in the ordinary course of our business. Beginning in 2007, we received a number of subpoenas from various government entities, including the U.S. Attorney’s Offices for the Eastern District of New York and the Western District of Washington, as well as the Attorneys General of New York and New Jersey. The federal subpoenas were issued pursuant to the Health Insurance Portability and Accountability Act of 1996 (18 U.S.C. 3486), and by a federal grand jury, while the Attorneys General subpoenas were issued pursuant to state specific statutes relating to consumer fraud laws and state false claims acts. In general, the subpoenas requested documents relating to the sales and marketing of our products, and our collection and dissemination of information reflecting clinical research as to the safety and efficacy of our ESAs. Based on representations in a U.S. government filing that became public in May 2009 relating to the Massachusetts Qui Tam Action (as defined in Note 18, Contingencies and commitments in the notes to our consolidated financial statements) and subsequent conversations with government prosecutors, we learned that the subpoenas we received from the U.S. Attorney’s Offices for the Eastern District of New York and the Western District of Washington relate to the Massachusetts Qui Tam Action and nine additional Qui Tam Actions (as defined in Note 18, Contingencies and commitments in the notes to our consolidated financial statements) pending against us in various federal jurisdictions. In October 2011 we announced that we had reached an agreement in principle to settle the allegations regarding our sales and marketing practices arising out of the ongoing civil and criminal investigations conducted by the U.S. Attorney’s Offices for the Eastern District of New York and the Western District of Washington. The proposed settlement involves numerous state and federal agencies and remains subject to continuing discussions regarding the components of the agreement, and the completion and execution of all required documentation. Until the proposed settlement becomes final, there can be no guarantee that these matters will be resolved by the agreement in principle. If the proposed settlement is not finalized as proposed, we would have to continue to explain and defend our actions to government entities involved, which would be burdensome, expensive and time-consuming for us and could result in criminal charges, civil penalties or other enforcement actions. In addition, while the agreement in principle includes the dismissal of the claims of the government in the Qui Tam Actions, the individual relators in the Qui Tam Actions have the opportunity to join in the proposed settlement or, if they object, to have the settlement evaluated in a federal court fairness hearing to determine whether it is fair, adequate and reasonable under all the circumstances. If the court determines that the settlement is not fair, adequate and reasonable, then we would have the option to continue to defend our actions in court, or to seek to negotiate a new settlement. We have been made aware that we are also a defendant in several other civil qui tam actions that remain under seal in the U.S. federal courts where they were filed. Included with these actions are allegations that our promotional, contracting, sales and marketing activities relating to ENBREL and Aranesp® caused the submission of various false claims under the Federal Civil False Claims Act and various State False Claims Acts. Certain of the allegations in these other actions are not encompassed in the proposed settlement discussed above. In addition, as described in Note 18, Contingencies and commitments in the notes to our consolidated financial statements, this proposed settlement does not cover a number of other litigation matters that will continue to be pending against us.

 

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Throughout these investigations, the government entities are asserting that we violated various state and federal laws. These investigations are very burdensome, expensive and time-consuming for us to explain and defend to these entities. Although we cannot predict whether additional proceedings may be initiated against us, or predict when these matters may be resolved, it is not unusual for investigations such as these to continue for a considerable period of time and to require management’s attention and significant legal expense. A determination that we are in violation of the various federal and state laws that govern the sales and marketing of our products could result in federal criminal liability and/or federal or state civil or administrative liability, and thus could result in substantial financial damages or criminal penalties and possible exclusion from future participation in the Medicare and Medicaid programs. In addition, we may see new governmental investigations of or actions against us citing novel theories of recovery. Any of these results could have a material adverse effect on our business and results of operations.

We rely on third-party suppliers for certain of our raw materials, medical devices and components.

We rely on unaffiliated third-party suppliers for certain raw materials, medical devices and components necessary for the manufacturing of our commercial and clinical products. Certain of those raw materials, medical devices and components are the proprietary products of those unaffiliated third-party suppliers and are specifically cited in our drug application with regulatory agencies so that they must be obtained from that specific sole source or sources and could not be obtained from another supplier unless and until the regulatory agency approved such supplier.

Among the reasons we may be unable to obtain these raw materials, medical devices and components include:

 

   

regulatory requirements or action by regulatory agencies or others;

 

   

adverse financial or other strategic developments at or affecting the supplier;

 

   

unexpected demand for or shortage of raw materials, medical devices or components;

 

   

labor disputes or shortages, including the effects of a pandemic flu outbreak, natural disaster, or otherwise;

 

   

failure to comply with our quality standards which results in quality and product failures, product contamination and/or recall; and

 

   

discovery of previously unknown or undetected imperfections in raw materials, medical devices or components.

These events could negatively impact our ability to satisfy demand for our products, which could materially and adversely affect our product use and sales and our business and operating results. For example, in prior years we have experienced shortages in certain components necessary for the formulation, fill and finish of certain of our products in our Puerto Rico facility. Further quality issues which result in unexpected additional demand for certain components may lead to shortages of required raw materials or components (such as we have experienced with EPOGEN® glass vials). We may experience or continue to experience these or other shortages in the future resulting in delayed shipments, supply constraints, contract disputes and/or stock-outs of our products. Also, certain of the raw materials required in the commercial and clinical manufacturing of our products are sourced from other countries and/or derived from biological sources, including mammalian tissues. In addition, one of our marketed products also uses bovine serum and human serum albumin. Some countries in which we market our products may restrict the use of certain biologically derived substances in the manufacture of drugs. We continue to investigate alternatives to certain biological sources and alternative manufacturing processes that do not require the use of certain biologically derived substances because such raw materials may be subject to contamination and/or recall.

A material shortage, contamination, recall and/or restriction of the use of certain biologically derived substances or other raw materials, which may be sourced from other countries and that are used in the manufacture of our products could adversely impact or disrupt the commercial manufacturing of our products or

 

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could result in a mandated withdrawal of our products from the market. This could negatively impact our ability to satisfy demand for our products, which could materially and adversely affect our product sales, business and operating results. Further, any disruptions or delays by us or by third-party suppliers or partners in converting to alternatives to certain biologically derived substances and alternative manufacturing processes or our ability to gain regulatory approval for the alternative materials and manufacturing processes could increase our associated costs or result in the recognition of an impairment in the carrying value of certain related assets, which could have a material and adverse effect on our business and results of operations.

Manufacturing difficulties, disruptions or delays could limit supply of our products and limit our product sales.

Manufacturing biologic human therapeutic products is difficult, complex and highly regulated. We currently manufacture all of our principal products and plan to manufacture many of our product candidates. In addition, we currently use third-party contract manufacturers to produce or assist in the production of ENBREL, Prolia®, Sensipar®/Mimpara®, Nplate®, XGEVA® and Vectibix® and plan to use contract manufacturers to produce or assist in the production of a number of our late-stage product candidates. Our ability to adequately and timely manufacture and supply our products is dependent on the uninterrupted and efficient operation of our facilities and those of our third-party contract manufacturers, which may be impacted by:

 

   

availability or contamination of raw materials, components and equipment used in the manufacturing process, particularly those for which we have no other source or supplier;

 

   

capacity of our facilities and those of our contract manufacturers;

 

   

contamination by microorganisms or viruses;

 

   

natural or other disasters, including hurricanes, earthquakes, volcanoes or fires;

 

   

labor disputes or shortages, including the effects of a pandemic flu outbreak, natural disaster, or otherwise;

 

   

degree of compliance with regulatory requirements;

 

   

changes in forecasts of future demand;

 

   

timing and actual number of production runs;

 

   

updating of manufacturing specifications;

 

   

production success rates and yields; and

 

   

timing and outcome of product quality testing.

If the efficient manufacture and supply of our products is interrupted, we may experience delayed shipments, supply constraints, stock-outs and/or recalls of our products. For example, over the past several years we have initiated a number of voluntary recalls of certain lots of our products. (See Our current products and products in development cannot be sold if we do not maintain or gain regulatory approval.) If we are at any time unable to provide an uninterrupted supply of our products to patients, we may lose patients and physicians may elect to prescribe competing therapeutics instead of our products, which could materially and adversely affect our product sales, business and results of operations.

Our manufacturing processes and those of our third-party contract manufacturers must undergo a potentially lengthy FDA or other regulatory approval process and are subject to continued review by the FDA and other regulatory authorities. It can take longer than five years to build, validate and license a new manufacturing plant and it can take longer than three years to qualify and license a new contract manufacturer. For example, in order to maintain supply and to satisfy anticipated future demand for denosumab, we are qualifying the expansion of our existing bulk protein facilities at our Puerto Rico site. In addition, in order mitigate the risk associated with the majority of our formulation and fill operations being performed in a single facility, we are completing the construction and qualification of a new formulation and filling facility at our Puerto Rico site, and are modifying

 

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and expanding our recently acquired formulation, fill and finish manufacturing site in Ireland. Upon completion, these facilities will require licensure by the various regulatory authorities.

If regulatory authorities determine that we or our third-party contract manufacturers or certain of our third-party service providers have violated regulations or if they restrict, suspend or revoke our prior approvals, they could prohibit us from manufacturing our products or conducting clinical trials or selling our marketed products until we or the affected third-party contract manufacturers or third-party service providers comply, or indefinitely. Because our third-party contract manufacturers and certain of our third-party service providers are subject to the FDA and foreign regulatory authorities, alternative qualified third-party contract manufacturers and third-party service providers may not be available on a timely basis or at all. If we or our third-party contract manufacturers or third-party service providers cease or interrupt production or if our third-party contract manufacturers and third-party service providers fail to supply materials, products or services to us, we may experience delayed shipments, supply constraints, stock-outs and/or recalls of our products. Additionally, we distribute a substantial volume of our commercial products through our primary distribution centers in Louisville, Kentucky for the United States and in Breda, the Netherlands for Europe and much of the rest of the world. We also conduct all the labeling and packaging of our products distributed in Europe and much of the rest of the world in Breda, the Netherlands. Our ability to timely supply products is dependent on the uninterrupted and efficient operations of our distribution and logistics centers, our third-party logistics providers and our labeling and packaging facility in Breda. Further, we rely on commercial transportation for the distribution of our products to our customers which may be negatively impacted by natural disasters or security threats.

We perform a substantial amount of our commercial manufacturing activities at our Puerto Rico manufacturing facility and a substantial amount of our clinical manufacturing activities at our Thousand Oaks, California manufacturing facility; if significant natural disasters or production failures occur at the Puerto Rico facility, we may not be able to supply these products or, at the Thousand Oaks facility, we may not be able to continue our clinical trials.

We currently perform all of the formulation, fill and finish for Neulasta®, NEUPOGEN®, Aranesp®, EPOGEN®, Prolia® and XGEVA® and substantially all of the formulation, fill and finish operations for ENBREL at our manufacturing facility in Juncos, Puerto Rico. We also currently perform all of the bulk manufacturing for Neulasta®, NEUPOGEN® and Aranesp® and the purification of bulk EPOGEN® material at this facility, and plan to perform substantially all of the bulk manufacturing for Prolia® and XGEVA® at the Puerto Rico facility once the facility has been approved by the FDA for that purpose. We perform substantially all of the bulk manufacturing and formulation, fill and finish, and packaging for product candidates to be used in clinical trials at our manufacturing facility in Thousand Oaks, California. The global supply of our products and product candidates is significantly dependent on the uninterrupted and efficient operation of these facilities. A number of factors could materially and adversely affect our operations, including:

 

   

power failures and/or other utility failures;

 

   

breakdown, failure or substandard performance of equipment;

 

   

improper installation or operation of equipment;

 

   

labor disputes or shortages, including the effects of a pandemic flu outbreak;

 

   

inability or unwillingness of third-party suppliers to provide raw materials and components;

 

   

natural or other disasters, including hurricanes, earthquakes or fires; and

 

   

failures to comply with regulatory requirements, including those of the FDA.

In the past, the Puerto Rico facility has experienced manufacturing component shortages and there was evidence of adverse trends in the microbial bioburden of the production environment that reduced the production output. The same or other problems may result in our being unable to supply these products, which could materially and adversely affect our product sales, business and operating results. Although we have obtained limited insurance to protect against certain business interruption losses, there can be no assurance that such

 

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coverage will be adequate or that such coverage will continue to remain available on acceptable terms, if at all. The extent of the coverage of our insurance could limit our ability to mitigate for lost sales and such losses could materially and adversely affect our product sales, business and operating results. Our Puerto Rico facility is also subject to the same difficulties, disruptions or delays in manufacturing experienced in our other manufacturing facilities. For example, the limited number of lots of ENBREL and EPOGEN® voluntarily recalled in 2009 and 2010 were manufactured at our Puerto Rico facility. In future inspections, our failure to adequately address the FDA’s expectations could lead to further inspections of the facility or regulatory actions. (See Manufacturing difficulties, disruptions or delays could limit supply of our products and limit our product sales.)

Our intellectual property positions may be challenged, invalidated, circumvented or expire, or we may fail to prevail in present and future intellectual property litigation.

Our success depends in part on our ability to obtain and defend patent rights and other intellectual property rights that are important to the commercialization of our products and product candidates. The patent positions of pharmaceutical and biotechnology companies can be highly uncertain and often involve complex legal, scientific and factual questions. Third parties may challenge, invalidate or circumvent our patents and patent applications relating to our products, product candidates and technologies. In addition, our patent positions might not protect us against competitors with similar products or technologies because competing products or technologies may not infringe our patents. For certain of our product candidates, there are third parties who have patents or pending patent applications that they may claim necessitate payment of a royalty or prevent us from commercializing these product candidates in certain territories. Patent disputes are frequent, costly and can preclude, delay or increase the cost of commercialization of products. We have been in the past, and may be in the future, involved in patent litigation. A determination made by a court, agency or tribunal concerning infringement, validity, enforceability, injunctive or economic remedy, or the right to patent protection, for example, are typically subject to appellate or administrative review. Upon review, such initial determinations may be afforded little or no deference by the reviewing tribunal and may be affirmed, reversed, or made the subject of reconsideration through further proceedings. A patent dispute or litigation may not discourage a potential violator from bringing the product that is alleged to infringe to market prior to a final resolution of the dispute or litigation. For example, until the Pennsylvania District Court entered final judgment and a permanent injunction against Teva on July 15, 2011 pursuant to a joint stipulation and settlement agreement between the parties, Teva had announced that it intended to sell its filgrastim product, upon approval from the FDA, in the United States without a license from us and prior to the expiration of our G-CSF patents. The period of time from inception until resolution of a patent dispute or litigation is subject to the availability and schedule of the court, agency or tribunal before which the dispute or litigation is pending. We may be subject to competition during this period and may not be able to fully recover for the losses, damages, and harms we incur from infringement by the competitor product even if we prevail. Moreover, if we lose or settle current or future litigations at certain stages or entirely, we could be subject to competition and/or significant liabilities, be required to enter into third-party licenses for the infringed product or technology or be required to cease using the technology or product in dispute. In addition, we cannot guarantee that such licenses will be available on terms acceptable to us, or at all.

Further, under the Hatch-Waxman Act, our products approved by the FDA under the Food, Drug and Cosmetic Act may be the subject of patent litigation with generic competitors before expiry of the five year period of data exclusivity provided for under the Hatch-Waxman Act and prior to the expiration of the patents listed for the product. Likewise, our biologic products may be the subject of patent litigation prior to the expiration of our patents and, with respect to competitors seeking approval as a biosimilar or interchangeable version of our products, prior to the twelve year exclusivity period provided under the Biologics Price Competition and Innovation Act of 2009.

Over the next several years, many of the existing patents on our principal products will expire. (See Item 1. Business — Marketed Products.) As our patents expire, competitors may be able to legally produce and market similar products or technologies, including biosimilars, which may have a material adverse effect on our product sales, business and results of operations. (See Item 7A. Management’s Discussion and Analysis of Financial Condition and Results of Operations — Financial Condition, Liquidity and Capital Resources.) We have received,

 

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and we continue to seek, additional patent protection relating to our products, including patents on our products, specific processes for making our products, formulations and particular uses of our products. However, competitors may be able to invalidate, design around or otherwise circumvent our patents and sell competing products. For example, while we do not expect biosimilars competition on ENBREL in the United States for the foreseeable future, there are a number of competing therapies currently on the market and more in clinical development that are different from ENBREL but are used to treat the same inflammatory diseases treated by ENBREL. Although we continue to develop new products, and obtain patent protection for these new product candidates, we may not be able to replace the revenue lost upon the expiration of the patents on our current products.

From time to time, U.S. and other policymakers have proposed reforming the patent laws and regulations of their countries. In September 2011, after years of Congressional debate regarding patent reform legislation, President Obama signed into law the America Invents Act (the Act) considered by many to be the most substantial revision of U.S. patent law since 1952. The Act’s various provisions will go into effect over an 18-month period. The Act changes the current “first-to-invent” system to a system that awards a patent to the “first-inventor-to-file” for an application for a patentable invention. This change alters the pool of available materials that can be used to challenge patents and eliminates the ability to rely on prior research work in order to lay claim to patent rights. Disputes as to whether the first filer is in fact the true inventor will be resolved through newly implemented derivation proceedings. The Act also creates mechanisms to allow challenges to newly issued patents in the patent office in post-grant proceedings and new inter partes reexamination proceedings. Although many of the changes bring U.S. law into closer harmony with European and other national patent laws, the new bases and procedures may make it easier for competitors to challenge our patents, which could result in increased competition and have a material adverse effect on our product sales, business and results of operations. The changes may also make it harder to challenge third-party patents and place greater importance on being the first inventor to file a patent application on an invention.

Our stock price is volatile.

Our stock price, like that of our peers in the biotechnology and pharmaceutical industries, is volatile. Our revenues and operating results may fluctuate from period to period for a number of reasons. Events such as a delay in product development or even a relatively small revenue shortfall may cause financial results for a period to be below our expectations or projections. As a result, our revenues and operating results and, in turn, our stock price may be subject to significant fluctuations.

We may not be able to access the capital and credit markets on terms that are favorable to us, or at all.

The capital and credit markets may experience extreme volatility and disruption which may lead to uncertainty and liquidity issues for both borrowers and investors. We may access the capital markets to supplement our existing funds and cash generated from operations in satisfying our needs for working capital; capital expenditure and debt service requirements; our plans to pay dividends and repurchase stock; and other business initiatives we plan to strategically pursue, including acquisitions and licensing activities. In the event of adverse capital and credit market conditions, we may not be able to obtain capital market financing on similar favorable terms, or at all, which could have a material adverse effect on our business and results of operations. Changes in credit ratings issued by nationally recognized credit rating agencies could adversely affect our cost of financing and have an adverse effect on the market price of our securities.

Guidelines and recommendations published by various organizations can reduce the use of our products.

Government agencies promulgate regulations and guidelines directly applicable to us and to our products. However, professional societies, HTA organizations, practice management groups, insurance carriers, physicians, private health/science foundations and organizations involved in various diseases from time to time may also publish guidelines or recommendations to healthcare providers, administrators and payers, and patient communities. Recommendations by government agencies or those other groups/organizations may relate to such matters as usage, dosage, route of administration and use of related therapies as well as reimbursement of our products by government and private payers. Recommendations or guidelines that are followed by patients,

 

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healthcare providers and payers could result in decreased use and/or dosage of our products. Some examples of agency and organizational guidelines include:

 

   

In August 2007, the National Kidney Foundation (NKF) distributed to the nephrology community final updated Kidney Disease Outcomes Quality Initiative (KDOQI) clinical practice guidelines and clinical practice recommendations for anemia in CKD. The NKF-KDOQI™ Anemia Work Group recommended in its 2007 Update to the NKF-KDOQI™ Anemia Management Guidelines that physicians target Hb in the range of 11 g/dL to 12 g/dL, and also stipulated that the target not be above 13 g/dL.

 

   

In December 2008, the KDIGO, a not-for-profit foundation managed by NKF, announced that it was developing a new global anemia guideline. The announcement stated that an updated anemia guideline is necessary in light of new study results, particularly the data from the TREAT trial, which had become available since the NKF-KDOQI™’s clinical practice guidelines and clinical practice recommendations for anemia in CKD were released. On September 30, 2011, the KDIGO released its draft global anemia clinical practice guidelines for public review and comment. KDIGO has indicated that final guidelines could be available by early 2012.

 

   

In February 2007, following the reported results from our Anemia of Cancer 103 Study, the U.S. Pharmacopoeia Dispensing Information Drug Reference Guides removed Aranesp® in the treatment of anemia of cancer.

In addition, HTA organizations, such as NICE in the UK and the Canadian Agency for Drugs and Technologies in Health, make reimbursement recommendations to payers in their jurisdictions based on the clinical effectiveness, cost-effectiveness and service impact of new, emerging and existing medicines and treatments.

Any recommendations or guidelines that result in decreased use, dosage or reimbursement of our products could materially and adversely affect our product sales, business and operating results. In addition, the perception by the investment community or stockholders that such recommendations or guidelines will result in decreased use and dosage of our products could adversely affect the market price for our common stock.

The commercialization of certain of our product candidates and the marketing of certain of our products is dependent in part on our partners.

We have entered into agreements with third parties to assist in the commercialization of certain of our product candidates and the marketing of certain of our products in specified geographic areas. (See Item 1. Business — Business Relationships.) Many of these agreements involve the sharing of certain decisions and a division of responsibilities, costs and benefits. If our partners fail to effectively deliver on their marketing and commercialization commitments to us or if we and our partners fail to coordinate our efforts effectively, sales of our products may be materially and adversely affected.

Our corporate compliance and risk mitigation programs cannot guarantee that we are in compliance with all potentially applicable U.S. federal and state regulations and all potentially applicable foreign regulations and/or that we effectively manage all operational risks.

The development, manufacturing, distribution, pricing, sales, marketing and reimbursement of our products, together with our general operations, are subject to extensive federal and state regulation in the United States and to extensive regulation in foreign countries. (See Our current products and products in development cannot be sold if we do not maintain or gain regulatory approval and manufacturing difficulties, disruptions or delays could limit supply of our products and limit our product sales.) While we have developed and instituted a corporate compliance program, we cannot guarantee that we, our employees, our consultants or our contractors are or will be in compliance with all potentially applicable U.S. federal and state regulations and/or laws or all potentially applicable foreign regulations and/or laws. If we or our agents fail to comply with any of those regulations and/or laws, a range of actions could result, including, but not limited to, the termination of clinical trials, the failure to approve a product candidate, restrictions on our products or manufacturing processes, withdrawal of our products from the market, significant fines, exclusion from government healthcare programs or other sanctions or litigation. Additionally, while we have implemented numerous risk mitigation measures, we cannot guarantee

 

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that we will be able to effectively mitigate all operational risks. If we fail to effectively mitigate all operational risks, our product supply may be negatively impacted, which could have a material and adverse effect on our product sales, business and results of operations.

Cost savings initiatives may result in the carrying value of certain existing manufacturing facilities or other assets becoming impaired or other related charges being incurred.

Our business continues to face many challenges. In response to these challenges, we have worked and continue to work to improve cost efficiencies and to reduce discretionary expenditures. As part of those efforts, we undertake cost savings initiatives to evaluate our processes and procedures in order to identify opportunities for achieving greater efficiencies in how we conduct our business. In particular, we evaluate our manufacturing operations to identify opportunities to increase production yields and/or success rates as well as capacity utilization. Depending on the timing and outcomes of these cost savings initiatives, the carrying value of certain manufacturing or other assets may not be fully recoverable and could result in the recognition of impairment and/or other related charges. The recognition of such charges, if any, could have a material adverse effect on our results of operations.

The adoption of new tax legislation or exposure to additional tax liabilities could affect our profitability.

We are subject to income and other taxes in the United States and other jurisdictions in which we do business. Our provision for income taxes and results of operations in the future could be adversely affected by changes to our operating structure, changes in the mix of earnings in countries with differing tax rates, changes in the valuation of deferred tax assets and liabilities, and changes in applicable tax laws, regulations or administrative interpretations thereof. For example, there are several proposals under consideration in the United States to reform tax law, including proposals that may reduce or eliminate the deferral of U.S. income tax on our unrepatriated foreign earnings. While it is uncertain how the U.S. Congress may address U.S. tax policy matters in the future, reform of U.S. taxation, including taxation of international income, continues to be a topic of discussion for the U.S. Congress and the Administration. A significant change to the U.S. tax system, such as a change to the taxation of international income, could have a material and adverse effect on our business and results of operations.

There can be no assurance that we will continue to declare cash dividends or repurchase stock.

On April 20, 2011, our Board of Directors adopted a dividend policy pursuant to which the Company would pay quarterly dividends on our common stock, and increased the total authorization for repurchases of our common stock to approximately $7.2 billion. On October 13, 2011, our Board of Directors increased the total authorization for repurchases of our common stock by approximately $6.1 billion to $10 billion, and in December 2011 we repurchased approximately $5 billion of our common stock in a modified Dutch auction tender offer, leaving approximately $5 billion remaining for future repurchases under our Board authorization. Whether we continue and the amount and timing of such dividends and/or stock repurchases are subject to capital availability and periodic determinations by our Board of Directors that cash dividends and/or stock repurchases are in the best interest of our stockholders and are in compliance with all respective laws and agreements of the Company applicable to the declaration and payment of cash dividends and the repurchase of stock. Future dividends and stock repurchases, including their timing and amount, may be affected by, among other factors: our views on potential future capital requirements for strategic transactions, including acquisitions; debt service requirements; our credit rating; changes to applicable tax laws or corporate laws; and changes to our business model. In addition, the amount we spend and the number of shares we are able to repurchase under our stock repurchase program may further be affected by a number of other factors, including the stock price and blackout periods in which we are restricted from repurchasing shares. Our dividend payments and/or stock repurchases may change from time to time, and we cannot provide assurance that we will continue to declare dividends and/or repurchase stock in any particular amounts or at all. A reduction in or elimination of our dividend payments and/or stock repurchases could have a negative effect on our stock price.

 

Item 1B. UNRESOLVED STAFF COMMENTS

None.

 

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Item 2. PROPERTIES

The following table summarizes our significant properties and their primary functions as of December 31, 2011. For additional information regarding manufacturing initiatives, see Item 1. Business  —  Manufacturing, Distribution and Raw Materials.

 

LOGO

 

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Our corporate headquarters are located in Thousand Oaks, California. In addition to the properties listed above, we have undeveloped land at certain U.S. locations, principally in Thousand Oaks, California; Longmont, Colorado; Louisville, Kentucky; Allentown, Pennsylvania; West Greenwich, Rhode Island; Seattle and Bothell, Washington; and in Juncos, Puerto Rico, to accommodate future expansion, as required. Excluded from the table above are leased properties that have been abandoned and certain buildings that we still own but are no longer used in our business. There are no material encumbrances on our properties.

We believe our facilities are suitable for their intended use and, in conjunction with our third-party contracting manufacturing agreements, provide adequate capacity. We also believe that our existing facilities, third-party contract manufacturing agreements and our anticipated additions are sufficient to meet our expected needs. (See Item 1A. Risk Factors — We perform a substantial amount of our commercial manufacturing activities at our Puerto Rico manufacturing facility and a substantial amount of our clinical manufacturing activities at our Thousand Oaks, California manufacturing facility; if significant natural disasters or production failures occur at the Puerto Rico facility, we may not be able to supply these products or, at the Thousand Oaks facility, we may not be able to continue our clinical trials, — We rely on third-party suppliers for certain of our raw materials, medical devices and components and — Manufacturing difficulties, disruptions or delays could limit supply of our products and limit our product sales.)

Item 3.     LEGAL PROCEEDINGS

Certain of the legal proceedings in which we are involved are discussed in Note 18, Contingencies and commitments, to our Consolidated Financial Statements in this Annual Report on Form 10-K, and are hereby incorporated by reference.

Item 4.     MINE SAFETY DISCLOSURES

Not applicable.

 

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PART II

 

Item 5. MARKET FOR REGISTRANT’S COMMON EQUITY, RELATED STOCKHOLDER MATTERS AND ISSUER PURCHASES OF EQUITY SECURITIES

Common stock

Our common stock trades on The NASDAQ Global Select Market under the symbol AMGN. As of February 10, 2012, there were approximately 9,153 holders of record of our common stock.

The following table sets forth, for the periods indicated, the range of high and low quarterly closing sales prices of the common stock as quoted on The NASDAQ Global Select Market:

 

Year ended December 31, 2011

   High      Low  

Fourth quarter

   $   64.74       $   53.90   

Third quarter

     58.28         48.27   

Second quarter

     61.17         53.08   

First quarter

     57.31         50.95   

Year ended December 31, 2010

             

Fourth quarter

   $ 57.96       $ 52.69   

Third quarter

     56.32         50.93   

Second quarter

     61.14         50.36   

First quarter

     60.09         55.71   

 

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Performance graph

The following graph shows the value of an investment of $100 on December 31, 2006, in each of Amgen common stock, the Amex Biotech Index, the Amex Pharmaceutical Index and Standard & Poor’s 500 Index (S&P 500). All values assume reinvestment of the pretax value of dividends paid by companies included in these indices and are calculated as of December 31 of each year. The historical stock price performance of the Company’s common stock shown in the performance graph is not necessarily indicative of future stock price performance.

Amgen vs. Amex Biotech, Amex Pharmaceutical and S&P 500 Indices

Comparison of Five-Year Cumulative Total Return

Value of Investment of $100 on December 31, 2006

 

LOGO

 

     12/31/2006      12/31/2007      12/31/2008      12/31/2009      12/31/2010      12/31/2011  

Amgen (AMGN)

   $   100.00       $ 67.98       $   84.54       $ 82.81       $ 80.37       $ 94.98   

Amex Biotech (BTK)

     100.00           104.28         85.80           124.91           172.04           144.79   

Amex Pharmaceutical (DRG)

     100.00         101.01         84.76         99.15         101.64         114.77   

S&P 500 (SPX)

     100.00         105.48         66.93         84.28         96.78         98.81   

The material in this performance graph is not soliciting material, is not deemed filed with the SEC, and is not incorporated by reference in any filing of the Company under the Securities Act or the Exchange Act, whether made on, before or after the date of this filing and irrespective of any general incorporation language in such filing.

Stock repurchase program

The Company intends to continue to return capital to stockholders through share repurchases, reflecting our confidence in the long-term value of the Company. The amount we spend, the number of shares repurchased and the timing of such repurchases will vary based on a number of factors, including the stock price, the availability of financing on acceptable terms, the amount and timing of dividend payments and blackout periods in which we are restricted from repurchasing shares; and the manner of purchases may include private block purchases, tender offers, as well as market transactions.

 

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During the three months and year ended December 31, 2011, we had one outstanding stock repurchase program. Our repurchase activity for the three months and year ended December 31, 2011, was as follows:

 

     Total
number of
shares
purchased
     Average
price  paid
per share(1)
     Total number
of  shares
purchased as
part of
publicly
announced
program
     Maximum $
value that may
yet be purchased
under the
program(2)
 

October 1 - October 31

     2,728,703       $ 53.99         2,728,703       $ 10,000,000,000   

November 1 - November 30

      —           —           —          10,000,000,000   

December 1 - December 31

     83,333,333         60.08         83,333,333         4,993,072,585   
  

 

 

       

 

 

    
     86,062,036         59.89         86,062,036      
  

 

 

       

 

 

    

January 1 - December 31

     144,331,565       $ 57.55         144,331,565      
  

 

 

       

 

 

    

 

(1) 

Average price paid per share includes related expenses.

 

(2) 

Following the repurchase of $147 million in additional shares in early October 2011, on October 13, 2011, our Board of Directors increased the authorization for repurchase of our common stock by $6.1 billion to an aggregate of $10 billion.

Dividends

We began paying quarterly cash dividends in 2011. On July 28 and October 13, 2011, the Board of Directors declared quarterly cash dividends of $0.28 per share of common stock, which were paid on September 8 and December 8, 2011, respectively. Additionally, on December 15, 2011, the Board of Directors declared a quarterly cash dividend of $0.36 per share of common stock, which will be paid on March 7, 2012, to all stockholders of record as of the close of business on February 15, 2012. We expect to continue to pay quarterly dividends, although the amount and timing of any future dividends are subject to approval by our Board of Directors.

 

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Item 6. SELECTED FINANCIAL DATA

 

     Years ended December 31,  

Consolidated Statement of Income Data:

   2011      2010      2009      2008      2007  
     (In millions, except per share data)  

Revenues:

              

Product sales

   $ 15,295       $ 14,660       $ 14,351       $ 14,687       $ 14,311   

Other revenues

     287         393         291         316         460   
  

 

 

    

 

 

    

 

 

    

 

 

    

 

 

 

Total revenues

     15,582         15,053         14,642         15,003         14,771   

Operating expenses(1):

              

Cost of sales (excludes amortization of certain acquired intangible assets presented separately)

     2,427         2,220         2,091         2,296         2,548   

Research and development

     3,167         2,894         2,864         3,030         3,266   

Selling, general and administrative

     4,486         3,983         3,820         3,789         3,361   

Amortization of certain acquired intangible assets

     294         294         294         294         298   

Write-off of acquired in-process research and development(2)

       —             —             —             —           590   

Other(3)

     896         117         67         380         728   

Net income(4)

     3,683         4,627         4,605         4,052         3,078   

Diluted earnings per share(4)

     4.04         4.79         4.51         3.77         2.74   

Dividends paid per share

     0.56           —             —             —             —     
     As of December 31,  

Consolidated Balance Sheet Data:

   2011      2010      2009      2008      2007  
     (In millions)  

Total assets

   $ 48,871       $ 43,486       $ 39,629       $ 36,427       $ 34,618   

Total debt(4)(5)(6)

     21,428         13,362         10,601         9,352         10,114   

Total stockholders’ equity(4)(6)

     19,029         23,944         22,667         20,885         18,512   

 

In addition to the following notes, see Item 7. Management’s Discussion and Analysis of Financial Condition and Results of Operations and the consolidated financial statements and accompanying notes and previously filed Annual Reports on Form 10-K for further information regarding our consolidated results of operations and financial position for periods reported therein and for known factors that will impact comparability of future results. Also, see Item 5. Market for Registrant’s Common Equity, Related Stockholder Matters and Issuer Purchases of Equity Securities for information regarding cash dividends declared per common share.

 

(1) 

On August 15, 2007, we announced a plan to restructure our worldwide operations in order to improve our cost structure. Under this plan in 2009, 2008 and 2007, we incurred restructuring charges of $70 million ($44 million, net of tax), $148 million ($111 million, net of tax) and $739 million ($576 million, net of tax), respectively, related primarily to staff separation costs, asset impairment charges, accelerated depreciation (primarily in 2007) and loss accruals for leases on certain facilities that will not be used in our business.

 

(2) 

As part of the accounting for the business combinations of Alantos Pharmaceutical Holding, Inc. and Ilypsa, Inc. in 2007, under the then existing accounting rules we recorded charges to write-off acquired in-process R&D (IPR&D) of $270 million and $320 million, respectively. The charges represent the estimated fair values of the IPR&D that, as of the respective acquisition dates, had not reached technological feasibility and had no alternative future use.

 

(3) 

In 2011, we recorded a $780 million legal settlement charge ($705 million, net of tax) in connection with an agreement in principle to settle allegations relating to our sales and marketing practices. In 2008, we recorded loss accruals for settlements of certain commercial legal proceedings aggregating $288 million, related principally to the settlement of the Ortho Biotech Products L.P. (Ortho Biotech) antitrust suit.

 

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(4) 

Effective January 1, 2009, we adopted a new accounting standard that changed the method of accounting for convertible debt that may be partially or wholly settled in cash. As required by this standard, we retrospectively applied this change in accounting to all prior periods for which we had applicable outstanding convertible debt. Under this method of accounting, the debt and equity components of our convertible notes are bifurcated and accounted for separately. The equity components of our convertible notes are included in Common stock and additional paid-in capital in the Consolidated Balance Sheets, with a corresponding reduction in the carrying values of these convertible notes as of the date of issuance or modification, as applicable. The reduced carrying values of our convertible notes are being accreted back to their principal amounts through the recognition of non-cash interest expense. This results in recognizing interest expense on these borrowings at effective rates approximating what we would have incurred had we issued nonconvertible debt with otherwise similar terms. Included in net income for 2011, 2010, 2009, 2008 and 2007 is the incremental non-cash interest expense of $143 million ($91 million, net of tax), $266 million ($168 million, net of tax), $250 million ($155 million, net of tax), $235 million ($144 million, net of tax) and $168 million ($88 million, net of tax), respectively, related to the adoption of the new accounting standard.

 

(5) 

See Note 14, Financing arrangements, to the Consolidated Financial Statements for discussion of our financing arrangements. In addition, in 2008 and 2007 we issued $1.0 billion and $4.0 billion, respectively, aggregate principal amount of notes. In 2008, we repaid our $2.0 billion of floating rate notes. In 2007, as a result of holders of substantially all of our outstanding zero-coupon 2032 Modified Convertible Notes exercising their put option, we repurchased the majority of the then outstanding convertible notes, at their then-accreted value of $1.7 billion.

 

(6) 

Throughout the five years ended December 31, 2011, we had a share repurchase program authorized by the Board of Directors through which we repurchased $8.3 billion, $3.8 billion, $3.2 billion, $2.3 billion and $5.1 billion, respectively, of Amgen common stock.

 

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Item 7. MANAGEMENT’S DISCUSSION AND ANALYSIS OF FINANCIAL CONDITION AND RESULTS OF OPERATIONS

Forward-looking statements

This report and other documents we file with the SEC contain forward-looking statements that are based on current expectations, estimates, forecasts and projections about us, our future performance, our business or others on our behalf, our beliefs and our management’s assumptions. In addition, we, or others on our behalf, may make forward-looking statements in press releases or written statements, or in our communications and discussions with investors and analysts in the normal course of business through meetings, webcasts, phone calls and conference calls. Such words as “expect,” “anticipate,” “outlook,” “could,” “target,” “project,” “intend,” “plan,” “believe,” “seek,” “estimate,” “should,” “may,” “assume” and “continue,” as well as variations of such words and similar expressions are intended to identify such forward-looking statements. These statements are not guarantees of future performance and involve certain risks, uncertainties and assumptions that are difficult to predict. We describe our respective risks, uncertainties and assumptions that could affect the outcome or results of operations in Item 1A. Risk Factors. We have based our forward-looking statements on our management’s beliefs and assumptions based on information available to our management at the time the statements are made. We caution you that actual outcomes and results may differ materially from what is expressed, implied or forecast by our forward-looking statements. Reference is made in particular to forward-looking statements regarding product sales, regulatory activities, clinical trial results, reimbursement, expenses, earnings per share (EPS), liquidity and capital resources, trends and planned dividends and stock repurchases. Except as required under the federal securities laws and the rules and regulations of the SEC, we do not have any intention or obligation to update publicly any forward-looking statements after the distribution of this report, whether as a result of new information, future events, changes in assumptions or otherwise.

Overview

The following management’s discussion and analysis (MD&A) is intended to assist the reader in understanding Amgen’s business. MD&A is provided as a supplement to, and should be read in conjunction with, our consolidated financial statements and accompanying notes. Our results of operations discussed in MD&A are presented in conformity with accounting principles generally accepted in the United States (GAAP).

We are the world’s largest independent biotechnology medicines company. We discover, develop, manufacture and market medicines for grievous illnesses. We concentrate on innovative novel medicines based on advances in cellular and molecular biology. Our mission is to serve patients. We operate in one business segment   —   human therapeutics. Therefore, our results of operations are discussed on a consolidated basis.

We earn revenues and income and generate cash primarily from sales of human therapeutic products in the areas of supportive cancer care, inflammation and nephrology. Our principal products include Neulasta®, NEUPOGEN®, ENBREL, Aranesp® and EPOGEN®. For additional information about our products, their approved indications and where they are marketed, see Item 1. Business  —  Marketed Products.

In 2011, we had several notable accomplishments, including achieving record U.S. and international product sales of $11.7 billion and $3.6 billion, respectively. We also paid our first ever dividends, aggregating $500 million paid in 2011. In December 2011, we declared a quarterly dividend of $0.36 per share of common stock payable in March 2012, representing a 29% increase over prior quarters. Additionally, in 2011, we repurchased approximately 15% of our stock outstanding as of December 31, 2010, for a total cost of $8.3 billion. Of this amount, $5 billion was purchased in a modified Dutch auction tender offer following an increase in our authorized stock repurchase program to $10 billion and our announcement that we intended to accelerate our repurchases, reflecting our confidence in the long-term value of the Company and the attractive interest rate environment. We issued $7.5 billion of debt, in part to fund the purchase of stock related to the tender offer. We expect to repurchase the remaining $5 billion of stock under our authorized stock repurchase program through open-market purchases.

We enter 2012 with various opportunities to continue growing our business. We believe the currently approved indications for XGEVA® and Prolia® represent significant commercial opportunities. In addition, receiving regulatory and/or reimbursement approvals in new geographic territories or for additional indications

 

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for these products may provide further opportunities for growth. Longer-term growth may also be achieved by expansion into emerging markets and Japan, by the successful development of our later stage pipeline and through strategic business development opportunities, such as our acquisitions of BioVex, Bergamo and our recently announced agreement to acquire Micromet. Our continued focus on increasing cost efficiencies, along with the significant savings that we will realize upon the expiration of our ENBREL co-promotion agreement with Pfizer in the fourth quarter of 2013, may assist in providing the necessary resources to fund many of these future opportunities.

Our business will, however, continue to face various challenges. Certain of our products will continue to face increasing competitive pressure, including in Europe as a result of biosimilars. In the United States, ENBREL will also continue to face increasing competition and our ESAs may begin facing competition in the near term. Additionally, over the next several years, many of the existing patents on our principal products will expire and, as a result, we expect to face increasing competition from biosimilars. We also believe our products and product candidates will continue to face regulatory and reimbursement challenges. In addition, the current global economic conditions continue to pose challenges to our business, including increased pressure to reduce healthcare expenditures.

Certain of the above challenges may have a material adverse impact on our sales, results of operations and liquidity. However, these effects may be offset by certain of the opportunities we have to grow our business, as discussed above.

Selected financial information

The following provides an overview of our results of operations as well as our financial condition (amounts in millions, except percentages and per-share data):

 

     2011          Change          2010  

Product sales:

        

U.S.

   $ 11,725         4 %       $ 11,254   

International

     3,570         5 %         3,406   
  

 

 

       

 

 

 

Total product sales

     15,295         4 %         14,660   

Other revenues

     287         (27)%         393   
  

 

 

       

 

 

 

Total revenues

   $ 15,582         4 %       $ 15,053   
  

 

 

       

 

 

 

Operating expenses

   $ 11,270         19 %       $ 9,508   

Operating income

   $ 4,312         (22)%       $ 5,545   

Net income

   $ 3,683         (20)%       $ 4,627   

Diluted EPS

   $ 4.04         (16)%       $ 4.79   

Diluted shares

     912         (5)%         965   

When discussing changes in product sales below, any reference to unit growth or decline refers to changes in the purchases of our products by healthcare providers, such as physicians or their clinics, dialysis centers, hospitals and pharmacies.

The increase in U.S. product sales for 2011 reflects overall growth for all marketed products except ESAs, which declined 17%. Excluding sales of ESAs, U.S. product sales increased 14%, driven primarily by unit growth and, to a lesser extent, increases in average net sales prices. International product sales for 2011 were negatively impacted by a decline in sales of Aranesp® of 5%. Excluding Aranesp® sales, international product sales grew 11%.

The decrease in other revenues for 2011 was due principally to certain milestone payments earned in 2010.

The increase in operating expenses for 2011 was driven primarily by a legal settlement charge and higher SG&A expenses.

The decrease in diluted EPS for 2011 was due to the reduction in net income, attributable primarily to lower operating income. This decrease in diluted EPS was offset partially by the favorable impact of our stock repurchase program, which reduced the number of shares used to compute diluted EPS.

 

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Although changes in foreign currency exchange rates result in increases or decreases in our reported international product sales, the benefit or detriment that such movements have on our international product sales is offset partially by corresponding increases or decreases in our international operating expenses and our related foreign currency hedging activities. Our hedging activities seek to offset the impacts, both positive and negative, that foreign currency exchange rate changes may have on our net income by hedging our net foreign currency exposure, primarily with respect to product sales denominated in the euro.

Our results of operations for 2011 were impacted by the Puerto Rico excise tax. Commencing January 1, 2011, Puerto Rico imposes a temporary excise tax on the acquisition of goods and services from a related manufacturer in Puerto Rico. This tax is currently scheduled to expire in 2016. We account for the excise tax as a manufacturing cost that is capitalized in inventory and expensed in cost of sales when the related products are sold. For U.S. income tax purposes, the excise tax results in foreign tax credits that are generally recognized in our provision for income taxes in the year in which the excise tax is incurred. This excise tax has had and will continue to have a significant adverse impact on our cost of sales and a significant favorable impact on our provision for income taxes. In addition, the overall impact of the excise tax will vary from period to period as a result of the timing difference between recognizing the expense and the applicable foreign tax credit. As a result of the excise tax, for 2011 cost of sales increased by $211 million, the provision for income taxes was reduced by $321 million and EPS was favorably impacted by $0.12.

As of December 31, 2011, our cash, cash equivalents and marketable securities totaled $20.6 billion, and total debt outstanding was $21.4 billion. Of our total cash, cash equivalents and marketable securities balance as of December 31, 2011, approximately $16.9 billion was generated from operations in foreign tax jurisdictions and is intended to be invested indefinitely outside of the United States. Under current tax laws, if these funds were repatriated for use in our U.S. operations, we would be required to pay additional income taxes at the tax rates then in effect.

Results of Operations

Product sales

Worldwide product sales were as follows (dollar amounts in millions):

 

     2011      Change      2010      Change      2009  

Neulasta®/NEUPOGEN ®

   $ 5,212         8 %       $ 4,844         4 %       $ 4,643   

ENBREL

     3,701         5 %         3,534         1 %         3,493   

Aranesp®

     2,303         (7)%         2,486         (6)%         2,652   

EPOGEN®

     2,040         (19)%         2,524         (2)%         2,569   

Other products

     2,039         60 %         1,272         28 %         994   
  

 

 

       

 

 

       

 

 

 

Total product sales

   $ 15,295         4 %       $ 14,660         2 %       $ 14,351   
  

 

 

       

 

 

       

 

 

 

Total U.S.

   $ 11,725         4 %       $ 11,254         1 %       $ 11,135   

Total International

     3,570         5 %         3,406         6 %         3,216   
  

 

 

       

 

 

       

 

 

 

Total product sales

   $ 15,295         4 %       $ 14,660         2 %       $ 14,351   
  

 

 

       

 

 

       

 

 

 

Product sales are influenced by a number of factors, some of which may impact the sales of certain of our existing products more significantly than others, including, but not necessarily limited to:

 

   

our contracting and pricing strategies;

 

   

recent and future reimbursement changes resulting from:

 

  ¡    

governmental or private organization regulations or guidelines relating to the use of our products;

 

  ¡    

legislative reform in federal, state and foreign jurisdictions;

 

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  ¡    

cost containment pressures; and

 

  ¡    

the mix of reimbursement from governmental and private payers;

 

   

clinical trial outcomes, including adverse events or results from clinical trials, including sub-analyses, studies or meta-analyses performed by us or by others (including our licensees or independent investigators), which could impact product safety labeling and may negatively impact healthcare provider prescribing behavior, use of our products, regulatory or private healthcare organization medical guidelines and reimbursement practices;

 

   

competitive products, including biosimilars;

 

   

physician and patient compliance with product dosing regimens;

 

   

changes in clinical practice, including those resulting from the development of new protocols, tests and/or treatments;

 

   

adoption of and adherence to risk management activities, such as a REMS, undertaken by us or required by the FDA or other regulatory authorities;

 

   

product label changes;

 

   

patient population growth;

 

   

segment growth and penetration;

 

   

new product launches and indications;

 

   

expansion into new international markets;

 

   

patent expirations and our ability to obtain and defend our patent and other intellectual property rights;

 

   

fluctuations in foreign currency exchange rates;

 

   

adequacy of product supply and distribution;

 

   

effectiveness of our marketing efforts, including those conducted under collaboration agreements;

 

   

concentration of customer purchasing power; and

 

   

acquisitions and divestures.

Our U.S. product sales are also subject to certain other influences throughout the year, including wholesaler and end-user buying patterns (e.g., holiday-driven wholesaler and end-user stocking, contract-driven buying and patients purchasing products later in the year after satisfying their annual insurance deductibles). Such factors can result in higher demand for our products and/or higher wholesaler inventory levels and, therefore, higher product sales for a given three-month period, generally followed by a reduction in demand and/or a drawdown in wholesaler inventories and a corresponding decline in product sales in the subsequent three-month period. For example, sales of certain of our products in the United States for the three months ended March 31 have been slightly lower relative to the immediately preceding three-month period, which we believe to be due, in part, to certain of these factors. While this can result in variability in quarterly product sales on a sequential basis, these effects have generally not been significant when comparing product sales in the three months ended March 31 with product sales in the corresponding period of the prior year.

In addition, general economic conditions may affect, or in some cases amplify, certain of these factors with a corresponding impact on our product sales.

See Item 1. Business  —  Marketed Products for a discussion of our principal products and their approved indications.

 

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Neulasta®/NEUPOGEN®

Total Neulasta®/NEUPOGEN® sales by geographic region were as follows (dollar amounts in millions):

 

     2011      Change      2010      Change      2009  

Neulasta®  —  U.S.

   $ 3,006         13 %       $ 2,654         5 %       $ 2,527   

NEUPOGEN® — U.S.

     959         3 %         932         3 %         901   
  

 

 

       

 

 

       

 

 

 

Total U.S. Neulasta®/NEUPOGEN®

     3,965         11 %         3,586         5 %         3,428   
  

 

 

       

 

 

       

 

 

 

Neulasta® — International

     946         5 %         904         9 %         828   

NEUPOGEN® — International

     301         (15)%         354         (9)%         387   
  

 

 

       

 

 

       

 

 

 

Total International Neulasta®/NEUPOGEN®

     1,247         (1)%         1,258         4 %         1,215   
  

 

 

       

 

 

       

 

 

 

Total Neulasta®/NEUPOGEN®

   $ 5,212         8 %       $ 4,844         4 %       $ 4,643   
  

 

 

       

 

 

       

 

 

 

The increase in U.S. sales of Neulasta®/NEUPOGEN® for 2011 was driven principally by an increase in the average net sales price and Neulasta® unit growth. The decrease in Neulasta®/NEUPOGEN® international sales was driven by a decline in NEUPOGEN® sales due, in part, to biosimilar competition, offset partially by an increase in Neulasta® sales due, in part, to continued conversion from NEUPOGEN®.

The increase in U.S. sales of Neulasta®/NEUPOGEN® for 2010 was driven principally by an increase in the average net sales price and, to a lesser extent, favorable changes in wholesaler inventories. The increase in international Neulasta®/NEUPOGEN® sales for 2010 reflects primarily growth in Neulasta®, principally from the continued conversion from NEUPOGEN®, offset partially by a decline in NEUPOGEN® sales due, in part, to biosimilar competition.

In addition to other factors mentioned in the Product sales section above, future Neulasta®/NEUPOGEN® sales will depend, in part, on the development of new protocols, tests and/or treatments for cancer and/or new chemotherapy treatments or alternatives to chemotherapy that may have reduced and may continue to reduce the use of chemotherapy in some patients.

See Item 1. Business — Marketed Products and Item 1A. Risk Factors for further discussion of certain of the above factors that could impact our future product sales.

ENBREL

Total ENBREL sales by geographic region were as follows (dollar amounts in millions):

 

     2011      Change      2010      Change      2009  

ENBREL — U.S.

   $ 3,458         5 %       $ 3,304         1 %       $ 3,283   

ENBREL — Canada

     243         6 %         230         10 %         210   
  

 

 

       

 

 

       

 

 

 

Total ENBREL

   $ 3,701         5 %       $ 3,534         1 %       $ 3,493   
  

 

 

       

 

 

       

 

 

 

The increase in ENBREL sales for 2011 reflects primarily an increase in the average net sales price.

The increase in ENBREL sales for 2010 reflects an increase in the average net sales price, offset partially by a low single-digit percentage point unit decline, resulting primarily from share declines in dermatology.

ENBREL continues to maintain a leading position in both the rheumatology and dermatology segments.

See Item 1. Business — Marketed Products and Item 1A. Risk Factors for further discussion of certain of the above factors that could impact our future product sales.

 

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Aranesp®

Total Aranesp® sales by geographic region were as follows (dollar amounts in millions):

 

     2011      Change      2010      Change      2009  

Aranesp® — U.S.

   $ 986         (11)%       $ 1,103         (12)%       $ 1,251   

Aranesp® — International

     1,317         (5)%         1,383         (1)%         1,401   
  

 

 

       

 

 

       

 

 

 

Total Aranesp®

   $ 2,303         (7)%       $ 2,486         (6)%       $ 2,652   
  

 

 

       

 

 

       

 

 

 

The decrease in U.S. Aranesp® sales for 2011 was due principally to a high-teens percentage point unit decline, offset partially by an increase in the average net sales price. The unit decline reflects segment contraction resulting from changes to reimbursement in 2011 and the June 2011 ESA label changes. The decrease in international Aranesp® sales for 2011 was due to a decrease in the average net sales price and a unit decline, reflecting segment contraction.

The decrease in U.S. Aranesp® sales for 2010 was due primarily to a unit decline, reflecting segment contraction. The decrease in international Aranesp® sales for 2010 was due primarily to a unit decline.

In addition to other factors mentioned in the Product sales section above, future Aranesp® sales will depend, in part, on such factors as:

 

   

regulatory developments, including the June 2011 ESA label changes and any other product label changes;

 

   

reimbursement developments, including LCDs;

 

   

changes in dose utilization as healthcare providers continue to refine their treatment practices in accordance with approved labeling; and

 

   

development of new protocols, tests and/or treatments for cancer and/or new chemotherapy treatments or alternatives to chemotherapy that may have reduced and may continue to reduce the use of chemotherapy in some patients.

Certain of the above factors may have a material adverse impact on future sales of Aranesp®.

See Item 1. Business — Significant Developments, Item 1. Business — Marketed Products and Item 1A. Risk Factors for further discussion of certain of the above factors that could impact our future product sales.

EPOGEN®

Total EPOGEN® sales were as follows (dollar amounts in millions):

 

     2011      Change      2010      Change      2009  

EPOGEN® — U.S.

   $ 2,040         (19)%       $ 2,524         (2)%       $ 2,569   
  

 

 

       

 

 

       

 

 

 

The decrease in EPOGEN® sales for 2011 was due primarily to a decrease in dose utilization related to changes to reimbursement in 2011 and the June 2011 ESA label changes, offset partially by an increase in the average net sales price and patient population growth.

The decrease in EPOGEN® sales for 2010 was due primarily to a unit decline and certain changes in accounting estimates. The unit decline reflects a decrease in dose utilization, offset partially by patient population growth.

In addition to other factors mentioned in the Product sales section above, future EPOGEN® sales will depend, in part, on such factors as:

 

   

potential peginesatide launch;

 

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reimbursement developments, including those resulting from:

 

  ¡    

CMS’s 2011 Final Rule on Bundling in Dialysis; and

 

  ¡    

other CMS activities, including recent changes related to the QIP;

 

   

regulatory developments, including the June 2011 ESA label changes and any other product label changes;

 

   

changes in dose utilization as healthcare providers continue to refine their treatment practices in accordance with approved labeling;

 

   

new contracts with dialysis centers; and

 

   

adoption of alternative therapies or development of new modalities to treat anemia associated with CRF.

Certain of the above factors may have a material adverse impact on future sales of EPOGEN®.

See Item 1. Business — Significant Developments, Item 1. Business — Marketed Products and Item 1A. Risk Factors for further discussion of certain of the above factors that could impact our future product sales.

Other products

Other product sales by geographic region were as follows (dollar amounts in millions):

 

     2011      Change      2010      Change      2009  

Sensipar®/Mimpara ® — U.S.

   $ 518         13 %       $ 459         7 %       $ 429   

Sensipar®/Mimpara ® — International

     290         14 %         255         15 %         222   

Vectibix® — U.S.

     122         6 %         115         19 %         97   

Vectibix® — International

     200         16 %         173         27 %         136   

Nplate® — U.S.

     163         26 %         129         65 %         78   

Nplate® — International

     134         34 %         100          —           32   

Prolia® — U.S.

     130          —           26          —            —    

Prolia® — International

     73          —           7          —            —    

XGEVA® — U.S.

     343          —           8          —            —    

XGEVA® — International

     8          —            —           —            —    

Other — International

     58          —            —           —            —    
  

 

 

       

 

 

       

 

 

 

Total other product sales

   $ 2,039         60 %       $ 1,272         28 %       $ 994   
  

 

 

       

 

 

       

 

 

 

Total U.S.  —  other products

   $ 1,276         73 %       $ 737         22 %       $ 604   

Total International  —  other products

     763         43 %         535         37 %         390   
  

 

 

       

 

 

       

 

 

 

Total other product sales

   $ 2,039         60 %       $ 1,272         28 %       $ 994   
  

 

 

       

 

 

       

 

 

 

See Item 1. Business — Significant Developments, Item 1. Business — Marketed Products and Item 1A. Risk Factors for further discussion of certain of the above factors that could impact our future product sales.

 

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Operating expenses

Operating expenses were as follows (dollar amounts in millions):

 

     2011      Change      2010      Change      2009  

Operating expenses:

              

Cost of sales (excludes amortization of certain acquired intangible assets presented separately)

   $ 2,427         9%       $ 2,220         6%       $ 2,091   

        % of product sales

     15.9%            15.1%            14.6%   

Research and development

   $ 3,167         9%       $ 2,894         1%       $ 2,864   

        % of product sales

     20.7%            19.7%            20.0%   

Selling, general and administrative

   $ 4,486         13%       $ 3,983         4%       $ 3,820   

        % of product sales

     29.3%            27.2%            26.6%   

Amortization of certain acquired intangible assets

   $ 294           —       $ 294           —       $ 294   

Other

   $ 896           —       $ 117           —       $ 67   

Cost of sales

Cost of sales, which excludes the amortization of certain acquired intangible assets, increased to 15.9% of product sales for 2011. Excluding the impact of the Puerto Rico excise tax, cost of sales would have been 14.5% of product sales compared with 15.1% for 2010. This decrease was driven by improved productivity, offset partially by certain expenses related to actions to improve cost efficiencies.

Cost of sales increased to 15.1% of product sales for 2010, driven primarily by higher bulk material costs and higher inventory write-offs due to voluntary EPOGEN®, PROCRIT® (epoetin alfa) and ENBREL recalls. These increases were offset partially by lower excess capacity charges and lower royalties, primarily for ENBREL.

Research and development

R&D costs are expensed as incurred and include primarily salaries, benefits and other staff-related costs; facilities and overhead costs; clinical trial and related clinical manufacturing costs; contract services and other outside costs; information systems’ costs and amortization of acquired technology used in R&D with alternative future uses. R&D expenses also include costs and cost recoveries associated with K-A and third-party R&D arrangements, including upfront fees and milestones paid to third parties in connection with technologies which had not reached technological feasibility and did not have an alternative future use. Net payment or reimbursement of R&D costs is recognized when the obligations are incurred or as we become entitled to the cost recovery.

The Company groups all of its R&D activities and related expenditures into three categories: (1) Discovery Research and Translational Sciences, (2) later stage clinical programs and (3) marketed products. These categories include the Company’s R&D activities as set forth in the following table:

 

Category

  

Description

Discovery Research and Translational Sciences

   R&D expenses incurred in activities substantially in support of early research through the completion of phase 1 clinical trials. These activities encompass our discovery research and translational sciences functions, including drug discovery, toxicology, pharmacokinetics and drug metabolism, and process development.

Later stage clinical programs

   R&D expenses incurred in or related to phase 2 and phase 3 clinical programs intended to result in registration of a new product or a new indication for an existing product in the United States or the EU.

Marketed products

   R&D expenses incurred in support of the Company’s marketed products that are authorized to be sold in the United States or the EU. Includes clinical trials designed to gather information on product safety (certain of which may be required by regulatory authorities) and their product characteristics after regulatory approval has been obtained, as well as the costs of obtaining regulatory approval of a product in a new market after approval in either the United States or the EU has been obtained.

 

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R&D expense by category was as follows (in millions):

 

     2011      2010      2009  

Discovery Research and Translational Sciences

   $ 1,125       $ 1,154       $ 1,157   

Later stage clinical programs

     983         832         1,000   

Marketed products

     1,059         908         707   
  

 

 

    

 

 

    

 

 

 

Total R&D expense.

   $ 3,167       $ 2,894       $ 2,864   
  

 

 

    

 

 

    

 

 

 

The increase in R&D expense for 2011 was driven primarily by an increase of $151 million in our marketed product support largely driven by our continued support for Prolia® and XGEVA® which, subsequent to their approvals during 2010, were categorized as marketed products rather than later stage clinical programs; and an increase of $151 million in our later stage clinical program support, including AMG 386, ganitumab (AMG 479), talimogene laherparepvec and AMG 145, offset partially by decreased support for Prolia® and XGEVA® as a result of their aforementioned approvals. These increases were offset partially by a decrease of $29 million in our Discovery Research and Translational Sciences activities, due primarily to reduced amortization expense related to R&D technology intangible assets acquired in business combinations in prior years.

The increase in R&D expense for 2010 was driven primarily by an increase of $201 million in our marketed product support largely driven by our support for Prolia® and XGEVA® which, subsequent to their approvals during 2010, were categorized as marketed products rather than later stage clinical programs and, to a lesser extent, lower cost recoveries from ongoing collaborations. This increase was offset by a reduction of $168 million in our later stage clinical programs as a result of the aforementioned approvals of Prolia® and XGEVA®, as well as licensing fees paid in 2009, and lower expenses associated with our Discovery Research and Translational Sciences activities of $3 million.

Certain amounts for 2010 have been reclassified to better conform to the above descriptions of R&D activities.

Selling, general and administrative

SG&A expenses are comprised primarily of salaries, benefits and other staff-related costs associated with sales and marketing, finance, legal and other administrative personnel; facilities and overhead costs; outside marketing, advertising and legal expenses; and other general and administrative costs. Advertising costs are expensed as incurred. SG&A expenses also include costs and cost recoveries associated with marketing and promotion efforts under certain collaboration arrangements. Net payment or reimbursement of SG&A costs is recognized when the obligations are incurred or we become entitled to the cost recovery. Beginning January 1, 2011, SG&A expenses also include the annual U.S. healthcare reform federal excise fee.

The increase in SG&A expense for 2011 was driven primarily by the U.S. healthcare reform federal excise fee of $151 million; higher ENBREL profit share expense of $104 million; increased expenses related to the launches of Prolia® and XGEVA® and expansion of our international operations of $89 million; and the unfavorable impact of foreign exchange of $67 million.

The increase in SG&A expense for 2010 was due primarily to higher promotional costs for Prolia® and other marketed products of $148 million, higher staff-related costs of $46 million and higher litigation expenses of $45 million, offset partially by charges of $29 million in 2009 for certain cost savings initiatives related to our 2007 restructuring plan.

 

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For the years ended December 31, 2011, 2010 and 2009, the expenses associated with the ENBREL profit share were $1,288 million, $1,184 million and $1,163 million, respectively.

Other

In 2011, we recorded a $780 million legal settlement charge in connection with an agreement in principle to settle allegations relating to our sales and marketing practices. In addition in 2011, as part of our continuing efforts to improve cost efficiencies in our operations, we recorded certain charges, primarily severance related, of $109 million. In 2010, we recorded a $118 million asset impairment charge for our manufacturing operations located in Fremont, California, associated with our continuing efforts to optimize our network of manufacturing facilities and improve cost efficiencies. In 2009, we recorded loss accruals for settlements of certain legal proceedings aggregating $33 million.

See Note 18, Contingencies and commitments, to the Consolidated Financial Statements for further discussion of our 2011 legal settlement.

Non-operating expenses/income and provision for income taxes

Non-operating expenses/income and provisions for income taxes were as follows (dollar amounts in millions):

 

     2011     2010     2009  

Interest expense, net

   $ 610      $ 604      $ 578   

Interest and other income, net

   $ 448      $ 376      $ 276   

Provisions for income taxes

   $ 467      $ 690      $ 599   

Effective tax rate

     11.3     13.0     11.5

Interest expense, net

Included in interest expense, net, for the years ended December 31, 2011, 2010 and 2009, is the impact of non-cash interest expense of $143 million, $266 million and $250 million, respectively, resulting from the change in the accounting for our convertible debt effective January 1, 2009. The reduction of non-cash interest expense in 2011 was offset by increased interest expense associated with recent borrowings.

Interest and other income, net

The increase in interest and other income, net, for 2011 was due primarily to higher net realized gains on sales of investments of $67 million.

The increase in interest and other income, net, for 2010 was due primarily to higher net realized gains on sales of investments of $48 million and higher interest income of $51 million, due principally to higher average cash, cash equivalents and marketable securities balances.

Income taxes

The decrease in our effective tax rate for 2011 was due primarily to the foreign tax credits associated with the Puerto Rico excise tax described below offset partially by the effect of the non-deductible U.S. healthcare reform federal excise fee in 2011, the non-deductible portion of the legal settlement reached in principle in 2011 and the favorable resolution in 2010 of certain prior years’ non-routine transfer pricing matters with tax authorities.

Commencing January 1, 2011, Puerto Rico imposes a temporary excise tax on the acquisition of goods and services from a related manufacturer in Puerto Rico. The excise tax is imposed over a six year period beginning in 2011 with the excise tax rate declining in each year (4% in 2011, 3.75% in 2012, 2.75% in 2013, 2.5% in 2014, 2.25% in 2015, and 1% in 2016). We account for the excise tax as a manufacturing cost that is capitalized in inventory and expensed in cost of sales when the related products are sold. For U.S. income tax purposes, the excise tax results in foreign tax credits that are generally recognized in our provision for income taxes in the year in which the excise tax is incurred. The effective tax rate for 2011 would have been approximately 18% without the impact of the tax credits associated with the Puerto Rico excise tax.

 

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The increase in our effective tax rate for 2010 was due primarily to the incremental favorable impact resulting from the resolution of certain prior years’ matters with tax authorities in 2009 compared to 2010; the unfavorable tax impact of changes in revenue and expense mix in 2010; and the tax impact from adjustments to deferred taxes arising from changes in California tax law enacted in 2009 and effective for subsequent periods. The resolution of prior years’ tax matters recognized in 2010 and 2009 reduced the effective tax rate by 3.1% and 4.2%, respectively.

As permitted under U.S. GAAP, we do not provide for U.S. income taxes on undistributed earnings of our foreign operations that are intended to be invested indefinitely outside of the United States.

See Summary of Critical Accounting Policies  —  Income taxes and Note 4, Income taxes, to the Consolidated Financial Statements for further discussion.

Recent accounting pronouncements

In June 2011, a new accounting standard was issued that changed the disclosure requirements for the presentation of other comprehensive income (OCI) in the financial statements, including the elimination of the option to present OCI in the statement of stockholders’ equity. OCI and its components will be required to be presented for both interim and annual periods either in a single financial statement, the statement of comprehensive income, or in two separate but consecutive financial statements, consisting of a statement of income followed by a separate statement presenting OCI. This standard is required to be applied retrospectively beginning January 1, 2012, except for certain provisions for which adoption was delayed.

Financial Condition, Liquidity and Capital Resources

Selected financial data was as follows as of December 31, 2011 and 2010 (in millions):

 

     2011      2010  

Cash, cash equivalents and marketable securities

   $ 20,641       $ 17,422   

Total assets

     48,871         43,486   

Current portion of long-term debt

     84         2,488   

Long-term debt

     21,344         10,874   

Stockholders’ equity

     19,029         23,944   

The Company intends to continue to return capital to stockholders through share repurchases and the payment of cash dividends, reflecting our confidence in the future cash flows of our business. The amount we spend, the number of shares repurchased and the timing of such repurchases will vary based on a number of factors, including the stock price, the availability of financing on acceptable terms, the amount and timing of dividend payments and blackout periods in which we are restricted from repurchasing shares; and the manner of purchases may include private block purchases, tender offers, as well as market transactions. Whether and when we declare dividends or repurchase stock, the size of any dividend and the amount of stock we repurchase could be affected by a number of additional factors. (See Item 1A. Risk Factors — There can be no assurance that we will continue to declare cash dividends or repurchase stock). In April 2011, the Board of Directors authorized us to repurchase up to an additional $5 billion of our common stock. Subsequently in October 2011, the Board of Directors increased the total authorization for stock repurchases by $6.1 billion to $10 billion. At that time, we announced our intent to accelerate our stock repurchase program, reflecting our confidence in the long-term value of the Company and the attractive interest rate environment. During 2011, we repurchased 144 million shares of our common stock at an aggregate cost of $8.3 billion, including $5 billion purchased in a modified Dutch auction tender offer. We expect to repurchase the remaining $5 billion of stock under our authorized stock repurchase program through open-market purchases. In April 2011, the Board of Directors also approved a dividend policy related to our common stock and subsequently declared quarterly cash dividends of $0.28 per share of common stock in July and October 2011, resulting in dividend payments aggregating $500 million in 2011. Additionally in December 2011, the Board of Directors declared a 29% increase in our quarterly cash dividend to $0.36 per share of common stock, payable in March 2012.

 

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We believe existing funds, cash generated from operations and existing sources of and access to financing are adequate to satisfy our needs for working capital; capital expenditure and debt service requirements; our plans to pay dividends and repurchase stock; and other business initiatives we plan to strategically pursue, including acquisitions and licensing activities, in each case for the foreseeable future. We anticipate that our liquidity needs can be met through a variety of sources, including cash provided by operating activities, sales of marketable securities, borrowings through commercial paper and/or our syndicated credit facility and access to other domestic and foreign debt markets and equity markets. With respect to our U.S. operations, we believe that existing funds intended for use in the United States; cash generated from our U.S. operations, including intercompany payments and receipts; and existing sources of and access to financing (collectively referred to as “U.S. funds”) are adequate to continue to meet our U.S. obligations (including our plans to repurchase stock and pay dividends with U.S. funds) for the foreseeable future. See Item 1A. Risk Factors — Current economic conditions may magnify certain risks that affect our business.

A significant portion of our operating cash flows is dependent upon the timing of payments from our customers located in the United States and, to a lesser extent, customers outside the United States, which include government owned or supported healthcare providers (government healthcare providers). Payments from these government healthcare providers are dependent, in part, upon the economic stability and creditworthiness of their applicable country. Deteriorating credit and economic conditions in parts of Southern Europe, particularly in Spain, Italy, Greece and Portugal, may continue to increase the average length of time it takes to collect payments, particularly in certain regions within these countries. However, the timing of payments from government healthcare providers has not nor is it expected to have a material adverse impact on our operating cash flows. To date we have not incurred any significant losses on collections of trade receivables from these government healthcare providers.

Over the next several years, many of the existing patents on our principal products will expire. As a result, we expect to face increasing competition from biosimilars that may have a material adverse impact on our product sales, results of operations and liquidity. Upon patent expiration for small molecule products, there is typically intense competition from generics manufacturers, which generally leads to significant and rapid declines in sales of the branded product. Given that our principal products are biologics, we do not believe the impact of biosimilar competition will be as significant as with small molecule products, in part because successful competitors must have a broad range of specialized skills and capabilities unique to biologics, including significant regulatory, clinical and manufacturing expertise, and since the products are similar, but not identical, the biosimilars will have to compete against a product with an established efficacy and safety record. As discussed above, we have many opportunities to grow our business, including the continued commercialization of XGEVA® and Prolia® and expansion into emerging markets and Japan, which we believe may offset the adverse financial impact of our principal products’ patent expiries.

Cash, cash equivalents and marketable securities

Of our total cash, cash equivalents and marketable securities balances as of December 31, 2011, approximately $16.9 billion was generated from operations in foreign tax jurisdictions and is intended to be invested indefinitely outside of the United States. Under current tax laws, if these funds were repatriated for use in our U.S. operations, we would be required to pay additional income taxes at the tax rates then in effect.

The primary objective of our investment portfolio is to enhance overall returns in an efficient manner while maintaining safety of principal, prudent levels of liquidity and acceptable levels of risk. Our investment policy limits debt security investments to certain types of debt and money market instruments issued by institutions with primarily investment grade credit ratings and places restrictions on maturities and concentration by asset class and issuer.

Financing arrangements

The current and noncurrent portions of our long-term borrowings at December 31, 2011, were $84 million and $21.3 billion, respectively. The current and noncurrent portions of our long-term borrowings at December 31, 2010, were $2.5 billion and $10.9 billion, respectively.

 

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We issued debt securities in various offerings during the three years ended December 31, 2011, including:

 

 

In 2011, we issued $10.5 billion aggregate principal amount of notes, comprised of the 1.875% 2014 Notes, the 2.30% 2016 Notes, the 2.50% 2016 Notes, the 4.375% 2018 euro Notes (€550 million aggregate principal amount), the 4.10% 2021 Notes, the 3.875% 2021 Notes, the 5.50% 2026 pound sterling Notes (£475 million aggregate principal amount), the 5.15% 2041 Notes and the 5.65% 2042 Notes.

 

 

In 2010, we issued $2.5 billion aggregate principal amount of notes, comprised of the 4.50% 2020 Notes, the 3.45% 2020 Notes, the 5.75% 2040 Notes and the 4.95% 2041 Notes.

 

 

In 2009, we issued $2.0 billion aggregate principal amount of notes, comprised of the 5.70% 2019 Notes and the 6.40% 2039 Notes.

In February 2011, our 0.125% 2011 Convertible Notes became due, and we repaid the $2.5 billion aggregate principal amount. No debt was due or repaid in 2010, and we repaid $1.0 billion aggregate principal amount of notes with a fixed interest rate of 4.00% in 2009.

To achieve a desired mix of fixed and floating interest rate debt, we enter into interest rate swap contracts that effectively convert a fixed rate interest coupon for certain of our debt issuances to a floating London Interbank Offered Rates (LIBOR) based coupon over the life of the respective note. These interest rate swap contracts qualify and are designated as fair value hedges. As of December 31, 2011 and 2010, we had interest rate swap contracts with an aggregate face value of $3.6 billion. See Note 14, Financing arrangements, and Note 17, Derivative instruments, to the Consolidated Financial Statements for further discussion of our interest rate swap contracts.

In order to hedge our exposure to foreign currency exchange rate risk associated with our pound sterling denominated long-term notes issued in 2011, we entered into cross currency swap contracts. These cross currency swap contracts qualify and are designated as cash flow hedges. Under the terms of these contracts, we receive interest payments in pounds sterling at a fixed rate of 5.5% on £475 million and pay interest in U.S. dollars at a fixed rate of 5.8% on $748 million, the aggregate notional amounts paid to/received from the counterparties upon exchange of currencies at the inception of these contracts. We will pay U.S. dollars to and receive pounds sterling from the counterparties at the maturity of the contracts for the same notional amounts. The terms of these contracts correspond to the related hedged notes, effectively converting the interest payments and principal repayment on these notes from pounds sterling to U.S. dollars.

As of December 31, 2011, we have a commercial paper program that allows us to issue up to $2.5 billion of unsecured commercial paper to fund our working capital needs. At December 31, 2011 and 2010, we had no amounts outstanding under our commercial paper program.

In December 2011, we entered into a $2.5 billion syndicated, unsecured, revolving credit agreement which is available for general corporate purposes or as a liquidity backstop to our commercial paper program. The commitments under the revolving credit agreement may be increased by up to $500 million with the agreement of the banks. Each bank which is a party to the agreement has an initial commitment term of five years. This term may be extended for up to two additional one-year periods with the agreement of the banks. Annual commitment fees for this agreement are 0.1% based on our current credit rating. We would be charged interest at LIBOR plus 0.9% for any amounts borrowed under this facility. As of December 31, 2011, no amounts were outstanding under this facility. In connection with the new revolving credit agreement we terminated our prior $2.3 billion revolving credit agreement that was scheduled to expire in November 2012.

In March 2011, we filed a shelf registration statement with the SEC to replace an existing shelf registration statement that was scheduled to expire in April 2011. This shelf registration statement allows us to issue unspecified amounts of debt securities; common stock; preferred stock; warrants to purchase debt securities, common stock, preferred stock or depository shares; rights to purchase common stock or preferred stock; securities purchase contracts; securities purchase units; and depository shares. Under this shelf registration statement, all of the securities available for issuance may be offered from time to time with terms to be determined at the time of issuance. This shelf registration statement expires in March 2014.

 

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In 1997, we established a $400 million medium-term note program under which medium-term debt securities may be offered from time to time with terms to be determined at the time of issuance. As of December 31, 2011 and 2010, no securities were outstanding under this medium-term note program.

Certain of our financing arrangements contain non-financial covenants. In addition, our revolving credit agreement includes a financial covenant with respect to the level of our borrowings in relation to our equity, as defined. We were in compliance with all applicable covenants under these arrangements as of December 31, 2011.

See Note 14, Financing arrangements, to the Consolidated Financial Statements for further discussion of our financing arrangements.

Cash flows

Our cash flow activity was as follows (in millions):

 

     2011     2010     2009  

Net cash provided by operating activities

   $ 5,119      $ 5,787      $ 6,336   

Net cash used in investing activities

     (786     (4,152     (3,202

Net cash used in financing activities

     (674     (1,232     (2,024

Operating

Cash provided by operating activities has been and is expected to continue to be our primary recurring source of funds. Cash provided by operating activities decreased during the 2011 due primarily to: increased interest payments; working capital increases related to the launch of Prolia® and XGEVA®; and the prepayment of certain royalties. The reduction in net income during 2011 was driven primarily by the accrual of the legal settlement charge of $780 million, which will be paid in a subsequent period. Cash provided by operating activities during 2010 decreased due primarily to the timing and amount of payments to taxing authorities.

Investing

Capital expenditures totaled $567 million, $580 million and $530 million in 2011, 2010 and 2009, respectively. Capital expenditures in 2011, 2010 and 2009 were associated primarily with manufacturing capacity expansions in Puerto Rico and other site developments. We currently estimate 2012 spending on capital projects and equipment to be approximately $700 million.

Cash used in investing activities during the year ended December 31, 2011, also included the cost of acquiring certain businesses totaling $701 million.

Net proceeds from marketable securities were $437 million for 2011, compared to net purchases of marketable securities of $3.5 billion for 2010 and $2.7 billion for 2009.

Financing

Cash used in financing activities during 2011 was due to the repurchases of our common stock of $8.3 billion, including $5 billion purchased in a modified Dutch auction tender offer in December 2011; repayment of long-term debt of $2.5 billion; and payment of dividends of $500 million, offset partially by the net proceeds from issuance of long-term debt of $10.4 billion, including $7.5 billion issued in November and December 2011, in part, to finance the repurchase of our common stock in the modified Dutch auction tender offer. Cash used in financing activities during 2010 was due to the repurchases of our common stock of $3.8 billion, offset partially by the net proceeds from issuance of long-term debt of $2.5 billion. Cash used in financing activities during 2009 was due to repurchases of our common stock of $3.2 billion and repayment of long-term debt of $1.0 billion, offset partially by the net proceeds from issuance of long-term debt of $2.0 billion.

 

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See Note 14, Financing arrangements, and Note 15, Stockholders’ equity, to the Consolidated Financial Statements for further discussion.

Off-Balance Sheet Arrangements

We do not have any off-balance sheet arrangements that are material or reasonably likely to become material to our consolidated financial position or consolidated results of operations.

Contractual Obligations

Contractual obligations represent future cash commitments and liabilities under agreements with third parties, and exclude contingent liabilities for which we cannot reasonably predict future payment. Additionally, the expected timing of payment of the obligations presented below is estimated based on current information. Timing of payments and actual amounts paid may be different depending on the timing of receipt of goods or services or changes to agreed-upon terms or amounts for some obligations.

The following table represents our contractual obligations as of December 31, 2011, aggregated by type (in millions):

 

     Payments due by period  
            Year      Years      Years      Years  

Contractual obligations

   Total      1      2 and 3      4 and 5      6 and beyond  

Long-term debt obligations (1) (2) (3)

   $ 37,521       $ 888       $ 6,131       $ 3,396       $ 27,106   

Operating lease obligations

     774         116         189         141         328   

Purchase obligations (4)

     2,992         865         420         243         1,464   

Unrecognized tax benefits (5)

      —           —           —           —           —    
  

 

 

    

 

 

    

 

 

    

 

 

    

 

 

 

Total contractual obligations

   $ 41,287       $ 1,869       $ 6,740       $ 3,780       $ 28,898   
  

 

 

    

 

 

    

 

 

    

 

 

    

 

 

 

 

(1)

The long-term debt obligation amounts also include future interest payments. Future interest payments are included on our financing arrangements at the fixed contractual coupon rates. To achieve a desired mix of fixed and floating interest rate debt, we enter into interest rate swap contracts that effectively convert a fixed rate interest coupon for certain of our debt issuances to a floating LIBOR-based coupon over the life of the respective note. We used an interest rate forward curve at December 31, 2011, in computing net amounts to be paid or received under our interest rate swap contracts which resulted in an aggregate net reduction in future interest payments of $366 million. See Note 14, Financing arrangements, to the Consolidated Financial Statements for further discussion of our interest swap contracts.

 

(2)

In order to hedge our exposure to foreign currency exchange rate risk associated with our pound sterling denominated long-term debt issued in December 2011, we entered into cross currency swap contracts that effectively convert interest payments and principal repayment on this debt from pounds sterling to U.S. dollars. For purposes of this table, we used the contracted exchange rates in the cross currency swap contracts to compute the net amounts of future interest and principal payments and on this debt. See Note 14, Financing arrangements, to the Consolidated Financial Statements for further discussion of our cross currency swap contracts.

 

(3)

The long-term debt obligations amounts include the repayment of principal on our euro denominated foreign currency debt at the foreign currency exchange rates in effect at December 31, 2011. See Note 14, Financing arrangements, to the Consolidated Financial Statements for further discussion of our long-term debt obligations.

 

(4)

Purchase obligations relate primarily to (i) our long-term supply agreements with third-party manufacturers, which are based on firm commitments for the purchase of production capacity; (ii) R&D commitments (including those related to clinical trials) for new and existing products; (iii) capital expenditures; and (iv) open purchase orders for the acquisition of goods and services in the ordinary course of business. Our obligation to pay certain of these amounts may be reduced based on certain future events.

 

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(5) 

Liabilities for unrecognized tax benefits (UTBs) (net of foreign tax credits and federal tax benefit of state taxes) and related accrued interest and penalties totaling approximately $912 million at December 31, 2011, are not included in the table above because, due to their nature, there is a high degree of uncertainty regarding the timing of future cash outflows and other events that extinguish these liabilities.

In addition to amounts in the table above, we are contractually obligated to pay additional amounts, which in the aggregate are significant, upon the achievement of various development, regulatory and commercial milestones for agreements we have entered into with third parties, including contingent consideration incurred with the acquisition of BioVex. These payments are contingent upon the occurrence of various future events, substantially all of which have a high degree of uncertainty of occurring. These contingent payments have not been included in the table above, and, except with respect to the fair value of the BioVex contingent consideration, are not recorded on our Consolidated Balance Sheets. As of December 31, 2011, the maximum amount that may be payable in the future for agreements we have entered into with third parties is approximately $3.6 billion, including $575 million in connection with the acquisition of BioVex (see Note 2, Business combinations, to the Consolidated Financial Statements).

Summary of Critical Accounting Policies

The preparation of our consolidated financial statements in conformity with U.S. GAAP requires management to make estimates and assumptions that affect the amounts reported in the financial statements and the notes to the financial statements. Some of those judgments can be subjective and complex, and therefore, actual results could differ materially from those estimates under different assumptions or conditions.

Product sales, sales deductions and returns

Revenues from sales of our products are recognized when the products are shipped and title and risk of loss have passed. Product sales are recorded net of accruals for estimated rebates, wholesaler chargebacks, cash discounts and other deductions (collectively, “sales deductions”) and returns, which are established at the time of sale.

We analyze the adequacy of our accruals for sales deductions quarterly. Amounts accrued for sales deductions are adjusted when trends or significant events indicate that adjustment is appropriate. Accruals are also adjusted to reflect actual results. Amounts recorded in Accrued liabilities in the Consolidated Balance Sheets for sales deductions were as follows (in millions):

 

     Rebates     Chargebacks     Other deductions     Total  

Balance as of January 1, 2009

   $ 653      $ 84      $ 139      $ 876   

Amounts charged against product sales

     1,663        2,424        552        4,639   

Payments

     (1,609     (2,380     (556     (4,545
  

 

 

   

 

 

   

 

 

   

 

 

 

Balance as of December 31, 2009

     707        128        135        970   

Amounts charged against product sales

     1,861        2,593        580        5,034   

Payments

     (1,724     (2,548     (588     (4,860
  

 

 

   

 

 

   

 

 

   

 

 

 

Balance as of December 31, 2010

     844        173        127        1,144   

Amounts charged against product sales

     1,795        2,626        670        5,091   

Payments

     (1,592     (2,600     (717     (4,909
  

 

 

   

 

 

   

 

 

   

 

 

 

Balance as of December 31, 2011

   $ 1,047      $ 199      $ 80      $ 1,326   
  

 

 

   

 

 

   

 

 

   

 

 

 

For the years ended December 31, 2011, 2010 and 2009, total sales deductions were 25%, 25% and 24% of gross product sales, respectively. Included in these amounts are immaterial adjustments related to prior-year sales due to changes in estimates. Such amounts represent 2% or less of the aggregate sales deductions charged against product sales for the three year ended December 31, 2011.

 

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In the United States, we utilize wholesalers as the principal means of distributing our products to healthcare providers, such as physicians or their clinics, dialysis centers, hospitals and pharmacies. Products we sell in the EU are distributed principally to hospitals and/or wholesalers depending on the distribution practice in each country where the product is sold. We monitor the inventory levels of our products at our wholesalers by using data from our wholesalers and other third parties, and we believe wholesaler inventories have been maintained at appropriate levels (generally two to three weeks) given end-user demand. Accordingly, historical fluctuations in wholesaler inventory levels have not significantly impacted our method of estimating sales deductions and returns.

Accruals for sales deductions are based primarily on estimates of the amounts earned or to be claimed on the related sales. These estimates take into consideration current contractual and statutory requirements, specific known market events and trends, internal and external historical data and forecasted customer buying patterns. Sales deductions are substantially product-specific and, therefore, for any given year, can be impacted by the mix of products sold.

Rebates include primarily amounts paid to payers and providers in the United States, including those paid to state Medicaid programs, and are based on contractual arrangements which vary by product, by payer and individual payer plans. We estimate the amount of rebate that will be paid based on the product sold, contractual terms, historical experience and wholesaler inventory levels and accrue these rebates in the period the related sale is recorded. We adjust the accrual as more information becomes available and to reflect actual experience. Estimating such rebates is complicated, in part, due to the time delay between the date of sale and the actual settlement of the liability, which for certain rebates can take up to one year and greater than one year for certain recent government programs. Rebates totaled $1.8 billion, $1.9 billion and $1.7 billion for the years ended December 31, 2011, 2010 and 2009, respectively. We believe the methodology we use to accrue for rebates is reasonable and appropriate given current facts and circumstances. However, actual results may differ. Changes in annual estimates related to prior annual periods have been less than 5% of the estimated rebate amounts charged against product sales for each of the three years ended December 31, 2011. A 5% change in our rebate estimate attributable to rebates recognized in 2011 would have had an impact of approximately $90 million, or approximately one-half of 1% of our 2011 product sales and a corresponding impact on our financial condition and liquidity.

Wholesaler chargebacks relate to our contractual agreements to sell products to healthcare providers in the United States at fixed prices that are lower than the prices we charge wholesalers. When the healthcare providers purchase our products through wholesalers at these reduced prices, the wholesaler charges us for the difference between their purchase price and the contractual price between Amgen and the healthcare providers. The provision for chargebacks is based on the expected sales by our wholesaler customers to healthcare providers. Those chargebacks from wholesalers totaled $2.6 billion, $2.6 billion and $2.4 billion for the years ended December 31, 2011, 2010 and 2009, respectively. Accruals for wholesaler chargebacks are less difficult to estimate than rebates and closely approximate actual results since chargeback amounts are fixed at the date of purchase by the healthcare providers, and we generally settle the liability for these deductions within a few weeks.

Product returns

Returns are estimated through comparison of historical return data to their related sales on a production lot basis. Historical rates of return are determined for each product and are adjusted for known or expected changes in the marketplace specific to each product, when appropriate. Historically, sales return provisions have been insignificant, amounting to less than 1.5% of gross product sales. Furthermore, changes in estimates for prior year sales return provisions have historically also been insignificant.

Income taxes

The Company provides for income taxes based on pretax income, applicable tax rates and tax planning opportunities available in the various jurisdictions in which it operates.

 

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We recognize the tax benefit from an uncertain tax position only if it is more likely than not that the tax position will be sustained on examination by the taxing authorities based on the technical merits of the position. The tax benefits recognized in the financial statements on a particular tax position are measured based on the largest benefit that is more likely than not to be realized upon settlement. The amount of UTBs is adjusted as appropriate for changes in facts and circumstances, such as significant amendments to existing tax law, new regulations or interpretations by the taxing authorities, new information obtained during a tax examination, or resolution of an examination. We believe our estimates for uncertain tax positions are appropriate and sufficient for any assessments that may result from examinations of our tax returns. We recognize both accrued interest and penalties, where appropriate, related to UTBs in income tax expense.

Certain items are included in the Company’s tax return at different times than they are reflected in the financial statements. Such timing differences create deferred tax assets and liabilities. Deferred tax assets are generally items that can be used as a tax deduction or credit in the tax return in future years but for which the Company has already recorded the tax benefit in the financial statements. The Company establishes valuation allowances against its deferred tax assets when the amount of expected future taxable income is not likely to support the use of the deduction or credit. Deferred tax liabilities are either: (i) a tax expense recognized in the financial statements for which payment has been deferred; or (ii) an expense for which the Company has already taken a deduction on the tax return, but has not yet recognized the expense in the financial statements.

The Company is a vertically integrated enterprise with operations in the U.S. and various foreign jurisdictions. The Company is subject to income tax in the foreign jurisdictions where it conducts activities based on the tax laws and principles of such jurisdictions and the functions, risks and activities performed therein. The Company’s pre-tax income is therefore attributed to domestic or foreign sources based on the operations performed in each location and the tax laws and principles of the respective taxing jurisdictions. For example, the Company conducts significant operations outside the United States in Puerto Rico pertaining to manufacturing, distribution and other related functions to meet its worldwide product demand. Income from the Company’s operations in Puerto Rico is subject to a tax incentive grant that expires in 2020.

Our effective tax rate reflects the impact of undistributed foreign earnings for which no U.S. taxes have been provided because such earnings are intended to be invested indefinitely outside the United States. Substantially all of this benefit is attributable to the Company’s foreign income associated with the Company’s operations conducted in Puerto Rico.

If future events, including material changes in cash, working capital and long-term investment requirements necessitate that certain assets associated with these earnings be repatriated to the United States, under current tax laws an additional tax provision and related liability would be required at the applicable income tax rates which could have a material adverse effect on both our future effective tax rate and our financial results.

Our operations are subject to the tax laws, regulations and administrative practices of the United States, U.S. state jurisdictions and other countries in which we do business. Significant changes in these rules could have a material adverse effect on the results of operations. (See Item 1A. Risk Factors  —  The adoption of new tax legislation or exposure to additional tax liabilities could affect our profitability.)

Contingencies

In the ordinary course of business, we are involved in various legal proceedings and other matters such as intellectual property disputes, contractual disputes, governmental investigations and class action suits which are complex in nature and have outcomes that are difficult to predict. Certain of these proceedings are discussed in Note 18, Contingencies and commitments, to the Consolidated Financial Statements. We record accruals for loss contingencies to the extent that we conclude that it is probable that a liability has been incurred and the amount of the related loss can be reasonably estimated. We consider all relevant factors when making assessments regarding these contingencies.

While it is not possible to accurately predict or determine the eventual outcomes of these items, an adverse determination in one or more of these items currently pending could have a material adverse effect on our consolidated results of operations, financial position or cash flows.

 

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Valuation of assets and liabilities in connection with business combinations

We have acquired and continue to acquire intangible assets in connection with business combinations. These intangible assets consist primarily of technology associated with currently marketed human therapeutic products and IPR&D product candidates. Discounted cash flow models are typically used to determine the fair values of these intangible assets for purposes of allocating consideration paid to the net assets acquired in a business combination. These models require the use of significant estimates and assumptions, including, but not limited to:

 

 

determining the timing and expected costs to complete in-process projects taking into account the stage of completion at the acquisition date;

 

 

projecting the probability and timing of obtaining marketing approval from the FDA and other regulatory agencies for product candidates;

 

 

estimating the timing of and future net cash flows from product sales resulting from completed products and in-process projects; and

 

 

developing appropriate discount rates to calculate the present values of the cash flows.

Significant estimates and assumptions are also required to determine the acquisition date fair values of any contingent consideration obligations incurred in connection with business combinations. In addition, we must revalue these obligations each subsequent reporting period until the related contingencies are resolved and record changes in their fair values in earnings. The acquisition date fair values of the various contingent consideration obligations incurred in the acquisition of BioVex (see Note 2, Business combinations, to the Consolidated Financial Statements) were determined using a combination of valuation techniques. Significant estimates and assumptions required for these valuations included, but were not limited to, the probability of achieving regulatory milestones, product sales projections under various scenarios and discount rates used to calculate the present value of the required payments. These estimates and assumptions are required to be updated in order to revalue these contingent consideration obligations each reporting period. Accordingly, subsequent changes in underlying facts and circumstances could result in changes in these estimates and assumptions, which could have a material impact on the estimated future fair values of these obligations.

We believe the fair values used to record intangible assets acquired and contingent consideration obligations incurred in connection with business combinations are based upon reasonable estimates and assumptions given the facts and circumstances as of the related valuation dates.

 

Item 7A. QUANTITATIVE AND QUALITATIVE DISCLOSURES ABOUT MARKET RISK

We are exposed to market risks that may result from changes in interest rates, foreign currency exchange rates and prices of equity instruments as well as changes in the general economic conditions in the countries where we conduct business. To reduce certain of these risks, we enter into various types of foreign currency and interest rate derivative hedging transactions as part of our risk management program. We do not use derivatives for speculative trading purposes.

In the capital and credit markets, strong demand for fixed income instruments led to historically low interest rates on corporate debt issuances during 2011. Short-term interest rates on U.S. Treasury instruments continued to decline due to a combination of the Federal Reserve’s monetary policies and the challenging macroeconomic environment. As a result, in the discussion that follows, we have assumed a hypothetical change in interest rates of 100 basis points from those at December 31, 2011 and 2010. Continued uncertainty surrounding European sovereign debt resulted in ongoing volatility in the foreign exchange markets, and we have consequently assumed a hypothetical 20% change in foreign currency exchange rates against the U.S. dollar based on its position relative to other currencies as of December 31, 2011 and 2010.

Interest rate sensitive financial instruments

Our portfolio of available-for-sale debt security investments at December 31, 2011 and 2010, was comprised of: U.S. Treasury securities and other government-related debt securities; corporate debt securities; mortgage- and

 

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asset-backed securities; money market mutual funds; and additionally at December 31, 2010, other short-term interest bearing securities, composed principally of commercial paper. The fair value of our investment portfolio of debt securities was $20.0 billion and $17.3 billion at December 31, 2011 and 2010, respectively. Duration is a sensitivity measure that can be used to approximate the change in the value of a security that will result from a 100 basis point change in interest rates. Applying a duration model, a hypothetical 100 basis point increase in interest rates at December 31, 2011 and 2010, would not have resulted in a material effect on the fair values of these securities on these dates. In addition, a hypothetical 100 basis point decrease in interest rates at December 31, 2011 and 2010, would not result in a material effect on the related income or cash flows in the respective ensuing year.

As of December 31, 2011, we had outstanding debt with a carrying value of $21.4 billion and a fair value of $23.0 billion. As of December 31, 2010, we had outstanding debt with a carrying value of $13.4 billion and a fair value of $14.5 billion. Our outstanding debt at December 31, 2011 and 2010, was comprised entirely of debt with fixed interest rates. Changes in interest rates do not affect interest expense or cash flows on fixed rate debt. Changes in interest rates would, however, affect the fair values of fixed rate debt. A hypothetical 100 basis point decrease in interest rates relative to interest rates at December 31, 2011, would have resulted in an increase of approximately $2.1 billion in the aggregate fair value of our outstanding debt on this date. A hypothetical 100 basis point decrease in interest rates relative to the interest rates at December 31, 2010, would have resulted in an increase of approximately $1.0 billion in the aggregate fair value of our outstanding debt on this date. The analysis for the debt does not consider the impact that hypothetical changes in interest rates would have on the related interest rate swap and cross currency swap contracts.

To achieve a desired mix of fixed and floating interest rate debt, we have entered into interest rate swap contracts, which qualify and have been designated for accounting purposes as fair value hedges, for certain of our fixed rate debt with notional amounts totaling $3.6 billion at December 31, 2011 and 2010. These derivative contracts effectively convert a fixed rate interest coupon to a floating rate LIBOR-based coupon over the life of the respective note. A hypothetical 100 basis point increase in interest rates relative to interest rates at December 31, 2011 and 2010, would have resulted in a reduction fair value of approximately $200 million on our interest rate swap contracts on these dates and would not result in a material effect on the related income or cash flows in the respective ensuing year. The analysis for the interest rate swap contracts does not consider the impact that hypothetical changes in interest rates would have on the related fair values of debt that these interest rate sensitive instruments were designed to offset.

As of December 31, 2011, we had open cross currency swap contracts with an aggregate notional amount of $748 million that hedge the entire principal amount of our pound sterling denominated debt and related interest payments. These contracts effectively convert payments on this debt to U.S. dollars and are designated for accounting purposes as cash flow hedges. A hypothetical 100 basis point adverse movement in interest rates relative to interest rates at December 31, 2011, would have resulted in approximately a $130 million reduction in the fair value of our cross currency swap contracts on this date but would not have a material effect on cash flows or income in the ensuing year.

Foreign currency sensitive financial instruments

Our international operations are affected by fluctuations in the value of the U.S. dollar as compared to foreign currencies, predominately the euro. Increases and decreases in our international product sales from movements in foreign currency exchange rates are offset partially by the corresponding increases or decreases in our international operating expenses. Increases and decreases in our foreign currency denominated assets from movements in foreign currency exchange rates are offset partially by the corresponding increases or decreases in our foreign currency denominated liabilities. To further reduce our net exposure to foreign currency exchange rate fluctuations on our results of operations, we enter into foreign currency forward, option and cross currency swap contracts.

As of December 31, 2011, we had outstanding debt with a carrying value and fair value of $1.5 billion that was denominated in pounds sterling and euros. A hypothetical 20% adverse movement in foreign currency exchange rates compared with the U.S. dollar relative to exchange rates at December 31, 2011, would have

 

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resulted in an increase in fair value of this debt of approximately $290 million on this date with a corresponding reduction in income in the ensuing year and would not result in a material effect on the related cash flows in the ensuing year. The analysis for this debt does not consider the impact that hypothetical changes in foreign exchange would have on the related cross currency swap contracts.

With regard to our cross currency swap contracts that are designated as cash flow hedges of our pound sterling denominated debt, a hypothetical 20% adverse movement in foreign currency exchange rates compared with the U.S. dollar relative to exchange rates at December 31, 2011, would have resulted in a reduction in the fair value of these contracts of approximately $210 million on this date and would not result in a material effect on the related cash flows in the ensuing year. The impact on income in the ensuing year of this hypothetical adverse movement in foreign currency exchange rates, which would equal the entire change in the carrying amount of the hedged debt, would be approximately $150 million.

We enter into foreign currency forward and options contracts that are designated for accounting purposes as cash flow hedges of certain anticipated foreign currency transactions. As of December 31, 2011, we had open foreign currency forward and options contracts, primarily euro-based, with notional amounts of $3.5 billion and $292 million, respectively. As of December 31, 2010, we had open foreign currency forward and options contracts, primarily euro-based, with notional amounts of $3.2 billion and $398 million, respectively. As of December 31, 2011 and 2010, the net unrealized gains on these contracts were not material. With regard to foreign currency forward and option contracts that were open at December 31, 2011, a hypothetical 20% adverse movement in foreign currency exchange rates compared with the U.S. dollar relative to exchange rates at December 31, 2011, would have resulted in a reduction in fair value of these contracts of approximately $700 million on this date and, in the ensuing year, a reduction in income and cash flows of approximately $330 million. With regard to contracts that were open at December 31, 2010, a hypothetical 20% adverse movement in foreign currency exchange rates compared with the U.S. dollar relative to exchange rates at December 31, 2010, would have resulted in a reduction in fair value of these contracts of approximately $670 million on this date and, in the ensuing year, a reduction in income and cash flows of approximately $330 million. The analysis does not consider the impact that hypothetical changes in foreign currency exchange rates would have on anticipated transactions that these foreign currency sensitive instruments were designed to offset.

As of December 31, 2011 and 2010, we had open foreign currency forward contracts with notional amounts totaling $389 million and $670 million, respectively, that hedged fluctuations of certain assets and liabilities denominated in foreign currencies but were not designated as hedges for accounting purposes. These contracts had no material net unrealized gains or losses at December 31, 2011 and 2010. With regard to these foreign currency forward contracts that were open at December 31, 2011, a hypothetical 20% adverse movement in foreign currency exchange rates compared with the U.S. dollar relative to exchange rates at December 31, 2011, would not have resulted in a material reduction in the fair value of these contracts on this date and would not result in a material effect on the related income or cash flows in the respective ensuing year. With regard to these foreign currency forward contracts that were open at December 31, 2010, a hypothetical 20% adverse movement in foreign currency exchange rates compared with the U.S. dollar relative to exchange rates at December 31, 2010, would have resulted in a reduction in fair value of these contracts on these dates of approximately $130 million and would not result in a material effect on the related income or cash flows in the ensuing year. The analysis does not consider the impact that hypothetical changes in foreign currency exchange rates would have on assets and liabilities that these foreign currency sensitive instruments were designed to offset.

Market price sensitive financial instruments

As of December 31, 2011 and 2010, we were also exposed to price risk on equity securities included in our portfolio of investments, which were acquired primarily for the promotion of business and strategic objectives. These investments are generally in small capitalization stocks in the biotechnology industry sector. Price risk relative to our equity investment portfolio as of December 31, 2011 and 2010, was not material.

Counterparty credit risks

Our financial instruments, including derivatives, are subject to counterparty credit risk which we consider as part of the overall fair value measurement. Our financial risk management policy limits derivative transactions by

 

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requiring transactions to be with institutions with investment grade credit ratings and requires placing exposure limits on the amount with any individual counterparty. In addition, we have an investment policy that limits investments to certain types of debt and money market instruments issued by institutions primarily with investment grade credit ratings and places restriction on maturities and concentrations by asset class and issuer.

 

Item 8. FINANCIAL STATEMENTS AND SUPPLEMENTARY DATA

The information required by this item is incorporated herein by reference to the financial statements and schedule listed in Item 15(a)1 and (a)2 of Part IV and included in this Annual Report on Form 10-K.

 

Item 9. CHANGES IN AND DISAGREEMENTS WITH ACCOUNTANTS ON ACCOUNTING AND FINANCIAL DISCLOSURES

None.

 

Item 9A. CONTROLS AND PROCEDURES

We maintain “disclosure controls and procedures,” as such term is defined under Exchange Act Rule 13a-15(e), that are designed to ensure that information required to be disclosed in Amgen’s Exchange Act reports is recorded, processed, summarized and reported within the time periods specified in the SEC’s rules and forms, and that such information is accumulated and communicated to Amgen’s management, including its Chief Executive Officer and Chief Financial Officer, as appropriate, to allow timely decisions regarding required disclosures. In designing and evaluating the disclosure controls and procedures, Amgen’s management recognized that any controls and procedures, no matter how well designed and operated, can provide only reasonable assurance of achieving the desired control objectives and in reaching a reasonable level of assurance Amgen’s management necessarily was required to apply its judgment in evaluating the cost-benefit relationship of possible controls and procedures. We have carried out an evaluation under the supervision and with the participation of our management, including Amgen’s Chief Executive Officer and Chief Financial Officer, of the effectiveness of the design and operation of Amgen’s disclosure controls and procedures. Based upon their evaluation and subject to the foregoing, the Chief Executive Officer and Chief Financial Officer concluded that our disclosure controls and procedures were effective as of December 31, 2011.

Management determined that, as of December 31, 2011, there were no changes in our internal control over financial reporting that occurred during the fiscal quarter then ended that have materially affected, or are reasonably likely to materially affect, our internal control over financial reporting.

Management’s Report on Internal Control over Financial Reporting

Management of the Company is responsible for establishing and maintaining adequate internal control over financial reporting, as such term is defined in Rule 13a-15(f) under the Securities Exchange Act of 1934. The Company’s internal control over financial reporting is designed to provide reasonable assurance regarding the reliability of financial reporting and the preparation of financial statements for external purposes in accordance with generally accepted accounting principles in the United States. However, all internal control systems, no matter how well designed, have inherent limitations. Therefore, even those systems determined to be effective can provide only reasonable assurance with respect to financial statement preparation and reporting.

Management assessed the effectiveness of the Company’s internal control over financial reporting as of December 31, 2011. In making this assessment, management used the criteria set forth by the Committee of Sponsoring Organizations of the Treadway Commission (COSO) in Internal Control-Integrated Framework. Based on our assessment, management believes that the Company maintained effective internal control over financial reporting as of December 31, 2011, based on the COSO criteria.

The effectiveness of the Company’s internal control over financial reporting has been audited by Ernst & Young LLP, an independent registered public accounting firm, as stated in their attestation report appearing below, which expresses an unqualified opinion on the effectiveness of the Company’s internal control over financial reporting as of December 31, 2011.

 

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Report of Independent Registered Public Accounting Firm

The Board of Directors and Stockholders of Amgen Inc.

We have audited Amgen Inc.’s (the “Company”) internal control over financial reporting as of December 31, 2011, based on criteria established in Internal Control — Integrated Framework issued by the Committee of Sponsoring Organizations of the Treadway Commission (the COSO criteria). Amgen Inc.’s management is responsible for maintaining effective internal control over financial reporting, and for its assessment of the effectiveness of internal control over financial reporting included in the accompanying Management’s Report on Internal Control over Financial Reporting. Our responsibility is to express an opinion on the Company’s internal control over financial reporting based on our audit.

We conducted our audit in accordance with the standards of the Public Company Accounting Oversight Board (United States). Those standards require that we plan and perform the audit to obtain reasonable assurance about whether effective internal control over financial reporting was maintained in all material respects. Our audit included obtaining an understanding of internal control over financial reporting, assessing the risk that a material weakness exists, testing and evaluating the design and operating effectiveness of internal control based on the assessed risk, and performing such other procedures as we considered necessary in the circumstances. We believe that our audit provides a reasonable basis for our opinion.

A company’s internal control over financial reporting is a process designed to provide reasonable assurance regarding the reliability of financial reporting and the preparation of financial statements for external purposes in accordance with generally accepted accounting principles. A company’s internal control over financial reporting includes those policies and procedures that (1) pertain to the maintenance of records that, in reasonable detail, accurately and fairly reflect the transactions and dispositions of the assets of the company; (2) provide reasonable assurance that transactions are recorded as necessary to permit preparation of financial statements in accordance with generally accepted accounting principles, and that receipts and expenditures of the company are being made only in accordance with authorizations of management and directors of the company; and (3) provide reasonable assurance regarding prevention or timely detection of unauthorized acquisition, use, or disposition of the company’s assets that could have a material effect on the financial statements.

Because of its inherent limitations, internal control over financial reporting may not prevent or detect misstatements. Also, projections of any evaluation of effectiveness to future periods are subject to the risk that controls may become inadequate because of changes in conditions, or that the degree of compliance with the policies or procedures may deteriorate.

In our opinion, Amgen Inc. maintained, in all material respects, effective internal control over financial reporting as of December 31, 2011, based on the COSO criteria.

We also have audited, in accordance with the standards of the Public Company Accounting Oversight Board (United States), the Consolidated Balance Sheets as of December 31, 2011 and 2010, and the related Consolidated Statements of Income, Stockholders’ Equity, and Cash Flows for each of the three years in the period ended December 31, 2011 of Amgen Inc. and our report dated February 29, 2012 expressed an unqualified opinion thereon.

/s/    Ernst & Young LLP

Los Angeles, California

February 29, 2012

 

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Item 9B. OTHER INFORMATION

Not applicable.

PART III

 

Item 10. DIRECTORS, EXECUTIVE OFFICERS AND CORPORATE GOVERNANCE OF THE REGISTRANT

Information about our Directors is incorporated by reference from the section entitled ITEM 1 — ELECTION OF DIRECTORS in our Proxy Statement for the 2012 Annual Meeting of Stockholders to be filed with the SEC within 120 days of December 31, 2011 (the Proxy Statement). Information about compliance with Section 16(a) of the Securities Exchange Act of 1934 is incorporated by reference from the section entitled OTHER MATTERS — Section 16(a) Beneficial Ownership Reporting Compliance in our Proxy Statement. Information about the procedures by which stockholders may recommend nominees for the Board of Directors is incorporated by reference from Appendix A — AMGEN INC. BOARD OF DIRECTORS GUIDELINES FOR DIRECTOR QUALIFICATIONS AND EVALUATIONS in our Proxy Statement. Information about our Audit Committee, members of the committee and our Audit Committee financial experts is incorporated by reference from the section entitled CORPORATE GOVERNANCE — Board Committees and Charters — Audit Committee in our Proxy Statement. Information about our executive officers is contained in the discussion entitled Item 1. Business — Executive Officers of the Registrant.

Code of Ethics

We maintain a code of ethics applicable to our principal executive officer, principal financial officer, principal accounting officer or controller, and other persons performing similar functions. To view this code of ethics free of charge, please visit our website at www.amgen.com (This website address is not intended to function as a hyperlink, and the information contained in our website is not intended to be a part of this filing). We intend to satisfy the disclosure requirements under Item 5.05 of Form 8-K regarding an amendment to, or waiver from, a provision of this code of ethics, if any, by posting such information on our website as set forth above.

 

Item 11. EXECUTIVE COMPENSATION

Information about director and executive compensation is incorporated by reference from the section entitled EXECUTIVE COMPENSATION in our Proxy Statement. Information about compensation committee matters is incorporated by reference from the sections entitled CORPORATE GOVERNANCE — Board Committees and Charters — Compensation and Management Development Committee and CORPORATE GOVERNANCE — Compensation Committee Report in our Proxy Statement.

 

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Item 12. SECURITY OWNERSHIP OF CERTAIN BENEFICIAL OWNERS AND MANAGEMENT AND RELATED STOCKHOLDER MATTERS

Securities Authorized for Issuance Under Existing Equity Compensation Plans

The following table sets forth certain information as of December 31, 2011, concerning our common stock that may be issued under any form of award granted under all of our equity compensation plans approved by stockholders and equity compensation plans not approved by stockholders in effect as of December 31, 2011 (including upon the exercise of options, pursuant to purchases of stock or upon vesting of awards of restricted stock units (RSUs) or performance units).

 

    (a)      (b)      (c)  

Plan Category

  Number of
Securities to be
Issued Upon
Exercise of
Outstanding
Options and Rights
     Weighted
Average
Exercise Price
Outstanding
Options and
Rights
     Number of
Securities Remaining
Available for Future
Issuance Under
Equity Compensation
Plans (Excluding
Securities Reflected
in Column (a))
 

Equity compensation plans approved by Amgen security holders:

       

2009 Equity Incentive Plan(1)

    25,145,740       $ 54.78         58,012,064   

Amended and Restated 1991 Equity Incentive Plan (2)

    10,937,360       $ 58.16           

Amended and Restated Employee Stock Purchase Plan(3)

          $         5,961,514   
 

 

 

       

 

 

 

Total Approved Plans

    36,083,100       $ 56.25         63,973,578   

Equity compensation plans not approved by Amgen security holders:

       

Amended and Restated 1993 Equity Incentive Plan(4)

    6,077       $ 52.60           

Amended and Restated 1999 Equity Incentive Plan(4)

    5,752,222       $ 65.37           

Amended and Restated 1997 Equity Incentive Plan(5)

    772,456       $ 51.71           

Amended and Restated 1997 Special Non-Officer Equity

       

Incentive Plan(6)

    3,136,770       $ 66.46           

Amended and Restated 1996 Incentive Stock Plan(7)

    290,500       $ 68.86           

Amended and Restated 1999 Incentive Stock Plan(7)

    1,271,686       $ 68.40           

Amended and Restated Assumed Avidia Equity Plan(8)

    11,415       $ 1.96           

Amgen Profit Sharing Plan for Employees in Ireland(9)

          $         192,180   
 

 

 

       

 

 

 

Total Unapproved Plans

    11,241,126       $ 65.06         192,180   
 

 

 

       

 

 

 

Total All Plans

    47,324,226       $ 59.11         64,165,758   
 

 

 

       

 

 

 

 

(1) 

The number under column (a) with respect to this plan includes approximately 13.06 million shares issuable upon the exercise of outstanding options with a weighted-average exercise price of approximately $54.78, approximately 8.03 million shares issuable upon the vesting of outstanding RSUs and approximately 4.05 million shares issuable upon the vesting of outstanding performance units. The performance units awarded in 2010 and 2011 continue to be subject to performance goals and the maximum number of units that could be earned is 200% of the units awarded in 2010 and 150% of the units awarded in 2011. The number under column (c) with respect to this plan represents the maximum number of shares that remain available for future issuance under this plan. This number may fluctuate depending on the nature of the award granted. Shares that are subject to awards of options or stock appreciation rights granted under the 2009 Plan will be counted against the pool of available shares under the 2009 Plan as one (1) share for every one (1) share granted. Shares that are subject to awards granted under the 2009 Plan other than options or

 

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stock appreciation rights will be counted against the pool of available shares under the 2009 Plan as 1.9 shares for every one (1) share granted. Furthermore, if any shares subject to an award under the 2009 Plan are forfeited or expire or an award under the 2009 Plan is settled for cash, then any shares subject to such award may, to the extent of such forfeiture, expiration or cash settlement, be used again for new grants under the 2009 Plan and the shares subject to such awards will be added back to the pool of available shares under the 2009 Plan as (i) one (1) share if such shares were subject to an option or stock appreciation right granted under the 2009 Plan and (ii) as 1.9 shares if such shares were subject to awards other than options or stock appreciation rights granted under the 2009 Plan.

 

(2) 

This plan has terminated as to future grants. The number under column (a) with respect to this plan includes approximately 10.04 million shares issuable upon the exercise of outstanding options with a weighted-average exercise price of approximately $58.16 and approximately 0.89 million shares issuable upon the vesting of outstanding RSUs.

 

(3) 

The purchases occurred on June 15, 2011, and December 15, 2011 (the Purchase Dates), with a purchase of 204,758 shares of Common Stock at a purchase price of $55.00 per shares on June 15, 2011, and 149,728 shares of Common Stock at a purchase price of $55.69 per share on December 15, 2011. Such purchases reflect 95% of the closing price of the Common Stock on the applicable Purchase Date.

 

(4) 

These plans have terminated as to future grants. These Plans were originally assumed pursuant to the terms of the merger agreement between Amgen and Immunex which was approved by our stockholders in May 2002. Both plans were previously approved by Immunex’s shareholders. The number under column (a) with respect to the Amended and Restated 1999 Equity Incentive Plan includes approximately 5.74 million shares issuable upon the exercise of outstanding options with a weighted-average exercise price of approximately $65.37 and approximately 12,000 shares issuable upon the vesting of outstanding RSUs.

 

(5) 

This plan has terminated as to future grants. This plan was originally assumed by Amgen in connection with the merger of Tularik with and into Amgen SF, LLC, a wholly owned subsidiary of Amgen, on August 13, 2004. This plan was previously approved by Tularik’s shareholders.

 

(6) 

This plan has terminated as to future grants.

 

(7) 

These plans have terminated as to future grants. These plans were originally assumed by Amgen in connection with the merger of Abgenix with and into Amgen Fremont Inc., a wholly owned subsidiary of Amgen, on April 1, 2006. The Amended and Restated 1996 Incentive Stock Plan (1996 Plan) was previously approved by Abgenix’s shareholders. The number under column (a) with respect to the 1996 Plan includes approximately 291,000 shares issuable upon the exercise of outstanding options with a weighted-average exercise price of approximately $68.86. The number under column (a) with respect to the Amended and Restated 1999 Incentive Stock Plan includes approximately 1.15 million shares issuable upon the exercise of outstanding options with a weighted-average exercise price of approximately $68.40 and approximately 119,000 shares issuable upon the vesting of outstanding RSUs.

 

(8) 

This plan has terminated as to future grants. This plan was originally assumed by Amgen in connection with the merger of Avidia, Inc. with and into Amgen Mountain View Inc., a wholly owned subsidiary of Amgen, on October 24, 2006.

 

(9) 

The Amgen Profit Sharing Plan for Employees in Ireland (the Profit Sharing Plan) was approved by the Board of Directors on July 28, 2011. The Profit Sharing Plan permits eligible employees of the Company’s subsidiaries located in Ireland, which participate in the Profit Sharing Plan, to apply a portion of their qualifying bonus and salary to the purchase the Company’s Common Stock on the open market at the market price by a third-party trustee as described in the Profit Sharing Plan. 7,820 shares were purchased on December 16, 2011.

 

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Security Ownership of Directors and Executive Officers and Certain Beneficial Owners

Information about security ownership of certain beneficial owners and management is incorporated by reference from the sections entitled SECURITY OWNERSHIP OF DIRECTORS AND EXECUTIVE OFFICERS and SECURITY OWNERSHIP OF CERTAIN BENEFICIAL OWNERS in our Proxy Statement.

 

Item 13. CERTAIN RELATIONSHIPS AND RELATED TRANSACTIONS AND DIRECTOR INDEPENDENCE

Information about certain relationships and related transactions and directors independence is incorporated by reference from the sections entitled CERTAIN RELATIONSHIPS AND RELATED TRANSACTIONS and CORPORATE GOVERNANCE — Board Independence in our Proxy Statement.

 

Item 14. PRINCIPAL ACCOUNTING FEES AND SERVICES

Information about the fees for professional services rendered by our independent registered public accountants is incorporated by reference from the section entitled AUDIT MATTERS — Independent Registered Public Accountants in our Proxy Statement.

 

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PART IV

 

Item 15. EXHIBITS AND FINANCIAL STATEMENT SCHEDULES

(a)1.     Index to Financial Statements

The following Consolidated Financial Statements are included herein:

 

     Page
number

Report of Independent Registered Public Accounting Firm

   F-1

Consolidated Statements of Income for each of the three years in the period ended December 31, 2011

   F-2

Consolidated Balance Sheets at December 31, 2011 and 2010

   F-3

Consolidated Statements of Stockholders’ Equity for each of the three years in the period ended December 31, 2011

   F-4

Consolidated Statements of Cash Flows for each of the three years in the period ended December 31, 2011

   F-5

Notes to Consolidated Financial Statements

   F-6 - F-55

(a)2.    Index to Financial Statement Schedules

The following Schedule is filed as part of this Annual Report on Form 10-K:

 

     Page
number

II. Valuation Accounts

   F-56

All other schedules are omitted because they are not applicable, not required or because the required information is included in the consolidated financial statements or notes thereto.

 

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(a)3.    Exhibits

 

Exhibit No.

  

Description

2.1   

Agreement and Plan of Merger, dated as of January 25, 2012, among Micromet, Inc., Amgen Inc., and Armstrong Acquisition Corp. (Filed as an exhibit to Form 8-K filed on January 26, 2012 and incorporated herein by reference.)

3.1   

Restated Certificate of Incorporation (As Restated December 7, 2005). (Filed as an exhibit to Form 10-K for the year ended December 31, 2005 on March 10, 2006 and incorporated herein by reference.)

3.2   

Certificate of Amendment of the Restated Certificate of Incorporation (As Amended May 24, 2007). (Filed as an exhibit to Form 10-Q for the quarter ended June 30, 2007 on August 9, 2007 and incorporated herein by reference.)

3.3   

Certificate of Correction of the Restated Certificate of Incorporation (As Corrected May 24, 2007). (Filed as an exhibit to Form 10-Q for the quarter ended June 30, 2007 on August 9, 2007 and incorporated herein by reference.)

3.4   

Certificate of Elimination of the Certificate of Designations of the Series A Junior Participating Preferred Stock (As Eliminated December 9, 2008). (Filed as an exhibit to Form 10-K for the year ended December 31, 2008 on February 27, 2009 and incorporated herein by reference.)

3.5   

Certificate of Amendment of the Restated Certificate of Incorporation (As Amended May 11, 2009). (Filed as an exhibit to Form 10-Q for the quarter ended June 30, 2009 on August 10, 2009 and incorporated herein by reference.)

3.6   

Certificate of Correction of the Restated Certificate of Incorporation (As Corrected May 11, 2009). (Filed as an exhibit to Form 10-Q for the quarter ended June 30, 2009 on August 10, 2009 and incorporated herein by reference.)

3.7   

Certificate of Correction of the Restated Certificate of Incorporation (As Corrected May 13, 2010). (Filed as an exhibit to Form 10-Q for the quarter ended June 30, 2010 on August 9, 2010.)

3.8   

Amended and Restated Bylaws of Amgen Inc. (As Amended and Restated October 6, 2009). (Filed as an exhibit to Form 8-K filed on October 7, 2009 and incorporated herein by reference.)

4.1   

Form of stock certificate for the common stock, par value $.0001 of the Company. (Filed as an exhibit to Form 10-Q for the quarter ended March 31, 1997 on May 13, 1997 and incorporated herein by reference.)

4.2   

Form of Indenture, dated January 1, 1992. (Filed as an exhibit to Form S-3 Registration Statement filed on December 19, 1991 and incorporated herein by reference.)

4.3   

Agreement of Resignation, Appointment and Acceptance dated February 15, 2008. (Filed as an exhibit to Form 10-K for the year ended December 31, 2007 on February 28, 2008 and incorporated herein by reference.)

4.4   

Two Agreements of Resignation, Appointment and Acceptance in the same form as the previously filed Exhibit 4.3 hereto are omitted pursuant to instruction 2 to Item 601 of Regulation S-K. Each of these agreements, which are dated December 15, 2008, replaces the current trustee under the agreements listed as Exhibits 4.9 and 4.15, respectively, with Bank of New York Mellon. Amgen Inc. hereby agrees to furnish copies of these agreements to the Securities and Exchange Commission upon request.

4.5   

First Supplemental Indenture, dated February 26, 1997. (Filed as an exhibit to Form 8-K on March 14, 1997 and incorporated herein by reference.)

4.6   

8-1/8% Debentures due April 1, 2097. (Filed as an exhibit to Form 8-K filed on April 8, 1997 and incorporated herein by reference.)

 

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Exhibit No.

  

Description

4.7   

Officer’s Certificate, dated as of January 1, 1992, as supplemented by the First Supplemental Indenture, dated as of February 26, 1997, establishing a series of securities entitled “8 1/8% Debentures due April 1, 2097.” (Filed as an exhibit to Form 8-K filed on April 8, 1997 and incorporated herein by reference.)

4.8   

Form of Liquid Yield Option™ Note due 2032. (Filed as an exhibit to Form 8-K on March 1, 2002 and incorporated herein by reference.)

4.9   

Indenture, dated as of March 1, 2002. (Filed as an exhibit to Form 8-K on March 1, 2002 and incorporated herein by reference.)

4.10   

First Supplemental Indenture, dated March 2, 2005. (Filed as an exhibit to Form 8-K filed on March 4, 2005 and incorporated herein by reference.)

4.11   

Indenture, dated as of August 4, 2003. (Filed as an exhibit to Form S-3 Registration Statement on August 4, 2003 and incorporated herein by reference.)

4.12   

Form of 4.85% Senior Notes due 2014. (Filed as an exhibit to Form 8-K on November 19, 2004 and incorporated herein by reference.)

4.13   

Officers’ Certificate, dated November 18, 2004, including forms of the 4.00% Senior Notes due 2009 and 4.85% Senior Notes due 2014. (Filed as an exhibit to Form 8-K on November 19, 2004 and incorporated herein by reference.)

4.14   

Form of Zero Coupon Convertible Note due 2032. (Filed as an exhibit to Form 8-K on May 6, 2005 and incorporated herein by reference.)

4.15   

Indenture, dated as of May 6, 2005. (Filed as an exhibit to Form 8-K on May 6, 2005 and incorporated herein by reference.)

4.16   

Indenture, dated as of February 17, 2006 and First Supplemental Indenture, dated as of June 8, 2006 (including form of 0.375% Convertible Senior Note due 2013). (Filed as exhibit to Form 10-Q for the quarter ended June 30, 2006 on August 9, 2006 and incorporated herein by reference.)

4.17   

Corporate Commercial Paper - Master Note between and among Amgen Inc., as Issuer, Cede & Co., as Nominee of The Depository Trust Company, and Citibank, N.A., as Paying Agent. (Filed as an exhibit to Form 10-Q for the quarter ended March 31, 1998 on May 13, 1998 and incorporated herein by reference.)

4.18   

Officers’ Certificate of Amgen Inc. dated as of May 30, 2007, including forms of the Company’s Senior Floating Rate Notes due 2008, 5.85% Senior Notes due 2017 and 6.375% Senior Notes due 2037. (Filed as an exhibit to Form 8-K on May 30, 2007 and incorporated herein by reference.)

4.19   

Officers’ Certificate of Amgen Inc. dated as of May 23, 2008, including forms of the Company’s 6.15% Senior Notes due 2018 and 6.90% Senior Notes due 2038. (Filed as exhibit to Form 8-K on May 23, 2009 and incorporated herein by reference.)

4.20   

Officers’ Certificate of Amgen Inc. dated as of January 16, 2009, including forms of the Company’s 5.70% Senior Notes due 2019 and 6.40% Senior Notes due 2039. (Filed as exhibit to Form 8-K on January 16, 2009 and incorporated herein by reference.)

4.21   

Officers’ Certificate of Amgen Inc. dated as of March 12, 2010, including forms of the Company’s 4.50% Senior Notes due 2020 and 5.75% Senior Notes due 2040. (Filed as exhibit to Form 8-K on March 15, 2010 and incorporated herein by reference.)

4.22   

Officers’ Certificate of Amgen Inc., dated as of September 16, 2010, including forms of the Company’s 3.45% Senior Notes due 2020 and 4.95% Senior Notes due 2041. (Filed as an exhibit to Form 8-K on September 17, 2010 and incorporated herein by reference.)

 

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Exhibit No.

  

Description

4.23   

Officers’ Certificate of Amgen Inc., dated as of June 30, 2011, including forms of the Company’s 2.30% Senior Notes due 2016, 4.10% Senior Notes due 2021 and 5.65% Senior Notes due 2042. (Filed as an exhibit to Form 8-K on June 30, 2011 and incorporated herein by reference.)

4.24   

Officers’ Certificate of Amgen Inc., dated as of November 10, 2011, including forms of the Company’s 1.875% Senior Notes due 2014, 2.50% Senior Notes due 2016, 3.875% Senior Notes due 2021 and 5.15% Senior Notes due 2041. (Filed as an exhibit to Form 8-K on November 10, 2011 and incorporated herein by reference.)

4.25   

Officers’ Certificate of Amgen Inc., dated as of December 5, 2011, including forms of the Company’s 4.375% Senior Notes due 2018 and 5.50% Senior Notes due 2026. (Filed as an exhibit to Form 8-K on December 5, 2011 and incorporated herein by reference.)

10.1+   

Amgen Inc. 2009 Equity Incentive Plan. (Filed as Appendix A to Amgen Inc.’s Proxy Statement on March 26, 2009 and incorporated herein by reference.)

10.2+   

Form of Stock Option Agreement for the Amgen Inc. 2009 Equity Incentive Plan. (As Amended on March 2, 2011.) (Filed as an exhibit to Form 10-Q for the quarter ended March 31, 2011 on May 10, 2011 and incorporated herein by reference.)

10.3+   

Form of Restricted Stock Unit Agreement for the Amgen Inc. 2009 Equity Incentive Plan. (As Amended on March 2, 2011.) (Filed as an exhibit to Form 10-Q for the quarter ended March 31, 2011 on May 10, 2011 and incorporated herein by reference.)

10.4+   

Amgen Inc. 2009 Performance Award Program. (As Amended and Restated on December 4, 2009.) (Filed as an exhibit to Form 10-K for the year ended December 31, 2009 on March 1, 2010 and incorporated herein by reference.)

10.5+   

Form of Performance Unit Agreement for the Amgen Inc. 2009 Performance Award Program. (As Amended on March 2, 2011.) (Filed as an exhibit to Form 10-Q for the quarter ended March 31, 2011 on May 10, 2011 and incorporated herein by reference.)

10.6+   

Amgen Inc. 2009 Director Equity Incentive Program. (Filed as an exhibit to Form 8-K on May 8, 2009 and incorporated herein by reference.)

10.7+   

Form of Grant of Non-Qualified Stock Option Agreement and Restricted Stock Unit Agreement for the Amgen Inc. 2009 Director Equity Incentive Program. (Filed as an exhibit to Form 8-K on May 8, 2009 and incorporated herein by reference.)

10.8+   

Amgen Supplemental Retirement Plan. (As Amended and Restated effective January 1, 2009.) (Filed as an exhibit to Form 10-Q for the quarter ended September 30, 2008 on November 7, 2008 and incorporated herein by reference.)

10.9+   

First Amendment to the Amgen Supplemental Retirement Plan, effective April 11, 2011. (Filed as an exhibit to Form 10-Q for the quarter ended June 30, 2011 on August 8, 2011 and incorporated herein by reference.)

10.10+*   

Second Amendment to the Amgen Supplemental Retirement Plan, effective October 12, 2011.

10.11+*    Third Amendment to the Amgen Supplemental Retirement Plan, executed December 16, 2011.
10.12+   

Amended and Restated Amgen Change of Control Severance Plan. (As Amended and Restated effective December 9, 2010 and subsequently amended effective March 2, 2011.) (Filed as an exhibit to Form 10-Q for the quarter ended March 31, 2011 on May 10, 2011 and incorporated herein by reference.)

10.13+   

Amgen Inc. Executive Incentive Plan. (As Amended and Restated effective January 1, 2009.) (Filed as an exhibit to Form 10-Q for the quarter ended September 30, 2008 on November 7, 2008 and incorporated herein by reference.)

10.14+   

Amgen Inc. Executive Nonqualified Retirement Plan. (As Amended and Restated effective January 1, 2009.) (Filed as an exhibit to Form 10-Q for the quarter ended September 30, 2008 on November 7, 2008 and incorporated herein by reference.)

 

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Exhibit No.

  

Description

10.15+   

First Amendment to the Amgen Inc. Executive Nonqualified Retirement Plan. (Filed as an exhibit to Form 10-Q for the quarter ended June 30, 2010 on August 9, 2010 and incorporated herein by reference.)

10.16+   

Amgen Nonqualified Deferred Compensation Plan. (As Amended and Restated effective January 1, 2009.) (Filed as an exhibit to Form 10-Q for the quarter ended September 30, 2008 on November 7, 2008 and incorporated herein by reference.)

10.17+   

First Amendment to the Amgen Nonqualified Deferred Compensation Plan, effective April 11, 2011. (Filed as an exhibit to Form 10-Q for the quarter ended June 30, 2011 on August 8, 2011 and incorporated herein by reference.)

10.18+*   

Second Amendment to the Amgen Nonqualified Deferred Compensation Plan, effective October 12, 2011.

10.19+   

2002 Special Severance Pay Plan for Amgen Employees. (Filed as an exhibit to Form 10-Q for the quarter ended June 30, 2002 on August 13, 2002 and incorporated herein by reference.)

10.20+   

Agreement between Amgen Inc. and Mr. Jonathan M. Peacock, dated July 5, 2010. (Filed as an exhibit to Form 10-Q for the quarter ended September 30, 2010 on November 8, 2010 and incorporated herein by reference.)

10.21+*   

Agreement between Amgen Inc. and Mr. Anthony C. Hooper, dated October 12, 2011.

10.22+   

Consulting Agreement, effective February 1, 2011, between Amgen Inc. and Mr. George Morrow. (Filed as an exhibit to Form 8-K on October 22, 2010 and incorporated herein by reference).

10.23   

Product License Agreement, dated September 30, 1985, and Technology License Agreement, dated, September 30, 1985 between Amgen and Ortho Pharmaceutical Corporation. (Filed as an exhibit to Form 10-Q for the quarter ended June 30, 2000 on August 1, 2000 and incorporated herein by reference.)

10.24   

Shareholders’ Agreement, dated May 11, 1984, among Amgen, Kirin Brewery Company, Limited and Kirin-Amgen, Inc. (Filed as an exhibit to Form 10-K for the year ended December 31, 2000 on March 7, 2001 and incorporated herein by reference.)

10.25   

Amendment No. 1 dated March 19, 1985, Amendment No. 2 dated July 29, 1985 (effective July 1, 1985), and Amendment No. 3, dated December 19, 1985, to the Shareholders’ Agreement dated May 11, 1984. (Filed as an exhibit to Form 10-Q for the quarter ended June 30, 2000 on August 1, 2000 and incorporated herein by reference.)

10.26   

Amendment No. 4 dated October 16, 1986 (effective July 1, 1986), Amendment No. 5 dated December 6, 1986 (effective July 1, 1986), Amendment No. 6 dated June 1, 1987, Amendment No. 7 dated July 17, 1987 (effective April 1, 1987), Amendment No. 8 dated May 28, 1993 (effective November 13, 1990), Amendment No. 9 dated December 9, 1994 (effective June 14, 1994), Amendment No. 10 effective March 1, 1996, and Amendment No. 11 effective March 20, 2000 to the Shareholders’ Agreement, dated May 11, 1984. (Filed as exhibits to Form 10-K for the year ended December 31, 2000 on March 7, 2001 and incorporated herein by reference.)

10.27   

Amendment No. 12 to the Shareholders’ Agreement, dated January 31, 2001. (Filed as an exhibit to Form 10-Q for the quarter ended June 30, 2005 on August 8, 2005 and incorporated herein by reference.)

10.28   

Amendment No. 13 to the Shareholders’ Agreement, dated June 28, 2007 (with certain confidential information deleted therefrom). (Filed as an exhibit to Form 10-Q for the quarter ended June 30, 2007 on August 9, 2007 and incorporated herein by reference.)

 

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Exhibit No.

  

Description

10.29   

Product License Agreement, dated September 30, 1985, and Technology License Agreement, dated September 30, 1985, between Kirin-Amgen, Inc. and Ortho Pharmaceutical Corporation. (Filed as an exhibit to Form 10-Q for the quarter ended June 30, 2000 on August 1, 2000 and incorporated herein by reference.)

10.30   

Research, Development Technology Disclosure and License Agreement: PPO, dated January 20, 1986, by and between Kirin Brewery Co., Ltd. and Amgen Inc. (Filed as an exhibit to Amendment No. 1 to Form S-1 Registration Statement on March 11, 1986 and incorporated herein by reference.)

10.31   

Assignment and License Agreement, dated October 16, 1986 (effective July 1, 1986, between Amgen and Kirin-Amgen, Inc. (Filed as an exhibit to Form 10-K for the year ended December 31, 2000 on March 7, 2001 and incorporated herein by reference.)

10.32   

G-CSF United States License Agreement, dated June 1, 1987 (effective July 1, 1986), Amendment No. 1, dated October 20, 1988, and Amendment No. 2, dated October 17, 1991 (effective November 13, 1990), between Kirin-Amgen, Inc. and Amgen Inc. (Filed as exhibits to Form 10-K for the year ended December 31, 2000 on March 7, 2001 and incorporated herein by reference.)

10.33   

G-CSF European License Agreement, dated December 30, 1986, between Kirin-Amgen and Amgen, Amendment No. 1 to Kirin-Amgen, Inc. / Amgen G-CSF European License Agreement, dated June 1, 1987, Amendment No. 2 to Kirin-Amgen, Inc. / Amgen G-CSF European License Agreement, dated March 15, 1998, Amendment No. 3 to Kirin-Amgen, Inc. / Amgen G-CSF European License Agreement, dated October 20, 1988, and Amendment No. 4 to Kirin-Amgen, Inc. / Amgen G-CSF European License Agreement, dated December 29, 1989, between Kirin-Amgen, Inc. and Amgen Inc. (Filed as exhibits to Form 10-K for the year ended December 31, 2000 on March 7, 2001 and incorporated herein by reference.)

10.34   

Agreement Regarding Governance and Commercial Matters, dated December 16, 2001, by and among American Home Products Corporation, American Cyanamid Company and Amgen Inc. (with certain confidential information deleted therefrom). (Filed as an exhibit to Amendment No. 1 to Form S-4 Registration Statement on March 22, 2002 and incorporated herein by reference.)

10.35   

Amended and Restated Promotion Agreement, dated as of December 16, 2001, by and among Immunex Corporation, American Home Products Corporation and Amgen Inc. (with certain confidential information deleted therefrom). (Filed as an exhibit to Amendment No. 1 to Form S-4 Registration Statement on March 22, 2002 and incorporated herein by reference.)

10.36   

Description of Amendment No. 1 to Amended and Restated Promotion Agreement, effective as of July 8, 2003, among Wyeth, Amgen Inc. and Immunex Corporation (with certain confidential information deleted therefrom). (Filed as an exhibit to Form 10-K for the year ended December 31, 2003 on March 11, 2004 and incorporated herein by reference.)

10.37   

Description of Amendment No. 2 to Amended and Restated Promotion Agreement, effective as of April 20, 2004, by and among Wyeth, Amgen Inc. and Immunex Corporation. (Filed as an exhibit to Form S-4/A on June 29, 2004 and incorporated herein by reference.)

10.38   

Amendment No. 3 to Amended and Restated Promotion Agreement, effective as of January 1, 2005, by and among Wyeth, Amgen Inc. and Immunex Corporation (with certain confidential information deleted therefrom). (Filed as an exhibit to Form 10-Q for the quarter ended March 31, 2005 on May 4, 2005 and incorporated herein by reference.)

10.39   

Confirmation of OTC Convertible Note Hedge related to 2013 Notes, dated February 14, 2006, to Amgen Inc. from Merrill Lynch International related to 0.375% Convertible Senior Notes Due 2013. (Filed as an exhibit to Form 10-K for the year ended December 31, 2005 on March 10, 2006 and incorporated herein by reference.)

10.40   

Confirmation of OTC Warrant Transaction, dated February 14, 2006, to Amgen Inc. from Merrill Lynch International for warrants expiring in 2013. (Filed as an exhibit to Form 10-K for the year ended December 31, 2005 on March 10, 2006 and incorporated herein by reference.)

 

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Exhibit No.

  

Description

10.41   

Collaboration Agreement, dated July 11, 2007, between Amgen Inc. and Daiichi Sankyo Company (with certain confidential information deleted therefrom). (Filed as an exhibit to Form 10-Q for the quarter ended September 30, 2007 on November 9, 2007 and incorporated herein by reference.)

10.42   

Credit Agreement, dated as of December 2, 2011, among Amgen Inc., with Citibank, N.A., as administrative agent, JPMorgan Chase Bank, N.A., as syndication agent, Citigroup Global Markets Inc. and J.P. Morgan Securities LLC as joint lead arrangers and joint book runners, and the other banks party thereto. (Filed as an exhibit to Form 8-K filed on December 2, 2011 and incorporated herein by reference.)

10.43   

Multi-product License Agreement with Respect to Japan between Amgen Inc. and Takeda Pharmaceutical Company Limited dated February 1, 2008 (with certain confidential information deleted therefrom). (Filed as an exhibit to Form 10-Q for the quarter ended March 31, 2008 on May 12, 2008 and incorporated herein by reference.)

10.44   

License Agreement for motesanib diphosphate between Amgen Inc. and Takeda Pharmaceutical Company Limited dated February 1, 2008 (with certain confidential information deleted therefrom). (Filed as an exhibit to Form 10-Q for the quarter ended March 31, 2008 on May 12, 2008 and incorporated herein by reference.)

10.45   

Supply Agreement between Amgen Inc. and Takeda Pharmaceutical Company Limited dated February 1, 2008 (with certain confidential information deleted therefrom). (Filed as an exhibit to Form 10-Q for the quarter ended March 31, 2008 on May 12, 2008 and incorporated herein by reference.)

10.46   

Sale and Purchase Agreement between Amgen Inc. and Takeda Pharmaceutical Company Limited dated February 1, 2008 (with certain confidential information deleted therefrom). (Filed as an exhibit to Form 10-Q for the quarter ended March 31, 2008 on May 12, 2008 and incorporated herein by reference.)

10.47   

Integrated Facilities Management Services Agreement, dated February 4, 2009, between Amgen Inc. and Jones Lang LaSalle Americas, Inc. (with certain confidential information deleted therefrom) (Previously filed as an exhibit to Form 10-K for the year ended December 31, 2008 on February 27, 2009.), as amended by Amendment Number 1 dated March 31, 2010 (with certain confidential information deleted therefrom), Amendment Number 2 dated May 12, 2011 (as corrected by the Letter Agreement) (with certain confidential information deleted therefrom), and Letter Agreement dated July 19, 2011. (Filed as an exhibit to Form 10-Q for the quarter ended June 30, 2011 on August 8, 2011 and incorporated herein by reference.)

10.48   

Amendment Number 3, dated July 1, 2011, to the Integrated Facilities Management Services Agreement, dated February 4, 2009, between Amgen Inc. and Jones Lang LaSalle Americas, Inc. (Filed as an exhibit to Form 10-Q for the quarter ended September 30, 2011 on November 4, 2011 and incorporated herein by reference.)

10.49   

Collaboration Agreement dated July 27, 2009 between Amgen Inc. and Glaxo Group Limited, a wholly owned subsidiary of GlaxoSmithKline plc (with certain confidential information deleted therefrom). (Filed as an exhibit to Form 10-Q for the quarter ended September 30, 2009 on November 6, 2009 and incorporated herein by reference.)

10.50   

Expansion Agreement dated July 27, 2009 between Amgen Inc. and Glaxo Group Limited, a wholly owned subsidiary of GlaxoSmithKline plc (with certain confidential information deleted therefrom). (Filed as an exhibit to Form 10-Q for the quarter ended September 30, 2009 on November 6, 2009 and incorporated herein by reference.)

10.51   

Amendment Number 1, dated September 20, 2010, to Expansion Agreement dated July 27, 2009 between Amgen Inc. and Glaxo Group Limited, a wholly owned subsidiary of GlaxoSmithKline plc (with certain confidential information deleted therefrom). (Filed as an exhibit to Form 10-Q for the quarter ended September 30, 2010 on November 8, 2010 and incorporated herein by reference.)

 

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Exhibit No.

 

Description

10.52 *  

Sourcing and Supply Agreement, dated November 15, 2011, by and between Amgen USA Inc., a wholly owned subsidiary of Amgen Inc., and DaVita Inc. (with certain confidential information deleted therefrom).

21*  

Subsidiaries of the Company

23  

Consent of the Independent Registered Public Accounting Firm. The consent is set forth on pages 105 and 106 of this Annual Report on Form 10-K.

24  

Power of Attorney. The Power of Attorney is set forth on pages 107 and 108 of this Annual Report on Form 10-K.

31*  

Rule 13a-14(a) Certifications.

32**  

Section 1350 Certifications.

101.INS*  

XBRL Instance Document.

101.SCH*  

XBRL Taxonomy Extension Schema Document.

101.CAL*  

XBRL Taxonomy Extension Calculation Linkbase Document.

101.LAB*  

XBRL Taxonomy Extension Label Linkbase Document.

101.PRE*  

XBRL Taxonomy Extension Presentation Linkbase Document.

101.DEF*  

XBRL Taxonomy Extension Definition Linkbase.

 

(*   =

filed herewith)

 

(** =

furnished herewith and not “filed” for purposes of Section 18 of the Securities Exchange Act of 1934, as amended)

 

(+   =

management contract or compensatory plan or arrangement)

 

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SIGNATURES

Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this Annual Report to be signed on its behalf by the undersigned, thereunto duly authorized.

 

 

AMGEN INC.

 

(Registrant)

Date: 02/29/2012

  By:   /S/    JONATHAN M. PEACOCK
    Jonathan M. Peacock
    Executive Vice President
    and Chief Financial Officer

 

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EXHIBIT 23

CONSENT OF INDEPENDENT REGISTERED PUBLIC ACCOUNTING FIRM

We consent to the incorporation by reference in the following Registration Statements:

 

 

Registration Statement (Form S-8 No. 333-159377) pertaining to the Amgen Inc. 2009 Equity Incentive Plan;

 

 

Registration Statement (Form S-8 No. 33-39183) pertaining to the Amended and Restated Employee Stock Purchase Plan;

 

 

Registration Statements (Form S-8 No. 33-39104, as amended by Form S-8 No. 333-144581) pertaining to the Amended and Restated Amgen Retirement and Savings Plan (formerly known as the Amgen Retirement and Savings Plan);

 

 

Registration Statements (Form S-8 Nos. 33-42072 and 333-144579) pertaining to the Amgen Inc. Amended and Restated 1991 Equity Incentive Plan;

 

 

Registration Statements (Form S-8 Nos. 33-47605 and 333-144580) pertaining to the Retirement and Savings Plan for Amgen Manufacturing, Limited (formerly known as the Retirement and Savings Plan for Amgen Manufacturing, Inc.);

 

 

Registration Statements (Form S-8 Nos. 333-44727, 333-62735, 333-56672 and 333-83824) pertaining to the Amgen Inc. Amended and Restated 1997 Special Non-Officer Equity Incentive Plan (formerly known as the Amgen Inc. 1997 Special Non-Officer Equity Incentive Plan);

 

 

Registration Statement (Form S-3 No. 333-19931) pertaining to debt securities of Amgen Inc.;

 

 

Registration Statement (Form S-3 No. 333-40405) pertaining to debt securities of Amgen Inc.;

 

 

Registration Statement (Form S-3 No. 333-53929) pertaining to the Amgen Inc. 1997 Special Non-Officer Equity Incentive Plan, the Amgen Inc. Amended and Restated 1991 Equity Incentive Plan, the Amended and Restated 1988 Stock Option Plan of Amgen Inc. and the Amended and Restated 1987 Directors’ Stock Option Plan;

 

 

Registration Statements (Form S-8 Nos. 333-81284 and 333-177868) pertaining to the Amgen Nonqualified Deferred Compensation Plan;

 

 

Registration Statements (Form S-3 No. 333-56664 and Amendment No. 1 thereto) pertaining to the Amgen Inc. 1997 Special Non-Officer Equity Incentive Plan, the Amgen Inc. Amended and Restated 1991 Equity Incentive Plan;

 

 

Registration Statement (Form S-3 No. 333-88834) pertaining to Amgen Inc.’s Liquid Yield Option™ Notes due 2032;

 

 

Registration Statements (Form S-3 No. 333-92450 and Amendment No. 1 thereto) pertaining to Amgen Inc.’s Common Stock;

 

 

Registration Statements (Form S-8 No. 333-92424 and Amendment No. 1 thereto) pertaining to the Amgen Inc. Amended and Restated 1993 Equity Incentive Plan (formerly known as the Immunex Corporation 1993 Stock Option Plan), the Amgen Inc. Amended and Restated 1999 Equity Incentive Plan (formerly known as the Immunex Corporation 1999 Stock Option Plan);

 

 

Registration Statements (Form S-3 No. 333-107639 and Amendment 1 thereto) relating to debt securities, common stock and associated preferred share repurchase rights, preferred stock, warrants to purchase debt securities, common stock or preferred stock, securities purchase contracts, securities purchase units and depositary shares of Amgen Inc. and in the related Prospectuses;

 

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Registration Statement (Form S-8 No. 333-118254) pertaining to the Amgen Inc. Amended and Restated 1997 Equity Incentive Plan (formerly known as the Tularik Inc. 1997 Equity Incentive Plan, as amended);

 

 

Registration Statement (Form S-3 No. 333-132286) relating to the potential resale of securities acquired from Amgen Inc. by selling security holders in unregistered private offerings;

 

 

Registration Statement (Form S-8 No. 333-132932) pertaining to the Amgen Inc. Amended and Restated 1996 Incentive Stock Plan (formerly known as Abgenix, Inc. 1996 Incentive Stock Plan, as amended and restated), the Amgen Inc. Amended and Restated 1999 Incentive Stock Plan (formerly known as Abgenix, Inc. 1999 Nonstatutory Stock Option Plan, as amended and restated);

 

 

Registration Statement (Form S-8 No. 333-133002) pertaining to the Amgen Inc. Amended and Restated 1999 Incentive Stock Plan (formerly known as Abgenix, Inc. 1999 Nonstatutory Stock Option Plan, as amended and restated);

 

 

Registration Statement (Form S-8 No. 333-138325) pertaining to the Amgen Inc. Amended and Restated Assumed Avidia Equity Incentive Plan (formerly known as the Avidia, Inc. Amended and Restated 2003 Equity Incentive Plan);

 

 

Registration Statement (Form S-4 No. 333-147482) relating to the possible exchange of unregistered Senior Floating Notes for registered Senior Floating Notes relating to the Prospectus of Amgen Inc. for the registration of Senior Floating Rate Notes due 2008, 5.85% Senior Notes due 2017, 6.375% Senior Notes Due 2037; and

 

 

Registration Statements (Form S-3 Nos. 333-150290 and 333-172617) relating to debt securities, common stock, preferred stock, warrants to purchase debt securities, common stock, preferred stock or depositary shares, rights to purchase common stock or preferred stock, securities purchase contracts, securities purchase units and depositary shares of Amgen Inc. and in the related Prospectuses.

 

 

Registration Statement (Form S-8 No. 333-176240) pertaining to the Amgen Profit Sharing Plan for Employees in Ireland;

of our reports dated February 29, 2012, with respect to the consolidated financial statements and schedule of Amgen Inc. and the effectiveness of internal control over financial reporting of Amgen Inc. included in this Annual Report (Form 10-K) of Amgen Inc. for the year ended December 31, 2011.

/s/ Ernst & Young LLP

Los Angeles, California

February 29, 2012

 

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EXHIBIT 24

POWER OF ATTORNEY

KNOW ALL MEN AND WOMEN BY THESE PRESENTS, that each person whose signature appears below constitutes and appoints Jonathan M. Peacock and Thomas J.W. Dittrich, or either of them, his or her attorney-in-fact, each with the power of substitution, for him or her in any and all capacities, to sign any amendments to this Report, and to file the same, with exhibits thereto and other documents in connection therewith, with the Securities and Exchange Commission, hereby ratifying and confirming all that each of said attorneys-in-fact, or his or her substitute or substitutes, may do or cause to be done by virtue hereof.

Pursuant to the requirements of the Securities Exchange Act of 1934, this report has been signed below by the following persons on behalf of the registrant and in the capacities and on the dates indicated:

 

Signature

  

Title

 

Date

/S/    KEVIN W. SHARER

Kevin W. Sharer

  

Chairman of the Board, Chief

Executive Officer and Director

(Principal Executive Officer)

  02/29/2012

/S/    JONATHAN M. PEACOCK

Jonathan M. Peacock

  

Executive Vice President and Chief

Financial Officer

(Principal Financial Officer)

  02/29/2012

/S/    THOMAS J.W. DITTRICH

Thomas J.W. Dittrich

  

Vice President Finance and Chief

Accounting Officer

(Principal

Accounting Officer)

  02/27/2012

/S/    ROBERT A. BRADWAY

Robert A. Bradway

   President, Chief Operating Officer and Director  

02/29/2012

/S/    DAVID BALTIMORE

David Baltimore

   Director   02/29/2012

/S/    FRANK J. BIONDI, JR.

Frank J. Biondi, Jr.

   Director   02/29/2012

/S/    VANCE D. COFFMAN

Vance D. Coffman

   Director   02/29/2012

/S/    FRANÇOIS DE CARBONNEL

François de Carbonnel

   Director   02/29/2012

/S/    REBECCA M. HENDERSON

Rebecca M. Henderson

   Director   02/29/2012

/S/    FRANK C. HERRINGER

Frank C. Herringer

   Director   02/23/2012

/S/    GILBERT S. OMENN

Gilbert S. Omenn

   Director   02/29/2012

 

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Signature

  

Title

 

Date

/S/    JUDITH C. PELHAM

Judith C. Pelham

   Director   02/29/2012

/S/    J. PAUL REASON

J. Paul Reason

   Director   02/29/2012

/S/    LEONARD D. SCHAEFFER

Leonard D. Schaeffer

   Director   02/29/2012

/S/    RONALD D. SUGAR

Ronald D. Sugar

   Director   02/29/2012

 

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Report of Independent Registered Public Accounting Firm

The Board of Directors and Stockholders of Amgen Inc.

We have audited the accompanying Consolidated Balance Sheets of Amgen Inc. (the “Company”) as of December 31, 2011 and 20010, and the related Consolidated Statements of Income, Stockholders’ Equity, and Cash Flows for each of the three years in the period ended December 31, 2011. Our audits also included the financial statement schedule listed in the Index at Item 15(a) 2. These financial statements and schedule are the responsibility of the Company’s management. Our responsibility is to express an opinion on these financial statements and schedule based on our audits.

We conducted our audits in accordance with the standards of the Public Company Accounting Oversight Board (United States). Those standards require that we plan and perform the audit to obtain reasonable assurance about whether the financial statements are free of material misstatement. An audit includes examining, on a test basis, evidence supporting the amounts and disclosures in the financial statements. An audit also includes assessing the accounting principles used and significant estimates made by management, as well as evaluating the overall financial statement presentation. We believe that our audits provide a reasonable basis for our opinion.

In our opinion, the financial statements referred to above present fairly, in all material respects, the consolidated financial position of Amgen Inc. at December 31, 2011 and 2010, and the consolidated results of its operations and its cash flows for each of the three years in the period ended December 31, 2011, in conformity with U.S. generally accepted accounting principles. Also, in our opinion, the related financial statement schedule, when considered in relation to the basic financial statements taken as a whole, presents fairly in all material respects the information set forth therein.

We also have audited, in accordance with the standards of the Public Company Accounting Oversight Board (United States), Amgen Inc.’s internal control over financial reporting as of December 31, 2011, based on criteria established in Internal Control — Integrated Framework issued by the Committee of Sponsoring Organizations of the Treadway Commission and our report dated February 29, 2012 expressed an unqualified opinion thereon.

/s/ Ernst & Young LLP

Los Angeles, California

February 29, 2012

 

F-1


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For the fiscal year ended December 31, 2011

AMGEN INC.

CONSOLIDATED STATEMENTS OF INCOME

Years ended December 31, 2011, 2010 and 2009

(In millions, except per share data)

 

     2011      2010      2009  

Revenues:

        

Product sales

   $ 15,295       $ 14,660       $ 14,351   

Other revenues

     287         393         291   
  

 

 

    

 

 

    

 

 

 

Total revenues

     15,582         15,053         14,642   
  

 

 

    

 

 

    

 

 

 

Operating expenses:

        

Cost of sales (excludes amortization of certain acquired intangible assets presented separately)

     2,427         2,220         2,091   

Research and development

     3,167         2,894         2,864   

Selling, general and administrative

     4,486         3,983         3,820   

Amortization of certain acquired intangible assets

     294         294         294   

Other

     896         117         67   
  

 

 

    

 

 

    

 

 

 

Total operating expenses

     11,270         9,508         9,136   
  

 

 

    

 

 

    

 

 

 

Operating income

     4,312         5,545         5,506   

Interest expense, net

     610         604         578   

Interest and other income, net

     448         376         276   
  

 

 

    

 

 

    

 

 

 

Income before income taxes

     4,150         5,317         5,204   

Provision for income taxes

     467         690         599   
  

 

 

    

 

 

    

 

 

 

Net income

   $ 3,683       $ 4,627       $ 4,605   
  

 

 

    

 

 

    

 

 

 

Earnings per share:

        

Basic

   $ 4.07       $ 4.82       $ 4.53   

Diluted

   $ 4.04       $ 4.79       $ 4.51   

Shares used in the calculation of earnings per share:

        

Basic

     905         960         1,016   

Diluted

     912         965         1,021   

See accompanying notes.

 

F-2


Table of Contents

AMGEN INC.

CONSOLIDATED BALANCE SHEETS

December 31, 2011 and 2010

(In millions, except per share data)

 

     2011     2010  
ASSETS   

Current assets:

    

Cash and cash equivalents

   $ 6,946      $ 3,287   

Marketable securities

     13,695        14,135   

Trade receivables, net

     2,896        2,335   

Inventories

     2,484        2,022   

Other current assets

     1,572        1,350   
  

 

 

   

 

 

 

Total current assets

     27,593        23,129   

Property, plant and equipment, net

     5,420        5,522   

Intangible assets, net

     2,584        2,230   

Goodwill

     11,750        11,334   

Other assets

     1,524        1,271   
  

 

 

   

 

 

 

Total assets

   $ 48,871      $ 43,486   
  

 

 

   

 

 

 
LIABILITIES AND STOCKHOLDERS’ EQUITY   

Current liabilities:

    

Accounts payable

   $ 642      $ 716   

Accrued liabilities

     5,028        3,366   

Current portion of long-term debt

     84        2,488   
  

 

 

   

 

 

 

Total current liabilities

     5,754        6,570   

Long-term debt

     21,344        10,874   

Other noncurrent liabilities

     2,744        2,098   

Contingencies and commitments

    

Stockholders’ equity:

    

Common stock and additional paid-in capital; $0.0001 par value; 2,750.0 shares authorized; outstanding — 795.6 shares in 2011 and 932.1 shares in 2010

     27,777        27,299   

Accumulated deficit

     (8,919     (3,508

Accumulated other comprehensive income

     171        153   
  

 

 

   

 

 

 

Total stockholders’ equity

     19,029        23,944   
  

 

 

   

 

 

 

Total liabilities and stockholders’ equity

   $ 48,871      $ 43,486   
  

 

 

   

 

 

 

See accompanying notes.

 

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AMGEN INC.

CONSOLIDATED STATEMENTS OF STOCKHOLDERS’ EQUITY

Years ended December 31, 2011, 2010 and 2009

(In millions)

 

    Number
of shares
of common
stock
    Common
stock and
additional
paid-in capital
    Accumulated
deficit
    Accumulated
other
comprehensive
income
    Total  

Balance at December 31, 2008

    1,047.5      $ 26,441      $ (5,673   $ 117      $ 20,885   

Comprehensive income:

         

Net income

                  4,605               4,605   

Other comprehensive loss, net of tax

                         (72     (72
         

 

 

 

Comprehensive income

            4,533   

Issuance of common stock in connection with the Company’s equity award programs

    6.3        190                      190   

Stock-based compensation

           324                      324   

Tax impact related to employee stock options

           (11                   (11

Repurchases of common stock

    (59.2            (3,254            (3,254
 

 

 

   

 

 

   

 

 

   

 

 

   

 

 

 

Balance at December 31, 2009

    994.6        26,944        (4,322     45        22,667   

Comprehensive income:

         

Net income

                  4,627               4,627   

Other comprehensive income, net of tax

                         108        108   
         

 

 

 

Comprehensive income

            4,735   

Issuance of common stock in connection with the Company’s equity award programs

    4.0        69                      69   

Stock-based compensation

           357                      357   

Tax impact related to employee stock options

           (71                   (71

Repurchases of common stock

    (66.5            (3,800            (3,800

Other

                  (13            (13
 

 

 

   

 

 

   

 

 

   

 

 

   

 

 

 

Balance at December 31, 2010

    932.1        27,299        (3,508     153        23,944   

Comprehensive income:

         

Net income

                  3,683               3,683   

Other comprehensive income, net of tax

                         18        18   
         

 

 

 

Comprehensive income

            3,701   

Dividends

                  (787            (787

Issuance of common stock in connection with the Company’s equity award programs

    7.8        230                      230   

Stock-based compensation

           337                      337   

Tax impact related to employee stock options

           (89                   (89

Repurchases of common stock

    (144.3            (8,307            (8,307
 

 

 

   

 

 

   

 

 

   

 

 

   

 

 

 

Balance at December 31, 2011

    795.6      $ 27,777      $ (8,919   $ 171      $ 19,029   
 

 

 

   

 

 

   

 

 

   

 

 

   

 

 

 

See accompanying notes.

 

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AMGEN INC.

CONSOLIDATED STATEMENTS OF CASH FLOWS

Years ended December 31, 2011, 2010 and 2009

(In millions)

 

     2011     2010     2009  

Cash flows from operating activities:

      

Net income

   $ 3,683      $ 4,627      $ 4,605   

Depreciation and amortization

     1,060        1,017        1,049   

Stock-based compensation expense

     341        353        284   

Deferred income taxes

     (399     (167     47   

Property, plant and equipment impairments

     6        118        21   

Dividend received from equity investee

                   110   

Other items, net

     63        140        111   

Changes in operating assets and liabilities, net of acquisitions:

      

Trade receivables, net

     (557     (210     (36

Inventories

     (383     153        (134

Other assets

     (133     36        (3

Accounts payable

     (95     142        71   

Accrued income taxes

     (20     (656     (142

Legal reserve

     780                 

Other liabilities

     773        234        353   
  

 

 

   

 

 

   

 

 

 

Net cash provided by operating activities

     5,119        5,787        6,336   
  

 

 

   

 

 

   

 

 

 

Cash flows from investing activities:

      

Purchases of property, plant and equipment

     (567     (580     (530

Cash paid for acquisitions, net of cash acquired

     (701              

Purchases of marketable securities

     (21,183     (14,602     (12,418

Proceeds from sales of marketable securities

     20,871        10,485        8,252   

Proceeds from maturities of marketable securities

     749        642        1,443   

Other

     45        (97     51   
  

 

 

   

 

 

   

 

 

 

Net cash used in investing activities

     (786     (4,152     (3,202
  

 

 

   

 

 

   

 

 

 

Cash flows from financing activities:

      

Repurchases of common stock

     (8,315     (3,786     (3,208

Repayment of debt

     (2,500            (1,000

Repayments of commercial paper

     (762              

Dividends paid

     (500              

Net proceeds from issuance of debt

     10,387        2,471        1,980   

Net proceeds from issuance of commercial paper

     762                 

Other

     254        83        204   
  

 

 

   

 

 

   

 

 

 

Net cash used in financing activities

     (674     (1,232     (2,024
  

 

 

   

 

 

   

 

 

 

Increase in cash and cash equivalents

     3,659        403        1,110   

Cash and cash equivalents at beginning of period

     3,287        2,884        1,774   
  

 

 

   

 

 

   

 

 

 

Cash and cash equivalents at end of period

   $ 6,946      $ 3,287      $ 2,884   
  

 

 

   

 

 

   

 

 

 

See accompanying notes.

 

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Table of Contents

AMGEN INC.

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS

December 31, 2011

1. Summary of significant accounting policies

Business

Amgen Inc. (including its subsidiaries, referred to as “Amgen,” “the Company,” “we,” “our” or “us”) is a global biotechnology medicines company that discovers, develops, manufactures and markets medicines for grievous illnesses. We concentrate on innovating novel medicines based on advances in cellular and molecular biology, and we operate in one business segment: human therapeutics.

Principles of consolidation

The consolidated financial statements include the accounts of Amgen as well as its wholly owned subsidiaries. We do not have any significant interests in any variable interest entities. All material intercompany transactions and balances have been eliminated in consolidation.

Use of estimates

The preparation of consolidated financial statements in conformity with accounting principles generally accepted in the United States requires management to make estimates and assumptions that affect the amounts reported in the consolidated financial statements and accompanying notes. Actual results may differ from those estimates.

Product sales

Product sales consist primarily of sales of Neulasta® (pegfilgrastim), NEUPOGEN® (Filgrastim), Enbrel® (etanercept), Aranesp® (darbepoetin alfa) and EPOGEN® (epoetin alfa). Sales of our products are recognized when shipped and title and risk of loss have passed. Product sales are recorded net of accruals for estimated rebates, wholesaler chargebacks, discounts and other deductions (collectively “sales deductions”) and returns. Taxes collected from customers and remitted to government authorities related to the sales of the Company’s products, primarily in Europe, are excluded from revenues.

We have the exclusive right to sell epoetin alfa for dialysis, certain diagnostics and all non-human, non-research uses in the United States. We sell epoetin alfa under the brand name EPOGEN®. We granted to Ortho Pharmaceutical Corporation (which has assigned its rights under the product license agreement to Janssen Biotech, Inc., formerly known as Centocor Ortho Biotech Products, L.P.), a subsidiary of Johnson & Johnson (J&J), a license relating to epoetin alfa for sales in the United States for all human uses except dialysis and diagnostics. This license agreement, which is perpetual, may be terminated for various reasons, including upon mutual agreement of the parties, or default. The parties are required to compensate each other for epoetin alfa sales that either party makes into the other party’s exclusive market, sometimes referred to as “spillover.” Accordingly, we do not recognize product sales we make into the exclusive market of J&J and do recognize the product sales made by J&J into our exclusive market. Sales in our exclusive market are derived from our sales to our customers, as adjusted for spillover. We are employing an arbitrated audit methodology to measure each party’s spillover based on estimates of and subsequent adjustments thereto of third-party data on shipments to and usage by end users.

Other revenues

Other revenues consist primarily of royalty income and corporate partner revenues. Royalties from licensees are based on third-party sales of licensed products and are recorded in accordance with contract terms when

 

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AMGEN INC.

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (Continued)

 

third-party results are reliably measurable and collectability is reasonably assured. Royalty estimates are made in advance of amounts collected using historical and forecasted trends. Corporate partner revenues are comprised of amounts earned from Kirin-Amgen, Inc. (K-A) for certain research and development (R&D) activities, which are earned as the R&D activities are performed. Corporate partner revenues also include license fees and milestone payments earned from K-A and from third parties. See Multiple-deliverable revenue arrangements, discussed below, Note 6, Collaborative arrangements, and Note 7, Related party transactions.

Muliple-deliverable revenue arrangements

Effective January 1, 2011, we adopted a new accounting standard that amends the guidance on the accounting for arrangements involving the delivery of more than one element. Pursuant to the new standard, each required deliverable is evaluated to determine whether it qualifies as a separate unit of accounting. For Amgen this determination is generally based on whether the deliverable has “stand-alone value” to the customer. The arrangement’s consideration that is fixed or determinable is then allocated to each separate unit of accounting based on the relative selling price of each deliverable. In general, the consideration allocated to each unit of accounting is recognized as the related goods or services are delivered, limited to the consideration that is not contingent upon future deliverables. The Company adopted this new accounting standard on a prospective basis for all multiple-deliverable revenue arrangements (MDRAs) entered into on or after January 1, 2011, and for any MDRAs that were entered into prior to January 1, 2011, but materially modified on or after that date.

For MDRAs entered into prior to January 1, 2011, (pre-2011 arrangements) and not materially modified thereafter, we continue to apply our prior accounting policy with respect to such arrangements. Under this policy, in general, revenue from non-refundable, up-front fees related to intellectual property rights/licenses, where we have continuing involvement and where standalone value could not be determined under the previous guidance, is recognized ratably over the estimated period of ongoing involvement. In general, the consideration with respect to the other deliverables is recognized when the goods or services are delivered.

Under all of our MDRAs, consideration associated with at-risk substantive performance milestones is recognized as revenue upon the achievement of the related milestone, as defined in the respective contracts.

The primary impact of adopting the new accounting standard is expected to be the earlier recognition of revenue associated with delivering rights to the underlying intellectual property. The adoption of this accounting standard did not have a material impact on our consolidated results of operations for the year ended December 31, 2011, or on our financial position as of December 31, 2011. Our consolidated results of operations for the year ended December 31, 2010, or our financial position as of December 31, 2010, also would not have been materially impacted if the accounting standard had been adopted on January 1, 2010. The impact of adopting this new accounting standard is dependent on the terms and conditions of any future arrangements that we may enter into that include multiple-deliverables and pre-2011 arrangements that are materially modified. Depending on the terms of any such arrangements, the adoption of this accounting standard may have a material impact on our consolidated results of operations or financial position.

Research and development costs

R&D costs are expensed as incurred and include primarily salaries, benefits and other staff-related costs; facilities and overhead costs; clinical trial and related clinical manufacturing costs; contract services and other outside costs; information systems’ costs and amortization of acquired technology used in R&D with alternative future uses. R&D expenses also include costs and cost recoveries associated with K-A and third-party R&D arrangements, including upfront fees and milestones paid to third parties in connection with technologies which

 

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AMGEN INC.

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (Continued)

 

had not reached technological feasibility and did not have an alternative future use. Net payment or reimbursement of R&D costs is recognized when the obligations are incurred or as we become entitled to the cost recovery. See Note 6, Collaborative arrangements, and Note 7, Related party transactions.

Selling, general and administrative costs

Selling, general and administrative (SG&A) expenses are comprised primarily of salaries, benefits and other staff-related costs associated with sales and marketing, finance, legal and other administrative personnel; facilities and overhead costs; outside marketing, advertising and legal expenses; and other general and administrative costs. Advertising costs are expensed as incurred. SG&A expenses also include costs and cost recoveries associated with marketing and promotion efforts under certain collaboration arrangements. Net payment or reimbursement of SG&A costs is recognized when the obligations are incurred or we become entitled to the cost recovery. See Note 6, Collaborative arrangements.

Beginning January 1, 2011, SG&A expenses also include the amortization of the annual fee mandated by the Patient Protection and Affordable Care Act and the companion Health Care and Education Reconciliation Act (the U.S. healthcare reform federal excise fee). The liability for the annual U.S. healthcare reform federal excise fee is estimated and recorded in full upon the first qualifying sale of our covered products with a corresponding deferred cost established that is amortized on a straight-line basis over the calendar year that it is payable.

Stock-based compensation

We have stock-based compensation plans under which various types of equity-based awards are granted, including stock options, restricted stock units (RSU) and performance units. The estimated fair values of stock option and RSU awards which are subject only to service conditions with graded vesting are generally recognized as compensation expense on a straight-line basis over the service period. The estimated fair values of performance unit awards are generally recognized as compensation expense on a straight-line basis from the grant date to the end of the performance period. See Note 3, Stock-based compensation.

Income taxes

We provide for income taxes based on pretax income, applicable tax rates and tax planning opportunities available in the various jurisdictions in which we operate.

We recognize the tax benefit from an uncertain tax position only if it is more likely than not that the tax position will be sustained on examination by the taxing authorities based on the technical merits of the position. The tax benefit recognized in the financial statements for a particular tax position is based on the largest benefit that is more likely than not to be realized upon settlement. The amount of unrecognized tax benefits (UTBs) is adjusted as appropriate for changes in facts and circumstances, such as significant amendments to existing tax law, new regulations or interpretations by the taxing authorities, new information obtained during a tax examination, or resolution of an examination. We recognize both accrued interest and penalties, where appropriate, related to UTBs in income tax expense. See Note 4, Income taxes.

Business combinations

Business combinations are accounted for using the acquisition method of accounting. Under the acquisition method, assets acquired, including in-process research and development (IPR&D) projects and liabilities assumed, are recorded at their respective fair values as of the acquisition date in our consolidated financial statements. The excess of the fair value of consideration transferred over the fair value of the net assets acquired

 

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Table of Contents

AMGEN INC.

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (Continued)

 

is recorded as goodwill. Contingent consideration obligations incurred in connection with a business combination are recorded at their fair values on the acquisition date and remeasured at their fair values each subsequent reporting period until the related contingencies are resolved. The resulting changes in fair values are recorded in earnings. See Note 2, Business combinations, and Note 16, Fair value measurement.

Cash equivalents

We consider cash equivalents to be only those investments which are highly liquid, readily convertible to cash and which mature within three months from the date of purchase.

Available-for-sale investments

We consider our investment portfolio available-for-sale and, accordingly, these investments are recorded at fair value with unrealized gains and losses generally recorded in other comprehensive income. See Note 9, Available-for-sale investments, and Note 16, Fair value measurement.

Inventories

Inventories are stated at the lower of cost or market. Cost, which includes amounts related to materials, labor and overhead, is determined in a manner that approximates the first-in, first-out method. Cost also includes the Puerto Rico excise tax enacted in 2011 related to our manufacturing operations in Puerto Rico. See Note 10, Inventories.

Derivatives

We recognize all of our derivative instruments as either assets or liabilities at fair value in the Consolidated Balance Sheets. The accounting for changes in the fair value of a derivative instrument depends on whether it has been formally designated and qualifies as part of a hedging relationship under the applicable accounting standards and, further, on the type of hedging relationship. For derivatives formally designated as hedges, we assess both at inception and quarterly thereafter, whether the hedging derivatives are highly effective in offsetting changes in either the fair value or cash flows of the hedged item. Our derivatives that are not designated and do not qualify as hedges are adjusted to fair value through current earnings. See Note 16, Fair value measurement, and Note 17, Derivative instruments.

Property, plant and equipment, net

Property, plant and equipment is recorded at historical cost, net of accumulated depreciation, amortization and, if applicable, impairment charges. We review our property, plant and equipment assets for impairment whenever events or changes in circumstances indicate that the carrying amount of an asset may not be recoverable. Depreciation is provided over the assets’ useful lives on a straight-line basis. Leasehold improvements are amortized on a straight-line basis over the shorter of their estimated useful lives or lease terms. See Note 11, Property, plant and equipment.

Intangible assets and goodwill

Finite-lived intangible assets are recorded at cost, net of accumulated amortization and, if applicable, impairment charges. Amortization of finite-lived intangible assets is provided over their estimated useful lives on a straight-line basis. We review our finite-lived intangible assets for impairment whenever events or changes in circumstances indicate that the carrying amount of an asset may not be recoverable. See Note 12, Intangible assets.

 

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Table of Contents

AMGEN INC.

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (Continued)

 

The estimated fair values of IPR&D projects acquired in a business combination which have not reached technological feasibility are capitalized and accounted for as indefinite-lived intangible assets subject to impairment testing until completion or abandonment of the project. Capitalized IPR&D projects are tested for impairment annually and whenever events or changes in circumstances indicate that the carrying amount may not be recoverable. Upon successful completion of the project, the capitalized amount is amortized over its estimated useful life. If a project is abandoned, all remaining capitalized amounts are written-off immediately.

Goodwill relates principally to our 2002 acquisition of Immunex Corporation (Immunex). We perform an impairment test of goodwill annually and whenever events or changes in circumstances indicate that the carrying amount may not be recoverable.

Convertible debt

The debt and equity components of convertible debt instruments that may be partially or wholly cash settled (cash settleable convertible notes), including our 0.125% 2011 Convertible Notes and 0.375% 2013 Convertible Notes, are bifurcated and accounted for separately. The debt component of cash settleable convertible notes, which excludes the associated equity conversion option, is recorded at fair value as of the issuance date. The difference between the amount allocated to the debt component and the proceeds received upon issuance of the debt is allocated to the equity component and recorded in Common stock and additional paid-in capital in the Consolidated Balance Sheets. The reduced or discounted carrying value of cash settleable convertible notes resulting from bifurcation is subsequently accreted back to its principal amount through the recognition of non-cash interest expense. This results in recognizing interest expense on the borrowing at an effective rate approximating what would have been incurred had nonconvertible debt with otherwise similar terms been issued. See Note 14, Financing arrangements.

Recent accounting pronouncements

In June 2011, a new accounting standard was issued that changed the disclosure requirements for the presentation of other comprehensive income (OCI) in the financial statements, including the elimination of the option to present OCI in the statement of stockholders’ equity. OCI and its components will be required to be presented for both interim and annual periods either in a single financial statement, the statement of comprehensive income, or in two separate but consecutive financial statements, consisting of a statement of income followed by a separate statement presenting OCI. This standard is required to be applied retrospectively beginning January 1, 2012, except for certain provisions for which adoption was delayed.

2. Business combinations

BioVex Group, Inc.

On March 4, 2011, we acquired all of the outstanding stock of BioVex Group, Inc. (BioVex), a privately held biotechnology company developing treatments for cancer and for the prevention of infectious disease, including talimogene laherparepvec (formerly referred to as OncoVEXGM-CSF), a novel oncolytic vaccine in phase 3 clinical development for the treatment of malignant melanoma. This transaction, which was accounted for as a business combination, provides us with an opportunity to expand our efforts to bring novel therapeutics to market. Upon its acquisition, BioVex became a wholly owned subsidiary of Amgen, and its operations have been included in our consolidated financial statements commencing on the acquisition date.

 

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Table of Contents

AMGEN INC.

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (Continued)

 

The aggregate acquisition date consideration to acquire BioVex consisted of (in millions):

 

 

Cash paid to former shareholders of BioVex

   $ 407   

Fair value of contingent consideration obligations

     190   
  

 

 

 

Total consideration

   $ 597   
  

 

 

 

In connection with this acquisition, we are obligated to make additional payments to the former shareholders of BioVex of up to $575 million contingent upon the achievement of various regulatory and sales milestones with regard to talimogene laherparepvec, including the filing of a Biologics License Application with the U.S. Food and Drug Administration (FDA); the first commercial sale in each of the United States and the European Union (EU) following receipt of marketing approval, which includes use of the product in specified patient populations; and upon achieving specified levels of sales. The estimated fair values of the contingent consideration obligations aggregated $190 million as of the acquisition date and were determined using a combination of valuation techniques. The contingent consideration obligations to make regulatory milestone payments were valued based on assumptions regarding the probability of achieving the milestones and making the related payments, with such amounts discounted to present value based on our credit risk. The contingent consideration obligations to make sales milestone payments were valued based on assumptions regarding the probability of achieving specified product sales thresholds to determine the required payments, with such amounts discounted to present value based on our credit risk.

We allocated the total consideration to the acquisition date fair values of assets acquired and liabilities assumed as follows (in millions):

 

 

Intangible assets — IPR&D

   $ 675   

Goodwill

     170   

Deferred tax liabilities

     (246

Other assets (liabilities) acquired, net

     (2
  

 

 

 

Total consideration

   $ 597   
  

 

 

 

Intangible assets are composed of the estimated fair value of acquired IPR&D related to talimogene laherparepvec. The estimated fair value was determined using a probability-weighted income approach, which discounts expected future cash flows to present value. The estimated net cash flows were discounted to present value using a discount rate of 11%, which is based on the estimated weighted-average cost of capital for companies with characteristics similar to those of BioVex. This is comparable to the estimated internal rate of return on BioVex operations and represents the rate that market participants would use to value the intangible assets. The projected cash flows from talimogene laherparepvec were based on certain key assumptions, including estimates of future revenue and expenses and taking into account the stage of development of talimogene laherparepvec at the acquisition date, the time and resources needed to complete development and the probabilities of obtaining marketing approval from the FDA and other regulatory agencies. IPR&D intangible assets acquired in a business combination are considered to be indefinite-lived until the completion or abandonment of the associated R&D efforts.

The estimated incremental R&D costs to be incurred to obtain necessary regulatory approvals for talimogene laherparepvec are not material. The major risks and uncertainties associated with the timely and successful completion of development and commercialization of this product candidate include our ability to confirm its safety and efficacy based on data from clinical trials, our ability to obtain necessary regulatory approvals and our ability to successfully complete these tasks within budgeted costs. We are not able to market a

 

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Table of Contents

AMGEN INC.

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (Continued)

 

human therapeutic without obtaining regulatory approvals, and such approvals require completing clinical trials that demonstrate a product candidate is safe and effective. Consequently, the eventual realized value of the acquired IPR&D may vary from its estimated fair value at the date of acquisition.

The excess of the acquisition date consideration over the fair values assigned to the assets acquired and the liabilities assumed of $170 million was recorded as goodwill, which is not deductible for tax purposes. Goodwill is attributable primarily to the deferred tax consequences of acquired IPR&D recorded for financial statement purposes.

Other acquisitions

During the year ended December 31, 2011, we also acquired the businesses described below, which were accounted for as business combinations, and accordingly, their operations have been included in our consolidated financial statements commencing on their respective acquisition dates.

On April 7, 2011, we acquired all of the outstanding stock of Laboratório Químico Farmacêutico Bérgamo Ltda (Bergamo), a privately held Brazilian pharmaceutical company. Upon its acquisition, Bergamo became a wholly owned subsidiary of Amgen.

On May 16, 2011, we acquired a manufacturing facility in Dun Laoghaire, Ireland, from Pfizer Inc. (Pfizer) (Dun Laoghaire). Under the terms of the agreement, most staff at the facility became Amgen employees, and we agreed to manufacture certain products for Pfizer at the facility for an interim period.

On June 15, 2011, we reacquired rights to distribute certain of our products in the Brazilian pharmaceutical market from our local distributor in Brazil and its parent company, Hypermarcas, and in connection therewith acquired all business operations relating to these products in Brazil.

The aggregate acquisition date consideration for these businesses was approximately $453 million, composed primarily of cash paid to the former owners of the businesses. The aggregate acquisition date consideration was allocated to (i) goodwill of $265 million, of which $130 million related to Bergamo was tax deductible: (ii) property, plant and equipment of $99 million; (iii) amortizable intangible assets composed primarily of licenses to distribute products and customer contracts of $58 million; and (iv) other assets, net of $31 million. The purchase price allocation for the Bergamo transaction is preliminary and will be finalized upon collection of information regarding certain tax-related items. Goodwill resulting from these acquisitions is attributable primarily to the benefits of immediate, direct access to the Brazilian market for expediting our international expansion efforts and geographic diversification to assist in risk mitigation efforts related to our manufacturing operations.

Pro forma supplemental consolidated results of operations for the years ended December 31, 2011 and 2010, that assumes the acquisitions of BioVex, Bergamo, Dun Laoghaire and Hypermarcas all occurred on January 1, 2010, are not provided because the impact would not be material to our consolidated results of operations either individually or in the aggregate.

In addition to the increase in goodwill for the acquisitions of the businesses discussed above, goodwill decreased by $19 million for the year ended December 31, 2011, due to changes in foreign currency exchange rates.

 

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Table of Contents

AMGEN INC.

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (Continued)

 

3. Stock-based compensation

Our 2009 Equity Incentive Plan (the 2009 Plan) provides for the grant of equity-based awards, including stock options, RSUs and performance units, to employees and consultants of Amgen, its subsidiaries and non-employee members of our Board of Directors. The 2009 Plan, which was approved by our stockholders on May 6, 2009, replaced our prior equity plans (the Prior Plans) and no further awards may be made under these Prior Plans. The 2009 Plan authorizes the issuance of 100 million shares of our common stock. Under the terms of the 2009 Plan, the pool of available shares that may be used for all types of awards, including those issued under our Prior Plans after December 31, 2008, and before May 6, 2009 (the stub period), is reduced by one share for each stock option granted and by 1.9 shares for other types of awards granted, including RSUs and performance units. If any shares subject to an award granted under our Prior Plans during the stub period or any awards granted under the 2009 Plan expire, or are forfeited, terminated or cancelled without the issuance of shares, the shares subject to such awards are added back to the pool of available shares under the 2009 Plan on the same basis that they were removed. As of December 31, 2011, the 2009 Plan provides for future grants and/or issuances of up to approximately 58 million shares of our common stock. Stock-based awards under our employee compensation plans are made with newly issued shares reserved for this purpose.

The following table reflects the components of stock-based compensation expense recognized in our Consolidated Statements of Income for the years ended December 31, 2011, 2010 and 2009 (in millions):

 

 

     2011     2010     2009  

Stock options

   $ 85      $ 124      $ 115   

Restricted stock units

     188        182        134   

Performance units

     68        47        35   
  

 

 

   

 

 

   

 

 

 

Total stock-based compensation expense, pre-tax

     341        353        284   

Tax benefit from stock-based compensation expense

     (124     (120     (97
  

 

 

   

 

 

   

 

 

 

Total stock-based compensation expense, net of tax

   $ 217      $ 233      $ 187   
  

 

 

   

 

 

   

 

 

 

Employee stock options and restricted stock units

Eligible employees generally receive a grant of stock options and/or RSUs annually with the size and type of award generally determined by the employee’s salary grade and performance level. In addition, certain management and professional level employees typically receive RSU grants upon commencement of employment. Our stock option and RSU grants provide for accelerated or continued vesting in certain circumstances as defined in the plans and related grant agreements, including upon death, disability, a change in control, termination in connection with a change in control and retirement of employees who meet certain service and/or age requirements. Stock options and RSUs granted prior to April 25, 2011, generally vest in equal amounts on each of the first four anniversaries of the grant date. Stock options and RSUs granted on and after April 25, 2011, generally vest in approximately equal amounts on the second, third and fourth anniversaries of the grant date.

Stock options

The exercise price for stock options is set at the closing price of our common stock on the date of grant and the related number of shares granted is fixed at that point in time. Awards granted to employees on and after April 26, 2010, expire 10 years from the date of grant; options granted to employees prior to that date expire seven years from the date of grant.

 

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Table of Contents

AMGEN INC.

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (Continued)

 

We use an option valuation model to estimate the grant date fair value of our employee stock options. The weighted-average assumptions used in the option valuation model and the resulting weighted-average estimated grant date fair values of our employee stock options were as follows for the years ended December 31, 2011, 2010 and 2009:

 

 

     2011      2010      2009  

Closing price of our common stock on grant date

   $ 54.66       $ 58.32       $ 50.65   

Expected volatility

     23.5%         28.0%         39.6%   

Expected life (in years)

     5.9         6.6         4.6   

Risk-free interest rate

     2.5%         3.2%         2.1%   

Expected dividend yield

     2.0%         0%         0%   

Fair value of stock options granted

   $ 11.39       $ 20.97       $ 18.35   

The expected volatility reflects the consideration of the implied volatility in publicly traded instruments associated with Amgen’s common stock during the period the options were granted. We believe implied volatility in these instruments is more indicative of expected future volatility than the historical volatility in the price of our common stock. We use historical data to estimate the expected life of the options. The risk-free interest rates for periods within the expected life of the option are based on the U.S. Treasury yield curve in effect during the period the options were granted. The expected dividend yield for options granted on and after April 25, 2011, was based on expectations regarding our policy of paying dividends announced in April 2011.

The following summarizes select information regarding our stock options during the year ended December 31, 2011:

 

 

     Options
(in millions)
    Weighted-
average
exercise price
     Weighted-
average
remaining
contractual
life (years)
     Aggregate
intrinsic
value
(in millions)
 

Balance unexercised at December 31, 2010

     46.8      $ 58.66         

Granted

     2.3      $ 54.66         

Exercised

     (5.0   $ 50.22         

Expired/forfeited

     (9.9   $ 60.43         
  

 

 

         

Balance unexercised at December 31, 2011

     34.2      $ 59.11         3.8       $ 245   
  

 

 

   

 

 

    

 

 

    

 

 

 

Vested or expected to vest at December 31, 2011

     33.8      $ 59.15         3.7       $ 242   
  

 

 

   

 

 

    

 

 

    

 

 

 

Exercisable at December 31, 2011

     23.6      $ 61.49         2.3       $ 135   
  

 

 

   

 

 

    

 

 

    

 

 

 

The total intrinsic value of options exercised during the three years ended December 31, 2011, 2010 and 2009, was $47 million, $15 million and $57 million, respectively.

Restricted stock units

The fair value of an RSU granted prior to April 25, 2011, is equal to the closing price of our common stock on the grant date. The fair values of RSUs granted on and after April 25, 2011, are based on the closing price of our common stock on the grant date reduced by the weighted average expected dividend yield of 1.9% over the weighted-average vesting period, discounted at a weighted-average risk-free interest rate of 1.0%. The weighted-

 

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AMGEN INC.

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (Continued)

 

average grant date fair values of RSUs granted in 2011, 2010 and 2009 were $51.83, $58.19 and $51.24, respectively. The following summarizes select information regarding our RSUs during the year ended December 31, 2011:

 

 

     Units
(in millions)
    Weighted-average
grant date
fair value
 

Balance nonvested at December 31, 2010

     9.3      $ 52.67   

Granted

     4.0      $ 51.83   

Vested

     (3.4   $ 52.06   

Forfeited

     (0.9   $ 52.77   
  

 

 

   

Balance nonvested at December 31, 2011

     9.0      $ 52.64   
  

 

 

   

The total fair values of shares associated with RSUs that vested during the year ended December 31, 2011, 2010 and 2009, were $176 million, $184 million and $139 million, respectively.

As of December 31, 2011, there was approximately $407 million of unrecognized compensation costs related to nonvested stock option and RSU awards, which is expected to be recognized over a weighted-average period of 1.7 years.

Performance units

Certain management-level employees also receive annual grants of performance units, which give the recipient the right to receive common stock that is contingent upon achievement of specified pre-established performance goals over the performance period, which is generally three years. The performance goals for the units granted in 2011, 2010 and 2009, which are accounted for as equity awards, are based upon Amgen’s annual stockholder return compared with a comparator group of companies, which are considered market conditions and are reflected in the grant date fair value of the units, and for units granted in 2010 and 2009, Amgen’s standalone financial performance, which are considered performance conditions. The expense recognized for the awards granted in 2011 is based on the grant date fair value of a unit multiplied by the number of units granted, net of estimated forfeitures. The expense recognized for the awards granted in 2010 and 2009 was based on the grant date fair value of a unit multiplied by the number of units expected to be earned with respect to the performance conditions, net of estimated forfeitures. Depending on the outcome of these performance goals, a recipient may ultimately earn a number of units greater or less than the number of units granted. Shares of our common stock are issued on a one-for-one basis for each performance unit earned. In general, participants vest in their performance unit awards at the end of the performance period. The performance award program provides for accelerated or continued vesting in certain circumstances as defined in the plan, including upon death, disability, a change in control and retirement of employees who meet certain service and/or age requirements.

We used payout simulation models to estimate the grant date fair value of performance units granted in 2011, 2010 and 2009. The weighted average assumptions used in these models and the resulting weighted average grant date fair values of our performance units were as follows for the years ended December 31, 2011, 2010 and 2009:

 

 

     2011      2010      2009  

Closing price of our common stock on grant date

   $ 51.67       $ 56.90       $ 47.63   

Volatility

     32.8%         34.7%         34.3%   

Risk-free interest rate

     1.2%         1.3%         1.2%   

Expected dividend yield

     0.1%         0%         0%   

Fair value of unit

   $ 49.50       $ 62.06       $ 48.22   

 

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AMGEN INC.

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (Continued)

 

The payout simulation models also assumed correlations of returns of the stock prices of our common stock and the common stocks of the comparator groups of companies and stock price volatilities of the comparator groups of companies.

As of December 31, 2011 and 2010, a total of 4.1 million and 2.7 million performance units were outstanding with weighted-average grant date fair values of $51.92 and $49.49 per unit, respectively. During the year ended December 31, 2011, 2.5 million performance units with a weighted average grant date fair value of $49.50 were granted, 0.4 million performance units with a grant date fair value of $48.22 vested and 0.2 million performance units with a weighted-average grant date fair value of $52.70 were forfeited.

The total fair values of performance units that vested during 2011, 2010 and 2009 were $25 million, $34 million and $29 million, respectively, based upon the number of performance units earned multiplied by the closing stock price of our common stock on the last day of the performance period. Performance unit awards granted for performance periods that ended prior to 2009 were accounted for as liability awards and were paid in the year after the performance period ended. Performance unit liability awards paid in 2009 aggregated $30 million.

As of December 31, 2011, there was approximately $90 million of unrecognized compensation cost related to the 2011 and 2010 performance unit grants that is expected to be recognized over a weighted-average period of approximately 1.1 years.

4. Income taxes

The provision for income taxes includes the following for the years ended December 31, 2011, 2010 and 2009 (in millions):

 

 

     2011     2010     2009  

Current provision:

      

Federal

   $ 618      $ 636      $ 325   

State

     58        52        85   

Foreign

     148        153        155   
  

 

 

   

 

 

   

 

 

 

Total current provision

     824        841        565   
  

 

 

   

 

 

   

 

 

 

Deferred (benefit) provision:

      

Federal

     (340     (196     92   

State

     (16     43        (59

Foreign

     (1     2        1   
  

 

 

   

 

 

   

 

 

 

Total deferred (benefit) provision

     (357     (151     34   
  

 

 

   

 

 

   

 

 

 

Total provision

   $ 467      $ 690      $ 599   
  

 

 

   

 

 

   

 

 

 

Deferred income taxes reflect the temporary differences between the carrying amounts of assets and liabilities for financial reporting purposes and the amounts used for income tax purposes, tax credit carryforwards and the tax effects of net operating loss carryforwards.

 

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AMGEN INC.

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (Continued)

 

Significant components of our deferred tax assets and liabilities are as follows as of December 31, 2011 and 2010 (in millions):

 

 

     2011     2010  

Deferred income tax assets:

    

Intercompany inventory related items

   $ 387      $ 306   

Expense accruals

     751        626   

Acquired net operating loss and credit carryforwards

     192        147   

Expenses capitalized for tax

     167        188   

Stock-based compensation

     241        269   

Deferred revenue

     133        117   

Other

     72        72   
  

 

 

   

 

 

 

Total deferred income tax assets

     1,943        1,725   

Valuation allowance

     (126     (80
  

 

 

   

 

 

 

Net deferred income tax assets

     1,817        1,645   
  

 

 

   

 

 

 

Deferred income tax liabilities:

    

Acquired intangibles

     (832     (739

Fixed assets

     (219     (181

Unremitted foreign earnings

     (61     (118

Other

     (110     (142
  

 

 

   

 

 

 

Total deferred income tax liabilities

     (1,222     (1,180
  

 

 

   

 

 

 

Total deferred income taxes, net

   $ 595      $ 465   
  

 

 

   

 

 

 

The valuation allowance for deferred tax assets increased by $46 million in 2011, due primarily to valuation allowances established as part of the BioVex and Dun Laoghaire acquisitions and the Company’s expectation that some state R&D credits will not be utilized, offset partially by the release of valuation allowance related to the expiration of state investment credits. The valuation allowance for deferred tax assets decreased by $12 million in 2010, due primarily to the utilization and expiration of certain acquired net operating loss carryforwards. Valuation allowances are provided when we believe our deferred tax assets are not recoverable based on an assessment of estimated future taxable income that incorporates ongoing, prudent and feasible tax planning strategies.

At December 31, 2011, we had $44 million of tax credit carryforwards available to reduce future federal income taxes for which a full valuation allowance has been provided. In addition, we had $176 million of tax credit carryforwards available to reduce future state income taxes and have provided a valuation allowance for $67 million of those state tax credit carryforwards. The majority of the state tax credit carryforwards have no expiry; the remainder expires between 2012 and 2025.

The reconciliation of the total gross amounts of UTBs (excluding interest, penalties, foreign tax credits and the federal tax benefit of state taxes related to UTBs) for the years ended December 31, 2011, 2010 and 2009, is as follows (in millions):

 

 

     2011     2010     2009  

Balance at beginning of year

   $ 920      $ 1,140      $ 1,113   

Additions based on tax positions related to the current year

     283        305        302   

Reductions for tax positions of prior years

     (7     (110     (215

Settlements

     (221     (415     (60
  

 

 

   

 

 

   

 

 

 

Balance at end of year

   $ 975      $ 920      $ 1,140   
  

 

 

   

 

 

   

 

 

 

 

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AMGEN INC.

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (Continued)

 

Substantially all of the UTBs as of December 31, 2011, if recognized, would affect our effective tax rate.

During the year ended December 31, 2011, we settled our examination with the Internal Revenue Service (IRS) related to certain transfer pricing tax positions for the years ended December 31, 2007, 2008 and 2009. As a result of these developments, we remeasured our UTBs accordingly.

During the year ended December 31, 2010, we settled our examination with the IRS related to certain transfer pricing tax positions for the years ended December 31, 2007 and 2008. In addition, we also settled issues under appeal with the IRS for the years ended December 31, 2005 and 2006, primarily related to the impact of transfer pricing adjustments on the repatriation of funds. During the year ended December 31, 2010, the IRS also agreed to Competent Authority relief for certain transfer pricing tax positions for the years ended December 31, 2002, through December 31, 2006. As a result of these developments, we remeasured our UTBs accordingly.

During the year ended December 31, 2009, we settled the examination of our U.S. income tax returns with the IRS for certain matters, primarily related to transfer pricing tax positions, for the years ended December 31, 2005 and 2006. Also during the year ended December 31, 2009, we settled the examination of our California state income tax returns for certain matters for the years ended December 31, 2004 and 2005. As a result of these developments, we remeasured our UTBs accordingly.

As of December 31, 2011, we believe it is reasonably possible that our gross liabilities for UTBs may decrease by approximately $270 million within the succeeding twelve months due to the resolution of federal and state audits.

Interest and penalties related to UTBs are included in our provision for income taxes. During 2011, 2010 and 2009, we accrued approximately $23 million, $41 million and $57 million, respectively, of interest and penalties through the income tax provision in the Consolidated Statements of Income. At December 31, 2011 and 2010, accrued interest and penalties associated with UTBs totaled approximately $105 million and $90 million, respectively.

The reconciliation between the federal statutory tax rate applied to income before income taxes and our effective tax rate for the years ended December 31, 2011, 2010 and 2009, is as follows:

 

 

     2011        2010        2009  

Federal statutory tax rate

     35.0 %           35.0 %           35.0 %   

Foreign earnings, including earnings invested indefinitely

     (19.4)%           (19.1)%           (19.6)%   

State taxes

     0.7 %           1.6 %           1.1 %   

Credits, Puerto Rico Excise Tax

     (6.5)%           0.0 %           0.0 %   

Credits, primarily research and experimentation

     (1.5)%           (0.9)%           (0.8)%   

Legal settlements

     2.2 %           0.0 %           0.0 %   

Audit settlements

     0.0 %           (3.1)%           (4.2)%   

Other, net

     0.8 %           (0.5)%           0.0 %   
  

 

 

      

 

 

      

 

 

 

Effective tax rate

     11.3 %           13.0 %           11.5 %   
  

 

 

      

 

 

      

 

 

 

We do not provide for U.S. income taxes on undistributed earnings of our foreign operations that are intended to be invested indefinitely outside of the United States. Substantially all of the benefit from foreign earnings on our effective tax rate results from foreign income associated with the Company’s operation conducted in Puerto Rico that is subject to a tax incentive grant that expires in 2020. At December 31, 2011, the

 

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AMGEN INC.

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (Continued)

 

cumulative amount of these earnings was approximately $19.5 billion. If these earnings were repatriated to the United States, we would be required to accrue and pay approximately $6.9 billion of additional income taxes based on the current tax rates in effect.

Our total foreign income before income taxes was approximately $2.6 billion, $3.1 billion and $3.1 billion for the years ended December 31, 2011, 2010 and 2009, respectively.

Commencing January 1, 2011, Puerto Rico imposes a temporary excise tax on the acquisition of goods and services from a related manufacturer in Puerto Rico. The excise tax is imposed over a six year period beginning in 2011 with the excise tax rate declining in each year (4% in 2011, 3.75% in 2012, 2.75% in 2013, 2.5% in 2014, 2.25% in 2015, and 1% in 2016). We account for the excise tax as a manufacturing cost that is capitalized in inventory and expensed in cost of sales when the related products are sold. For U.S. income tax purposes, the excise tax results in foreign tax credits that are generally recognized in our provision for income taxes in the year in which the excise tax is incurred.

One or more of our legal entities file income tax returns in the U.S. federal jurisdiction, various U.S. state jurisdictions and certain foreign jurisdictions. Our income tax returns are routinely audited by the tax authorities in those jurisdictions. Significant disputes may arise with these tax authorities involving issues of the timing and amount of deductions, the use of tax credits and allocations of income among various tax jurisdictions because of differing interpretations of tax laws and regulations. We are no longer subject to U.S. federal income tax examinations for tax years ending on or before December 31, 2006, or to California state income tax examinations for tax years ending on or before December 31, 2003.

Income taxes paid during the years ended December 31, 2011, 2010 and 2009, totaled $595 million, $1,344 million and $497 million, respectively.

5. Earnings per share

The computation of basic earnings per share (EPS) is based on the weighted-average number of our common shares outstanding. The computation of diluted EPS is based on the weighted-average number of our common shares outstanding and dilutive potential common shares, which principally include: shares that may be issued under our stock option, RSU and performance unit awards, determined using the treasury stock method; our outstanding convertible notes, as discussed below; and our outstanding warrants (collectively “dilutive securities”). The convertible note hedges purchased in connection with the issuance of our convertible notes are excluded from the calculation of diluted EPS because their impact is always anti-dilutive. For further information regarding our convertible notes and warrants, see Note 14, Financing arrangements.

Upon conversion of our convertible notes, the principal amount would be settled in cash, and the excess of the conversion value, as defined, over the principal amount may be settled in cash and/or shares of our common stock. Therefore, only the shares of our common stock potentially issuable with respect to the excess of the notes’ conversion value over their principal amount, if any, are considered as dilutive potential common shares for purposes of calculating diluted EPS. For the years ended December 31, 2011, 2010 and 2009, the conversion values for our convertible notes were less than the related principal amounts and, accordingly, no shares were assumed to be issued for purposes of computing diluted EPS.

 

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AMGEN INC.

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (Continued)

 

The computation for basic and diluted EPS was as follows (in millions, except per share data):

 

 

     2011      2010      2009  

Income (Numerator):

        

Net income for basic and diluted EPS

   $ 3,683       $ 4,627       $ 4,605   
  

 

 

    

 

 

    

 

 

 

Shares (Denominator):

        

Weighted-average shares for basic EPS

     905         960         1,016   

Effect of dilutive securities

     7         5         5   
  

 

 

    

 

 

    

 

 

 

Weighted-average shares for diluted EPS

     912         965         1,021   
  

 

 

    

 

 

    

 

 

 

Basic EPS

   $ 4.07       $ 4.82       $ 4.53   

Diluted EPS

   $ 4.04       $ 4.79       $ 4.51   

For the years ended December 31, 2011, 2010 and 2009, there were employee stock-based awards, calculated on a weighted-average basis, to purchase 33 million, 43 million and 42 million shares of our common stock, respectively, that are not included in the computation of diluted EPS because their impact would have been anti-dilutive. In addition, shares of our common stock that may be issued upon exercise of our warrants are not included in the computation of diluted EPS for any of the periods presented above because their impact would have been anti-dilutive.

6. Collaborative arrangements

A collaborative arrangement is a contractual arrangement that involves a joint operating activity. These arrangements involve two or more parties who are both: (i) active participants in the activity; and (ii) exposed to significant risks and rewards dependent on the commercial success of the activity.

From time to time, we enter into collaborative arrangements for the R&D, manufacture and/or commercialization of products and product candidates. These collaborations generally provide for non-refundable upfront license fees, regulatory and commercial performance milestone payments, cost sharing, royalty payments and/or profit sharing. Our collaboration agreements are performed on a “best efforts” basis with no guarantee of either technological or commercial success and each is unique in nature. Our significant arrangements are discussed below.

Pfizer Inc.

We are in a collaboration with Pfizer to co-promote ENBREL in the United States and Canada. The rights to market ENBREL outside of the United States and Canada are reserved to Pfizer. Under the agreement, a management committee comprised of equal representation from Amgen and Pfizer is responsible for overseeing the marketing and sales of ENBREL, including strategic planning, the approval of an annual marketing plan, product pricing and the establishment of a brand team. Amgen and Pfizer share in the agreed-upon selling and marketing expenses approved by the joint management committee. We currently pay Pfizer a percentage of annual gross profits on our ENBREL sales in the United States and Canada attributable to all approved indications on a scale that increases as gross profits increase; however, we maintain a majority share of ENBREL profits. After expiration of the agreement in the fourth quarter of 2013, we will be required to pay Pfizer a declining percentage of annual net ENBREL sales in the United States and Canada for three years, ranging from 12% to 10%. The amounts of such payments are anticipated to be significantly less than what would be owed based on the terms of the current ENBREL profit share.

 

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AMGEN INC.

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (Continued)

 

We have determined that we are the principal participant in the collaboration with Pfizer to market ENBREL in the United States and Canada. Accordingly, we record our product sales of ENBREL to third parties net of estimated returns, rebates and other deductions. For the years ended December 31, 2011, 2010 and 2009, ENBREL sales aggregated $3.7 billion, $3.5 billion and $3.5 billion, respectively.

During the years ended December 31, 2011, 2010 and 2009, the ENBREL profit share expense was $1,288 million, $1,184 million and $1,163 million, respectively, and is included in Selling, general and administrative expense in the Consolidated Statements of Income. In addition, cost recoveries from Pfizer for their share of the selling and marketing expense were $84 million, $87 million and $75 million for the years ended December 31, 2011, 2010 and 2009, respectively, and are included in Selling, general and administrative expense in the Consolidated Statements of Income.

Glaxo Group Limited

We are in a collaboration with Glaxo Group Limited (Glaxo), a wholly owned subsidiary of GlaxoSmithKline plc, for the commercialization of denosumab for osteoporosis indications in Europe, Australia, New Zealand and Mexico (the Primary Territories). We have retained the rights to commercialize denosumab for all indications in the United States and Canada and for oncology indications in the Primary Territories. Under a related agreement, Glaxo will commercialize denosumab for all indications in countries, excluding Japan, where we did not have a commercial presence at the commencement of the agreement, including China, Brazil, India, Taiwan and South Korea (the Expansion Territories). In the Expansion Territories, Glaxo is responsible for all development and commercialization costs and will purchase denosumab from us to meet demand. In the future, we have the option of expanding our role in the commercialization of denosumab in the Primary Territories and certain of the Expansion Territories.

In the Primary Territories, we share equally in the commercialization profits and losses related to the collaboration after accounting for expenses, including an amount payable to us in recognition of our discovery and development of denosumab. Glaxo is also responsible for bearing a portion of the cost of certain specified development activities in the Primary Territories.

The collaboration agreement with Glaxo for the Primary Territories will expire in 2022 and the related agreement for the Expansion Territories will expire in 2024, unless either agreement is terminated earlier in accordance with its terms.

As the principal participant in the Primary Territories, Amgen records related product sales to third parties net of estimated returns, rebates and other deductions. During the years ended December 31, 2011 and 2010, product sales in the Primary Territories for osteoporosis indications were $62 million and $5 million, respectively. In the Expansion Territories, we record product sales to Glaxo. During the years ended December 31, 2011 and 2010, product sales of denosumab to Glaxo for the Expansion Territories were not material.

During the years ended December 31, 2011, 2010 and 2009, the net recoveries from Glaxo were $30 million, $46 million and $29 million, respectively, and are included in Selling, general and administrative expense in the Consolidated Statements of Income. In addition, during 2010, we received payments aggregating $75 million for the achievement of certain commercial milestones, which were recognized upon the achievement of the related milestone events as Other revenue in our Consolidated Statement of Income. Under these agreements, we also received an initial payment of $45 million during the year ended December 31, 2009, which was deferred and is being recognized as Other revenue in our Consolidated Statements of Income, over our estimated period of continuing involvement of approximately 13 years.

 

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AMGEN INC.

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (Continued)

 

Takeda Pharmaceutical Company Limited

We are in a collaboration with Takeda Pharmaceutical Company Limited (Takeda), which provides Takeda the exclusive rights to develop and commercialize for the Japanese market up to 12 molecules from our portfolio across a range of therapeutic areas, including oncology and inflammation (collectively the “Japanese market products”) and for the worldwide development and commercialization of our product candidate, motesanib, in the oncology area. The Japanese market products include: (i) Vectibix®, which received regulatory approval in Japan, in 2010, for unresectable, advanced or recurrent colorectal cancer with wild-type KRAS, (ii) AMG 386, which is in a phase 3 trial for recurrent ovarian cancer, and (iii) ganitumab (AMG 479), which is in a phase 3 trial for first-line metastatic pancreatic cancer. Through collaboration committees, the parties jointly coordinate and oversee Takeda’s development and commercialization of the Japanese market products in Japan. The parties share responsibility for the development of motesanib outside Japan and Takeda is responsible for development in Japan. Additionally, Amgen shall be responsible for commercialization of motesanib in North America and Takeda shall be responsible for commercialization outside of North America. Each party has the right to participate in the commercialization of motesanib in the other party’s territory. In addition, under the collaboration Amgen will manufacture and supply Takeda motesanib and the Japanese market products for both clinical and commercial purposes. In 2011, we announced that the motesanib pivotal phase 3 trial (MONET1) did not meet its primary objective of demonstrating an improvement in overall survival.

For the Japanese market products Takeda is obligated to pay Amgen up to an additional $60 million of future worldwide development costs for these products in 2012 and a reduced amount of such costs, thereafter. Takeda will be solely responsible for all development and commercialization costs of these products in Japan and will pay Amgen royalties on future sales in Japan. Amgen has the right to participate in the promotion of these products in Japan. With respect to motesanib, Takeda is obligated to pay 60% of future worldwide development costs (excluding Japan, for which Takeda shall bear all such costs), and the parties will share equally all other costs and profits resulting from the commercialization of motesanib outside Japan. If approved for sale, Amgen will receive royalties on future sales of motesanib in Japan.

The collaboration agreements will continue in effect unless terminated earlier in accordance with their terms.

In connection with the collaboration, Amgen received upfront payments of $300 million in 2008 which were deferred and are being recognized as Other revenue in our Consolidated Statements of Income, over our estimated period of continuing involvement of approximately 20 years. Additionally, during 2010, we received payments aggregating $55 million for the achievement of certain regulatory milestones which were recognized as Other revenue in our Consolidated Statement of Income upon the achievement of the related milestone events. We may also receive numerous individually immaterial milestones aggregating $472 million upon the achievement of various substantive success-based development and regulatory approval milestones. The receipt of these amounts, however, is contingent upon the occurrence of various future events which have a high degree of uncertainty of occurring.

During the years ended December 31, 2011, 2010 and 2009, cost recoveries from Takeda were $83 million, $91 million and $112 million, respectively, and are included in Research and development expense in the Consolidated Statements of Income. In addition, for the years December 31, 2011 and 2010, we recognized royalties on sales of Vectibix® in Japan of $20 million and $7 million, respectively.

Daiichi Sankyo Company, Limited

We are in a collaboration with Daiichi Sankyo Company, Limited (Daiichi Sankyo), which provides Daiichi Sankyo the exclusive rights to develop and commercialize denosumab in Japan for osteoporosis, oncology and

 

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AMGEN INC.

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (Continued)

 

certain other indications. As part of the agreement, Amgen received exclusive worldwide rights to certain Daiichi Sankyo intellectual property to the extent applicable to denosumab. Through collaboration committees, the parties jointly coordinate and oversee Daiichi Sankyo’s development and commercialization of denosumab in Japan.

Under the terms of the agreement, Daiichi Sankyo assumed all related development and commercialization costs in Japan and agreed to reimburse Amgen for certain worldwide development costs related to denosumab. As of December 31, 2009, Daiichi Sankyo had substantially satisfied its obligations to reimburse Amgen for these costs. If approved for sale, Amgen will receive royalties on future sales of denosumab recorded by Daiichi Sankyo in Japan.

Pursuant to the terms of the agreement, we paid Daiichi Sankyo milestone payments aggregating $60 million, in 2010, as a result of various regulatory approvals of denosumab. The milestone payments were capitalized within Intangible assets, net in the Consolidated Balance Sheets and are being amortized over 11 years and the amortization expense is included in Cost of sales (excludes amortization of certain acquired intangible assets) in the Consolidated Statements of Income.

The collaboration agreement will expire in 2027 unless terminated earlier in accordance with its terms.

During the years ended December 31, 2011, 2010 and 2009, cost recoveries from Daiichi Sankyo were $4 million, $3 million and $64 million, respectively. The cost recoveries are included in Research and development expense in the Consolidated Statements of Income.

Other

We have various other collaborations, in addition to those discussed above, that are not individually significant to our business at this time. Pursuant to the terms of those agreements, we may be required to pay or we may receive additional amounts upon the achievement of various development, regulatory and commercial milestones which in the aggregate could be significant. We may also incur or have reimbursed to us significant R&D costs if the related product candidate were to advance to late stage clinical trials. In addition, if any products related to these collaborations are approved for sale, we may be required to pay or we may receive significant royalties on future sales. The payment of these amounts, however, is contingent upon the occurrence of various future events, which have a high degree of uncertainty of occurring.

7. Related party transactions

We own a 50% interest in K-A, a corporation formed in 1984 with Kirin Holdings Company, Limited (Kirin) for the development and commercialization of certain products based on advanced biotechnology. All of our rights to manufacture and market certain products including pegfilgrastim, granulocyte colony-stimulating factor, darbepoetin alfa, recombinant human erythropoietin and romiplostim are pursuant to exclusive licenses from K-A, which we currently market under the brand names Neulasta®, NEUPOGEN®, Aranesp®, EPOGEN®, and Nplate®, respectively.

We account for our interest in K-A using the equity method and include our share of K-A’s profits or losses in Selling, general and administrative expense in the Consolidated Statements of Income. For the years ended December 31, 2011, 2010 and 2009, our share of K-A’s profits was $47 million, $71 million and $72 million, respectively. During 2009, we received $110 million in dividends from K-A. At both December 31, 2011 and 2010, the carrying value of our equity method investment in K-A, net of dividends received, was approximately $0.4 billion and is included in noncurrent Other assets in the Consolidated Balance Sheets.

 

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AMGEN INC.

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (Continued)

 

K-A’s revenues consist of royalty income related to its licensed technology rights. K-A receives royalty income from us, as well as from Kirin, J&J and F. Hoffmann-La Roche Ltd. (Roche) under separate product license contracts for certain geographic areas outside of the United States. During the years ended December 31, 2011, 2010 and 2009, K-A earned royalties from us of $298 million, $322 million and $327 million, respectively. These amounts are included in Cost of sales (excludes amortization of certain acquired intangible assets) in the Consolidated Statements of Income.

K-A’s expenses consist primarily of costs related to R&D activities conducted on its behalf by Amgen and Kirin. K-A pays Amgen and Kirin for such services at negotiated rates. During the years ended December 31, 2011, 2010 and 2009, we earned revenues from K-A of $130 million, $96 million and $102 million, respectively, for certain R&D activities performed on K-A’s behalf. These amounts are recognized as Other revenues in the Consolidated Statements of Income. We may also receive numerous individually immaterial milestones aggregating $125 million upon the achievement of various substantive success-based development and regulatory approval milestones contingent upon the occurrence of various future events, most of which have a high degree of uncertainty of occurring. During the years ended December 31, 2011, 2010 and 2009, we recorded cost recoveries from K-A of $85 million, $88 million and $96 million, respectively, related to certain third-party costs. These amounts are included in Research and development expense in the Consolidated Statements of Income.

As of December 31, 2011 and 2010, we owed K-A $75 million and $62 million, respectively, which are included in Accrued liabilities in the Consolidated Balance Sheets.

8. Cost savings initiatives and restructuring

Manufacturing operations optimization

As part of our continuing efforts to optimize our network of manufacturing facilities and improve cost efficiencies, on January 18, 2011, we entered into an agreement whereby Boehringer Ingelheim (BI) agreed to acquire our rights in and substantially all assets at our manufacturing facility located in Fremont, California. The transaction was approved by Amgen’s Board of Directors in December 2010 and closed in March 2011. In connection with the closing of this transaction, BI has assumed our obligations under certain of the facility’s operating lease contracts and has entered into an agreement to manufacture certain quantities of our marketed product Vectibix® for us at this facility through December 31, 2012 (the supply period).

We considered the transaction with BI to be a potential indicator of impairment, and accordingly, we performed an impairment analysis of the carrying values of the related fixed assets as of December 31, 2010. Based on this analysis, we determined that no future economic benefit would be received from a manufacturing line at the facility that had not yet been completed. As a result, we wrote off its entire carrying value, which aggregated $118 million during the year ended December 31, 2010. This amount is included in Other operating expenses in the Consolidated Statement of Income. The carrying values of the remaining fixed assets, aggregating approximately $133 million at December 31, 2010, were determined to be fully recoverable.

Due to the lack of sufficient initial investment by BI in the acquisition of this facility and our ongoing involvement with these operations, the transaction did not meet the accounting requirements to be treated as a sale involving real estate. As a result, the related assets continue to be carried on our Consolidated Balance Sheets.

 

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AMGEN INC.

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (Continued)

 

As a result of this transaction, we reduced the estimated useful lives of the remaining fixed assets to coincide with the supply period. During the year ended December 31, 2011, we recorded incremental depreciation of approximately $42 million in excess of what otherwise would have been recorded. In addition, due to the assignment to BI of the obligations under certain of the facility’s operating leases, we recorded charges of approximately $23 million during the year ended December 31, 2011, with respect to the lease period beyond the end of the supply period. These amounts are recorded in Cost of sales (excludes amortization of certain acquired intangible assets presented separately) in the Consolidated Statement of Income.

Other cost savings initiatives

As part of our continuing efforts to improve cost efficiencies in our operations, we recorded certain charges, primarily severance-related, aggregating approximately $109 million during the year ended December 31, 2011, which are included in Other operating expenses in the Consolidated Statement of Income.

Restructuring

On August 15, 2007, we announced a plan to restructure our worldwide operations in order to improve our cost structure. This restructuring plan was primarily the result of regulatory and reimbursement developments that began in 2007 involving erythropoiesis-stimulating agents (ESAs), including our marketed ESAs, Aranesp® and EPOGEN®, and the resulting impact on our operations. As of December 31, 2009, we completed all of the actions included in our restructuring plan and subsequently identified initiatives. During the year ended December 31, 2009, we recorded charges associated with these actions aggregating $70 million, comprised primarily of staff separation costs of $25 million, included principally in Other operating expenses in the Consolidated Statement of Income, and integration-related costs of $32 million, which were included principally in Selling, general and administrative expenses in the Consolidated Statement of Income.

9. Available-for-sale investments

The amortized cost, gross unrealized gains, gross unrealized losses and estimated fair values of available-for-sale investments by type of security were as follows (in millions):

 

 

Type of security as of December 31, 2011

   Amortized
cost
     Gross
unrealized
gains
     Gross
unrealized
losses
    Estimated
fair value
 

U.S. Treasury securities

   $ 3,878       $ 68       $      $ 3,946   

Other government-related debt securities:

          

Obligations of U.S. government agencies and FDIC-guaranteed bank debt

     1,548         23                1,571   

Foreign and other

     441         9                450   

Corporate debt securities:

          

Financial

     2,493         30         (15     2,508   

Industrial

     3,077         79         (10     3,146   

Other

     280         9         -        289   

Mortgage- and asset-backed securities

     1,789         6         (10     1,785   

Money market mutual funds

     6,266                        6,266   
  

 

 

    

 

 

    

 

 

   

 

 

 

Total debt security investments

     19,772         224         (35     19,961   

Equity securities

     42                        42   
  

 

 

    

 

 

    

 

 

   

 

 

 

Total available-for-sale investments

   $ 19,814       $ 224       $ (35   $ 20,003   
  

 

 

    

 

 

    

 

 

   

 

 

 

 

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AMGEN INC.

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (Continued)

 

Type of security as of December 31, 2010

   Amortized
cost
     Gross
unrealized
gains
     Gross
unrealized
losses
    Estimated
fair value
 

U.S. Treasury securities

   $ 5,044       $ 50       $ (14   $ 5,080   

Other government-related debt securities:

          

Obligations of U.S. government agencies and FDIC-guaranteed bank debt

     2,158         51         (1     2,208   

Foreign and other

     837         16         (1     852   

Corporate debt securities:

          

Financial

     2,252         53         (9     2,296   

Industrial

     2,441         71         (5     2,507   

Other

     307         10         (1     316   

Mortgage- and asset-backed securities

     841         5         (5     841   

Money market mutual funds

     3,030                        3,030   

Other short-term interest-bearing securities

     147                        147   
  

 

 

    

 

 

    

 

 

   

 

 

 

Total debt security investments

     17,057         256         (36     17,277   

Equity securities

     50                 (2     48   
  

 

 

    

 

 

    

 

 

   

 

 

 

Total available-for-sale investments

   $ 17,107       $ 256       $ (38   $ 17,325   
  

 

 

    

 

 

    

 

 

   

 

 

 

The fair values of available-for-sale investments by classification in the Consolidated Balance Sheets were as follows as of December 31, 2011 and 2010 (in millions):

 

 

Classification in the Consolidated Balance Sheets

   2011      2010  

Cash and cash equivalents

   $ 6,266       $ 3,142   

Marketable securities

     13,695         14,135   

Other assets — noncurrent

     42         48   
  

 

 

    

 

 

 

Total available-for-sale investments

   $ 20,003       $ 17,325   
  

 

 

    

 

 

 

Cash and cash equivalents in the table above excludes cash of $680 million and $145 million as of December 31, 2011 and 2010, respectively.

The fair values of available-for-sale debt security investments by contractual maturity were as follows as of December 31, 2011 and 2010 (in millions):

 

 

Contractual maturity

   2011      2010  

Maturing in one year or less

   $ 6,811       $ 4,118   

Maturing after one year through three years

     6,346         6,736   

Maturing after three years through five years

     5,710         5,812   

Maturing after five years

     1,094         611   
  

 

 

    

 

 

 

Total debt securities

   $ 19,961       $ 17,277   
  

 

 

    

 

 

 

For the years ended December 31, 2011, 2010 and 2009, realized gains totaled $191 million, $115 million and $104 million, respectively, and realized losses totaled $37 million, $25 million and $62 million, respectively. The cost of securities sold is based on the specific identification method.

The primary objective of our investment portfolio is to enhance overall returns in an efficient manner while maintaining safety of principal, prudent levels of liquidity and acceptable levels of risk. Our investment policy

 

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AMGEN INC.

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (Continued)

 

limits debt security investments to certain types of debt and money market instruments issued by institutions with primarily investment grade credit ratings and places restrictions on maturities and concentration by asset class and issuer.

We review our available-for-sale investments for other-than-temporary declines in fair value below our cost basis each quarter and whenever events or changes in circumstances indicate that the cost basis of an asset may not be recoverable. This evaluation is based on a number of factors including, the length of time and the extent to which the fair value has been below our cost basis and adverse conditions related specifically to the security, including any changes to the credit rating of the security. As of December 31, 2011 and 2010, we believe the cost bases for our available-for-sale investments were recoverable in all material respects.

10. Inventories

Inventories consisted of the following as of December 31, 2011 and 2010 (in millions):

 

 

     2011      2010  

Raw materials

   $ 158       $ 128   

Work in process

     1,802         1,382   

Finished goods

     524         512   
  

 

 

    

 

 

 

Total inventories

   $ 2,484       $ 2,022   
  

 

 

    

 

 

 

11. Property, plant and equipment

Property, plant and equipment consisted of the following as of December 31, 2011 and 2010 (dollar amounts in millions):

 

 

     Useful life (in years)      2011      2010  

Land

           $ 366       $ 361   

Buildings and improvements

     10-40         3,463         3,392   

Manufacturing equipment

     8-12         1,897         1,802   

Laboratory equipment

     8-12         1,016         955   

Other

     3-15         3,745         3,547   

Construction in progress

             744         631   
     

 

 

    

 

 

 

Property, plant and equipment, gross

        11,231         10,688   

Less accumulated depreciation and amortization

        (5,811)         (5,166)   
     

 

 

    

 

 

 

Property, plant and equipment, net

      $ 5,420       $ 5,522   
     

 

 

    

 

 

 

During the years ended December 31, 2011, 2010 and 2009, we recognized depreciation and amortization charges associated with our property, plant and equipment of $679 million, $594 million and $624 million, respectively.

 

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AMGEN INC.

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (Continued)

 

12. Intangible assets

Finite-lived and indefinite-lived identifiable intangible assets consisted of the following as of December 31, 2011 and 2010 (in millions):

 

 

    2011     2010  
    Gross
carrying
amount
    Accumulated
amortization
    Intangible
assets, net
    Gross
carrying
amount
    Accumulated
amortization
    Intangible
assets, net
 

Finite-lived intangible assets:

           

Acquired product technology rights:

           

Developed product technology

  $ 2,872      $ (1,811)      $ 1,061      $ 2,872      $ (1,619)      $ 1,253   

Core technology

    1,348        (850)        498        1,348        (760)        588   

Trade name

    190        (120)        70        190        (107)        83   

Acquired R&D technology rights

    350        (350)               350        (329)        21   

Other acquired intangible assets

    686        (406)        280        627        (342)        285   
 

 

 

   

 

 

   

 

 

   

 

 

   

 

 

   

 

 

 

Total finite-lived intangible assets

    5,446        (3,537)        1,909        5,387        (3,157)        2,230   

Indefinite-lived intangible assets — IPR&D

    675               675                        
 

 

 

   

 

 

   

 

 

   

 

 

   

 

 

   

 

 

 

Total identifiable intangible assets

  $ 6,121      $ (3,537)      $ 2,584      $ 5,387      $ (3,157)      $ 2,230   
 

 

 

   

 

 

   

 

 

   

 

 

   

 

 

   

 

 

 

Amortization of finite-lived intangible assets is provided over their estimated useful lives ranging from 5 to 15 years on a straight-line basis.

Acquired product technology rights relate to the identifiable intangible assets acquired in connection with the 2002 Immunex acquisition and the related amortization expense is included in Amortization of certain acquired intangible assets in the Consolidated Statements of Income. Acquired R&D technology rights consist of technology used in R&D with alternative future uses and the related amortization expense is included in Research and development expense in the Consolidated Statements of Income. The amortization expense related to other acquired intangible assets is included principally in Cost of sales (excludes amortization of certain acquired intangible assets) and Selling, general and administrative expense in the Consolidated Statements of Income. During the years ended December 31, 2011, 2010 and 2009, we recognized amortization charges associated with our finite-lived intangible assets of $380 million, $423 million and $425 million, respectively. The total estimated amortization for each of the next five years for our intangible assets is $354 million, $359 million, $340 million, $327 million and $317 million in 2012, 2013, 2014, 2015 and 2016, respectively.

IPR&D relates to identifiable intangible assets acquired in connection with the acquisition of BioVex. (See Note 2, Business combinations — BioVex Group, Inc.)

 

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AMGEN INC.

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (Continued)

 

13. Accrued liabilities

Accrued liabilities consisted of the following as of December 31, 2011 and 2010 (in millions):

 

 

     2011      2010  

Sales deductions

   $ 1,326       $ 1,144   

Employee compensation and benefits

     916         764   

Sales returns reserve

     339         339   

Legal reserve

     780           

Other

     1,667         1,119   
  

 

 

    

 

 

 

Total accrued liabilities

   $ 5,028       $ 3,366   
  

 

 

    

 

 

 

See Note 18, Contingencies and commitments, for further discussion of the legal reserve.

14. Financing arrangements

The carrying values and the fixed contractual coupon rates of our long-term borrowings were as follows as of December 31, 2011 and 2010 (in millions):

 

 

     2011      2010  

0.125% convertible notes due 2011 (0.125% 2011 Convertible Notes)

   $       $ 2,488   

0.375% convertible notes due 2013 (0.375% 2013 Convertible Notes)

     2,346         2,213   

1.875% notes due 2014 (1.875% 2014 Notes)

     1,000           

4.85% notes due 2014 (4.85% 2014 Notes)

     1,000         1,000   

2.30% notes due 2016 (2.30% 2016 Notes)

     748           

2.50% notes due 2016 (2.50% 2016 Notes)

     999           

5.85% notes due 2017 (5.85% 2017 Notes)

     1,099         1,099   

6.15% notes due 2018 (6.15% 2018 Notes)

     499         499   

4.375% euro denominated notes due 2018 (4.375% 2018 euro Notes)

     714           

5.70% notes due 2019 (5.70% 2019 Notes)

     998         998   

4.50% notes due 2020 (4.50% 2020 Notes)

     300         300   

3.45% notes due 2020 (3.45% 2020 Notes)

     897         897   

4.10% notes due 2021 (4.10% 2021 Notes)

     998           

3.875% notes due 2021 (3.875% 2021 Notes)

     1,745           

5.50% pound sterling denominated notes due 2026 (5.50% 2026 pound sterling Notes)

     739           

6.375% notes due 2037 (6.375% 2037 Notes)

     899         899   

6.90% notes due 2038 (6.90% 2038 Notes)

     499         499   

6.40% notes due 2039 (6.40% 2039 Notes)

     996         996   

5.75% notes due 2040 (5.75% 2040 Notes)

     697         696   

4.95% notes due 2041 (4.95% 2041 Notes)

     595         595   

5.15% notes due 2041 (5.15% 2041 Notes)

     2,232           

5.65% notes due 2042 (5.65% 2042 Notes)

     1,244           

Other notes, including our zero-coupon convertible notes

     184         183   
  

 

 

    

 

 

 

Total debt

     21,428         13,362   

Less current portion

     (84)         (2,488)   
  

 

 

    

 

 

 

Total noncurrent debt

   $ 21,344       $ 10,874   
  

 

 

    

 

 

 

 

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AMGEN INC.

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (Continued)

 

Debt repayments

In February 2011, our 0.125% 2011 Convertible Notes became due, and we repaid the $2.5 billion aggregate principal amount. As these convertible notes were cash settleable, their debt and equity components were bifurcated and accounted for separately. The discounted carrying value of the debt component resulting from the bifurcation was accreted back to the principal amount over the period the notes were outstanding. The total aggregate amount repaid, including the amount related to the debt discount of $643 million resulting from the bifurcation, is included in Cash flows from financing activities in the Consolidated Statement of Cash Flows. No debt was due or repaid in 2010, and we repaid $1.0 billion aggregate principal amount of notes with a fixed interest rate of 4.00% in 2009.

Debt issuances

We issued debt securities in various offerings during the three years ended December 31, 2011, including:

 

   

In 2011, we issued $10.5 billion aggregate principal amount of notes, comprised of the 1.875% 2014 Notes, the 2.30% 2016 Notes, the 2.50% 2016 Notes, the 4.375% 2018 euro Notes (€550 million aggregate principal amount), the 4.10% 2021 Notes, the 3.875% 2021 Notes, the 5.50% 2026 pound sterling Notes (£475 million aggregate principal amount), the 5.15% 2041 Notes and the 5.65% 2042 Notes.

 

   

In 2010, we issued $2.5 billion aggregate principal amount of notes, comprised of the 4.50% 2020 Notes, the 3.45% 2020 Notes, the 5.75% 2040 Notes and the 4.95% 2041 Notes.

 

   

In 2009, we issued $2.0 billion aggregate principal amount of notes, comprised of the 5.70% 2019 Notes and the 6.40% 2039 Notes.

Debt issuance costs incurred in connection with these debt offerings in 2011, 2010 and 2009 totaled $55 million, $17 million and $13 million, respectively. These debt issuance costs are being amortized over the respective lives of the notes, and the related charge is included in Interest expense, net, in the Consolidated Statements of Income.

All of our debt issuances other than our 0.375% 2013 Convertible Notes and Other notes may be redeemed at any time at our option, in whole or in part, at the principal amount of the notes being redeemed plus accrued interest and a make-whole amount, as defined. In addition, except with respect to our 0.375% 2013 Convertible Notes, the 4.85% 2014 Notes and Other notes, in the event of a change in control triggering event, as defined, we may be required to purchase for cash all or a portion of these debt issuances at a price equal to 101% of the principal amount of the notes plus accrued interest.

Convertible Notes

In 2006, we issued $5.0 billion principal amount of convertible notes at par. While outstanding, the notes are convertible into shares of our common stock upon the occurrence of specified events. In February 2011, $2.5 billion principal amount of the convertible notes (the 0.125% 2011 Convertible Notes) became due and were repaid in full. While outstanding, the conversion rate on the 0.125% 2011 Convertible Notes was 12.5247 shares per $1,000 principal amount of notes, which represented a conversion price of approximately $79.84 per share. The conversion rate on the $2.5 billion principal amount of convertible notes, which mature in February 2013 (the 0.375% 2013 Convertible Notes), was 12.7473 shares per $1,000 principal amount of notes at December 31, 2011, which represents a conversion price of approximately $78.45 per share. This conversion rate is adjusted as we make specified types of distributions, including paying cash dividends on our common stock, or enter into

 

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AMGEN INC.

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (Continued)

 

certain other transactions with respect to our common stock. The 0.375% 2013 Convertible Notes may only be converted: (i) during any calendar quarter if the closing price of our common stock exceeds 130% of the then conversion price per share during a defined period at the end of the previous quarter, (ii) if we make specified distributions to holders of our common stock or specified corporate transactions occur or (iii) within one month prior to the maturity date. Upon conversion, a holder would receive the conversion value equal to the conversion rate multiplied by the volume weighted-average price of our common stock during a specified period following the conversion date. The conversion value will be paid in: (i) cash equal to the lesser of the principal amount of the note or the conversion value, as defined, and (ii) cash, shares of our common stock, or a combination of cash and shares of our common stock, at our option, to the extent the conversion value exceeds the principal amount of the note (the excess conversion value). In addition, upon a change in control, as defined, the holders may require us to purchase for cash all or a portion of their notes for the principal amount of the notes plus accrued interest. As of December 31, 2011, the 0.375% 2013 Convertible Notes were not convertible. While outstanding, the 0.125% 2011 Convertible Notes had terms similar to the 0.375% 2013 Convertible Notes.

Concurrent with the issuance of the 0.375% 2013 Convertible Notes, we purchased a convertible note hedge. The convertible note hedge allows us to receive shares of our common stock and/or cash from the counterparty to the transaction equal to the amounts of common stock and/or cash related to the excess conversion value that we would issue and/or pay to the holders of the 0.375% 2013 Convertible Notes upon conversion. This convertible note hedge will terminate at the earlier of the maturity of the 0.375% 2013 Convertible Notes or the first day none of these notes remain outstanding due to conversion or otherwise. We also purchased a convertible note hedge with similar terms in connection with the issuance of the 0.125% 2011 Convertible Notes, which terminated unexercised when these notes were repaid.

Also concurrent with the issuance of the 0.375% 2013 Convertible Notes, we sold warrants to acquire 31.5 million shares of our common stock in May 2013 (the settlement date) at an exercise price of $107.90 per share. If the average price of our common stock during a defined period ending on or about the settlement date exceeds the exercise price of the warrants, the warrants will be net settled, at our option, in cash or shares of our common stock. In connection with the issuance of the 0.125% 2011 Convertible Notes, we sold warrants to purchase 31.3 million shares of our stock on similar terms, which expired unexercised in May 2011.

Because the convertible note hedges and warrants can be settled at our option in cash or shares of our common stock, and these contracts meet all of the applicable criteria for equity classification under the applicable accounting standards, the cost of the convertible note hedges and net proceeds from the sale of the warrants are classified in Stockholders’ equity in the Consolidated Balance Sheets. In addition, because both of these contracts are classified in Stockholders’ equity and are indexed to our common stock, they are not accounted for as derivatives.

As required for cash settleable convertible notes, the debt and equity components of the 0.375% 2013 Convertible Notes were bifurcated and accounted for separately. The resulting discounted carrying value of the debt is being accreted back to the principal amount through the scheduled maturity date, resulting in the recognition of non-cash interest expense. After giving effect to this bifurcation, the effective interest rate on this borrowing is 6.35%. For the years ended December 31, 2011, 2010 and 2009, total interest expense for the 0.375% 2013 Convertibles Notes was $143 million, $134 million, and $127 million, respectively, including non-cash interest expense of $133 million, $125 million, and $118 million, respectively. While outstanding, the 0.125% 2011 Convertible Notes were accounted for in the same manner, resulting in an effective interest rate of 6.24%. For the years ended December 31, 2011, 2010 and 2009, total interest expense for the 0.125% 2011 Convertible Notes was $13 million, $149 million, and $140 million, respectively, including non-cash interest expense of $12 million, $146 million, and $136 million, respectively.

 

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AMGEN INC.

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (Continued)

 

The principal balance, unamortized discount and net carrying amount of the liability and equity components of our 0.375% 2013 Convertible Notes were as follows as of December 31, 2011 and 2010 (in millions):

 

 

     Liability component      Equity component  

0.375% 2013 Convertible Notes

   Principal
balance
     Unamortized
discount
     Net carrying
amount
     Net carrying
amount
 

December 31, 2011

   $ 2,500       $ 154       $ 2,346       $ 829   

December 31, 2010

   $ 2,500       $ 287       $ 2,213       $ 829   

Other

Other notes include zero-coupon convertible notes due in 2032 with a carrying value of $84 million and $83 million at December 31, 2011 and 2010, respectively, and notes due in 2097 with a carrying value of $100 million.

Interest rate swaps

To achieve a desired mix of fixed and floating interest rate debt, we enter into interest rate swap contracts that effectively convert a fixed rate interest coupon for certain of our debt issuances to a floating London Interbank Offered Rate (LIBOR)-based coupon over the life of the respective note. These interest rate swap contracts qualify and are designated as fair value hedges. The effective interest rates on these notes after giving effect to the related interest rate swap contracts and the notional amounts of these interest rate swap contracts were as follows as of December 31, 2011 and 2010 (dollar amounts in millions):

 

 

          Notional amount  
    

Effective interest rate

   2011      2010  

4.85% 2014 Notes

   LIBOR + 0.3%    $ 1,000       $ 1,000   

5.85% 2017 Notes

   LIBOR + 2.5%      1,100         1,100   

6.15% 2018 Notes

   LIBOR + 1.8%      500         500   

5.70% 2019 Notes

   LIBOR + 2.6%      1,000         1,000   
     

 

 

    

 

 

 
      $ 3,600       $ 3,600   
     

 

 

    

 

 

 

Cross currency swaps

In order to hedge our exposure to foreign currency exchange rate risk associated with our pound sterling denominated long-term notes issued in 2011, we entered into cross currency swap contracts. These cross currency swap contracts qualify and are designated as cash flow hedges. Under the terms of these contracts, we receive interest payments in pounds sterling at a fixed rate of 5.5% on £475 million and pay interest in U.S. dollars at a fixed rate of 5.8% on $748 million, the aggregate notional amounts paid to/received from the counterparties upon exchange of currencies at the inception of these contracts. We will pay U.S. dollars to and receive pounds sterling from the counterparties at the maturity of the contracts for the same notional amounts. The terms of these contracts correspond to the related hedged notes, effectively converting the interest payments and principal repayment on these notes from pounds sterling to U.S. dollars.

 

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AMGEN INC.

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (Continued)

 

Shelf registration statements and other facilities

As of December 31, 2011, we have a commercial paper program that allows us to issue up to $2.5 billion of unsecured commercial paper to fund our working capital needs. At December 31, 2011 and 2010, we had no amounts outstanding under our commercial paper program.

In December 2011, we entered into a $2.5 billion syndicated, unsecured, revolving credit agreement which is available for general corporate purposes or as a liquidity backstop to our commercial paper program. The commitments under the revolving credit agreement may be increased by up to $500 million with the agreement of the banks. Each bank which is a party to the agreement has an initial commitment term of five years. This term may be extended for up to two additional one-year periods with the agreement of the banks. Annual commitment fees for this agreement are 0.1% based on our current credit rating. We would be charged interest at LIBOR plus 0.9% for any amounts borrowed under this facility. As of December 31, 2011, no amounts were outstanding under this facility. In connection with the new revolving credit agreement we terminated our prior $2.3 billion revolving credit agreement that was scheduled to expire in November 2012.

In March 2011, we filed a shelf registration statement with the U.S. Securities and Exchange Commission to replace an existing shelf registration statement that was scheduled to expire in April 2011. This shelf registration statement allows us to issue unspecified amounts of debt securities; common stock; preferred stock; warrants to purchase debt securities, common stock, preferred stock or depository shares; rights to purchase common stock or preferred stock; securities purchase contracts; securities purchase units; and depository shares. Under this shelf registration statement, all of the securities available for issuance may be offered from time to time with terms to be determined at the time of issuance. This shelf registration statement expires in March 2014.

In 1997, we established a $400 million medium-term note program under which medium-term debt securities may be offered from time to time with terms to be determined at the time of issuance. As of December 31, 2011 and 2010, no securities were outstanding under this medium-term note program.

Certain of our financing arrangements contain non-financial covenants. In addition, our revolving credit agreement includes a financial covenant with respect to the level of our borrowings in relation to our equity, as defined. We were in compliance with all applicable covenants under these arrangements as of December 31, 2011.

Contractual maturities of long-term debt obligations

The aggregate contractual maturities of all long-term debt obligations due subsequent to December 31, 2011, are as follows (in millions):

 

 

Maturity date

   Amount  

2012(1)

   $ 84   

2013(2)

     2,500   

2014

     2,000   

2015

       

2016

     1,750   

Thereafter

     15,312   
  

 

 

 

Total

   $ 21,646   
  

 

 

 

 

 

(1) 

This amount represents the accreted value of our zero-coupon convertible notes due in 2032 which will be redeemed on March 1, 2012.

 

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AMGEN INC.

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (Continued)

 

(2) 

This amount represents the principal amount for our 0.375% 2013 Convertible Notes after full accretion of the debt discount.

Interest costs

Interest costs are expensed as incurred, except to the extent such interest is related to construction in progress, in which case interest is capitalized. Interest expense, net, for the years ended December 31, 2011, 2010 and 2009, was $610 million, $604 million and $578 million, respectively. Interest costs capitalized for the years ended December 31, 2011, 2010 and 2009, were $22 million, $33 million and $32 million, respectively. Interest paid, net of interest rate swaps, during the years ended December 31, 2011, 2010 and 2009, totaled $446 million, $323 million and $293 million, respectively.

15. Stockholders’ equity

Stock repurchase program

Activity under our stock repurchase program was as follows for the years ended December 31, 2011, 2010 and 2009 (in millions):

 

 

     2011     2010      2009  
     Shares      Dollars     Shares      Dollars      Shares      Dollars  

First quarter

           $        29.1       $ 1,684         37.5       $ 1,997   

Second quarter

     12.9         732        10.3         616                   

Third quarter

     45.4         2,421        6.6         364                   

Fourth quarter

     86.0         5,154 (1)      20.5         1,136         21.7         1,211   
  

 

 

    

 

 

   

 

 

    

 

 

    

 

 

    

 

 

 

Total stock repurchases

     144.3       $ 8,307        66.5       $ 3,800         59.2       $ 3,208   
  

 

 

    

 

 

   

 

 

    

 

 

    

 

 

    

 

 

 

 

 

(1) 

Includes the repurchase of 83.3 million shares of our common stock at an average price paid per share of $60.08 including related expenses, for an aggregate cost of $5.0 billion, under a modified Dutch auction tender offer.

In April 2011, the Board of Directors authorized us to repurchase up to an additional $5.0 billion of our common stock under our stock repurchase program, and in October 2011, the Board of Directors further increased the total authorization for stock repurchases by $6.1 billion to $10.0 billion. As of December 31, 2011, $5.0 billion remained available under the program.

In July and October 2011, the Board of Directors declared quarterly cash dividends of $0.28 per share of common stock, which were paid in September and December 2011, respectively. Additionally, on December 15, 2011, the Board of Directors declared a quarterly cash dividend of $0.36 per share of common stock, which will be paid on March 7, 2012, to all stockholders of record as of the close of business on February 15, 2012.

 

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AMGEN INC.

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (Continued)

 

Accumulated other comprehensive income

The components of Accumulated Other Comprehensive Income (AOCI) are as follows for the years ended December 31, 2011, 2010 and 2009 (in millions):

 

 

     Foreign
currency
translation
    Cash flow
hedges
    Available-for-sale
securities
    Other     AOCI  

Balance as of December 31, 2008

   $ 25      $ 50      $ 49      $ (7   $ 117   

Foreign currency translation adjustments

     25                             25   

Unrealized (losses) gains

            (213     116        (12     (109

Reclassification adjustments to income

            8        (42            (34

Other

                          5        5   

Income taxes

     (10     73        (28     6        41   
  

 

 

   

 

 

   

 

 

   

 

 

   

 

 

 

Balance as of December 31, 2009

     40        (82     95        (8     45   

Foreign currency translation adjustments

     (29                          (29

Unrealized gains

            186        155        1        342   

Reclassification adjustments to income

            (46     (90            (136

Income taxes

     11        (55     (25            (69
  

 

 

   

 

 

   

 

 

   

 

 

   

 

 

 

Balance as of December 31, 2010

     22        3        135        (7     153   

Foreign currency translation adjustments

     (6                          (6

Unrealized (losses) gains

            (51     125        2        76   

Reclassification adjustments to income

            112        (154            (42

Other

                          (8     (8

Income taxes

     5        (21     14               (2
  

 

 

   

 

 

   

 

 

   

 

 

   

 

 

 

Balance as of December 31, 2011

   $ 21      $ 43      $ 120      $ (13   $ 171   
  

 

 

   

 

 

   

 

 

   

 

 

   

 

 

 

Income tax expense or benefit for unrealized gains and losses and the related reclassification adjustments to income for cash flow hedges was a $20 million benefit and $41 million expense in 2011, a $71 million expense and $16 million benefit in 2010 and a $76 million benefit and $3 million expense in 2009, respectively. Income tax expense/benefit for unrealized gains and losses and the related reclassification adjustments to income for available-for-sale securities was a $45 million expense and $59 million benefit for 2011, a $60 million expense and $35 million benefit in 2010 and a $44 million expense and $16 million benefit in 2009, respectively.

Other

In addition to common stock, our authorized capital includes 5 million shares of preferred stock, $0.0001 par value. As of December 31, 2011 and 2010, no shares of preferred stock were issued or outstanding.

16. Fair value measurement

To determine the fair value of our financial assets and liabilities we use valuation approaches within a hierarchy that maximizes the use of observable inputs and minimizes the use of unobservable inputs by requiring that observable inputs be used when available. Observable inputs are inputs that market participants would use in pricing the asset or liability based on market data obtained from sources independent of the Company. Unobservable inputs are inputs that reflect the Company’s assumptions about the inputs that market participants

 

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AMGEN INC.

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (Continued)

 

would use in pricing the asset or liability and are developed based on the best information available in the circumstances. The fair value hierarchy is divided into three levels based on the source of inputs as follows:

 

Level 1

     

Valuations based on unadjusted quoted prices in active markets for identical assets or liabilities that the Company has the ability to access

Level 2

     

Valuations for which all significant inputs are observable, either directly or indirectly, other than level 1 inputs

Level 3

     

Valuations based on inputs that are unobservable and significant to the overall fair value measurement

The availability of observable inputs can vary among the various types of financial assets and liabilities. To the extent that the valuation is based on models or inputs that are less observable or unobservable in the market, the determination of fair value requires more judgment. In certain cases, the inputs used for measuring fair value may fall into different levels of the fair value hierarchy. In such cases, for financial statement disclosure purposes, the level in the fair value hierarchy within which the fair value measurement is categorized is based on the lowest level of input used that is significant to the overall fair value measurement.

The fair value of each major class of the Company’s financial assets and liabilities measured at fair value on a recurring basis was as follows (in millions):

 

 

Fair value measurement as of December 31, 2011, using:

  Quoted prices in
active markets for
identical assets

(Level 1)
    Significant other
observable
inputs

(Level 2)
    Significant
unobservable
inputs

(Level 3)
    Total  

Assets:

       

Available-for-sale investments:

       

U.S. Treasury securities

  $ 3,946      $      $      $ 3,946   

Other government-related debt securities:

       

Obligations of U.S. government agencies and FDIC-guaranteed bank debt

           1,571               1,571   

Foreign and other

           450               450   

Corporate debt securities:

       

Financial

           2,508               2,508   

Industrial

           3,146               3,146   

Other

           289               289   

Mortgage- and asset-backed securities

           1,785               1,785   

Money market mutual funds

    6,266                      6,266   

Equity securities

    42                      42   

Derivatives:

       

Foreign currency contracts

           172               172   

Interest rate swap contracts

           377               377   
 

 

 

   

 

 

   

 

 

   

 

 

 

Total assets

  $ 10,254      $ 10,298      $      $ 20,552   
 

 

 

   

 

 

   

 

 

   

 

 

 

Liabilities:

       

Derivatives:

       

Foreign currency contracts

  $      $ 48      $      $ 48   

Cross currency swap contracts

           26               26   

Contingent consideration obligations in connection with a business combination

                  190        190   
 

 

 

   

 

 

   

 

 

   

 

 

 

Total liabilities

  $      $ 74      $ 190      $ 264   
 

 

 

   

 

 

   

 

 

   

 

 

 

 

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AMGEN INC.

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (Continued)

 

 

Fair value measurement as of December 31, 2010, using:

   Quoted prices in
active  markets for
identical assets

(Level 1)
     Significant  other
observable

inputs
(Level 2)
     Significant
unobservable

inputs
(Level 3)
     Total  

Assets:

           

Available-for-sale investments:

           

U.S. Treasury securities

   $ 5,080       $       $  —       $ 5,080   

Other government-related debt securities:

           

Obligations of U.S. government agencies and FDIC-guaranteed bank debt

             2,208                 2,208   

Foreign and other

             852                 852   

Corporate debt securities:

           

Financial

             2,296                 2,296   

Industrial

             2,507                 2,507   

Other

             316                 316   

Mortgage- and asset-backed securities

             841                 841   

Money market mutual funds

     3,030                         3,030   

Other short-term interest-bearing securities

             147                 147   

Equity securities

     48                         48   

Derivatives:

           

Foreign currency contracts

             154                 154   

Interest rate swap contracts

             195                 195   
  

 

 

    

 

 

    

 

 

    

 

 

 

Total assets

   $ 8,158       $ 9,516       $       $  17,674   
  

 

 

    

 

 

    

 

 

    

 

 

 

Liabilities:

           

Derivatives:

           

Foreign currency contracts

   $       $ 103       $       $ 103   
  

 

 

    

 

 

    

 

 

    

 

 

 

Total liabilities

   $       $ 103       $       $ 103   
  

 

 

    

 

 

    

 

 

    

 

 

 

The fair values of our U.S. Treasury securities, money market mutual funds and equity securities are based on quoted market prices in active markets with no valuation adjustment.

Substantially all of our other government related and corporate debt securities are investment grade with maturity dates of five years or less from the balance sheet date. Our other government related debt securities portfolio is composed of securities with weighted-average credit ratings of AA+ by Standard & Poor’s (S&P) and AAA or equivalent by Moody’s Investors Service, Inc. (Moody’s) or Fitch, Inc. (Fitch); and our corporate debt securities portfolio has a weighted-average credit rating of A- by S&P and A or equivalent by Moody’s or Fitch. We estimate the fair values of these securities by taking into consideration valuations obtained from third-party pricing services. The pricing services utilize industry standard valuation models, including both income- and market-based approaches, for which all significant inputs are observable, either directly or indirectly, to estimate fair value. These inputs include reported trades of and broker/dealer quotes on the same or similar securities; issuer credit spreads; benchmark securities; and other observable inputs.

Our mortgage and asset backed securities portfolio is composed entirely of senior tranches, with credit ratings of AAA or equivalent by S&P, Moody’s or Fitch. We estimate the fair values of these securities by taking into consideration valuations obtained from third-party pricing services. The pricing services utilize industry standard valuation models, including both income- and market-based approaches, for which all significant inputs are observable, either directly or indirectly, to estimate fair value. These inputs include reported trades of and

 

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AMGEN INC.

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (Continued)

 

broker/dealer quotes on the same or similar securities; issuer credit spreads; benchmark securities; prepayment/default projections based on historical data; and other observable inputs.

We value our other short-term interest bearing securities at amortized cost, which approximates fair value given their near-term maturity dates.

Substantially all of our foreign currency forward and option derivatives contracts have maturities of three years or less and all are with counterparties that have a minimum credit rating of A- or equivalent by S&P, Moody’s or Fitch. We estimate the fair values of these contracts by taking into consideration valuations obtained from a third-party valuation service that utilizes an income-based industry standard valuation model for which all significant inputs are observable, either directly or indirectly. These inputs include foreign currency rates, LIBOR, swap rates and obligor credit default swap rates. In addition, inputs for our foreign currency option contracts also include implied volatility measures. These inputs, where applicable, are at commonly quoted intervals. As of December 31, 2011 and 2010, we had open foreign currency forward contracts with notional amounts of $3.5 billion and $3.2 billion, respectively, and open foreign currency option contracts with notional amounts of $292 million and $398 million, respectively, that were primarily euro-based and were designated as cash flow hedges. In addition, as of December 31, 2011 and 2010, we had $389 million and $670 million, respectively, of open foreign currency forward contracts to reduce exposure to fluctuations in value of certain assets and liabilities denominated in foreign currencies that were primarily euro-based and that were not designated as hedges. (See Note 17, Derivative instruments.)

Our interest rate and cross currency swap contracts are with counterparties that have a minimum credit rating of A- or equivalent by S&P, Moody’s or Fitch. We estimate the fair values of these contracts by taking into consideration valuations obtained from a third-party valuation service that utilizes an income-based industry standard valuation model for which all significant inputs are observable either directly or indirectly. These inputs include foreign currency rates, LIBOR, swap rates, obligor credit default swap rates and cross currency basis swap spreads. We had interest rate swap contracts with an aggregate notional amount of $3.6 billion as of December 31, 2011 and 2010, that were designated as fair value hedges. We had cross currency swap contracts on all of our 5.50% 2026 pound sterling Notes as of December 31, 2011, that were designated as cash flow hedges. (See Note 17, Derivative instruments.)

Contingent consideration obligations in connection with a business combination result from our acquisition of BioVex in March 2011. The fair value measurements of these obligations are based on significant unobservable inputs, and accordingly, such amounts are considered Level 3 measurements. There were no changes in assumptions that had a material impact on the estimated fair values of these obligations during the period from the acquisition date to December 31, 2011, and accordingly, there was no significant impact on net income for this period. For a description of the valuation methodology and related assumptions used for estimating the fair values of these obligations, see Note 2, Business combinations.

There have been no transfers of assets or liabilities between the fair value measurement levels, and there were no material remeasurements to fair value during the years ended December 31, 2011 and 2010, of assets and liabilities that are not measured at fair value on a recurring basis, except as discussed in Note 8, Cost savings initiatives and restructuring, regarding an impairment of fixed assets that we recognized in 2010.

Summary of the fair value of other financial instruments

Cash equivalents

The estimated fair values of cash equivalents approximate their carrying values due to the short-term nature of these financial instruments.

 

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AMGEN INC.

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (Continued)

 

Borrowings

We estimate the fair values of our convertible notes by using an income-based industry standard valuation model for which all significant inputs are observable either directly or indirectly, including benchmark yields adjusted for our credit risk (Level 2). The fair value of our convertible notes represent only the liability components of these instruments, as their equity components are included in Common stock and additional paid-in capital in the Consolidated Balance Sheets. We estimate the fair values of our other long-term notes by taking into consideration indicative prices obtained from a third-party financial institution that utilizes industry standard valuation models, including both income- and market-based approaches, for which all significant inputs are observable either directly or indirectly. These inputs include reported trades of and broker/dealer quotes on the same or similar securities; credit spreads; benchmark yields; and other observable inputs (Level 2). As of December 31, 2011 and 2010, the aggregate fair values of our long-term debt were $23.0 billion and $14.5 billion, respectively, and the carrying values were $21.4 billion and $13.4 billion, respectively.

17. Derivative instruments

The Company is exposed to foreign currency exchange rate and interest rate risks related to its business operations. To reduce our risks related to these exposures, we utilize certain derivative instruments, including foreign currency forward, foreign currency option, cross currency swap, forward interest rate and interest rate swap contracts. We do not use derivatives for speculative trading purposes.

Cash flow hedges

We are exposed to possible changes in the values of certain anticipated foreign currency cash flows resulting from changes in foreign currency exchange rates, associated primarily with our euro-denominated international product sales. Increases or decreases in the cash flows associated with our international product sales due to movements in foreign currency exchange rates are offset partially by the corresponding increases and decreases in our international operating expenses resulting from these foreign currency exchange rate movements. To further reduce our exposure to foreign currency exchange rate fluctuations on our international product sales, we enter into foreign currency forward and option contracts to hedge a portion of our projected international product sales primarily over a three-year time horizon, with, at any given point in time, a higher percentage of nearer-term projected product sales being hedged than in successive periods. As of December 31, 2011, 2010 and 2009, we had open foreign currency forward contracts with notional amounts of $3.5 billion, $3.2 billion and $3.4 billion and open foreign currency option contracts with notional amounts of $292 million, $398 million and $376 million, respectively. These foreign currency forward and option contracts, primarily euro-based, have been designated as cash flow hedges, and accordingly, the effective portion of the unrealized gains and losses on these contracts are reported in AOCI and reclassified to earnings in the same periods during which the hedged transactions affect earnings.

In order to hedge our exposure to foreign currency exchange rate risk associated with our pound sterling denominated long-term notes issued in 2011, we entered into cross currency swap contracts. Under the terms of these contracts, we receive interest payments in pounds sterling at a fixed rate of 5.5% on £475 million and pay interest in U.S. dollars at a fixed rate of 5.8% on $748 million, the aggregate notional amounts paid to/received from the counterparties upon exchange of currencies at the inception of these contracts. We will pay U.S. dollars to and receive pounds sterling from the counterparties at the maturity of the contracts for the same notional amounts. The terms of these contracts correspond to the related hedged notes, effectively converting the interest payments and principal repayment on these notes from pounds sterling to U.S. dollars. These cross currency

 

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AMGEN INC.

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (Continued)

 

swap contracts have been designated as cash flow hedges, and accordingly, the effective portion of the unrealized gains and losses on these contracts are reported in AOCI and reclassified to earnings in the same periods during which the hedged debt affects earnings.

In connection with the anticipated issuance of long-term fixed-rate debt, we occasionally enter into forward interest rate contracts in order to hedge the variability in cash flows due to changes in the applicable Treasury rate between the time we enter into these contracts and the time the related debt is issued. Gains and losses on such contracts, which are designated as cash flow hedges, are reported in AOCI and amortized into earnings over the lives of the associated debt issuances.

The effective portion of the unrealized gain/(loss) recognized in OCI for our derivative instruments designated as cash flow hedges was as follows (in millions):

 

 

     Years ended December 31,  

Derivatives in cash flow hedging relationships

     2011       2010       2009    

Foreign currency contracts

   $ (25   $ 191      $ (202

Cross currency swap contracts

     (26              

Forward interest rate contracts

            (5     (11
  

 

 

   

 

 

   

 

 

 

Total

   $ (51   $ 186      $ (213
  

 

 

   

 

 

   

 

 

 

The location in the Consolidated Statements of Income and the effective portion of the gain/(loss) reclassified from AOCI into earnings for our derivative instruments designated as cash flow hedges was as follows (in millions):

 

 

          Years ended December 31,  

Derivatives in cash flow hedging relationships

  

Statements of Income location

     2011       2010       2009    

Foreign currency contracts

   Product sales    $ (108   $ 47      $ (7

Cross currency swap contracts

   Interest and other income, net      (3              

Forward interest rate contracts

   Interest expense, net      (1     (1     (1
     

 

 

   

 

 

   

 

 

 

Total

      $ (112   $ 46      $ (8
     

 

 

   

 

 

   

 

 

 

No portions of our cash flow hedge contracts are excluded from the assessment of hedge effectiveness, and the ineffective portions of these hedging instruments were approximately $1 million of gain for the year ended December 31, 2011, and approximately $1 million of loss for both the years ended December 31, 2010 and 2009. As of December 31, 2011, the amounts expected to be reclassified from AOCI into earnings over the next 12 months are approximately $75 million of net gains on foreign currency and cross currency swap contracts and approximately $1 million of losses on forward interest rate contracts.

Fair value hedges

To achieve a desired mix of fixed and floating interest rates on our long-term debt, we have entered into interest rate swap contracts, which qualify and have been designated as fair value hedges. The terms of these interest rate swap contracts correspond to the related hedged debt instruments and effectively convert a fixed interest rate coupon to a floating LIBOR-based coupon over the lives of the respective notes. The rates on these swaps range from LIBOR plus 0.3% to LIBOR plus 2.6%. As of December 31, 2011, 2010 and 2009, we had interest rate swap contracts with aggregate notional amounts of $3.6 billion, $3.6 billion and $1.5 billion,

 

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AMGEN INC.

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (Continued)

 

respectively. The interest rate swap contracts as of December 31, 2011 and 2010, were for our 4.85% 2014 Notes, 5.85% 2017 Notes, 6.15% 2018 Notes and 5.70% 2019 Notes, and, as of December 31, 2009, for our 4.85% 2014 Notes and 6.15% 2018 Notes. For derivative instruments that are designated and qualify as fair value hedges, the unrealized gain or loss on the derivative resulting from the change in fair value during the period as well as the offsetting unrealized loss or gain of the hedged item resulting from the change in fair value during the period attributable to the hedged risk is recognized in current earnings. For the years ended December 31, 2011 and 2010, we included unrealized losses on the hedged debt of $182 million and $105 million, respectively, in the same line item, Interest expense, net, in the Consolidated Statements of Income, as the offsetting unrealized gains of $182 million and $105 million, respectively, on the related interest rate swap contracts. For the year ended December 31, 2009, we included the unrealized gain on the hedged debt of $116 million in the same line item, Interest expense, net, in the Consolidated Statement of Income, as the offsetting unrealized loss of $116 million on the related interest rate swap contracts.

Derivatives not designated as hedges

We enter into foreign currency forward contracts that are not designated as hedging transactions to reduce our exposure to foreign currency fluctuations of certain assets and liabilities denominated in foreign currencies. These exposures are hedged on a month-to-month basis. As of December 31, 2011, 2010 and 2009, the total notional amounts of these foreign currency forward contracts, primarily euro-based, were $389 million, $670 million and $414 million, respectively.

The location in the Consolidated Statements of Income and the amount of gain/(loss) recognized in earnings for the derivative instruments not designated as hedging instruments was as follows (in millions):

 

 

          Years ended December 31,  

Derivatives not designated as hedging instruments

  

Statements of Income location

   2011     2010      2009  

Foreign currency contracts

   Interest and other income, net    $ (1   $ 32       $ (24
     

 

 

   

 

 

    

 

 

 

 

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AMGEN INC.

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (Continued)

 

The fair values of both derivatives designated as hedging instruments and derivatives not designated as hedging instruments included in the Consolidated Balance Sheets were as follows (in millions):

 

 

    

Derivative assets

    

Derivative liabilities

 

December 31, 2011

  

Balance Sheet location

   Fair value     

Balance Sheet location

   Fair value  

Derivatives designated as hedging instruments:

           

Interest rate swap contracts

  

Other current assets/ Other noncurrent assets

   $ 377      

Accrued liabilities/ Other noncurrent liabilities

   $   

Cross currency swap contracts

  

Other current assets/ Other noncurrent assets

          

Accrued liabilities/ Other noncurrent liabilities

     26   

Foreign currency contracts

  

Other current assets/ Other noncurrent assets

     172      

Accrued liabilities/ Other noncurrent liabilities

     48   
     

 

 

       

 

 

 

Total derivatives designated as hedging instruments

        549            74   
     

 

 

       

 

 

 

Derivatives not designated as hedging instruments:

           

Foreign currency contracts

  

Other current assets

          

Accrued liabilities

       
     

 

 

       

 

 

 

Total derivatives not designated as hedging instruments

                     
     

 

 

       

 

 

 

Total derivatives

      $ 549          $ 74   
     

 

 

       

 

 

 
    

Derivative assets

    

Derivative liabilities

 

December 31, 2010

  

Balance Sheet location

   Fair value     

Balance Sheet location

   Fair value  

Derivatives designated as hedging instruments:

           

Interest rate swap contracts

  

Other current assets/ Other noncurrent assets

   $ 195      

Accrued liabilities/ Other noncurrent liabilities

   $   

Foreign currency contracts

  

Other current assets/ Other noncurrent assets

     154      

Accrued liabilities/ Other noncurrent liabilities

     103   
     

 

 

       

 

 

 

Total derivatives designated as hedging instruments

        349            103   
     

 

 

       

 

 

 

Derivatives not designated as hedging instruments:

           

Foreign currency contracts

  

Other current assets

          

Accrued liabilities

       
     

 

 

       

 

 

 

Total derivatives not designated as hedging instruments

                     
     

 

 

       

 

 

 

Total derivatives

      $ 349          $ 103   
     

 

 

       

 

 

 

 

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Our derivative contracts that were in liability positions as of December 31, 2011, contain certain credit risk related contingent provisions that would be triggered if (i) we were to undergo a change in control and (ii) our or the surviving entity’s creditworthiness deteriorates, which is generally defined as having either a credit rating that is below investment grade or a materially weaker creditworthiness after the change in control. If these events were to occur, the counterparties would have the right, but not the obligation, to close the contracts under early-termination provisions. In such circumstances, the counterparties could request immediate settlement of these contracts for amounts that approximate the then current fair values of the contracts.

The cash flow effects of our derivatives contracts for the three years ended December 31, 2011, are included within Net cash provided by operating activities in the Consolidated Statements of Cash Flows.

18. Contingencies and commitments

Contingencies

In the ordinary course of business, we are involved in various legal proceedings and other matters, including those discussed in this Note, that are complex in nature and have outcomes that are difficult to predict.

We record accruals for loss contingencies to the extent that we conclude that it is probable that a liability has been incurred and the amount of the related loss can be reasonably estimated. We evaluate, on a quarterly basis, developments in legal proceedings and other matters that could cause an increase or decrease in the amount of the liability that has been accrued previously. As more fully described below, in the three months ended September 30, 2011, excluding fees paid to our external counsel, the Company recorded a $780 million legal settlement charge associated with the proposed settlement of the allegations arising out of the previously disclosed federal civil and criminal investigations pending in the U.S. Attorney’s Offices for the Eastern District of New York and the Western District of Washington. The charge is included in Other operating expenses in the Consolidated Statements of Income.

Our legal proceedings range from cases brought by a single plaintiff to a class action with thousands of putative class members. These legal proceedings, as well as other matters, involve various aspects of our business and a variety of claims (including but not limited to patent infringement, marketing, pricing and trade practices and securities law), some of which present novel factual allegations and/or unique legal theories. Except for the proposed settlement of the litigation referenced above, in each of the matters described in this filing, plaintiffs seek an award of a not-yet-quantified amount of damages or an amount that is not material. In addition, a number of the matters pending against us are at very early stages of the legal process (which in complex proceedings of the sort faced by us often extend for several years). As a result, some pending matters have not yet progressed sufficiently through discovery and/or development of important factual information and legal issues to enable us to estimate a range of possible loss, if any. While it is not possible to accurately predict or determine the eventual outcomes of these items, an adverse determination in one or more of these items currently pending, including further adverse determinations associated with the pending investigations described above, could have a material adverse effect on our consolidated results of operations, financial position or cash flows.

Certain of our legal proceedings and other matters are discussed below:

Roche U.S. International Trade Commission Complaint

On April 11, 2006, Amgen filed a complaint with the U.S. International Trade Commission (ITC) in Washington D.C. requesting that the ITC institute an investigation of the importation of pegylated erythropoietin

 

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(alternatively referred to as peg-EPO or MIRCERA®) into the United States as Amgen believes that importation of peg-EPO is unlawful because peg-EPO, and the method of its manufacture, are covered by Amgen’s EPO patents. Amgen asked the ITC to issue a permanent exclusion order that would prohibit importation of peg-EPO into the United States. The ITC instituted an investigation naming Roche Holding Ltd., F. Hoffmann-La Roche Ltd., Roche Diagnostics GmbH, and Hoffmann-La Roche Inc. (collectively, Roche) as respondents in the investigation. On July 7, 2006, the Administrative Law Judge (ALJ) at the ITC issued a summary determination that Roche’s importation and use of peg-EPO in the United States had been subject to a clinical trial exemption to patent infringement under 35 U.S.C. 271(e)(1). On August 31, 2006, the ITC adopted the ALJ’s summary determination terminating the investigation.

On October 11, 2006, Amgen filed a petition for review of the ITC’s decision with the U.S. Court of Appeals for the Federal Circuit (the Federal Circuit Court). On March 19, 2008, the Federal Circuit Court reversed the ITC’s dismissal of the investigation on jurisdictional grounds. In response to Roche’s request for rehearing, on April 30, 2009, the Federal Circuit Court vacated the ITC’s dismissal of the ITC investigation for non-infringement. The Federal Circuit Court remanded the case back to the ITC for further proceedings to determine if patent infringement had occurred and to provide a remedy, if appropriate.

Amgen had previously filed a separate lawsuit in November 2006 in the U.S. District Court for the District of Massachusetts (the Massachusetts District Court) against F. Hoffmann-La Roche Ltd., Roche Diagnostics GmbH and Hoffmann-La Roche Inc. (collectively, Roche Defendants) seeking a declaration by the Massachusetts District Court that the importation, use, sale or offer to sell peg-EPO infringes Amgen’s EPO patents, specifically U.S. Patent Nos. 5,547,933; 5,621,080; 5,955,422; 5,756,349; 5,618,698 and 5,441,868. After a jury trial and an appeal, on December 22, 2009, the Massachusetts District Court entered final judgment and a permanent injunction against the Roche Defendants prohibiting the Roche Defendants from infringing the five Amgen patents-in-suit. The judgment was accompanied by the Roche Defendants’ admission that the patents involved in the lawsuit are valid, enforceable and infringed by the Roche Defendant’s peg-EPO product, and by Amgen allowing Roche to begin selling peg-EPO in the United States in mid-2014 under terms of a limited license agreement. The settlement terms did not include any financial payments between the parties. Thereafter, in the ITC matter Amgen filed a motion for summary determination of violation with a request for entry of a limited exclusion order. The Roche respondents notified the ITC that they were not opposing Amgen’s motion. On March 11, 2011, the ITC issued an order to show cause why the investigation should not be terminated without a determination of violation or by way of consent order in view of the resolution of the Massachusetts District Court proceedings. In response, on April 21, 2011, the parties filed a joint response requesting termination of the investigation on the basis of a proposed Consent Order and Stipulation. On October 17, 2011, the ITC terminated the investigation without entry of a consent order on the basis of the December 2009 settlement between the parties and resolution of the parallel litigation in the Massachusetts District Court.

Average Wholesale Price (AWP) Litigation

Amgen and its wholly owned subsidiary Immunex Inc. are named as defendants, either separately or together, in numerous civil actions broadly alleging that they, together with many other pharmaceutical manufacturers, reported prices for certain products in a manner that allegedly inflated reimbursement under Medicare and/or Medicaid programs and commercial insurance plans, including co-payments paid to providers who prescribe and administer the products. The complaints generally assert varying claims under the Medicare and Medicaid statutes, as well as state law claims for deceptive trade practices, common law fraud and various related state law claims. The complaints seek an undetermined amount of damages, as well as other relief, including declaratory and injunctive relief.

The AWP litigation was commenced against Amgen and Immunex on December 19, 2001 with the filing of Citizens for Consumer Justice, et al. v. Abbott Laboratories, Inc., et al. Additional cases have been filed since

 

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that time. Most of these actions, as discussed below, have been consolidated, or are in the process of being consolidated, in a federal Multi-District Litigation proceeding (the MDL Proceeding), captioned In Re: Pharmaceutical Industry Average Wholesale Price Litigation MDL No. 1456 and pending in the Massachusetts District Court.

The following cases have been consolidated into the MDL Proceeding, and include cases brought by consumer classes and certain state and local governmental entities:

Citizens for Consumer Justice, et al., v. Abbott Laboratories, Inc., et al.; Teamsters Health & Welfare Fund of Philadelphia, et al., v. Abbott Laboratories, Inc., et al.; Action Alliance of Senior Citizens of Greater Philadelphia v. Immunex Corporation; Constance Thompson, et al., v. Abbott Laboratories, Inc., et al.; Ronald Turner, et al., v. Abbott Laboratories, Inc., et al.; Congress of California Seniors v. Abbott Laboratories, Inc., et al.

In the MDL Proceeding, the Massachusetts District Court has set various deadlines relating to motions to dismiss the complaints, discovery, class certification, summary judgment and other pre-trial issues. For the private class action cases, the Massachusetts District Court has divided the defendant companies into a Track I group and a Track II group. Both Amgen and Immunex are in the Track II group. On March 2, 2006, plaintiffs filed a fourth amended master consolidated complaint, which did not include their motion for class certification as to the Track II group. On September 12, 2006, a hearing before the Massachusetts District Court was held on plaintiffs’ motion for class certification as to the Track II group defendants, which include Amgen and Immunex. On March 7, 2008, the Track II defendants reached a tentative class settlement of the MDL Proceeding, which was subsequently amended on April 3, 2008. The tentative Track II settlement relates to claims against numerous defendants, including Abbott Laboratories, Inc., Amgen Inc., Aventis Pharmaceuticals Inc., Hoechst Marion Roussel, Inc., Baxter Healthcare Corporation, Baxter International Inc., Bayer Corporation, Dey, Inc., Fujisawa Healthcare, Inc., Fujisawa USA, Inc., Immunex Corporation, Pharmacia Corporation, Pharmacia & Upjohn LLC (f/k/a Pharmacia & Upjohn, Inc.), Sicor, Inc., Gensia, Inc., Gensia Sicor Pharmaceuticals, Inc., Watson Pharmaceuticals, Inc. and ZLB Behring, L.L.C. Following repeated hearings on the sufficiency of the notice given by the plaintiffs, the Massachusetts District Court approved the Track II settlement on December 8, 2011, and dismissed with prejudice the fourth amended master consolidated complaint effective January 31, 2012.

The following AWP litigation case is not part of the MDL Proceeding:

State of Louisiana v. Abbott Laboratories, Inc., et al.    The State of Louisiana filed a complaint against Amgen and several other pharmaceutical manufacturers, on November 3, 2010, in the Parish of East Baton Rouge, 19th Judicial District (the Louisiana Court). Amgen was served the complaint on November 9, 2010. The complaint alleges that the manufacturers misrepresented product pricing information reported to the state by falsely inflating those prices. On May 12, 2011, Amgen and the other defendants filed joint exceptions seeking to dismiss the complaint. On October 27, 2011 the Louisiana Court denied the defendants’ joint exceptions.

Federal Securities Litigation — In re Amgen Inc. Securities Litigation

The six federal class action stockholder complaints filed against Amgen Inc., Kevin W. Sharer, Richard D. Nanula, Dennis M. Fenton, Roger M. Perlmutter, Brian M. McNamee, George J. Morrow, Edward V. Fritzky, Gilbert S. Omenn and Franklin P. Johnson, Jr., (the Federal Defendants) in the U.S. District Court for the Central District of California (the California Central District Court) on April 17, 2007 (Kairalla v. Amgen Inc., et al.), May 1, 2007 (Mendall v. Amgen Inc., et al., & Jaffe v. Amgen Inc., et al.), May 11, 2007 (Eldon v. Amgen Inc.,

 

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et al.), May 21, 2007 (Rosenfield v. Amgen Inc., et al.) and June 18, 2007 (Public Employees’ Retirement Association of Colorado v. Amgen Inc., et al.) were consolidated by the California Central District Court into one action captioned In re Amgen Inc. Securities Litigation. The consolidated complaint was filed with the California Central District Court on October 2, 2007. The consolidated complaint alleges that Amgen and these officers and directors made false statements that resulted in: (i) deceiving the investing public regarding Amgen’s prospects and business; (ii) artificially inflating the prices of Amgen’s publicly traded securities and (iii) causing plaintiff and other members of the class to purchase Amgen publicly traded securities at inflated prices. The complaint also makes off-label marketing allegations that, throughout the class period, the Federal Defendants improperly marketed Aranesp® and EPOGEN® for off-label uses while aware that there were alleged safety signals with these products. The plaintiffs seek class certification, compensatory damages, legal fees and other relief deemed proper. The Federal Defendants filed a motion to dismiss on November 8, 2007. On February 4, 2008, the California Central District Court granted in part, and denied in part, the Federal Defendants’ motion to dismiss the consolidated amended complaint. Specifically, the California Central District Court granted the Federal Defendants’ motion to dismiss as to individual defendants Fritzky, Omenn, Johnson, Fenton and McNamee, but denied the Federal Defendants’ motion to dismiss as to individual defendants Sharer, Nanula, Perlmutter and Morrow.

A class certification hearing before the California Central District Court, was held on July 17, 2009 and on August 12, 2009, the California Central District Court granted plaintiffs’ motion for class certification. On August 28, 2009, Amgen filed a petition for permission to appeal with the U.S. Court of Appeals for the Ninth Circuit (the Ninth Circuit Court) under Rule 23(f), regarding the Order on Class Certification and the Ninth Circuit Court granted Amgen’s permission to appeal on December 11, 2009. On February 2, 2010, the California Central District Court granted Amgen’s motion to stay the underlying action pending the outcome of the Ninth Circuit Court 23(f) appeal. On October 14, 2011, the appeal under Rule 23(f) was argued before the Ninth Circuit Court and on December 28, 2011, the Ninth Circuit Court denied the appeal. On January 3, 2012, Amgen filed a motion to stay the mandate and the Ninth Circuit Court granted the motion and stayed the mandate on January 12, 2012. The staying of the mandate effectively stays the underlying action in the California Central District Court for ninety days pending the filing of a writ of certiorari with the U.S. Supreme Court. Amgen has until March 27, 2012 to file a petition for certiorari with the U.S. Supreme Court.

State Derivative Litigation

Larson v. Sharer, et al.

The three state stockholder derivative complaints filed against Amgen Inc., Kevin W. Sharer, George J. Morrow, Dennis M. Fenton, Brian M. McNamee, Roger M. Perlmutter, David Baltimore, Gilbert S. Omenn, Judith C. Pelham, Frederick W. Gluck, Jerry D. Choate, J. Paul Reason, Frank J. Biondi, Jr., Leonard D. Schaeffer, Frank C. Herringer, Richard D. Nanula, Willard H. Dere, Edward V. Fritzky, Franklin P. Johnson, Jr. and Donald B. Rice as defendants (the State Defendants) on May 1, 2007 (Larson v. Sharer, et al., & Anderson v. Sharer, et al.), and August 13, 2007 (Weil v. Sharer, et al.) in the Superior Court of the State of California, Ventura County (the Superior Court) were consolidated by the Superior Court under one action captioned Larson v. Sharer, et al. The consolidated complaint was filed on July 5, 2007. The complaint alleges that the State Defendants breached their fiduciary duties, wasted corporate assets, were unjustly enriched and violated the California Corporations Code. Plaintiffs allege that the State Defendants failed to disclose and/or misrepresented results of Aranesp® clinical studies, marketed both Aranesp® and EPOGEN® for off-label uses and that these actions or inactions caused stockholders to suffer damages. The complaints also allege insider trading by the State Defendants. The plaintiffs seek treble damages based on various causes of action, reformed corporate governance, equitable and/or injunctive relief, restitution, disgorgement of profits, benefits and other compensation, and legal costs.

 

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An amended consolidated complaint was filed on March 13, 2008, adding Anthony Gringeri as a State Defendant and removing the causes of action for insider selling and misappropriation of information, violation of California Corporations Code Section 25402 and violation of California Corporations Code Section 25403. On July 14, 2008, the Superior Court dismissed without prejudice the consolidated state derivative class action. The judge also ordered a stay of any re-filing of an amended complaint until the federal court has determined whether any securities fraud occurred.

Birch v. Sharer, et al.

On January 23, 2009, a stockholder derivative lawsuit titled Birch v. Sharer, et al. was filed in the Superior Court of the State of California, Los Angeles County (the Los Angeles Superior Court) naming Amgen Inc., Kevin W. Sharer, David Baltimore, Frank J. Biondi, Jr., Jerry D. Choate, Vance D. Coffman, Frederick W. Gluck, Frank C. Herringer, Gilbert S. Omenn, Judith C. Pelham, J. Paul Reason, Leonard D. Schaeffer and Tom Zindrick as defendants. The complaint alleges derivative claims for breach of fiduciary duty based on a purported failure to implement adequate internal controls and to oversee the Company’s operations, which plaintiff claims resulted in numerous lawsuits and investigations over a number of years. Plaintiff seeks damages on behalf of Amgen, including costs and expenses, allegedly incurred, among other things, in connection with wrongful termination lawsuits and potential violations of the Health Insurance Portability and Accountability Act. On February 25, 2009, the case was reassigned to a judge in the Complex Department of the Los Angeles Superior Court. Amgen and the individual defendants filed motions to dismiss on June 23, 2009.

Oral argument on Amgen and the individual defendants’ motions to dismiss were heard on September 25, 2009 before the Los Angeles Superior Court and the court granted the motions to dismiss but allowed the plaintiff an opportunity to amend her complaint by October 21, 2009. Plaintiff filed a request for dismissal without prejudice with the court on October 23, 2009. On October 29, 2009, Amgen received from plaintiff a stockholder demand on the Board of Directors to take action to remedy breaches of fiduciary duties by the directors and certain executive officers of the Company. Ms. Birch alleged that the directors and certain executive officers violated their core fiduciary principles, causing Amgen to suffer damages. She demanded that the Board of Directors take action against each of the officers and directors to recover damages and to correct deficiencies in the Company’s internal controls that allowed the misconduct to occur. The Board of Directors completed its investigation and determined in its business judgment that it was not in the best interests of the Company to pursue the claims made in the demand against any of the individuals mentioned in the demand. Therefore, the Board voted to reject the demand and communicated this to Ms. Birch on May 19, 2010.

On February 8, 2010, plaintiff filed another stockholder demand lawsuit in the Los Angeles Superior Court against the same defendants in the original lawsuit but also added Board of Director members François de Carbonnel and Rebecca Henderson. The allegations in the new complaint are nearly identical to those in the previously filed complaint. The case filed on February 8, 2010 by plaintiff Birch was assigned to the Complex Division of the Los Angeles Superior Court. On June 30, 2010, Amgen filed its demurrer to plaintiff’s complaint with the Complex Division of the Los Angeles Superior Court. On September 29, 2010, the Complex Division of the Los Angeles Superior Court denied Amgen’s and the individual defendants’ demurrers finding that the plaintiff had adequately pled wrongful refusal. Amgen and the individual defendants filed answers on October 29, 2010. On December 9, 2010, the Complex Division of the Los Angeles Superior Court stayed the underlying action and Amgen and the individual defendants filed a motion for judgment on the pleadings/motion for summary judgment. The motion for the judgment on the pleadings was heard on January 31, 2011 and the Complex Division of the Los Angeles Superior Court dismissed the entire lawsuit with prejudice against both Amgen and the individual defendants without leave to amend. On February 24, 2011, plaintiff filed a notice of appeal with the California State Appellate Court. The briefing schedule for the appeal was issued by the California State Appellate Court and plaintiff’s opening brief was filed September 7, 2011. The opposition brief from Amgen and the individual defendants was filed on November 21, 2011. No date has been set for oral argument.

 

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Federal Derivative Litigation

On May 7, 2007, the stockholder derivative lawsuit of Durgin v. Sharer, et al., was filed in the California Central District Court and named Amgen Inc., Kevin W. Sharer, George J. Morrow, Dennis M. Fenton, Brian M. McNamee, Roger M. Perlmutter, David Baltimore, Gilbert S. Omenn, Judith C. Pelham, Frederick W. Gluck, Jerry D. Choate, J. Paul Reason, Frank J. Biondi, Jr., Leonard D. Schaeffer, Frank C. Herringer, Richard D. Nanula, Edward V. Fritzky and Franklin P. Johnson, Jr. as defendants. The complaint alleges the same claims and requests the same relief as in the three state stockholder derivative complaints now consolidated as Larson v. Sharer, et al. The case has been stayed for all purposes until thirty days after a final ruling on the motion to dismiss by the California Central District Court in the In re Amgen Inc. Securities Litigation action.

On September 21, 2007, the stockholder derivative lawsuit of Rosenblum v. Sharer, et al., was filed in the California Central District Court. This lawsuit was brought by the stockholder who previously made a demand on the Amgen Board on May 14, 2007. The complaint alleges that the defendants breached their fiduciary duties, wasted corporate assets and were unjustly enriched. Plaintiffs allege that the defendants failed to disclose and/or misrepresented results of Aranesp® clinical studies, marketed both Aranesp® and EPOGEN® for off-label uses and that these actions or inactions as well as the Amgen market strategy caused damage to the Company resulting in several inquiries, investigations and lawsuits that are costly to defend. The complaint also alleges insider trading by the defendants. The plaintiffs seek treble damages based on various causes of action, reformed corporate governance, equitable and/or injunctive relief, restitution, disgorgement of profits, benefits and other compensation, and legal costs. The case was stayed for all purposes until thirty days after a final ruling on the motion to dismiss by the California Central District Court in the In re Amgen Inc. Securities Litigation action.

Thereafter, on May 1, 2008, plaintiff in Rosenblum v. Sharer, et al., filed an amended complaint which removed Dennis Fenton as a defendant and also eliminated the claims for insider selling by defendants. On July 28, 2008, the California Central District Court heard Amgen and the defendants’ motion to dismiss and motion to stay. On July 30, 2008, the California Central District Court granted Amgen and the defendants’ motion to dismiss without prejudice and also granted a stay of the case pending resolution of the In re Amgen Inc. Securities Litigation action.

ERISA Litigation

On August 20, 2007, the ERISA class action lawsuit of Harris v. Amgen Inc., et al., was filed in the California Central District Court and named Amgen Inc., Kevin W. Sharer, Frank J. Biondi, Jr., Jerry Choate, Frank C. Herringer, Gilbert S. Omenn, David Baltimore, Judith C. Pelham, Frederick W. Gluck, Leonard D. Schaeffer, Jacqueline Allred, Raul Cermeno, Jackie Crouse, Lori Johnston, Michael Kelly and Charles Bell as defendants. Plaintiffs claim that Amgen and the individual defendants breached their fiduciary duties by failing to inform current and former employees who participated in the Amgen Retirement and Savings Plan and the Retirement and Savings Plan for Amgen Manufacturing Limited of the alleged off-label promotion of both Aranesp® and EPOGEN® while a number of studies allegedly demonstrated safety concerns in patients using ESAs. On February 4, 2008, the California Central District Court dismissed the complaint with prejudice as to plaintiff Harris, who had filed claims against Amgen Inc. The claims alleged by the second plaintiff, Ramos, were also dismissed but the court granted the plaintiff leave to amend his complaint. On February 1, 2008, the plaintiffs appealed the decision by the California Central District Court to dismiss the claims of both plaintiffs Harris and Ramos to the Ninth Circuit Court, which remains pending before the Ninth Circuit Court. On May 19, 2008, plaintiff Ramos in the Harris v. Amgen Inc., et al., action filed another lawsuit captioned Ramos v. Amgen Inc., et al., in the California Central District Court. The lawsuit is another ERISA class action. The Ramos v. Amgen Inc., et al., matter names the same defendants in the Harris v. Amgen Inc., et al., matter plus four new defendants: Amgen Manufacturing Limited, Richard Nanula, Dennis Fenton and the Fiduciary Committee.

 

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Pursuant to the parties’ stipulation, the Ramos matter has been stayed pending the outcome of the Harris matter appeal. Oral argument before the Ninth Circuit Court on the plaintiffs’ appeal of the California Central District Court’s dismissal of the plaintiffs’ claims occurred on May 8, 2009. On July 14, 2009, the Ninth Circuit Court reversed the California Central District Court’s decision and remanded the case back to the district court. In the meantime, a third ERISA class action was filed by Don Hanks on June 2, 2009 in the California Central District Court alleging the same ERISA violations as in the Harris and Ramos lawsuits.

On October 13, 2009, the California Central District Court granted plaintiffs Harris’ and Ramos’ motion to be appointed interim co-lead counsel. Plaintiffs filed an amended complaint on November 11, 2009 and added two additional plaintiffs, Jorge Torres and Albert Cappa. Amgen filed a motion to dismiss the amended/consolidated complaint, and on March 2, 2010, the California Central District Court dismissed the entire lawsuit without prejudice. Plaintiffs filed an amended complaint on March 23, 2010. Amgen then filed another motion to dismiss on April 20, 2010. On June 16, 2010, the California Central District Court entered an order dismissing the entire lawsuit with prejudice. On June 24, 2010, the plaintiffs filed a notice of appeal with the Ninth Circuit Court. Petitioner’s opening brief was served on December 20, 2010 and Amgen’s answering brief was filed on February 2, 2011. Oral argument occurred on February 17, 2012.

Government Investigations and Qui Tam Actions

On May 10, 2007, Amgen received a subpoena from the Attorney General of the State of New York seeking documents related to Amgen’s promotional activities, sales and marketing activities, medical education, clinical studies, pricing and contracting, license and distribution agreements and corporate communications. Amgen fully cooperated in responding to the subpoena.

Beginning in late 2007, Amgen received a number of subpoenas from the U.S. Attorney’s Offices for the Eastern District of New York and the Western District of Washington, pursuant to the Health Insurance Portability and Accountability Act (18 U.S.C. 3486), for broad production of documents relating to its products and clinical trials. Amgen fully cooperated with the government’s document requests. Over the next several years, numerous current and former Amgen employees received civil and grand jury subpoenas to provide testimony on a wide variety of subjects. We refer herein to these investigations being conducted by the U.S. Attorney’s Offices for the Eastern District of New York and the Western District of Washington as the Federal Investigations.

On January 14, 2008, Amgen received a subpoena from the New Jersey Attorney General’s Office for production of documents relating to one of its products. Amgen completed its response per the terms of the subpoena.

A U.S. government filing in the Massachusetts District Court concerning the partially unsealed complaint filed pursuant to the Qui Tam provisions of the Federal Civil False Claims Act and on behalf of 17 named states and the District of Columbia under their respective State False Claims Acts (the Massachusetts Qui Tam Action) became public on or about May 7, 2009. The filing stated that the relator in the Massachusetts Qui Tam Action is a former Amgen employee. Further, the filing represented that, in addition to the Massachusetts Qui Tam Action, there were nine other actions under the False Claim Act pending under seal against Amgen, including eight pending in the U.S. District Court for the Eastern District of New York and one pending in the U.S. District Court for the Western District of Washington (together, the Qui Tam Actions). In the filing made public on May 7, 2009, the U.S. government represented that these ten Qui Tam Actions alleged that Amgen engaged in a wide variety of illegal marketing practices with respect to various Amgen products and that these were joint civil and criminal investigations being conducted by a wide variety and large number of federal and state agencies.

 

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On September 1, 2009, the U.S. government filed a notice of non-intervention and 14 states and the District of Columbia filed notices of intervention in the Massachusetts Qui Tam Action. On October 30, 2009, 14 states and the District of Columbia filed an amended complaint in the Massachusetts District Court entitled The United States of America, States of California, Delaware, Florida, Georgia, Hawaii, Illinois, Indiana, Louisiana, Michigan, Nevada, New Hampshire, New Mexico, New York, Tennessee and Texas and the Commonwealths of Massachusetts and Virginia and the District of Columbia, ex rel Kassie Westmoreland v. Amgen Inc., Integrated Nephrology Network, AmerisourceBergen Specialty Group, ASD Healthcare and AmerisourceBergen Corporation. The relator, Kassie Westmoreland, also filed a second amended complaint with the Massachusetts District Court on the same day. The complaints alleged violations of the federal Anti-Kickback Statute and violations of state false claims act statutes with regard to Amgen’s marketing of overfill in vials of Aranesp® and with regard to Amgen’s relationship with the Integrated Nephrology Network (INN), a group purchasing organization. The relator’s seconded amended complaint also alleged that Amgen retaliated against and wrongfully terminated Ms. Westmoreland.

On January 20, 2010, the states of Florida and Texas voluntarily dismissed their complaints against Amgen. On February 12, 2010, February 16, 2010 and February 18, 2010, respectively, the states of New Hampshire, Louisiana and Nevada voluntarily dismissed their complaints against Amgen. On February 23, 2010, the state of Delaware voluntarily dismissed its complaint against Amgen. Also, on February 23, 2010, the Massachusetts District Court granted Amgen’s motion to stay and sever the relator’s employment claims.

On April 23, 2010, the Massachusetts District Court dismissed all of the claims of the relator, on behalf of the federal government and the states of New Mexico and Georgia, and all of the claims of the remaining states, for failure to state valid legal grounds upon which relief could be granted. On May 26, 2010, the Massachusetts District Court granted leave for the relator to file a fourth amended complaint. On May 24, 2010, the states of New York, Massachusetts, Michigan, California, Illinois, and Indiana (the States) filed notices of intent to appeal the Massachusetts District Court’s judgment to the U.S. Court of Appeals for the First Circuit (the First Circuit Court).

On September 20, 2010, the Massachusetts District Court entered a written ruling denying Amgen’s motions to dismiss the relator’s fourth amended complaint. On April 11, 2011, the Massachusetts District Court heard summary judgment arguments on the fourth amended complaint from Amgen, INN and the relator. On July 22, 2011, the First Circuit Court issued a written decision reversing the Massachusetts District Court’s dismissal of the claims of the states of California, Illinois, Indiana, Massachusetts, New Mexico, and New York and affirming the dismissal of the claims of Georgia.

In March 2011, the U.S. Attorney’s Office of the Western District of Washington informed Amgen that the subject matter of its investigation would be transferred to the U.S. Attorney’s Office of the Eastern District of New York.

On October 24, 2011, Amgen announced it had reached an agreement in principle to settle allegations relating to its sales and marketing practices arising out of the Federal Investigations. In connection with the agreement in principle, Amgen recorded a $780 million charge in the three months ended September 30, 2011. This amount represents Amgen’s currently estimable loss with respect to these matters. If the ongoing discussions are successfully concluded, Amgen expects that the proposed settlement will resolve the Federal Investigations, the related state Medicaid claims and the claims in U.S. ex rel. Westmoreland v. Amgen, et al. and the other nine Qui Tam Actions in a manner that will not result in exclusion from U.S. federally-funded health care programs. In connection with the settlement discussions, the Massachusetts District Court vacated the previously scheduled trial date and administratively closed that case. The relators in the Qui Tam Actions have

 

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AMGEN INC.

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (Continued)

 

the opportunity to join in the proposed settlement or, if they object, to have the settlement evaluated in a federal court fairness hearing to determine whether it is fair, adequate and reasonable under all the circumstances. The proposed settlement remains subject to continuing discussions regarding the components of the agreement and the completion and execution of all required documentation, and until the proposed settlement becomes final, there can be no guarantee that these matters will be resolved by the agreement in principle.

In addition, on September 19, 2011, Amgen filed a petition for certiorari with the U.S. Supreme Court in the U.S. ex rel. Westmoreland v. Amgen, et al. matter. The petition sought leave to appeal the First Circuit Court’s reinstatement of the claims of the states of California, Illinois, Indiana, Massachusetts, New Mexico and New York, which had been dismissed by the Massachusetts District Court. However, as described above, Amgen expects that these state claims will be resolved if the ongoing settlement discussions are successfully concluded. Accordingly, on December 12, 2011, Amgen withdrew its petition for certiorari and the U.S. Supreme Court subsequently dismissed the petition on December 29, 2011.

As part of the settlement discussions described above, Amgen was made aware that it is a defendant in several other civil qui tam actions. These other qui tam actions are in addition to the Qui Tam Actions described above. One of these other qui tam actions, U.S. ex rel. May v. Amgen, et al. was filed by Samuel May on June 6, 2010, in the U.S. District Court for the Northern District of California, and was unsealed in connection with it being dismissed by the Court on January 5, 2012 for failure to prosecute the matter. The remaining other qui tam actions remain under seal in the U.S. federal courts in which they were filed. Included with these other actions (including the May action) are allegations that Amgen’s promotional, contracting, sales and marketing activities relating to Enbrel® and Aranesp® caused the submission of various false claims under the Federal Civil False Claims Act and various State False Claims Acts. Certain of the allegations in these remaining other actions are not encompassed in the proposed settlement described above, and Amgen intends to cooperate fully with the government in its investigation of these new allegations. Amgen continues to explore with the government whether these remaining matters will be resolved in connection with the proposed settlement discussed above.

U.S. ex rel. Streck v. Allergan, et al.

A complaint filed in the U.S. District Court for the Eastern District of Pennsylvania against Amgen and numerous other pharmaceutical manufacturers, pursuant to the Qui Tam provisions of the Federal Civil False Claims Act and on behalf of 24 named states and the District of Columbia under their respective State False Claims Acts, was unsealed and became public on or about June 6, 2011. The plaintiff, Ronald Streck, alleges that from 2004 to the present, defendants failed to report accurate pricing data to Medicare and Medicaid, including data used to calculate average sales price and average manufacturer’s price, thereby causing the federal and state governments to reimburse defendants at inflated rates and causing the manufacturers to underpay Medicaid rebates. This matter, in which the federal government has declined to intervene, is not affected by the proposed settlement described above. On September 7, 2011, plaintiff filed a fourth amended complaint and on December 9, 2011, defendants filed a joint motion to dismiss the plaintiff’s complaint.

 

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AMGEN INC.

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (Continued)

 

Commitments

We lease certain facilities and equipment related primarily to administrative, R&D, sales and marketing activities under non-cancelable operating leases that expire through 2032. The following table summarizes the minimum future rental commitments under non-cancelable operating leases as of December 31, 2011 (in millions):

 

 

2012

   $ 116   

2013

     104   

2014

     85   

2015

     76   

2016

     65   

Thereafter

     328   
  

 

 

 

Total minimum operating lease commitments

   $ 774   
  

 

 

 

Included in the table above are future rental commitments for abandoned leases in the amount of $254 million. Rental expense on operating leases for the years ended December 31, 2011, 2010 and 2009, was $131 million, $115 million and $114 million, respectively.

In addition, we have minimum contractual purchase commitments with third-party manufacturers through 2014 that total $157 million as of December 31, 2011. Amounts purchased under these contractual purchase commitments for the years ended December 31, 2011, 2010 and 2009, were $87 million, $68 million and $207 million, respectively.

19. Segment information

We operate in one business segment — human therapeutics. Therefore, results of our operations are reported on a consolidated basis for purposes of segment reporting, consistent with internal management reporting. Enterprise-wide disclosures about product sales, revenues and long-lived assets by geographic area, and revenues from major customers are presented below.

 

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AMGEN INC.

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (Continued)

 

Revenues

Revenues were as follows for the years ended December 31, 2011, 2010 and 2009 (in millions):

 

 

     2011      2010      2009  

Product sales:

        

Neulasta® — U.S.

   $ 3,006       $ 2,654       $ 2,527   

NEUPOGEN® — U.S.

     959         932         901   

Neulasta® — International

     946         904         828   

NEUPOGEN® — International

     301         354         387   

ENBREL — U.S.

     3,458         3,304         3,283   

ENBREL — Canada

     243         230         210   

Aranesp® — U.S.

     986         1,103         1,251   

Aranesp® — International

     1,317         1,383         1,401   

EPOGEN® — U.S.

     2,040         2,524         2,569   

Sensipar® — U.S.

     518         459         429   

Sensipar® (Mimpara®) — International

     290         255         222   

Vectibix® — U.S.

     122         115         97   

Vectibix® — International

     200         173         136   

Nplate® — U.S.

     163         129         78   

Nplate® — International

     134         100         32   

Prolia® — U.S.

     130         26           

Prolia® — International

     73         7           

XGEVA® — U.S.

     343         8           

XGEVA® — International

     8                   

Other — International

     58                   
  

 

 

    

 

 

    

 

 

 

Total product sales

     15,295         14,660         14,351   

Other revenues

     287         393         291   
  

 

 

    

 

 

    

 

 

 

Total revenues

   $ 15,582       $ 15,053       $ 14,642   
  

 

 

    

 

 

    

 

 

 

Geographic information

Outside the United States, we sell products principally in Europe and Canada. The geographic classification of product sales was based upon the location of the customer. The geographic classification of all other revenues was based upon the domicile of the entity from which the revenues were earned.

Certain geographical information with respect to revenues and long-lived assets (consisting of property, plant and equipment) was as follows (in millions):

 

     Years ended December 31,  
     2011      2010      2009  

Revenues:

        

United States

   $ 11,985       $ 11,636       $ 11,421   

International countries

     3,597         3,417         3,221   
  

 

 

    

 

 

    

 

 

 

Total revenues

   $ 15,582       $ 15,053       $ 14,642   
  

 

 

    

 

 

    

 

 

 

 

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AMGEN INC.

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (Continued)

 

 

     December 31,  
     2011      2010  

Long-lived assets:

     

United States

   $ 3,144       $ 3,248   

Puerto Rico

     1,993         2,079   

International countries

     283         195   
  

 

 

    

 

 

 

Total long-lived assets

   $ 5,420       $ 5,522   
  

 

 

    

 

 

 

Major customers

In the United States, we sell primarily to pharmaceutical wholesale distributors. We utilize those wholesale distributors as the principal means of distributing our products to healthcare providers. In Europe, we sell principally to healthcare providers and/or pharmaceutical wholesale distributors depending on the distribution practice in each country. We monitor the financial condition of our larger customers, and we limit our credit exposure by setting credit limits and, for certain customers, by requiring letters of credit.

We had product sales to three customers each accounting for more than 10% of total revenues for the years ended December 31, 2011, 2010 and 2009. For 2011, on a combined basis, these customers accounted for 72% and 90% of worldwide gross revenues and U.S. gross product sales, respectively, as noted in the following table. Certain information with respect to these customers for the years ended December 31, 2011, 2010 and 2009, was as follows (dollar amounts in millions):

 

 

     2011      2010      2009  

AmerisourceBergen Corporation:

        

Gross product sales

   $ 7,574       $ 7,678       $ 7,179   

% of total gross revenues

     36%         38%         37%   

% of U.S. gross product sales

     45%         47%         46%   

McKesson Corporation:

        

Gross product sales

   $ 4,591       $ 3,913       $ 3,694   

% of total gross revenues

     22%         19%         19%   

% of U.S. gross product sales

     27%         24%         24%   

Cardinal Health, Inc:

        

Gross product sales

   $ 3,021       $ 2,813       $ 2,841   

% of total gross revenues

     14%         14%         15%   

% of U.S. gross product sales

     18%         17%         18%   

At December 31, 2011 and 2010, amounts due from these three customers each exceeded 10% of gross trade receivables, and accounted for 60% and 54%, respectively, of net trade receivables on a combined basis. At December 31, 2011 and 2010, 39% and 44%, respectively, of trade receivables, net were due from customers located outside the United States, primarily in Europe. Our total allowance for doubtful accounts as of December 31, 2011 and 2010, was not material.

20. Subsequent event

On January 26, 2012, we announced that we had entered into an agreement to acquire Micromet, Inc. (Micromet), a publicly held biotechnology company focused on the discovery, development and commercialization of innovative antibody-based therapies for the treatment of cancer. The acquisition includes blinatumomab, a Bispecific T cell Engager (BiTE) antibody in phase 2 clinical development for acute lymphoblastic leukemia and BiTE antibody technology, which is proprietary to Micromet, which provides an

 

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AMGEN INC.

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (Continued)

 

innovative platform for future clinical research. Blinatumomab is also in clinical development for the treatment of non-Hodgkin’s lymphoma and could have applications in other hematologic malignancies. In connection with this acquisition, which will be accounted for as a business combination, we have commenced a tender offer to acquire all of the outstanding shares of Micromet’s common stock at a price of $11 per share in cash, which values Micromet at approximately $1.16 billion. Upon its acquisition, Micromet will become a wholly owned subsidiary of Amgen. This acquisition will provide us with an opportunity to further expand our oncology pipeline. Micromet will be included in our consolidated financial statements commencing on the acquisition date. The acquisition, which is subject to customary closing conditions, is expected to close during the three months ended March 31, 2012.

21. Quarterly financial data (unaudited)

 

 

      2011 Quarters ended  

(In millions, except per share data)

   December 31      September  30(1)      June 30      March 31  

Product sales

   $ 3,907       $ 3,877       $ 3,893       $ 3,618   

Gross profit from product sales

     3,251         3,272         3,291         3,054   

Net income

     934         454         1,170         1,125   

Earnings per share:

           

Basic

   $ 1.09       $ 0.50       $ 1.26       $ 1.21   

Diluted

   $ 1.08       $ 0.50       $ 1.25       $ 1.20   
      2010 Quarters ended  

(In millions, except per share data)

   December  31(2)      September  30(3)      June 30      March 31  

Product sales

   $ 3,760       $ 3,759       $ 3,613       $ 3,528   

Gross profit from product sales

     3,188         3,172         3,060         3,020   

Net income

     1,022         1,236         1,202         1,167   

Earnings per share:

           

Basic

   $ 1.09       $ 1.29       $ 1.25       $ 1.19   

Diluted

   $ 1.08       $ 1.28       $ 1.25       $ 1.18   

 

(1) 

We recorded a $780 million legal settlement charge ($705 million, net of tax) in connection with an agreement in principle to settle allegations relating to our sales and marketing practices.

 

(2) 

We recorded $113 million of income tax benefit as the result of resolving certain transfer pricing issues with tax authorities for prior periods and a $118 million ($74 million, net of tax) asset impairment charge associated with a strategic decision to optimize our network of manufacturing facilities and improve cost efficiencies.

 

(3) 

We recorded $38 million of income tax benefit as the result of resolving certain transfer pricing issues with tax authorities for prior periods.

See Note 4, Income taxes, and Note 18, Contingencies and commitments, for further discussion of the items described above.

 

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SCHEDULE VALUATION ACCOUNTS

SCHEDULE II

AMGEN INC.

VALUATION ACCOUNTS

Years ended December 31, 2011, 2010 and 2009

(In millions)

 

Allowance for doubtful accounts

   Balance at
beginning
of period
     Additions
charged to
costs and
expenses
    Other
additions
     Deductions      Balance
at end
of
period
 

Year ended December 31, 2011

   $ 42       $ 17      $       $ 5       $ 54   

Year ended December 31, 2010

   $ 32       $ 10      $       $       $ 42   

Year ended December 31, 2009

   $ 38       $ (6   $       $       $ 32   

 

F-56

Second Amendment to the Amgen Supplemental Retirement Plan

Exhibit 10.10

SECOND AMENDMENT TO THE

AMGEN INC. SUPPLEMENTAL RETIREMENT PLAN

AS AMENDED AND RESTATED EFFECTIVE JANUARY 1, 2009

The Amgen Inc. Supplemental Retirement Plan (As Amended and Restated Effective January 1, 2009) (the “Plan”) is hereby amended, effective October 12, 2011, as follows:

 

  1. Article II is amended to add the following two definitions alphabetically and to renumber the definitions accordingly:

2.6 Change of Control Plan shall mean the Amgen Inc. Change of Control Severance Plan, as amended and restated, effective as of December 9, 2010 (and any subsequent amendments thereto).

2.19 Qualifying Termination shall mean your termination of employment within two (2) years following a Change of Control (as defined in the Change of Control Plan) (i) by the Company other than for Cause (as defined in the Change of Control Plan), Disability (as defined in the Change of Control Plan) or as a result of your death, or (ii) by you for Good Reason (as defined in the Change of Control Plan). No termination can qualify as a Qualifying Termination if there is no Change of Control Plan in effect at the time of the termination.

 

  2. Section 4.2 is amended and restated as follows:

4.2 Credits. For each year you are eligible, the Company will credit your Account with your share of Plan Credits in an amount equal to (i) ten percent (10%), multiplied by (ii) your Compensation for the year that is not recognized under the Retirement Plan either because it is in excess of the Salary Cap, or deferred under the NQDC, or both. In addition, if your employment terminates as a result of a Qualifying Termination, the Company may determine, in its sole discretion, to credit an amount determined under the Change in Control Plan to any Participant’s Account. Notwithstanding anything herein (including Article 5) or in the Change of Control Plan to the contrary, any Plan Credits resulting from a Qualifying Termination (and any Earnings thereon) will be paid to you in a lump sum as soon as administratively practicable during the Plan Year immediately following the Plan Year in which your Separation from Service occurs, but in no event more than two and one-half months after the end of the calendar year in which your Separation from Service occurs.


  3. Section 4.4 is amended and restated as follows:

4.4 Vesting of Your Account. Your Account will become fully vested upon termination of your employment with the Company (1) on or after (a) your Normal Retirement Date, (b) the date of your Disability, or (c) your death or (2) that is a Qualifying Termination. If your employment with the Company is terminated for any other reason, your Account will be vested in accordance with the following schedule:

 

Years of Service

  

Vested Percentage

Less than 3        0%
3 or more    100%

Notwithstanding the foregoing vesting schedule, if a portion of your Compensation for a year consists of amounts that were deferred under the NQDC, then a portion of that year’s Plan Credits in an amount equal to (i) 10%, multiplied by (ii) the amount of Compensation deferred under the NQDC that would have been taken into account under the Retirement Plan if it had not been deferred, shall be immediately vested.

Any portion of your Account that is not vested on your termination of employment will be permanently forfeited. All Accounts will be subject to the creditors of the Company in the event of the insolvency of the Company.

 

  4. Section 5.1 is amended to add the following sentence to the end thereof to read as follows:

Notwithstanding anything in this Section 5.1 or the balance of Article 5 to the contrary, the time and form of payment of any Plan Credits resulting from a Qualifying Termination (and any Earnings thereon), which will be treated as a right to receive a separate and distinct payment, shall be paid to you pursuant to and be governed by Section 4.2.

 

  5. The list of Participating and Subsidiaries and Affiliates of Amgen Inc. in Appendix A is amended and restated to read as follows:

 

  1. Amgen USA Inc. – January 1, 2002

 

  2. BioVex, Inc. – April 11, 2011

 

  3. Immunex Corporation – January 1, 2003

 

  4. Immunex Manufacturing Corporation – January 1, 2003

 

  5. Immunex Rhode Island Corporation – January 1, 2003

 

  6. Amgen Worldwide Services, Inc. – January 1, 2004

 

  7. Amgen SF, LLC – January 1, 2005

To record this Second Amendment to the Plan as set forth herein, the Company has caused its authorized officer to execute this document this 13th day of October, 2011.

 

AMGEN INC.
By:  

/s/ Brian McNamee

Brian McNamee
Senior Vice President, Human Resources

 

2

Third Amendment to the Amgen Supplemental Retirement Plan

Exhibit 10.11

THIRD AMENDMENT TO THE

AMGEN INC. SUPPLEMENTAL RETIREMENT PLAN

AS AMENDED AND RESTATED EFFECTIVE JANUARY 1, 2009

The Amgen Inc. Supplemental Retirement Plan (As Amended and Restated Effective January 1, 2009) (the “Plan”) is hereby amended, effective January 1, 2012, as follows:

 

  1. Section 1.1 “Purpose” will be amended and restated as follows:

The purpose of this Plan is to provide benefits to employees of the Company and certain of its affiliates and subsidiaries whose Matching Contributions and Nonelective Contributions are limited under the Retirement Plan or the AML Plan (each as defined below), whether because of statutory limitations or because of employee deferrals to the Amgen Nonqualified Deferred Compensation Plan (the “NQDC”), or both. The Company intends that the Plan will provide benefits to a select group of management or highly compensated employees. The Plan is intended to be an unfunded “top hat” plan meeting the requirements of Sections 201(2), 301(a)(3), 401(a)(1) and 4021(b)(6) of ERISA. The Plan is not intended to be a plan described in Section 401(a) of the Code and/or Section 1081.01(a) or the Puerto Rico Code.

 

  2. The first two sentences of “Article II DEFINITIONS” will be amended and restated as follows:

For the purposes of this Plan, the following terms, when capitalized, have the following meanings. Any capitalized term in this Plan that is not defined in this Article II has the meaning given such term in the Retirement Plan (or the AML Plan with respect to Puerto Rico Participants).

 

  3. A new Section 2.2A that reads as follows is added:

AML Plan means the Savings Plan for Amgen Manufacturing, Limited.

 

  4. Section 2.7 is amended and restated as follows:

Code means the Internal Revenue Code of 1986, as amended from time to time, and any applicable IRS Regulations promulgated thereunder and any successor thereto. References to any section of the Code include reference to any comparable or succeeding provisions or regulations that amends, supplements or replaces the section.

 

  5. Section 2.10 is amended and restated as follows:

Compensation has the same meaning as the term “Deferral Compensation” has under the Retirement Plan (or with respect to Puerto Rico Participants, as the term “Compensation” has under the AML Plan), except that, for purposes of this Plan, Compensation is not limited by the Salary Cap and includes amounts that are deferred into the NQDC.


  6. A new Section 2.11 that read as follows is added:

ERISA means the Employee Retirement Income Security Act of 1974, as amended from time to time.

 

  7. Section 2.15 is amended and restated as follows:

Section 2.15 Reserved

 

  8. A new Section 2.17A that reads as follows is added:

Puerto Rico Code means The Internal Revenue Code for a New Puerto Rico, as amended from time to time, and any applicable regulation thereunder and any successor thereto. Reference to any section or subsection of the Internal Revenue Code for a New Puerto Rico includes reference to any comparable or succeeding provisions that amends, supplements or replaces that section.

 

  9. A new Section 2.17B that reads as follows is added:

Puerto Rico Participant means each eligible employee who effective on or after January 1, 2012, is an active participant in the AML Plan.

 

  10. Section 2.19 is amended and restated as follows:

Qualifying Termination shall mean your termination of employment within two (2) years following a Change of Control (as defined in the Change of Control Plan) (i) by the Company other than for Cause (as defined in the Change of Control Plan), Disability (as defined in the Change of Control Plan) or as a result of your death, or (ii) by you for Good Reason (as defined in the Change of Control Plan). Your termination of employment will not qualify as a Qualifying Termination if you are not covered by the Change of Control Plan at the time of your termination or if there is no Change of Control Plan in effect at the time of your termination.

 

  11. Section 2.21 is amended and restated as follows:

Salary Cap means the highest level of compensation that can be considered for the purpose of calculating benefits under Section 401(a)(17) of the Code (or Puerto Rico Code Section 1081.01(a)(12) in the case of Puerto Rico Participants).

 

  12. Section 4.2 is amended and restated as follows:

Credits. For each year you are eligible, the Company will credit your Account with your share of Plan Credits in an amount equal to (i) ten percent (10%) (nine percent (9%) for Puerto Rico Participants), multiplied by (ii) your Compensation for the year that is not recognized under the Retirement Plan (or the AML Plan with respect to Puerto Rico Participants) either because it is in excess of the Salary Cap, or deferred under the


NQDC, or both. In addition, if your employment terminates as a result of a Qualifying Termination, the Company may determine, in its sole discretion, to credit an amount determined under the Change in Control Plan to any Plan participant’s Account. Notwithstanding anything herein (including Article 5) or in the Change of Control Plan to the contrary, any Plan Credits resulting from a Qualifying Termination (and any Earnings thereon) will be paid to you in a lump sum as soon as administratively practicable during the Plan Year immediately following the Plan Year in which your Separation from Service occurs, but in no event more than two and one-half months after the end of the calendar year in which your Separation from Service occurs.

 

  13. Section 3.1 is amended to add the following sentence at the end thereof:

Effective January 1, 2012, Puerto Rico Participants are eligible to participate (and only on a prospective basis) to the extent they satisfy on or after such date the eligibility requirements under this Section.

 

  14. Section 5.6 is amended to add the following subsection (d) to the end thereof to read as follows:

 

  (d) If there is an inclusion in income under Section Code 457A with respect to any portion of your Account, such inclusion is treated as a payment for purposes of the short-term deferral rule under §1.409A-1(b)(4). If the short-term deferral rule under §1.409A-1(b)(4) is satisfied, the amount included in income will be distributed to you during the taxable year in which such income inclusion occurs. If the short-term deferral rule under §1.409A-1(b)(4) is not satisfied, the amount included in income will be accelerated to the extent permitted under applicable IRS guidance.

 

  15. Section 7.1 is amended and restated as follows:

7.1 Committee; Duties. This Plan is administered by the Committee, or its duly appointed delegate or delegates, who may or may not be employees of the Company. The Committee (or its delegates) shall have all rights, powers and authority with respect to the administration and operation of the Plan, including, without limitation (i) the sole discretion and authority to make such rules, interpretations and computations and shall take such other actions to administer the Plan as it may deem appropriate, (ii) the sole discretion and authority to interpret the Plan and conclusively to determine all questions arising under the Plan, including questions relating to eligibility and benefits, (iii) the power to maintain and keep adequate records concerning the Plan and its proceedings and acts in such form and detail as the Committee may decide; provided, however, nothing in this Section 7.1 shall be construed to impose any fiduciary duty on the Committee or its delegates under ERISA. The decisions or actions of the Committee with respect to any question arising out of or in connection with the administration, interpretation or application of the Plan and the rules or regulations promulgated hereunder will be final, conclusive and binding upon all persons having any interest in the Plan.


  16. Section 7.3 is amended and restated as follows:

Section 7.3 CLAIMS AND REVIEW PROCEDURES

 

  (a) Applications for Benefits. Any application for benefits under the Plan shall be submitted to the Company at its principal office. Such application shall be in writing on the prescribed form and shall be signed by the applicant. All claims must be made within 180 days of the event that gives rise to a claim for benefits, including, without limitation, the receipt of a benefit statement that is labeled as a final determination (or labeled in terms substantially similar) of your benefits as of a certain date or states a claim for benefits may be filed within 180 days.

 

  (b) Denial of Applications. In the event that any application for benefits is denied in whole or in part, the Company shall notify the applicant in writing or electronically of the right to a review of the denial. Such written notice shall set forth, in a manner calculated to be understood by the applicant, specific reasons for the denial, specific references to the Plan provisions on which the denial was based, a description of any information or material necessary to perfect the application, an explanation of why such material is necessary, an explanation of the Plan’s review procedure, and a statement of the applicant’s right to bring a civil action under Section 502(a) of ERISA following an adverse benefit determination on review. Such notice shall be given to the applicant within 90 days after the Company receives the application, unless special circumstances require an extension of time for processing the application. In no event shall such an extension exceed a period of 90 days from the end of the initial 90 day period. If such an extension is required, written notice thereof shall be furnished to the applicant before the end of the initial 90 day period. Such notice shall indicate the special circumstances requiring an extension of time and the date by which the Company expects to render a decision. If notice is not given to the applicant within the period prescribed by this Section 7.3(b), the application shall be deemed to have been denied for purposes of Section 7.3(d) upon the expiration of such period.

 

  (c) Requests for Review. Any person whose application for benefits is denied in whole or in part (or such person’s duly authorized representative) may appeal the denial by submitting to the Company a request for a review of such application within 90 days after receiving written notice of the denial. The Company shall give the applicant or such representative an opportunity to review pertinent documents (except legally privileged materials) in preparing such request for review and to submit issues and comments in writing. The request for review shall be in writing and shall be addressed to the Company’s principal office. The request for review shall set forth all of the grounds on which it is based, all facts in support of the request, and any other matters which the applicant deems pertinent. The Company may require the applicant to submit such additional facts, documents or other material as it may deem necessary or appropriate in making its review.


  (d) Decisions on Review. The Company shall act upon each request for review within 60 days after receipt thereof, unless special circumstances require an extension of time for processing, but in no event shall the decision on review be rendered more than 120 days after the Company receives the request for review. If such an extension is required, written notice thereof shall be furnished to the applicant before the end of the initial 90 day period. The Company shall give prompt, written or electronic notice of its decision to the applicant and to the Company. In the event that the Company confirms the denial of the application for benefits in whole or in part, such notice shall set forth, in a manner calculated to be understood by the applicant, the specific reasons for such denial, specific references to the Plan provisions on which the decision is based, and a statement of the applicant’s right to bring a civil action under Section 502(a) of ERISA following an adverse benefit determination on review. To the extent that the Company overrules the denial of the application for benefits, such benefits shall be paid to the applicant.

 

  (e) Rules and Procedures. The Company shall adopt such rules and procedures, consistent with ERISA and the Plan, as it deems necessary or appropriate in carrying out its responsibilities under this Section 7.3.

 

  (f) Exhaustion of Administrative Remedies. No legal or equitable action for benefits under the Plan shall be brought unless and until the claimant (i) has submitted a written application for benefits in accordance with Section 7.3(a); (ii) has been notified that the application is denied; (iii) has filed a written request for a review of the application in accordance with Section 7.3(c); and (iv) has been notified in writing or electronically that the Company has affirmed the denial of the application. If the claimant has entered into an arbitration agreement with the Company, the provisions of that arbitration agreement will govern following the claimant’s compliance with the foregoing provisions of this Section 7.3, and shall be the sole and exclusive remedy following compliance with the foregoing provisions. No arbitration or civil action for benefits under the Plan may be brought more than one year following the notification that the appeal was denied in whole or in part, or the event that gave rise to the claim for benefits (including, without limitation, receipt of a benefit statement that is labeled as a final determination (or labeled in terms substantially similar) of your benefits as of a certain date or states you may file a claim for benefits within 180 days), whichever is later. If no arbitration agreement is applicable, any legal or equitable action for benefits under the Plan must be brought in the United States District Court that includes the city or is nearest to the city in which the participant was last employed by the Company.

 

17. References in the following Sections of the Plan to “the Retirement Plan” shall be changed to “the Retirement Plan (or the AML Plan with respect to Puerto Rico Participants)”:

Sections 3.1, 4.3, 4.4, 6.1, 6.2.


  18. The list of Participating Subsidiaries and Affiliates of Amgen Inc. in Appendix A is amended to add the following to the end thereof:

“8. Amgen Manufacturing, Limited – January 1, 2012”

To record this Third Amendment to the Plan as set forth herein, the Company has caused its authorized officer to execute this document this 16th day of December 2011.

 

AMGEN INC.
By:  

/s/ Brian McNamee

Title:   SVP, Human Resources
Second Amendment to the Amgen Nonqualified Deferred Compensation Plan

Exhibit 10.18

SECOND AMENDMENT TO THE

AMGEN NONQUALIFIED DEFERRED COMPENSATION PLAN

AS AMENDED AND RESTATED EFFECTIVE JANUARY 1, 2009

The Amgen Nonqualified Deferred Compensation Plan as Amended and Restated Effective January 1, 2009 (the “Plan”) is hereby amended, effective October 12, 2011, as follows:

 

  1. Section 3.1 is amended to add a subsection (d) to read as follows:

 

  (d) If a Participant received a hardship distribution from the 401(k) Plan or the 1165(e) Plan (as defined in Section 3.3) and, as a result of such hardship distribution, the Participant is prohibited from making deferrals to the 401(k) Plan or 1165(e) Plan, as applicable, for all or any portion of any subsequent Plan Year, such Participant shall be prohibited from making any deferrals to the Plan for such Plan Year, notwithstanding anything in Section 3.2 or 8.6 to the contrary. Any deferral for a subsequent Plan Year to which this subsection (d) does not apply must be made in accordance with Section 3.2.

 

  2. The list of Employers in Appendix A is amended and restated to read as follows:

Amgen Manufacturing, Limited

Amgen SF, LLC

Amgen USA Inc.

Amgen Worldwide Services, Inc.

BioVex, Inc.

Immunex Corporation

Immunex Manufacturing Corporation

Immunex Rhode Island Corporation

To record this Second Amendment to the Plan as set forth herein, the Company has caused its authorized officer to execute this document this 13th day of October, 2011.

 

AMGEN INC.
By:  

/s/ Brian McNamee

  Brian McNamee
  Senior Vice President, Human Resources
Agreement between Amgen Inc. and Mr. Anthony C. Hooper

Exhibit 10.21

October 12, 2011

Mr. Anthony C. Hooper

XXXXXXXXXXXX

XXXXXXXXXXXX

Dear Anthony:

On behalf of Amgen Inc. (Amgen or the Company), I am pleased to offer you the position of Executive Vice President, Global Commercial Operations, Level 11, reporting to Robert A. Bradway. This offer and the compensation listed are subject to your appointment by our Board of Directors (the Board) and the Compensation and Management Development Committee (the Compensation Committee) providing final approval of the compensation listed in this letter.

Your salary will be paid bi-weekly in the amount of $36,538.46, with 26 pay periods in one year, subject to federal and state and other applicable tax deductions and withholdings.

You will be entitled to a sign-on bonus of $1,000,000 less federal and state tax deductions and other applicable withholdings. This amount will be paid 30 days after you report to Amgen for full time employment (your Start Date), subject to your execution of the enclosed “Sign-On Bonus Agreement for New Hire Staff Members,” and further subject to your being actively employed by Amgen on the payment date. The sign-on bonus must be repaid by you in full if you voluntarily resign your employment for any reason, or if Amgen terminates your employment with Cause (as defined below), at any time prior to the two year anniversary of your Start Date, as provided in the attached Sign-On Bonus Agreement for New Hire Staff Members.

You will be granted as of the Effective Grant Date (as defined below) time-vested restricted stock units (RSUs) valued at $2,475,000 (based on the average daily closing price of Amgen common stock, $.0001 par value per share (the Common Stock) for the 60 trading days immediately preceding the Effective Grant Date. For these purposes, the Effective Grant Date shall be the day that is two business days after the date of the release of Amgen’s 2011 third quarter earnings and is expected to fall on October 27, 2011 provided you are actively employed by Amgen on that date; in the event you are not actively employed by Amgen on that date, the Effective Grant Date shall be a date that is as soon as possible after your Start Date, as determined by an award committee, authorized by the Board in accordance with Amgen’s equity awards policy. Upon each applicable vesting date (which shall be on each of March 2, 2012; March 2, 2013; March 2, 2014 and March 2, 2015), you will receive a number of shares of Common Stock equal to the number of RSUs that vest, less any shares that are withheld to satisfy applicable taxes. This grant will vest as to whole shares at a rate of 50% on March 2, 2012, and the remaining 50% in equal one-thirds (1/3rd) on March 2, 2013, on March 2, 2014 and on March 2, 2015, contingent upon your acceptance of the grant in accordance with Amgen’s grant acceptance policy and your being actively employed by Amgen through each vesting date (except as otherwise specified in the related RSU grant agreement). No fractional shares may be awarded.

You will be granted on the Effective Grant Date three awards denominated in performance units (PUs) with varying performance goals and performance periods. The first PU award shall be valued at $1,925,000 (the First PU Award), the second PU award shall be valued at $1,925,000 (the Second PU Award) and the third PU award shall be valued at $1,925,000 (the Third PU Award). The number of PUs granted shall be based on these values and the average daily closing price of the Common Stock for the 60 trading days immediately preceding the Effective Grant Date. The PUs shall be awarded pursuant to Amgen’s 2009 Performance Award Program, with the specific terms and performance goals as approved by the Compensation Committee (Performance Goals), and shall be contingent upon your acceptance of the grant in accordance with Amgen’s grant acceptance policy and your being actively employed by Amgen on the Effective Grant Date. The number of PUs earned shall be determined by the extent to which Amgen achieves the Performance Goals. In general, the Performance Goals shall be based on Amgen’s total shareholder return (TSR) compared to the


average TSR of the companies in a comparator group as designated by the Compensation Committee for the specified performance period. The PUs earned shall equal the PUs granted multiplied by the payout percentage (the Payout Percentage), derived from the comparison of Amgen’s TSR and the average TSR of the companies in the relevant comparator group for the relevant performance period, and shall be between 0% and 150% of the PUs granted. The performance period of the First PU Award shall commence on the Effective Grant Date and end on December 31, 2012; the performance period of the Second PU Award shall commence on the Effective Grant Date and end on December 31, 2013 and the performance period of the Third PU Award shall commence on the Effective Grant Date and end on December 31, 2014. All PUs shall be deemed earned as of the last day of the performance period (Vesting Date) and, when the Compensation Committee has certified the extent to which the Performance Goals have been achieved and the corresponding number of PUs earned, shall be payable on or prior to the March 15th immediately following the end of the performance period, subject to certain exceptions for delayed payment as provided under Section 409A of the Internal Revenue Code of 1986, as amended, and further subject to your being actively employed with Amgen through each Vesting Date (except as otherwise specified in the related PU grant agreement).

The RSUs, PUs and other equity awards will be subject to the terms and conditions set forth in the applicable grant agreements.

Beginning in 2012, you will be eligible to receive stock options, RSUs and/or PUs as part of Amgen’s Long-Term Incentive (LTI) program. Grants under the LTI program are discretionary as approved by the Compensation Committee.

For the 2011 cash bonus, you will be eligible to participate in Amgen’s Global Management Incentive Plan (the GMIP) pursuant to the terms of the GMIP. Your annual target incentive opportunity will be 80% of your actual base salary earned at Amgen during 2011. Your actual GMIP bonus may be more or less than this target amount, and may vary based on Company performance and the Compensation Committee’s assessment of your individual performance and contribution. For the sake of clarity, your target bonus opportunity is based on your actual salary for 2011 and thus it reflects a pro-ration based on the number of days you work for Amgen in 2011. You must be actively employed through the last regularly scheduled business day of a performance year to be eligible for that year’s GMIP bonus.

Further, in 2012, at the earlier of ten business days after (i) the filing of your current employer’s 2012 proxy statement or (ii) your provision of satisfactory documentation of the 2011 annual cash bonus calculations your current employer used for its Named Executive Officers (NEOs) and the amount your current employer pays you as 2011 base salary, you shall be paid an amount equal to any difference between the bonus you would have earned for 2011 at your current employer using your annualized 2011 base salary paid by your current employer multiplied by the bonus payout percentage based on actual financial and operational performance against objective targets at your current employer as used for its NEOs, multiplied by an individual performance factor of 1.35, less any 2011 bonus amounts you are actually paid by your current employer and less any 2011 bonus amounts paid by Amgen as a result of your participation in the 2011 GMIP. This payment is subject to your being actively employed with Amgen on the date of payment.

In 2012, management will nominate you for inclusion in the Amgen Executive Incentive Plan (the EIP). The EIP is the annual cash incentive plan in which officers of the Company at your level typically participate, and inclusion is determined and approved by the Compensation Committee during the first quarter of each calendar year. Actual awards under our EIP are determined using pre-established Company goals and results measured under our GMIP. Your annual target incentive opportunity (80% of your base salary earnings during the plan year) will not change as the result of your participation in the EIP.

You are also eligible to participate in the Amgen Nonqualified Deferred Compensation Plan (the DCP) to voluntarily defer, on a pre-tax basis, a portion of your annual earnings, including base salary and/or GMIP bonus. Shortly after commencing your employment at Amgen, you will receive an enrollment e-mail regarding the DCP plan for Amgen. A Q&A regarding the DCP is enclosed.

You will be eligible to participate in the Amgen Inc. Change in Control Severance Plan as amended from time-to-time (the COC), as a Group I Participant according to the terms of the COC. If, upon your termination, you are eligible to receive severance benefits under the COC and you are also eligible to receive severance benefits from another plan, agreement or policy, you will be paid the greater of the amount from that plan, agreement or policy or the amount provided in the COC, but not both amounts. A copy of the COC is enclosed as Attachment 2.

 

2


If, within the first three years of your employment with Amgen, Amgen terminates your employment without “Cause”, as defined below, you will be entitled to the benefits described in this paragraph (the Termination Paragraph), provided that you sign a general release of claims in the form furnished to you by Amgen as a condition to receipt of such payments. The following are such benefits: (1) two (2) times the sum of (i) your annual base salary then in effect and (ii) 80% of your annual base salary then in effect paid in a lump sum as soon as administratively practicable, but in no event later than March 15 of the year following the year in which Amgen terminates your employment and (2) if you elect continuation coverage under the Amgen group medical and dental plans for yourself and your qualified beneficiaries under the Consolidated Omnibus Budget Reconciliation Act of 1985 (COBRA), Amgen will pay the cost of such coverage until the earlier to occur of the following: (A) eighteen (18) months following your termination of employment or (B) the date on which you are no longer eligible for such COBRA coverage. Notwithstanding the previous sentence, with regard to such COBRA continuation coverage, if the Company determines in its sole discretion that it cannot provide the foregoing benefit without potentially violating applicable law (including, without limitation, Section 2716 of the Public Health Service Act), the Company shall in lieu thereof provide to you a taxable monthly payment in an amount equal to the monthly COBRA premium that you would be required to pay to continue your and your covered dependent’s group insurance coverages in effect on the date of termination (which amount shall be based on the premiums for the first month of COBRA coverage). Please note that this Termination Paragraph does not alter the at-will nature of your employment at Amgen. For purposes of this paragraph, Amgen shall include Amgen and any Amgen’s subsidiary and affiliate companies (for the avoidance of doubt, a transfer of employment to one of Amgen’s subsidiary or affiliate companies shall not be deemed a termination of your employment without “Cause”).

As an executive at Amgen, you will be eligible for the following: first-class air transportation while traveling on company business; an annual physical examination; and, reimbursement for up to $15,000 (gross) per year for financial counseling, tax preparation and related services.

You will also have the opportunity to participate in our comprehensive benefits program, as in effect from time-to-time in accordance with the terms of Amgen’s plans. Amgen’s excellent health care plan currently includes medical, dental and vision coverage for you and your eligible dependents. Amgen currently pays the major expense for these programs while staff members share through payroll deductions. Please be advised that in order for you and your dependents to be eligible for Amgen’s medical coverage you must:

 

  1. Report to work at Amgen or another location to which you are required to travel and perform the regular duties of your employment.

 

  2. Contact the Amgen Benefits Center at 1-800-97AMGEN, to enroll within 31 days of your Start Date.

 

  3. Meet all other eligibility requirements under the plan.

You will be eligible to participate in the Amgen Retirement and Savings Plan, which is a 401(k) plan that provides an opportunity for you to save a percentage of your pay (based on Internal Revenue Service limits) on a tax-deferred basis. Amgen will also contribute to your 401(k) account to help you save for your future financial goals. These benefits, services and programs are summarized in the enclosed brochure called “A Guide to Total Rewards at Amgen,” and may be changed or discontinued by Amgen from time-to-time.

The Company will be performing a background check and will require you to take a drug test. It is a condition of your employment that the Company receives satisfactory results from both the background check and the drug test.

Enclosed and included as part of this offer (Attachment 1) is information regarding Amgen’s Proprietary Information and Inventions Agreement, the Immigration Reform & Control Act and a packet of materials entitled “Arbitration of Disputes” which includes a Mutual Agreement to Arbitrate Claims. Provided that the basis is not related to an actual violation of these or any other agreement with Amgen, Amgen agrees to compensate you for Specified Forfeitures and agrees to indemnify and hold you harmless against any Specified Claim, in each case valued as of the Start Date. You agree that you shall submit a claim to Amgen for any Specified Claims and Specified Forfeitures as soon as possible upon notice of the triggering event(s). Such compensation and indemnification is subject to your being actively employed with Amgen on the date of

 

3


payment. Also enclosed and included, as part of this offer in Attachment 1, is information regarding Amgen’s New Staff Member Letter and Certification. This offer is contingent upon you truthfully and accurately completing the Certification, and returning it to the Company before or on your first day of employment.

This offer of employment is contingent upon your completing the items described in Attachment 1 and upon your ability to perform for Amgen all of the duties of your position without restriction from, or violation of, any enforceable contractual obligations owed to any former employer or entity for whom you worked or provided service(s).

Also enclosed and included, as part of this offer (Offer Letter Benefit Summary), is information about the main points of the relocation assistance that Amgen will provide to you to relocate to the “local area.” Please note that relocation assistance is contingent upon your execution of the enclosed “Relocation Agreement for New Hire Staff Members” and that relocation benefits are limited to one benefits package per household. In addition, you are required to reimburse Amgen for the gross amount of the cost of the relocation benefits (according to the attached schedule) if you resign employment for any reason within two years of your Start Date.

You will be contacted by a Relocation Counselor to initiate your relocation benefits within 3 business days after receipt of your signed acceptance of this offer and your signed New Hire Relocation Agreement.

For purposes of the Termination Paragraph, “Cause” means: (i) unfitness for service, inattention to or neglect of duties, or incompetence; (ii) dishonesty; (iii) disregard or violation of the policies or procedures of Amgen; (iv) refusal or failure to follow lawful directions of the Company; (v) illegal, unethical or immoral conduct; (vi) breach of the attached Amgen Proprietary Information and Inventions Agreement; or (vii) any other reason set forth in California Labor Code Section 2924, in all cases, as determined by Amgen, in its sole and absolute discretion. For purposes hereof, “Specified Claim” means any claim resulting from your work for Amgen for recoupment of previously earned or vested compensation or benefits; provided that “earned compensation” does not include any equity awards that were not vested as of the date of the termination of your employment and were not subject to any right to acceleration upon such termination. For purposes hereof, “Specified Forfeitures” means the cancellation or forfeiture of any vested compensation or benefit due to your work for Amgen or the denial of vesting of any compensation or benefit that would have vested upon your termination but for your work for Amgen.

By signing this letter, you understand and agree that your employment with Amgen is at-will. Therefore, your employment can terminate, with or without cause, and with or without notice, at any time, at your option or Amgen’s option, and Amgen can terminate or change all other terms and conditions of your employment, with or without cause, and with or without notice, at any time. This at-will relationship will remain in effect throughout your employment with either Amgen Inc. or any of its subsidiaries or affiliates. This letter and its enclosures constitute the entire agreement, arrangement and understanding between you and Amgen on the nature and terms of your employment with Amgen, including, but not limited to, the kind, character and existence of your proposed job duties, the length of time your employment will last and the compensation you will receive. This letter and its enclosures supersede any prior or contemporaneous agreement, arrangement or understanding on this subject matter. By executing this letter as provided below, you expressly acknowledge the termination of any such prior agreement, arrangement or understanding, except as referenced in this letter and/or its enclosures. Also, by your execution of this letter, you affirm that no one has made any written or verbal statement that contradicts the provisions of this letter or its enclosures. The at-will nature of your employment, as set forth in this paragraph, can be modified only by a written agreement signed by both Amgen’s Senior Vice President of Human Resources and you which expressly alters it. This at-will relationship may not be modified by any oral or implied agreement or by any Company policies, practices or patterns of conduct.

This offer letter shall be interpreted and administered in a manner such that any amount or benefit payable hereunder shall be paid or provided in a manner that is exempt from Section 409A of the Internal Revenue Code of 1986, as amended (together with any Department of Treasury regulations and other interpretive guidance issued thereunder, including without limitation any such regulations or other guidance that may be issued after the date hereof, Section 409A). None of the amounts or benefits payable hereunder are intended to constitute “nonqualified deferred compensation” within the meaning of Section 409A of the Internal Review Code of 1986, as amended. However, notwithstanding any other provision of this offer letter, if at any time

 

4


Amgen determines that any amounts or benefits payable hereunder may be subject to Section 409A, Amgen shall have the right in its sole discretion (without any obligation to do so or to indemnify you or any other person for failure to do so) to adopt such amendments to this offer letter, or take any other actions, as Amgen determines are necessary or appropriate either for such amounts or benefits to be exempt from the application of Section 409A or to comply with the requirements of Section 409A.

The complete terms of the plans, programs and policies referenced to in this letter are set forth in their respective documents, which are maintained by the Company. The Company reserves the right to amend or terminate any of these plans, programs or policies at any time, in its sole discretion. In the event of any difference between this offer letter and the provisions of the respective plan, program or policy document, the respective plan, program, or policy document will govern.

You have made an excellent impression on the staff at Amgen. We are enthusiastic about the contribution you can make, and we believe that Amgen can provide you with attractive opportunities for personal achievement and growth. I look forward to your favorable reply by October 13, 2011. If you accept our offer, please sign and date the copy of the letter and return it in the enclosed envelope to our Staffing Department along with the completed and signed Proprietary Information and Inventions Agreement and the Mutual Agreement to Arbitrate Claims. Please retain the original offer letter for your records. If you have any questions regarding this offer, please contact Greg XXXXXXX at (805) 447-XXXX.

Sincerely,

LOGO

Robert A. Bradway

President and Chief Operating Officer

RAB:ett

Enclosures

 

/s/ Anthony C. Hooper                         10/14/2011

Signature of Acceptance                             Date
10/26/2011
Anticipated Start Date

 

5


ATTACHMENT 1

In order to accept our offer you will be required to:

 

  A) Complete, date and sign the enclosed Amgen Proprietary Information and Inventions Agreement and return it with your signed offer letter.

 

  B) Sign and date the Amgen New Staff Member Letter and Certification and return it with your signed offer letter.

 

  C) Date and sign the enclosed Mutual Agreement to Arbitrate Claims and return it with your signed offer letter.

 

  D) You will be required to provide Amgen with proof of your identity and eligibility for employment per requirements of the Immigration Reform and Control Act of 1986 within 3 (three) days of hire. Information pertaining to this Act and required proof are enclosed.

 

  E) Sign and date the Consumer Disclosure and Authorization Form (Disclosure Regarding Background Check Investigation

 

6


AMGEN NEW STAFF MEMBER LETTER AND CERTIFICATION

Welcome to Amgen (the “Company”). The Company has no need to learn and does not want any proprietary, confidential or trade secret information that belongs to any prior employers. Please review and comply with the following instructions and policies, and execute the Certification below.

 

   

Carefully read the Company’s Proprietary Information and Inventions Agreement (“PIIA”) that you have executed, and make sure that you understand your obligations under the terms of the PIIA.

 

   

You may not bring any material to the Company from your prior employers in hard copy, in electronic format or in any other form.

 

   

Prior to commencing any work for the Company, conduct a search of your personal computer(s), email accounts, and any other electronic storage devices you possess, as well as any files you maintain in hard copy, for information or materials belonging to your prior employers. You are instructed to destroy, delete or return any such information or materials belonging to your prior employers, consistent with any obligations you have to the prior employers.

 

   

Do not disclose to or provide the Company with any customer lists you obtained from or during your employment with your prior employers. When interacting with doctors or other members of the healthcare industry with whom you may have had contact in connection with any of your prior employment, clearly indicate to such persons that you are an Amgen staff member, and focus on the Company’s products rather than using or discussing information related to your prior employment.

 

   

If you have any doubts regarding whether you may take, disclose, upload, access, or use any information in your possession, you must err on the side of not taking, disclosing, uploading, accessing or using the information.

 

   

Do not begin any work for the Company before your employment with your prior employers has officially ended.

 

   

After commencing work for the Company, do not request that any employee of your prior employers provide you with, or take any other steps to obtain, any information of your prior employers.

 

   

Under no circumstances are you permitted to connect to a Company computer any electronic storage device containing information relating to your prior employers. Likewise, in performing work for the Company, you are not permitted to use, disclose, access or upload any such information. If you discover that any confidential, proprietary, or trade secret information of your prior employers has been uploaded to any Company computer or email system(s), immediately inform Human Resources.

 

   

The Company may monitor and/or conduct an audit of your use of Company computer systems, and you should not have any expectation of privacy in data sent, stored or received on any Company systems.

Disclose and identify below all agreements relating to your current or prior employment that may affect your eligibility to become employed by and/or to perform work for the Company, including non-competition agreement(s), agreements relating to the solicitation of employees or customers, or other restrictive agreements (collectively, “Restrictive Agreements”), regardless of whether you believe these agreements are enforceable, or apply to your potential employment with the Company, or have expired, and provide a copy to Human Resources. If “none,” please so indicate. Do not leave blank.

 

7


 

Name of Agreement

       

Employer

       

Date signed

PSU, Restricted Stock and

     

BMS

     

2007 - 2011

Annual Stock Option allocations

     

 

     

 

(Attach additional sheets, if necessary)            

 

   

If you are subject to an agreement not to solicit employees of your prior employers, you should refrain from doing so. If you are contacted by a former colleague about employment opportunities with the Company, you should refer such inquiries/candidates to Amgen’s Staffing Department.

 

   

Do not use any email account (including Company email accounts), text messages, Instant Messaging, or any other method of written communication to store or discuss information relating to your prior employers or to recruit or solicit employees of your former employers.

 

   

Immediately inform your Human Resources Business Partner if you are contacted by any former employer regarding your work for Amgen and/or any non-competition agreements, agreements that relate to the solicitation of employees or customers, or any other restrictive agreements you entered into in connection with any previous employment.

CERTIFICATION

I understand that the above list is only a summary and does not purport to include all of my continuing obligations to the Company. By signing below I certify that I have and will continue to comply with the above instructions and policies.

I hereby agree that the Company may, at its sole option and discretion contact my prior employer(s) to determine whether any Restrictive Agreements exist and, if so, their applicable terms. I acknowledge that the Company may revoke its offer or terminate my employment if it determines in its reasonable business judgment that I have failed to disclose or am otherwise subject to an enforceable Restrictive Agreement.

Nothing in this Letter and Certification is intended to alter, or shall have any impact on, my status as an at-will employee of the Company. In addition to its right to terminate my employment, the Company shall have the right to suspend me from work without pay during its investigation into the existence and/or enforceability of any restrictions on my ability to perform work for the Company.

I agree:

 

/s/ Anthony C. Hooper

Signature of Staff Member

Anthony C. Hooper

Print Name of Staff Member

10/14/2011

Date

 

8


AMGEN SIGN-ON BONUS AGREEMENT

FOR

NEW HIRE STAFF MEMBERS

I, Anthony C. Hooper, agree to accept my sign-on bonus payment (“Bonus”) from Amgen on the following terms.

 

1. The amount of the Bonus is described in the offer letter (as may be amended) provided separately to me.

 

2. The Bonus will generally be paid to me after thirty (30) days following the date on which I report to Amgen for full time employment with Amgen. If I am not still employed as of the date the Bonus is to be paid, the Bonus will not be paid either in part or in full.

 

3. The Bonus is intended to facilitate my acceptance of employment with Amgen. While the Bonus is provided by Amgen in its business interests as part of its employee recruitment program, I acknowledge that the Bonus is not reimbursable to me as a matter of law under California Labor Code section 2802 or any similar statute.

 

4. Amgen is providing me with the Bonus with the expectation that I will not in the short term resign my employment. I understand and acknowledge that the bonus is being given for purposes of retention and conditioned upon my continued service for at least two years of active employment following the start date of my employment with Amgen. While, as an at-will employee, I am free to resign at any time, I agree to reimburse Amgen for the gross amount of my Bonus if I resign my employment for any reason within two years of the start date of my employment. Amgen is also providing the Bonus with the expectation that there will not occur a termination for Cause (as defined below). Thus, I agree to reimburse Amgen for the gross amount of my Bonus if my employment is terminated by Amgen for Cause within two years of the start date of my employment. I also agree that in the event of such a resignation or termination for Cause, the amount to be reimbursed shall be due in full and payable by me immediately in cash (i.e., by check, wire transfer, or similar immediate payment) without further notice or demand by Amgen, and that Amgen shall have the right to offset against compensation then owing to me. Additionally, any Bonus monies that were to be paid at an agreed upon future date but have not yet been paid are not earned and are forfeited upon resignation or termination from the company.

For these purposes, “Cause” means (i) unfitness for service, inattention to or neglect of duties, or incompetence; (ii) dishonesty; (iii) disregard or violation of the policies or procedures of Amgen; (iv) refusal or failure to follow lawful directions of the Company; (v) illegal, unethical or immoral conduct; (vi) breach of the attached Amgen Proprietary Information and Inventions Agreement; or (vii) any other reason set forth in California Labor Code Section 2924, in all cases, as determined by Amgen, in its sole and absolute discretion.

 

5. Generally, a new hire sign-on bonus is considered ordinary wage income to the recipient. I understand that Amgen will report to appropriate federal and state taxing authorities all income that Amgen considers to be subject to taxation and will withhold appropriate taxes in accordance with federal and state regulations. I understand that it is my obligation to declare all income and pay all taxes owed on such income, if any.

 

6. In the event that I fail to reimburse Amgen for my Bonus as required by this agreement and Amgen initiates proceedings to recover such Bonus, the prevailing party in such a suit shall be awarded its reasonable costs and attorney’s fees.

 

7. I understand that this agreement shall be governed by the law of the State of California.

 

8. Nothing in this agreement will be construed as an employment contract or to guarantee me employment at Amgen for any fixed term. I understand that my employment at Amgen is at will.

 

9. The provisions of this agreement are severable. If any part is found to be unenforceable, all other provisions shall remain fully valid and enforceable.

 

I agree:       Amgen Inc:

/s/ Anthony C. Hooper

   

/s/ Amie Krause

Signature of Staff Member     Signature of Authorized Representative

Anthony C. Hooper

   

Senior Staffing Manager

Print Name of Staff Member     Title of Representative

10/14/2011

   

10/18/2011

Date     Date

 

9


AMGEN RELOCATION AGREEMENT

FOR

NEW HIRE STAFF MEMBERS

I, Anthony C. Hooper, agree to accept certain relocation benefits from Amgen on the following terms.

 

1. The relocation benefits to be provided to me are outlined in the Amgen Relocation Policy that applies to staff members at my grade level.

 

2. I will obtain relocation benefits from Amgen by following the procedures outlined in the Amgen Relocation Policy that applies to staff members at my grade level.

 

3. I understand that I may obtain an estimate of my relocation costs from Amgen/Amgen’s third-party relocation vendor and that the actual cost of my relocation may be more or less than the estimate I am provided. I further understand that I can obtain detailed information about the actual services and costs being incurred during my relocation by contacting Amgen/Amgen’s third-party relocation vendor.

 

4. The relocation benefits are to facilitate my move as a result of my decision to accept an offer of employment with Amgen. I acknowledge that the cost of these benefits is not required to be reimbursed to me as a matter of law under California Labor Code section 2802 or any similar statute.

 

5. Amgen provides the relocation benefits with the expectation that I will not in the short term resign my employment. I understand and acknowledge that the relocation benefits are being given for purposes of retention and are conditioned upon my continued service through 730 days of active employment from the start date of my employment with Amgen. While, as an at-will employee, I am free to resign at any time, I agree to reimburse Amgen for the gross amount of the cost of the relocation benefits (according to the schedule below) if I resign my employment for any reason within 730 days of the date I report to Amgen for full time employment. Upon my resignation, the amount to be reimbursed shall be immediately due and payable by me without further notice or demand, and that Amgen shall have the right to offset against compensation then owing to me. The schedule for reimbursement is as follows:

 

Days Since Start Date

   % of Gross Cost of Relocation Benefits to be
Reimbursed to Amgen
 

0 to 365 days

     100

366- 450 days

       75

451 - 540 days

       50

541 - 730 days

       25

Over 730 days

         0

 

6. I understand that Amgen will report to federal and state taxing agencies all income that Amgen considers to be subject to taxation. I understand that it is my obligation to declare all income and pay all taxes owed on such income, if any.

 

7. In the event that I fail to make a reimbursement required by this agreement and Amgen initiates proceedings to recover such reimbursement, the prevailing party in such a suit shall be awarded its reasonable costs and attorney’s fees.

 

8. I understand that this agreement shall be governed by the law of the State of California.

 

9. Nothing in this agreement will be construed as an employment contract or to guarantee me employment at Amgen for any fixed term. I understand that my employment at Amgen is at will. Nor does this agreement guarantee me reimbursement of any particular relocation expenses. I understand that reimbursement is governed by the Amgen Relocation Policy and that I must comply with the procedures in that policy.

 

10. The provisions of this agreement are severable. If any part is found to be unenforceable, all other provisions shall remain fully valid and enforceable.

 

I agree:       Amgen Inc:

/s/ Anthony C. Hooper

   

/s/ Amie Krause

Signature of Staff Member     Signature of Authorized Representative

Anthony C. Hooper

   

Senior Staffing Manager

Print Name of Staff Member     Title of Representative

10/14/2011

    10/18/2011

Date

    Date

 

10


ATTACHMENT 2

AMGEN INC.

CHANGE OF CONTROL SEVERANCE PLAN

AMGEN INC., a Delaware corporation, has established this Change of Control Severance Plan, as amended and restated, effective as of December 9, 2010, as subsequently amended effective March 2, 2011 (the “Plan”) for the benefit of certain key employees of Amgen Inc. and Covered Subsidiaries (as defined below).

The purposes of the Plan are as follows:

 

  (1) To reinforce and encourage the continued attention and dedication of members of the Company’s management to their assigned duties without the distraction arising from the possibility of a change of control of the Company;

 

  (2) To enable and encourage the Company’s management to focus their attention on obtaining the best possible deal for the Company’s stockholders and to make an independent evaluation of all possible transactions, without being influenced by their personal concerns regarding the possible impact of various transactions on the security of their jobs and benefits; and

 

  (3) To provide severance benefits to any Participant (as defined below) who incurs a termination of employment under the circumstances described herein within a certain period following a Change of Control (as defined below).

 

  1. Defined Terms. For purposes of the Plan, the following terms shall have the meanings indicated below:

 

  (A) “Accountants” shall mean the Company’s independent registered public accountants serving immediately prior to the Change of Control; provided, however, that in the event that the Accountants are also serving as accountant or auditor for the individual, entity or group effecting the Change of Control, the Administration Committee shall appoint another nationally recognized public accounting firm to make the calculations required hereunder (which accounting firm shall then be referred to as the Accountants hereunder).

 

  (B) “Administration Committee” shall mean the committee which is responsible for administering the Plan, as described in Section 3(A) hereof.

 

  (C) “Amgen Retirement Savings Plan” shall mean the Amgen Retirement and Savings Plan, As Amended and Restated Effective January 1, 2010, or any successor plan.

 

  (D) “Amgen Supplemental Retirement Plan” shall mean the Amgen Inc. Supplemental Retirement Plan, Amended and Restated Effective January 1, 2009, or any successor plan.

 

  (E) “Benefits Continuation Period” shall mean the earlier to occur of (i) the expiration of a Participant’s eligibility for coverage under COBRA, and (ii) the expiration of the eighteen (18) month period immediately following the Participant’s Date of Termination.

 

  (F) “Benefits Multiple” shall mean (i) with respect to each Group I Participant, two (2), (ii) with respect to each Group II Participant, two (2), and (iii) with respect to each Group III Participant, one (1).

 

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  (G) “Board” shall mean the Board of Directors of the Company.

 

  (H) “Cash Severance Payment” shall mean a lump sum cash payment in an amount equal to the product of (x) the Participant’s Benefits Multiple, and (y) the sum of (i) the Participant’s annual base salary as in effect immediately prior to the Date of Termination or, if higher, as in effect immediately prior to the Change of Control, plus (ii) the Participant’s targeted annual bonus for the year in which such Date of Termination occurs (determined as the product of the Participant’s annual base salary and the Participant’s target annual bonus percentage, each as in effect immediately prior to the Date of Termination or, if higher, as in effect immediately prior to the Change of Control).

 

  (I) “Cause,” with respect to any Participant, shall mean (i) the Participant’s conviction of a felony, or (ii) the engaging by the Participant in conduct that constitutes willful gross neglect or willful gross misconduct in carrying out the Participant’s duties, resulting, in either case, in material economic harm to the Company, unless the Participant believed in good faith that such conduct was in, or not contrary to, the best interests of the Company. For purposes of clause (ii) above, no act, or failure to act, on the Participant’s part shall be deemed “willful” unless done, or omitted to be done, by the Participant not in good faith.

 

  (J) A “Change of Control” of the Company shall be deemed to have occurred at any of the following times:

 

  (i) upon the acquisition (other than from the Company) by any person, entity or “group,” within the meaning of Section 13(d)(3) or 14(d)(2) of the Exchange Act (excluding, for this purpose, the Company or its affiliates, or any employee benefit plan of the Company or its affiliates which acquires beneficial ownership of voting securities of the Company), of beneficial ownership (within the meaning of Rule 13d-3 promulgated under the Exchange Act) of fifty percent (50%) or more of either the then outstanding shares of Common Stock or the combined voting power of the Company’s then outstanding voting securities entitled to vote generally in the election of directors; or

 

  (ii) at the time individuals who, as of December 9, 2010, constitute the Board (the “Incumbent Board”) cease for any reason to constitute at least a majority of the Board, provided, that any person becoming a director subsequent to December 9, 2010, whose election, or nomination for election by the Company’s stockholders, was approved by a vote of at least a majority of the directors then comprising the Incumbent Board (other than an election or nomination of an individual whose initial assumption of office is in connection with an actual or threatened election contest relating to the election of the directors of the Company) shall be, for purposes of the Plan, considered as though such person were a member of the Incumbent Board; or

 

  (iii) immediately prior to the consummation by the Company of a reorganization, merger, consolidation, (in each case, with respect to which persons who were the stockholders of the Company immediately prior to such reorganization, merger or consolidation do not, immediately thereafter, own more than fifty percent (50%) of the combined voting power entitled to vote generally in the election of directors of the reorganized, merged or consolidated company’s then outstanding voting securities) or a liquidation or dissolution of the Company or the sale of all or substantially all of the assets of the Company; or

 

  (iv) the occurrence of any other event which the Incumbent Board in its sole discretion determines constitutes a Change of Control.

 

12


  (K) “Change of Control Period” shall mean the period beginning on the date of a Change of Control and ending on the second anniversary of such Change of Control.

 

  (L) “COBRA” shall mean the Consolidated Omnibus Budget Reconciliation Act of 1985, as amended.

 

  (M) “Code” shall mean the Internal Revenue Code of 1986, as amended from time to time.

 

  (N) “Common Stock” shall mean the common stock of the Company, par value $0.0001 per share.

 

  (O) “Company” shall mean Amgen Inc., a Delaware corporation, and, except in determining under Section 1(J) hereof whether or not any Change of Control of the Company has occurred, shall include any successor to its business and/or assets. “Company” shall exclude any disregarded entity pursuant Treasury Regulations section 301.7701-3, unless the Plan is amended to designate the disregarded entity’s employees as Participants.

 

  (P) “Compensation Committee” shall mean the Compensation and Management Development Committee of the Board.

 

  (Q) “Confidential Information” shall mean information disclosed to the Participant or known by the Participant as a consequence of or through his or her relationship with the Company, about the customers, employees, business methods, public relations methods, organization, procedures or finances, including, without limitation, information of or relating to customer lists, of the Company and its affiliates.

 

  (R) “Covered Subsidiaries” shall mean those Subsidiaries of the Company which are incorporated in any of the fifty states of the United States or the District of Columbia, except as otherwise determined in writing by the Administration Committee in its sole discretion and designated on Annex A attached hereto as maintained by the Administration Committee.

 

  (S) “Date of Termination” shall mean with respect to any purported termination of a Participant’s employment (other than by reason of the Participant’s death), (i) if the Participant’s employment is terminated for Disability, the date upon which a Notice of Termination is given, and (ii) if the Participant’s employment is terminated for any other reason, whether voluntarily or involuntarily, the date that the Participant’s employment terminates, as specified in the Notice of Termination (which shall be within sixty (60) days from the date such Notice of Termination is given).

 

  (T) “Disability” shall be determined in accordance with the Company’s long-term disability plan as in effect immediately prior to a Change of Control.

 

  (U) “Exchange Act” shall mean the Securities Exchange Act of 1934, as amended from time to time.

 

13


  (V) “Good Reason,” with respect to any Participant, shall mean the occurrence (without the Participant’s express written consent) of any of the following conditions, but only if (1) the Participant provides written notice to the Company of the existence of the condition within thirty (30) days of the initial existence of the condition; (2) the Company fails to remedy the condition within the thirty (30)-day period following the Company’s receipt of the notice delivered pursuant to clause (1); and (3) the Participant actually terminates employment within thirty (30) days following the expiration of the thirty (30)-day period described above in clause (2):

(i) any adverse and material diminution in the Participant’s authority, duties or responsibilities as they existed immediately prior to the Change of Control or as the same may be increased from time to time thereafter;

(ii) the Company’s material reduction of the Participant’s annual base salary as in effect immediately prior to the Change of Control;

(iii) relocation of the Company’s offices at which the Participant is employed immediately prior to the Change of Control which increases the Participant’s daily commute by more than one-hundred (100) miles on a round trip basis; or

(iv) any other action or inaction by the Company that constitutes a material breach of the agreement under which the Participant provides services.

A Participant’s right to terminate his or her employment for Good Reason shall not be affected by the Participant’s incapacity due to physical or mental illness.

 

  (W) “Group I Participants” shall mean those staff members of the Company, who hold the title of senior vice president or equivalent and above, and any other senior executive-level staff members of the Company and the Covered Subsidiaries whom the Administration Committee has designated as Group I Participants, as such group shall be constituted immediately prior to a Change of Control. At or before the occurrence of a Change of Control, the Company shall notify the Group I Participants in writing of their status as Participants in the Plan.

 

  (X) “Group II Participants” shall mean those management-level staff members of the Company and the Covered Subsidiaries at Level 8 or equivalent and above and who are not Group I Participants, as such group shall be constituted immediately prior to a Change of Control. At or before the occurrence of a Change of Control, the Company shall notify the Group II Participants in writing of their status as Participants in the Plan.

 

  (Y) “Group III Participants” shall mean those management-level staff members of the Company and the Covered Subsidiaries at Level 7 or equivalent, as such group shall be constituted immediately prior to a Change of Control. At or before the occurrence of a Change of Control, the Company shall notify the Group III Participants in writing of their status as Participants in the Plan.

 

  (Z) “Notice of Termination” shall mean a notice which shall indicate the specific termination provision in the Plan relied upon and shall set forth in reasonable detail the facts and circumstances claimed to provide a basis for termination of the Participant’s employment under the provision so indicated.

 

  (AA) “Participants” shall mean, collectively, the Group I Participants, the Group II Participants and the Group III Participants.

 

  (BB) “Proprietary Information Agreement” shall mean the Company’s form of Proprietary Information and Inventions Agreement in the form in effect immediately prior to a Change of Control.

 

  (CC) Subsidiary” shall mean any entity (other than the Company), in an unbroken chain of entities beginning with the Company if each of the entities other than the last entity in the unbroken chain beneficially owns, at the time of the determination, securities or interests representing more than fifty percent (50%) of the total combined voting power of all classes of securities or interests in one of the other entities in such chain.

 

14


  2. Effective Date and Term of Plan. The Plan, as amended and restated, shall be effective as of December 9, 2010 and shall continue in effect through December 31, 2014; provided, however, that commencing on December 31, 2014 and on each December 31 thereafter, the Plan shall automatically be extended for one additional year by adding one year to the last day of the term as then in effect unless, not later than November 30 of such year, the Company shall have given notice to the Participants that the term of the Plan will not be extended; provided, further, that if a Change of Control occurs during the original or any extended term of the Plan, the term of the Plan shall continue in effect for a period of not less than twenty-four (24) months beyond the month in which such Change of Control occurred.

 

  3. Administration.

 

  (A) The Plan shall be interpreted, administered and operated by the Compensation Committee, except that if the Compensation Committee determines that a Change of Control is likely to occur, the Compensation Committee shall appoint a person or group of persons who shall constitute the Administration Committee after the occurrence of the Change of Control, which Administration Committee shall have the power to interpret, administer and operate the Plan after the occurrence of the Change of Control. The Administration Committee shall have complete authority, in its sole discretion subject to the express provisions of the Plan, to determine who shall be a Participant, to interpret the Plan, to prescribe, amend and rescind rules and regulations relating to it, and to make all other determinations necessary or advisable for the administration of the Plan. The Administration Committee may delegate any of its duties hereunder to such person or persons from time to time as it may designate.

 

  (B) All expenses and liabilities which members of the Administration Committee incur in connection with the administration of the Plan shall be borne by the Company. The Administration Committee may employ attorneys, consultants, accountants, appraisers, brokers, or other persons in connection with such administration, and the Administration Committee, the Company and the Company’s officers and directors shall be entitled to rely upon the advice, opinions or valuations of any such persons. No member of the Compensation Committee, the Administration Committee or the Board shall be personally liable for any action, determination or interpretation made in good faith with respect to the Plan, and all members of the Compensation Committee, the Administration Committee and the Board shall be fully protected by the Company in respect of any such action, determination or interpretation.

 

  4. Benefits Provided.

 

  4.1 Termination After Change of Control. If a Participant’s employment is terminated during a Change of Control Period (a) by the Company other than for Cause or Disability, or (b) by the Participant for Good Reason, the Company shall pay the Participant the amounts, and provide the Participant with the benefits, described in this Section 4.1.

 

  (A) Cash Severance Payment. In lieu of any further salary payments to the Participant for periods subsequent to the Date of Termination and in lieu of any severance benefit otherwise payable to the Participant (other than accrued vacation and similar benefits otherwise payable upon termination of employment pursuant to Company policies and programs), the Company shall pay to the Participant the Cash Severance Payment.

 

  (B)

Benefits. Subject to subsection (B) of Section 11.6 hereof, if, as a result of the Participant’s termination of employment, the Participant becomes entitled to, and timely

 

15


  elects to continue, health care (including any applicable vision benefits) and/or dental coverage under COBRA, the Company shall provide the Participant and his or her dependents with Company-paid group health and dental insurance continuation coverage under COBRA during the Benefits Continuation Period.

 

  (C) The Company shall pay to the Participant any earned but unpaid portion of the Participant’s base salary as of the Date of Termination at the rate in effect at the time Notice of Termination is given, plus all other amounts to which the Participant is entitled under any compensation plan or practice of the Company at the time such payments are due.

 

  (D) The Participant shall be fully vested in his or her accrued benefits under the Amgen Retirement Savings Plan and the Amgen Supplemental Retirement Plan, as applicable. The Company shall provide the Participant with either, in the Company’s sole discretion, a lump-sum cash payment or a contribution to the Amgen Supplemental Retirement Plan, in an amount equal to the sum of (1) the product of $2,500 and the Benefits Multiple and (2) the product of (x) 0.10, (y) the sum of (i) the Participant’s annual base salary as in effect immediately prior to the Date of Termination or, if higher, as in effect immediately prior to the Change of Control, plus (ii) the Participant’s targeted annual bonus for the year in which such Date of Termination occurs (determined as the product of the Participant’s annual base salary and the Participant’s target annual bonus percentage, each as in effect immediately prior to the Date of Termination or, if higher, as in effect immediately prior to the Change of Control) and (z) the Benefits Multiple. Subject to subsection (B) of Section 11.6 hereof, payment under this Section 4.1(D) will be made within 45 days (or as soon thereafter as is administratively practicable) after the Date of Termination, but in no event more than two and one-half months after the end of the calendar year in which the Date of Termination occurs.

 

  (E) In any situation where under applicable law the Company has the power to indemnify (or advance expenses to) the Participant in respect of any judgments, fines, settlements, loss, cost or expense (including attorneys’ fees) of any nature related to or arising out of the Participant’s activities as an agent, employee, officer or director of the Company or in any other capacity on behalf of or at the request of the Company, the Company shall promptly on written request, indemnify (and advance expenses to) the Participant to the fullest extent permitted by applicable law. Such agreement by the Company shall not be deemed to impair any other obligation of the Company respecting the Participant’s indemnification otherwise arising out of this or any other agreement or promise of the Company or under any statute.

 

  (F) For the four (4) year period immediately following the Date of Termination, the Company shall furnish each Participant who was a director and/or officer of the Company at any time prior to the Date of Termination with directors’ and/or officers’ liability insurance, as applicable, insuring the Participant against insurable events which occur or have occurred while the Participant was a director or officer of the Company, such insurance to have policy limits aggregating not less than the amount in effect immediately prior to the Change of Control, and otherwise to be in substantially the same form and to contain substantially the same terms, conditions and exceptions as the liability insurance policies provided for officers and directors of the Company in force from time to time, provided, however, that if the aggregate annual premiums for such insurance at any time during such period exceed one hundred and fifty percent (150%) of the per annum rate of premium currently paid by the Company for such insurance, then the Company shall provide the maximum coverage that will then be available at an annual premium equal to one hundred and fifty percent (150%) of such rate.

 

16


4.2

 

  (A) All calculations required to be made under Section 4.1 hereof, including the amount of the Cash Severance Payment and the assumptions to be utilized in arriving at such calculations shall be made by the Accountants. The Accountants shall provide the Participant and the Company with detailed supporting calculations with respect to such calculations at least fifteen (15) business days prior to the date of the Change of Control (or as soon as practicable in the event that the Accountants have less than fifteen (15) business days advance notice of the potential occurrence of the Change of Control) with respect to the impact of any payment which will be made to the Participant before, at or immediately after the Change of Control and from time to time thereafter to the extent that the Participant may become entitled to receive any additional payments or benefits which would affect the amount of any “excess parachute payments” within the meaning of Section 280G(b)(1) of the Code payable to the Participant in order that the Participant may determine whether it is in the best interest of the Participant to waive the receipt of any or all amounts which may constitute “excess parachute payments.” Any calculation by the Accountants shall be binding upon the Company and the Participant. All fees and expenses of the Accountants under this Section 4.2 shall be borne solely by the Company.

 

  (B) Notwithstanding any other provision of this Plan, in the event that any payment or benefit received or to be received by the Participant, including any payment or benefit received in connection with a termination of the Participant’s employment, whether pursuant to the terms of this Plan or any other plan, arrangement or agreement, (all such payments and benefits, including the payments and benefits under Section 4 hereof, being hereinafter referred to as the “Total Payments”) would be subject (in whole or part), to the excise tax imposed under Section 4999 of the Code (the “Excise Tax”), then, after taking into account any reduction in the Total Payments provided by reason of Section 280G of the Code in such other plan, arrangement or agreement, the payments under this Plan shall be reduced in the order specified below, to the extent necessary so that no portion of the Total Payments is subject to the Excise Tax but only if (i) the net amount of such Total Payments, as so reduced (and after subtracting the net amount of federal, state and local income taxes on such reduced Total Payments and after taking into account the phase out of itemized deductions and personal exemptions attributable to such reduced Total Payments) is greater than or equal to (ii) the net amount of such Total Payments without such reduction (but after subtracting the net amount of federal, state and local income taxes on such Total Payments and the amount of Excise Tax to which the Participant would be subject in respect of such unreduced Total Payments and after taking into account the phase out of itemized deductions and personal exemptions attributable to such unreduced Total Payments). The payments and benefits under this Plan shall be reduced in the following order: (A) reduction of any cash severance payments otherwise payable to the Participant that are exempt from Section 409A of the Code; (B) reduction of any other cash payments or benefits otherwise payable to the Participant that are exempt from Section 409A of the Code, but excluding any payments attributable to any acceleration of vesting or payments with respect to any equity award that are exempt from Section 409A of the Code; (C) reduction of any other payments or benefits otherwise payable to the Participant on a pro-rata basis or such other manner that complies with Section 409A of the Code, but excluding any payments attributable to any acceleration of vesting and payments with respect to any equity award that are exempt from Section 409A of the Code; and (D) reduction of any payments attributable to any acceleration of vesting or payments with respect to any equity award that are exempt from Section 409A of the Code, in each case beginning with payments that would otherwise be made last in time.

 

  (C)

For purposes of determining whether and the extent to which the Total Payments will be subject to the Excise Tax, (i) no portion of the Total Payments the receipt or enjoyment of which the Executive shall have waived at such time and in such manner as not to constitute a “payment” within the meaning of Section 280G(b) of the Code shall be taken into account; (ii) no portion of the Total Payments shall be taken into account which, in

 

17


  the written opinion of the Accountants, does not constitute a “parachute payment” within the meaning of Section 280G(b)(2) of the Code (including by reason of Section 280G(b)(4)(A) of the Code) and, in calculating the Excise Tax, no portion of such Total Payments shall be taken into account which, in the opinion of the Accountants, constitutes reasonable compensation for services actually rendered, within the meaning of Section 280G(b)(4)(B) of the Code, in excess of the Base Amount (as defined in Section 280G(b)(3) of the Code) allocable to such reasonable compensation; and (iii) the value of any non-cash benefit or any deferred payment or benefit included in the Total Payments shall be determined by the Accountants in accordance with the principles of Sections 280G(d)(3) and (4) of the Code.

 

  4.3 Subject to subsection (B) of Section 11.6 hereof, the cash payments provided in subsections (A), (C) and (D) of Section 4.1 hereof shall be made by the fifth (5th) day following the receipt by the Participant of the Accountants’ calculation, but in no event later than March 15 of the calendar year following the calendar year in which the Participant’s employment is terminated. As a result of uncertainty in the application of Section 280G and Section 4999 of the Code at the time of the initial calculation by the Accountants hereunder, it is possible that the Cash Severance Payment made by the Company will have been less than the Company should have paid pursuant to Section 4.1(A) hereof, as the case may be (the amount of any such deficiency, the “Underpayment”) or more than the Company should have paid pursuant to Section 4.1(A) hereof, as the case may be (the amount of any such overage, the “Overpayment”). In the event of an Underpayment, the Company shall pay the Participant the amount of such Underpayment (together with interest at 120% of the rate provided in Section 1274(b)(2)(B) of the Code) not later than five (5) business days after the amount of such Underpayment is subsequently determined, provided, however, such Underpayment shall not be paid later than the end of the calendar year following the calendar year in which the Participant remitted the related taxes. In the event of an Overpayment, the amount of such Overpayment shall constitute a loan by the Company to the Participant, payable not later than five (5) business days after the amount of such Overpayment is subsequently determined (together with interest at 120% of the rate provided in Section 1274(b)(2)(B) of the Code).

 

  4.4 At the time that any payments are made under the Plan, the Company shall provide the Participant with a written statement setting forth the manner in which such payments were calculated and the basis for such calculations including, without limitation, any opinions or other advice the Company has received from its counsel, the Accountants or other advisors or consultants (and any such opinions or advice which are in writing shall be attached to the statement).

 

  5. Termination Procedures.

 

  5.1 Notice of Termination. Any purported termination of a Participant’s employment following a Change of Control (other than by reason of death) shall be communicated by written Notice of Termination from one party to the other party in accordance with Section 8 hereof. Further, no termination for Cause shall be effective without (a) reasonable notice to the Participant setting forth the reasons for the Company’s intention to terminate which specifies the particulars thereof in detail, and (b) in the case of clause (ii) of the definition of Cause above, an opportunity for the Participant to cure such Cause within twenty (20) days after receipt of such notice. With respect to the Group I Participants, the Notice of Termination must include a written statement that a majority of the entire membership of the Board has determined that the Participant was guilty of the conduct constituting Cause. With respect to Group II Participants and Group III Participants, the Notice of Termination must include a written statement by one of the Participant’s direct or indirect supervisors that the supervisor has determined that the Participant was guilty of conduct constituting Cause.

 

18


  6. No Mitigation. The Company agrees that, in order for a Participant to be eligible to receive the payments and other benefits described herein, the Participant is not required to seek other employment or to attempt in any way to reduce any amounts payable to the Participant by the Company pursuant to Section 4 hereof. Further, the amount of any payment or benefit provided for in the Plan shall not be reduced by any compensation earned by the Participant as the result of employment by another employer, by retirement benefits, by offset against any amount claimed to be owed by the Participant to the Company, or otherwise.

 

  7. Successors; Binding Agreement.

7.1

 

  (A) The Company shall require any successor (whether direct or indirect, by purchase, merger, consolidation or otherwise) to all or substantially all of the business and/or assets of the Company to expressly assume the Plan and all obligations of the Company hereunder in the same manner and to the same extent that the Company would be so obligated if no such succession had taken place.

 

  (B) This Plan shall inure to the benefit of and shall be binding upon the Company, its successors and assigns, but without the prior written consent of the Participants the Plan may not be assigned other than in connection with the merger or sale of any part of the business and/or assets of the Company or similar transaction in which the successor or assignee assumes (whether by operation of law or express assumption) all obligations of the Company hereunder.

 

  7.2 This Plan shall inure to the benefit of and be enforceable by the Participant’s personal or legal representatives, executors, administrators, successors, heirs, distributees, devisees, legatees or other beneficiaries. If a Participant shall die while any amount would still be payable to such Participant hereunder (other than amounts which, by their terms, terminate upon the death of the Participant) if such Participant had continued to live, all such amounts, unless otherwise provided herein, shall be paid in accordance with the terms of the Plan to the executors, personal representatives or administrators of such Participant’s estate.

 

  8. Notices. For the purpose of the Plan, notices and all other communications provided for in the Plan shall be in writing and shall be deemed to have been duly given when delivered or mailed by United States registered mail, return receipt requested, postage prepaid, addressed, if to a Participant, to the address on file with the Company and, if to the Company, to the address set forth below, or to such other address as either party may have furnished to the other in writing in accordance herewith, except that notice of change of address shall be effective only upon actual receipt:

One Amgen Center Drive

Thousand Oaks, California 91320-1789

Attention: Corporate Secretary

 

  9. Claims Procedures; Expenses.

 

  9.1 The Participant’s assertion of a right to benefits under, in connection with, or in any way related to the Plan constitutes Participant’s agreement to resolve covered disputes against any person or entity pursuant to this Section 9.

 

19


  9.2 Claim for Benefits. A Participant may file with the Administration Committee a written claim for benefits under the Plan. The Administration Committee shall, within a reasonable time not to exceed ninety (90) days, unless special circumstances require an extension of time of not more than an additional ninety (90) days (in which event a Participant will be notified of the delay during the first ninety (90) day period), provide adequate notice in writing to any Participant whose claim for benefits shall have been denied, setting forth the following in a manner calculated to be understood by the Participant: (i) the specific reason or reasons for the denial; (ii) specific reference to the provision or provisions of the Plan on which the denial is based; (iii) a description of any additional material or information required to perfect the claim, and an explanation of why such material or information is necessary; and (iv) information as to the steps to be taken in order that the denial of the claim may be reviewed, including a statement of the Participant’s right to bring an action under Section 502(a) of the Employee Retirement Income Security Act of 1974, as amended (“ERISA”) following an adverse determination of the claim.

 

  9.3 Review of Claims. If a Participant’s claim has been denied and the Participant wishes to submit a request for a review of such claim, the Participant must follow the claims review procedure below:

 

  (A) Upon the denial of a claim for benefits, a Participant may file a request for review of the claim, in writing, with the Administration Committee or any person or persons to whom the Administration Committee has delegated its duties hereunder, including a claims processor;

 

  (B) The Participant must file the claim for review not later than 60 days after the Participant has received written notification of the denial of the claim;

 

  (C) The Participant has the right to review and obtain copies of all relevant documents relating to the denial of the claim and to submit any issues and comments, in writing, to the Administration Committee;

 

  (D) If the claim is denied, the Administration Committee must provide the Participant with written notice of this denial within 60 days after the Administration Committee’s receipt of the Participant’s written claim for review. There may be times when this 60-day period may be extended. This extension may only be made, however, when there are special circumstances that are communicated to the Participant in writing within the 60-day period. If there is an extension, a decision will be made as soon as possible, but not later than 120 days after receipt by the Administration Committee of the claim for review; and

 

  (E) The Administration Committee’s decision on the claim for review will be communicated to the Participant in writing, and if the claim for review is denied in whole or part, the decision will include: (i) the specific reason or reasons for the denial; (ii) specific reference to the provision or provisions of the Plan on which the denial is based; (iii) a statement that the Participant may receive, upon request and free of charge, reasonable access to and copies of, all documents, records and other information relevant to the claim; and (iv) a statement of the Participant’s right to bring an action under Section 502(a) of ERISA.

 

  9.4

Expenses, Legal Fees. The Company shall pay to the Participant all reasonable expenses (including reasonable attorneys’ fees and legal expenses) incurred by the Participant with respect to any dispute or controversy arising under or in connection with the Plan (including, without limitation, all such fees and expenses, if any, incurred in contesting or disputing any termination of the Participant’s employment or in seeking to obtain or enforce any right or benefit provided by the Plan, or in connection with any tax audit or

 

20


  proceeding to the extent attributable to the application of Section 4999 of the Code to any payment or benefit provided hereunder) if the Participant prevails on any material issue which is in dispute with respect to such dispute or controversy. The Company shall make such payments no later than the last day of the Participant’s taxable year immediately following the taxable year in which the expenses are incurred.

 

  10. Confidentiality; Non-Solicitation.

 

  10.1 Confidentiality. With respect to each Participant, during the Participant’s Benefits Continuation Period, the Participant shall not directly or indirectly disclose or make available to any person, firm, corporation, association or other entity for any reason or purpose whatsoever, any Confidential Information. Upon termination of a Participant’s employment with the Company, all Confidential Information in the Participant’s possession that is in written or other tangible form (together with all copies or duplicates thereof, including computer files) shall be returned to the Company and shall not be retained by the Participant or furnished to any third party, in any form except as provided herein; provided, however, that the Participant shall not be obligated to treat as confidential, or return to the Company copies of any Confidential Information that (i) was publicly known at the time of disclosure to the Participant, (ii) becomes publicly known or available thereafter other than by any means in violation of the Plan or any other duty owed to the Company by any person or entity, or (iii) is lawfully disclosed to the Participant by a third party. In addition, each Participant shall be subject to the Company’s policies regarding proprietary information and inventions, as set forth in the Proprietary Information Agreement.

 

  10.2 Non-Solicitation. In addition to each Participant’s obligations under the Proprietary Information Agreement, during a Participant’s Benefits Continuation Period, the Participant shall not, either on the Participant’s own account or jointly with or as a manager, agent, officer, employee, consultant, partner, joint venturer, owner or stockholder or otherwise on behalf of any other person, firm or corporation, directly or indirectly solicit or attempt to solicit away from the Company any of its officers or employees or offer employment to any person who is an officer or employee of the Company; provided, however, that a general advertisement to which an employee of the Company responds shall in no event be deemed to result in a breach of this Section 10.2.

 

  10.3 Breach; Violation. In the event that a Participant breaches or violates any provision of Section 10.1 or 10.2 hereof, the Participant shall thereupon forfeit any right and interest of the Participant to receive payments or benefits hereunder, and the Company shall thereupon have no further obligation to provide such payments or benefits to the Participant hereunder.

 

  10.4 Survival of Provisions. The provisions of this Section 10 shall survive the termination or expiration of the applicable Participant’s employment with the Company and shall be fully enforceable thereafter. If it is determined by a court of competent jurisdiction in any state that any restriction in this Section 10 is excessive in duration or scope or is unreasonable or unenforceable under the laws of that state, it is the intention of the parties that such restriction may be modified or amended by the court to render it enforceable to the maximum extent permitted by the law of that state.

 

  11. Miscellaneous.

 

  11.1 No Waiver. No waiver by the Company or any Participant, as the case may be, at any time of any breach by the other party of, or of any lack of compliance with, any condition or provision of the Plan to be performed by such other party shall be deemed a waiver of similar or dissimilar provisions or conditions at the same or at any prior or subsequent time. All other plans, policies and arrangements of the Company in which the Participant participates during the term of the Plan shall be interpreted so as to avoid the duplication of benefits paid hereunder.

 

21


  11.2 No Right to Employment. Nothing contained in the Plan or any documents relating to the Plan shall (i) confer upon any Participant any right to continue as a Participant or in the employ of the Company or a subsidiary, (ii) constitute any contract or agreement of employment, or (iii) interfere in any way with the at-will nature of the Participant’s employment with the Company.

 

  11.3 Termination and Amendment of Plan. The Company shall have the right to amend (and to amend or cancel any amendments), or, subject to Section 2 hereof, terminate the Plan at any time by resolution of the Board; provided, however, that after a Change of Control, the Company may not terminate the Plan and no amendment to the Plan shall be made which removes any Participant from participation in the Plan, which amends subsection (W), (X) or (Y) of Section 1 hereof or which adversely affects a Participant’s interests without the express written consent of the Participant(s) so affected. Subject to Section 10.3 hereof, notwithstanding anything contained herein to the contrary, all obligations accrued by Participants prior to any termination of the Plan must be satisfied in full in accordance with the terms hereof.

 

  11.4 Benefits not Assignable. Except as otherwise provided herein or by law, no right or interest of any Participant under the Plan shall be assignable or transferable, in whole or in part, either directly or by operation of law or otherwise, including, without limitation, by execution, levy, garnishment, attachment, pledge or in any manner; no attempted assignment or transfer thereof shall be effective; and no right or interest of any Participant under the Plan shall be liable for, or subject to, any obligation or liability of such Participant. When a payment is due under the Plan to a Participant who is unable to care for his or her affairs, payment may be made directly to his or her legal guardian or personal representative.

 

  11.5 Tax Withholding. The Company shall withhold from any payments made to a Participant under this Plan all federal, state and local income, employment and other taxes that the Company reasonably determines to be required to be withheld by the Company in connection with such payments, in amounts and in a manner to be determined in the sole discretion of the Company. Except to the extent specifically provided within this Plan or any separate written agreement between a Participant and the Company, a Participant shall be solely responsible for the satisfaction of any taxes with respect to the benefits payable to the Participant under this Plan (including, but not limited to, employment taxes imposed on employees and additional taxes on nonqualified deferred compensation).

 

  11.6 Code Section 409A.

 

  (A) Generally. Although the Company intends and expects that the Plan and its payments and benefits will not give rise to taxes imposed under Section 409A of the Code, neither the Company, nor its employees, directors, or agents shall have any obligation to mitigate or to hold any Participant harmless from any or all of such taxes.

 

  (B)

Section 409A Six-Month Delayed Payment Rule. If any payments or benefits that become payable under this Plan on account of the Participant’s termination of employment constitute a deferral of compensation under Code Section 409A, such payments or benefits will be provided when the Participant incurs a “separation from service” within the meaning of Treasury Regulation § 1.409A-1(h) or successor provision (“Separation from Service”). If, at the time of the Participant’s Separation from Service, the Participant is a “specified employee” (within the meaning of Section 409A of the Code and Treasury Regulation Section 1.409A-1(i) or successor provision), the Company will

 

22


  not pay or provide any “Specified Benefits” (as defined herein) during the six-month period beginning with the date of the Participant’s Separation from Service (the “409A Suspension Period”). In the event of a Participant’s death, however, the Specified Benefits shall be paid to the Participant’s Beneficiary without regard to the 409A Suspension Period. For purposes of this Plan, “Specified Benefits” are any payments or benefits that would be subject to Section 409A additional taxes if the Company were to pay them, pursuant to this Plan, on account of the Participant’s “separation from service.” Within 14 calendar days after the end of the 409A Suspension Period, the Participant shall be paid a lump-sum payment in cash equal to any Specified Benefits delayed during the 409A Suspension Period.

 

  11.7 California Law. This Plan shall be construed, interpreted and the rights of the parties determined in accordance with the laws of the State of California, to the extent not preempted by federal law, which shall otherwise control.

 

  11.8 Validity. The invalidity or unenforceability of any provision of the Plan shall not affect the validity or enforceability of any other provision of the Plan, which shall remain in full force and effect. If the Plan shall for any reason be or become unenforceable by either party, the Plan shall thereupon terminate and become unenforceable by the other party as well.

 

23


ANNEX A

AMGEN INC. CHANGE OF CONTROL SEVERANCE PLAN

SUBSIDIARIES EXCLUDED FROM THE DEFINITION “COVERED SUBSIDIARIES”

Effective March 2, 2011, the following designated Subsidiaries shall be excluded from the definition “Covered Subsidiaries” in the Amgen Inc. Change of Control Severance Plan (the “Plan”) and such designation shall remain in effect until modified by the Administration Committee as defined in the Plan:

NONE

 

24

Sourcing and Supply Agreement

Exhibit 10.52

Note: Redacted portions have been marked with [*]. The redacted portions are subject to a request for

confidential treatment that has been filed with the Securities and Exchange Commission.

SOURCING AND SUPPLY AGREEMENT

This Sourcing and Supply Agreement (this “Agreement”) is made by and between Amgen USA Inc. (“Amgen”), a wholly-owned subsidiary of Amgen Inc., and DaVita Inc. (“Dialysis Center”) to set forth the terms and conditions upon which Dialysis Center Purchasers shall purchase EPOGEN® (Epoetin alfa) and Amgen shall provide discounts and pay rebates to Dialysis Center on EPOGEN. Each of Amgen and Dialysis Center are referred to herein as a “Party” and together as the “Parties”. Amgen Inc. is a party to this Agreement for the purposes set forth in Sections 3.1, 8.2, 9.4, 9.5.1, and 11.14 of this Agreement. Capitalized terms used herein and not otherwise defined herein shall have the meaning set forth in Section 1.

RECITALS

WHEREAS, Amgen is a leading innovator in the field of ESAs with expertise in the field of anemia management and the ability to manufacture and supply safe and efficacious ESAs for the treatment of dialysis patients;

WHEREAS, Dialysis Center is a leading provider of dialysis services in the Territory with expertise in establishing and delivering state-of-the-art, quality-of-care standards, practices and procedures for the care of patients undergoing dialysis;

WHEREAS, Dialysis Center desires to select one ESA supplier to meet its primary ESA needs on a long term basis for patients undergoing dialysis;

WHEREAS, Dialysis Center has evaluated the ESAs available for commercial use and those in clinical development, including potential [*] ESAs, and has determined that EPOGEN® (Epoetin alfa) will be its preferred ESA for managing anemia for patients undergoing dialysis;

WHEREAS, the Parties wish to enter into this Agreement to, among other things, provide for Dialysis Center’s selection of Amgen as the Dialysis Center Purchasers’ supplier of EPOGEN to meet the Dialysis Center Purchasers’ requirements for EPOGEN for the treatment of dialysis patients during the Term, on all of the terms provided herein;

WHEREAS, Dialysis Center seeks stable, predictable and competitive pricing over a seven year period, which it can achieve through the discounts, rebates and other price concessions set forth herein;

WHEREAS, in order to provide Dialysis Center with such pricing over a seven year period, Amgen will make substantial long-term investments and forego other potential opportunities to scale and schedule its manufacturing capacity and supply of EPOGEN for Dialysis Center Purchasers in accordance with Dialysis Center Purchasers’ anticipated demand for EPOGEN for use in the Territory as provided under this Agreement;

NOW THEREFORE, in consideration of the foregoing recitals and of the mutual promises and covenants set forth herein, and for other good and valuable consideration, the receipt and sufficiency of which is hereby acknowledged, and intending to be legally bound, each Party hereby agrees as follows:

 

1.

DEFINITIONS

When used with initial capitals herein, the following terms shall have the meaning ascribed to them below:

 

Page 1 of 136


1.1.

Actual Supply Shortfall” has the meaning set forth in Section 2.5.

 

1.2.

Added Dialysis Center Purchaser” has the meaning set forth in Section 2.8.2.

 

1.3.

Added Dialysis Center Purchaser Effective Date” has the meaning set forth in Section 2.8.2.

 

1.4.

Added Dialysis Center Purchaser Transaction Date” means with respect to each Added Dialysis Center Purchaser: (a) in the case of a new Dialysis Center Affiliate, the effective date of the acquisition or establishment of the new Dialysis Center Affiliate; or (b) in the case of a new Managed Center, the earlier of (i) the effective date of the contract pursuant to which a dialysis facility becomes a Managed Center or (ii) the date Dialysis Center first provides services to a dialysis facility that results in such facility becoming a Managed Center, in each case after the Term Start Date.

 

1.5.

Administrator” has the meaning set forth in Section 9.2.1.

 

1.6.

Affiliate” of a given entity shall mean an entity that controls, is controlled by, or under common control with such given entity. Control shall mean ownership of more than fifty percent (50%) of the voting stock of an entity or, for non-stock entities, the right to more than fifty percent (50%) of the profits of such entity.

 

1.7.

[*]” has the meaning set forth in Section 2.5.1.

 

1.8.

Alternative ESA” means an ESA that is available for use in the Territory that is not EPOGEN or Aranesp.

 

1.9.

Alternative ESA Purchase Amount” has the meaning set forth in Section 2.1.1.

 

1.10.

Alternative ESA Purchase Event” has the meaning set forth in Section 2.1.1.

 

1.11.

Alternative ESA Purchase Event Share of Sales” shall be calculated as follows

        [*]

A = Committed Unit Purchases of Amgen ESAs during the [*] which an Alternative ESA Purchase Event has occurred

B = Committed Unit Purchases of Amgen ESAs during the [*] which such Alternative ESA Purchase Event has occurred

C = Committed Unit Purchases of Alternative ESAs during the [*] which an Alternative ESA Purchase Event has occurred

D = Committed Unit Purchases of Alternative ESAs during the [*] which such Alternative ESA Purchase Event has occurred

 

1.12.

Amgen Business Representative” has the meaning set forth in Section 4.1.

 

1.13.

[*]” means [*] for use with patients receiving Dialysis Services, which [*] is the subject of a written agreement between the Parties or their Affiliates.

 

1.14.

Amgen ESA Risk Evaluation Program” has the meaning set forth in Section 11.18.

 

1.15.

Amgen ESAs Share of Sales” shall mean Committed [*] Purchases of Amgen ESAs during the Quarter divided by the sum of Committed [*] Purchases of Amgen ESAs and Committed [*] Purchases of Alternative ESAs during the Quarter.

 

Page 2 of 136


Amgen ESAs Share of Sales Illustration:

Committed [*] Purchases of Amgen ESAs

÷

Committed [*] Purchases of Amgen ESAs + Committed [*] Purchases of Alternative ESAs

 

1.16.

Amgen Indemnitees” has the meaning set forth in Section 9.5.2.

 

1.17.

Appeal Procedures” has the meaning set forth in Section 9.2.3.

 

1.18.

Aranesp” means Amgen’s proprietary darbepoetin alfa product that is marketed by Amgen in the Territory under the trademark Aranesp®.

 

1.19.

Arbitrator” has the meaning set forth in Section 9.2.1.

 

1.20.

Authorized Removal Occurrence” has the meaning set forth in Section 2.8.3.

 

1.21.

Authorized Wholesalers” shall mean those wholesalers listed on Exhibit B, as such list may be modified pursuant to Section 2.7.

 

1.22.

Authorized Wholesaler List” has the meaning set forth in Section 2.7.

 

1.23.

Available EPOGEN SKUs” have the meaning set forth in Section 2.4.5.

 

1.24.

Award” has the meaning set forth in Section 9.2.3.

 

1.25.

Base Invoice Discount” means the base invoice discount described in Section 2.1 of Exhibit A.

 

1.26.

Base Rate Rebate” means the base rebate described in Section 3.1 of Exhibit A.

 

1.27.

Baseline [*]” has the meaning set forth in Section 2.1.2.

 

1.28.

[*] Rebate” means the [*] rebate described in Section 3.2 of Exhibit A.

 

1.29.

Best Price” has the meaning set forth in Section 3.6.

 

1.30.

[*] Rebate” means the [*] rebate described in Section 3.3 of Exhibit A.

 

1.31.

Business Representatives” has the meaning set forth in Section 4.1.

 

1.32.

Certification” has the meaning set forth in Section 5.2.

 

1.33.

Committed [*] Purchases of Amgen ESAs” means, for any period, the aggregate amounts in [*] of EPOGEN and Aranesp purchased by all Dialysis Center Committed Purchasers during such period for use in providing Dialysis Services, net of product returns and adjustments, which aggregate [*] data have been independently confirmed by Amgen through the Relevant Information.

 

1.34.

Committed [*] Purchases of Alternative ESAs” means, for any period, the aggregate amounts in [*] of all Alternative ESAs purchased by all Dialysis Center Committed Purchasers from any source during such period for use in providing Dialysis Services, (provided that any Alternative ESA provided to a Dialysis Center Committed Purchaser at no or nominal cost from any source shall be considered a purchase), adjusted to be an equivalent [*] of EPOGEN (in [*]) based on the [*] (if the [*] is clearly set forth therein) or otherwise as reasonably determined pursuant to Section 2.1.2, and which aggregate [*] data have been independently confirmed by Amgen through the Relevant Information.

 

1.35.

Compensation Data” has the meaning set forth in Section 6.1.

 

1.36.

Confidential Information” has the meaning set forth in Section 11.14.

 

Page 3 of 136


1.37.

Data” means the data set forth on Schedule 1 provided by Dialysis Center to Amgen pursuant to the terms and conditions of Section 5 and Exhibit A.

 

1.38.

Debarred Party” has the meaning set forth in Section 10.2.3.

 

1.39.

Designated Affiliates” shall mean any Affiliate of Dialysis Center listed on Exhibit C, as such list may be modified pursuant to Section 2.8.1.

 

1.40.

Designated Affiliates List” has the meaning set forth in Section 2.8.1.

 

1.41.

Dialysis Center Business Representative” has the meaning set forth in Section 4.1.

 

1.42.

Dialysis Center Committed Purchasers” has the meaning set forth in Section 2.8.5.

 

1.43.

Dialysis Center Committed Purchasers List” has the meaning set forth in Section 2.8.5.

 

1.44.

Dialysis Center Indemnitees” has the meaning set forth in Section 9.5.1.

 

1.45.

Dialysis Center Purchasers” shall mean Dialysis Center, the Designated Affiliates, and the Managed Centers. Dialysis Center Purchasers include Added Dialysis Center Purchasers from and after the Added Dialysis Center Purchaser Effective Date.

 

1.46.

Dialysis Services” means services related to the treatment of patients receiving renal dialysis, including hemodialysis, peritoneal dialysis, nocturnal dialysis, and home hemodialysis in the Territory during the Term.

 

1.47.

Disclosing Party” has the meaning set forth in Section 11.14.

 

1.48.

Discounts” means all rebates and discounts set forth on Exhibit A that may be earned by the Dialysis Center Purchasers pursuant to the terms and conditions set forth in this Agreement, which shall be earned, calculated and vested as provided in Exhibit A.

 

1.49.

Disputes” has the meaning set forth in Section 9.1.

 

1.50.

[*]” has the meaning set forth in Section 2.1.2.

 

1.51.

EPOGEN” means Amgen’s proprietary epoetin alfa product that is marketed by Amgen in the Territory under the trademark EPOGEN®.

 

1.52.

EPOGEN Equivalent Quantity” has the meaning set forth in Section 2.1.1.

 

1.53.

ESAs” shall mean agents that stimulate erythropoiesis.

 

1.54.

FDA” has the meaning set forth in Section 8.3.

 

1.55.

FDA Website” has the meaning set forth in Section 11.18.

 

1.56.

Firm” has the meaning set forth in Section 3.2.

 

1.57.

Forecast Shortfall” has the meaning set forth in Section 2.4.2.

 

1.58.

Forecast Shortfall Amount” has the meaning set forth in Section 2.4.2.

 

1.59.

Force Majeure Event” has the meaning set forth in Section 11.8.

 

1.60.

Governmental Authority” shall mean in respect of any individual or entity, any government administrative agency, commission or other governmental authority, body or instrumentality, or any federal, state, or local governmental regulatory body having legal jurisdiction over that individual or entity.

 

1.61.

Gross Purchases of Amgen ESAs” means, for any period, the aggregate gross amounts paid for purchases of EPOGEN and Aranesp by all Dialysis Center Purchasers during such period for use in providing Dialysis Services, calculated by using [*] in effect on

 

Page 4 of 136


 

each date of purchase, net of product returns and adjustments, which aggregate sales data have been independently confirmed by Amgen through the Relevant Information.

 

1.62.

Hearing” has the meaning set forth in Section 9.2.3.

 

1.63.

HIPAA” shall mean the Health Insurance Portability and Accountability Act of 1996 and its implementing regulations, each as may be amended.

 

1.64.

IMS” means IMS Health Incorporated, a Delaware corporation and its Affiliates.

 

1.65.

Indemnified Party” has the meaning set forth in Section 9.6.1.

 

1.66.

Indemnifying Party” has the meaning set forth in Section 9.6.1.

 

1.67.

Individually Identifiable Health Information” shall have the meaning specified in HIPAA.

 

1.68.

Initial [*]” has the meaning set forth in Section 2.1.2.

 

1.69.

[*]” means an [*] for EPOGEN, Aranesp or an Alternative ESA, as applicable, based on its measured biological activity or effect.

 

1.70.

Joint Project” has the meaning set forth in Section 7.1.

 

1.71.

Joint Project Committee” has the meaning set forth in Section 7.1.

 

1.72.

Law” means, individually and collectively, any and all applicable laws, ordinances, rules, regulations, directives, administrative circulars, guidances and other pronouncements having the effect of law of any Governmental Authority.

 

1.73.

Liquidated Damages” has the meaning set forth in Section 10.3.

 

1.74.

Managed Center” shall mean a dialysis facility that is not an Affiliate of Dialysis Center but for which Dialysis Center or an Affiliate of Dialysis Center provides management services or administrative services in which it controls the selection or procurement of ESAs.

 

1.75.

Managed Centers List” has the meaning set forth in Section 2.8.1.

 

1.76.

Material Label Change” means a material amendment, change, revision, and/or modification to the Chronic Kidney Disease section of the Boxed Warning of the US prescribing information for EPOGEN as it relates to dialysis use.

 

1.77.

Minimum Forecast Commitment” has the meaning set forth in Section 2.4.2.

 

1.78.

[*] Rebate” means the [*] rebate described in Section 3.4 of Exhibit A.

 

1.79.

Non-Disclosing Party” has the meaning set forth in Section 11.14.

 

1.80.

Notice of Added Dialysis Center Purchaser” has the meaning set forth in Section 2.8.2.

 

1.81.

Objection Notice” has the meaning set forth in Section 3.2.

 

1.82.

Other Agreement(s)” has the meaning set forth in Section 2.2.

 

1.83.

Other Agreement Early Termination Date” has the meaning set forth in Section 2.2.

 

1.84.

Party” and “Parties” have the meaning set forth in the preamble hereto.

 

1.85.

[*]” has the meaning set forth in Section 5.5.

 

1.86.

Permitted Percentage Variances” has the meaning set forth in Section 2.4.3.

 

1.87.

Permitted Variance Period” has the meaning set forth in Section 2.4.3.

 

1.88.

Policies and Procedures” has the meaning set forth in Section 2.8.6.

 

1.89.

Project Plan” has the meaning set forth in Section 7.1.

 

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1.90.

Project Proposal” has the meaning set forth in Section 7.1.

 

1.91.

Purchase Commitment” has the meaning set forth in Section 2.1.

 

1.92.

Qualified Gross Purchases of EPOGEN” shall mean the amount of EPOGEN purchased by Dialysis Center Purchasers during the Term from an Authorized Wholesaler (or from Amgen pursuant to Section 2.7) for use in providing Dialysis Services, and confirmed by Amgen through sales tracking data. Qualified Gross Purchases of EPOGEN shall be calculated using the [*] in effect at the time of the relevant purchase, net of product returns and adjustments.

 

1.93.

Quarter” shall mean each calendar quarter during the Term (i.e., January 1 through March 31, April 1 through June 30, July 1 through September 30, and/or October 1 through December 31, as applicable).

 

1.94.

Recall” has the meaning set forth in Section 11.19.

 

1.95.

Relevant Information” means the Data, all sales tracking data, Self-Reported Purchase Data, Compensation Data and other relevant information, including relevant Third Party reporting agency data.

 

1.96.

Research Study” has the meaning set forth in Section 5.5.

 

1.97.

Rolling Forecast” has the meaning set forth in Section 2.4.1.

 

1.98.

Rolling Forecasts” has the meaning set forth in Section 2.4.1.

 

1.99.

Rules” has the meaning set forth in Section 9.2.1.

 

1.100.

Self-Reported Purchase Data” means all [*] purchased of each ESA and the number of patients who received each such ESA from Dialysis Center Purchasers and such other related data as may be specified on Exhibit SR-1.

 

1.101.

[*]” has the meaning set forth in Section 5.5.

 

1.102.

Supply Commitment” has the meaning set forth in Section 2.1.

 

1.103.

Supply Shortfall” has the meaning set forth in Section 2.5.

 

1.104.

Supply Shortfall Notice” has the meaning set forth in Section 2.5.

 

1.105.

Supply Shortfall Quarter” has the meaning set forth in Section 2.5.

 

1.106.

Term” means the period commencing on the Term Start Date and ending on the Term End Date.

 

1.107.

Term End Date” shall mean December 31, 2018.

 

1.108.

Term Start Date” shall mean January 1, 2012.

 

1.109.

Termination Date” means the date upon which this Agreement shall have been terminated in accordance with the terms and conditions of this Agreement pursuant to Section 10.2.

 

1.110.

Territory” means the United States, and its territories and possessions, including Puerto Rico.

 

1.111.

Third Party” means any individual or entity other than a Party or an Affiliate of a Party (or, in the case of Dialysis Center, a Managed Center).

 

1.112.

Third Party Claim(s)” has the meaning set forth in Section 9.5.1.

 

1.113.

[*]” shall mean the [*] for EPOGEN to [*] as established by [*] in its [*] from time to time, not including prompt pay or other discounts, rebates, or reductions in [*].

 

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2. PURCHASE AND SUPPLY COMMITMENTS

 

2.1.

Purchase and Supply Commitments. Subject to the terms and conditions of this Agreement, (i) the Dialysis Center Committed Purchasers shall purchase from Amgen through one or more Authorized Wholesalers those quantities of EPOGEN that are needed to meet an Amgen ESAs Share of Sales of at least ninety percent (90%) during each Quarter of the Term (the “Purchase Commitment”), and (ii) Amgen shall ensure that during each Quarter of the Term [*] percent ([*]%) of the [*] for each such Quarter is available for purchase by the Dialysis Center Purchasers from one or more Authorized Wholesalers (the “Supply Commitment”). Subject to Section 2.3.2 and Section 2.3.3, Amgen acknowledges and agrees that nothing in this Agreement shall prohibit any Dialysis Center Committed Purchaser from purchasing an amount of EPOGEN necessary to satisfy the Purchase Commitment in a particular Quarter regardless of whether such EPOGEN was actually administered by the Dialysis Center Committed Purchasers to their patients for the provision of Dialysis Services during such Quarter.

 

  2.1.1.

Alternative ESA Purchases. If in any Quarter the Dialysis Center Committed Purchasers do not meet the Purchase Commitment (an “Alternative ESA Purchase Event”), then Dialysis Center shall (i) within thirty (30) days of the end of any such applicable Quarter provide notice to Amgen of such Alternative ESA Purchase Event, including the Committed [*] Purchases of Alternative ESAs in such Quarter and (ii) within thirty (30) days of the end of the Quarter immediately following the Quarter in which the Alternative ESA Purchase Event occurred, the Committed [*] Purchases of Alternative ESAs in such subsequent Quarter. If Dialysis Center provides such notice pursuant to this Section 2.1.1, or if Amgen, in its sole discretion, through the use of Relevant Information determines that there has been an Alternative ESA Purchase Event, then Amgen shall have the right to deliver to Dialysis Center a notice that sets forth the “EPOGEN Equivalent Quantity,” which shall be that quantity of EPOGEN (in [*]) [*] but for the Alternative ESA Purchase Event (based on the [*] (if the [*] is clearly set forth therein), or otherwise as reasonably determined by Amgen through the Relevant Information as set forth in Section 2.1.2). In the event the Alternative ESA Purchase Event Share of Sales is equal to or greater than ninety percent (90%), then Dialysis Center shall be deemed to have met the Purchase Commitment for the Quarter in which the Alternative ESA Purchase Event occurred. If the Alternative ESA Purchase Event Share of Sales is less than ninety percent (90%) for any reason, including a Force Majeure Event related to Dialysis Center and/or the Dialysis Center Purchasers, and not the result of a Supply Shortfall, then Amgen shall deliver to Dialysis Center a notice, and Dialysis Center shall pay to Amgen within thirty (30) days of its receipt of such notice, an amount (the “Alternative ESA Purchase Amount”) indicated by Amgen (as determined by Amgen based on the Relevant Information) in such notice equal to (a) the EPOGEN Equivalent Quantity multiplied by (b) [*] of EPOGEN earned by the Dialysis Center Committed Purchasers during such Quarter. At Amgen’s option, any Alternative ESA Purchase Amount may be offset in whole or in part against any Discounts earned by the Dialysis Center Purchasers on Qualified Gross Purchases of EPOGEN in the applicable Quarter or any subsequent Quarter.

 

  2.1.2.

If a Party, in its reasonable discretion, feels that the Dialysis Center Committed Purchasers potentially may not meet the Purchase Commitment due to purchases of Alternative ESAs by the Dialysis Center Committed Purchasers in a Quarter, then Amgen shall in consultation with Dialysis Center determine the appropriate methodology to be used to determine the [*] (in [*]) of an Alternative ESA that was

 

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used by the Dialysis Center Committed Purchasers patients’ during the applicable measurement period that is equivalent to a [*] (in [*]) of EPOGEN that was used by the Dialysis Center Committed Purchasers patients’ during the applicable measurement period (the “[*]”) and Dialysis Center shall reasonably cooperate with Amgen and provide any other reasonable data, including [*] of ESAs utilized during the applicable measurement period, necessary to complete the determination. If Dialysis Center has a reasonable objection to the methodology proposed by Amgen, the Parties shall appoint a mutually agreeable Third Party to determine the methodology to be used with the costs of such Third Party to be borne equally by the Parties. The initial [*] for any particular Alternative ESA as determined by either the Parties or the Third Party appointed by the Parties, as applicable, pursuant to this Section 2.1.2 (the “Initial [*]”) shall only apply to the Quarter immediately preceding the Initial [*]. The determination of the [*] for each particular Alternative ESA shall be recalculated for each of the first [*] after the Initial [*] for such Alternative ESA and the calculation of the [*] for such Alternative ESA after each Quarter during such [*] period shall only apply to the immediately preceding Quarter after each such recalculation. The [*] for a particular Alternative ESA for all periods after such [*] period shall be the [*] determined as of the end of the [*] Quarter after the Initial [*] for such Alternative ESA (the “Baseline [*]”); provided, either Party may, no more frequently than once per calendar year, request a recalculation of the Baseline [*], which recalculation shall be applied prospectively, if such Party reasonably believes that the Baseline [*] has materially changed over time, in which event the requesting Party shall bear the costs of any Third Party appointed by the Parties in connection therewith.

 

2.2.

Purchase Commitment Transition Period for Added Dialysis Center Purchasers. If, after the Term Start Date, there is a new Added Dialysis Center Purchaser pursuant to Section 2.8.2, that is a Dialysis Center Committed Purchaser, Dialysis Center shall use its commercially reasonable efforts to cause such Added Dialysis Center Purchaser to meet the Purchase Commitment as soon as practicable, but such Added Dialysis Center Purchaser shall not be obligated to meet the Purchase Commitment until [*] days after the Added Dialysis Center Purchaser Effective Date. If, as of the Added Dialysis Center Purchaser Effective Date regarding an Added Dialysis Center Purchaser, such Added Dialysis Center Purchaser was a party to a written agreement with a Third Party which includes an obligation on the part of such Added Dialysis Center Purchaser to exclusively purchase an Alternative ESA to meet a majority of its ESA requirements for the provision of Dialysis Services in the Territory (an “Other Agreement(s)”) and Dialysis Center can demonstrate via reasonable evidence to Amgen that such Other Agreement was entered into by such Added Dialysis Center Purchaser at least [*] days prior to the Added Dialysis Center Purchaser Transaction Date, then such Added Dialysis Center Purchaser shall not be subject to the Purchase Commitment until [*] days after such time that such Other Agreement(s) can be terminated and/or amended to terminate such obligation with respect to the Alternative ESAs without such Added Dialysis Center Purchaser and/or Dialysis Center and/or any of its Affiliates paying any damages and/or other amounts to such Third Party (the “Other Agreement Early Termination Date”); provided that Dialysis Center shall use its best efforts to terminate such Other Agreement as soon Dialysis Center can do so without such Added Dialysis Center Purchaser and/or Dialysis Center and/or any of its Affiliates paying any damages and/or other amounts to such Third Party. Amgen shall not be obligated to meet the Supply Commitment for any Added Dialysis Center Purchaser until the expiration of the [*] day period after the Added Dialysis Center Purchaser Effective Date or, in the case of an

 

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Added Dialysis Center Purchaser that is a party to an Other Agreement, [*] days after the Other Agreement Early Termination Date.

 

2.3.

Eligible Purchases.

 

  2.3.1.

Purchases from Authorized Wholesaler. Only purchases of EPOGEN made by a Dialysis Center Purchaser from an Authorized Wholesaler shall be eligible to receive the Discounts provided under this Agreement.

 

  2.3.2.

Own Use. The Dialysis Center Purchasers shall purchase EPOGEN under this Agreement solely for their own use in providing Dialysis Services, and only purchases made by Dialysis Center Purchasers for such use shall be eligible for the Discounts provided under this Agreement and shall be considered Committed [*] Purchases of Amgen ESAs. Dialysis Center on behalf of itself and each other Dialysis Center Purchaser covenants that none of them shall seek to procure any of the Discounts available under this Agreement for any purchases of EPOGEN not for its or their use in providing Dialysis Services, and Dialysis Center shall promptly notify Amgen in the event Amgen shall have provided any Dialysis Center Purchaser with any Discounts hereunder for any EPOGEN that was not used by them for the provision of Dialysis Services.

 

  2.3.3.

Maximum Quarterly Purchase Increases. Notwithstanding any other provision of this Agreement, no Discounts earned by Dialysis Center shall apply to Qualified Gross Purchases of EPOGEN for any Quarter that exceed [*] percent ([*]%) of the Qualified Gross Purchases of EPOGEN in the immediately preceding Quarter unless Amgen, in its sole discretion, determines that such increase is necessary for Dialysis Center to meet its Purchase Commitment for any such Quarter. Such calculation shall be adjusted to remove from the calculation the effect of any change in [*], or increases/decreases in the number of Dialysis Center Purchasers during the relevant comparison periods.

 

2.4.

Quantity Forecasts and Minimum Forecast Commitment.

 

  2.4.1.

Rolling Forecast. Each Quarter during the Term, Dialysis Center shall submit in writing to Amgen a rolling [*] month forecast setting forth on a month-by-month basis the aggregate quantities in [*] of EPOGEN by Available EPOGEN SKU that Dialysis Center has determined in good faith are required for all Dialysis Center Purchasers for each month in the forecast period, starting with an initial [*] month forecast beginning as of [*] which shall be delivered to Amgen by [*] (each, a “Rolling Forecast” and collectively the “Rolling Forecasts”). With the exception of the initial Rolling Forecast, Dialysis Center shall submit each Rolling Forecast by no later than the [*] of the [*] of each Quarter during the Term (e.g., by [*] Dialysis Center shall submit a Rolling Forecast for the [*] month period from [*] through [*]). The Rolling Forecasts shall not reflect any EPOGEN requirements for periods after the Term End Date. If Dialysis Center has not timely delivered a Rolling Forecast as provided above, the Rolling Forecast previously in effect shall remain in effect for the periods covered thereby. The purpose of this Section 2.4.1 is to allow Amgen adequate time to adjust its manufacturing planning and operations to properly reflect the anticipated mix of Available EPOGEN SKUs.

 

  2.4.2.

Minimum Forecast Commitment. Without reducing or limiting the Purchase Commitment set forth in Section 2.1, the forecasted quantities of each Available EPOGEN SKU for months [*] of each Rolling Forecast shall constitute the Dialysis Center Purchasers’ aggregate minimum purchase commitment of [*] of EPOGEN by Available EPOGEN SKU (the “Minimum Forecast Commitment”). If

 

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the Dialysis Center Purchasers purchase an aggregate quantity in [*] of EPOGEN by Available EPOGEN SKU during any Quarter that is less than the Minimum Forecast Commitment for any such Quarter (the quantity of any such difference, the “Forecast Shortfall”), then Amgen shall notify Dialysis Center of the Forecast Shortfall in writing. If the Dialysis Center Purchasers purchase a quantity in [*] of EPOGEN by Available EPOGEN SKU during the Quarter in which the Forecast Shortfall occurred and the immediately following Quarter in the aggregate that is less than the aggregate Minimum Forecast Commitments for such two Quarters, Amgen shall notify Dialysis Centers of such failure in writing, and within thirty (30) days of Dialysis Center’s receipt of such notice, it shall pay to Amgen an amount equal to [*] percent ([*]%) of (i) the Forecast Shortfall for the applicable Quarter multiplied by (ii) [*] less the Discounts per [*] of EPOGEN for each Available EPOGEN SKU earned by the Dialysis Center Purchasers during such Quarter (the “Forecast Shortfall Amount”). At Amgen’s option, any Forecast Shortfall Amount may be offset in whole or in part against any Discounts earned by the Dialysis Center Purchasers on purchases of EPOGEN in the applicable Quarter or any subsequent Quarter.

 

  2.4.3.

Forecast Variance. Each Rolling Forecast provided by Dialysis Center may [*] quantities of each Available EPOGEN SKU only for new months [*] and may [*] quantities of each Available EPOGEN SKU in the new months [*] from the corresponding months in the immediately prior Rolling Forecast by the “Permitted Percentage Variances” in the table below. The Permitted Percentage Variances for the months of each Rolling Forecast (the “Permitted Variance Period”) are as follows:

 

Months

     [ *]      [ *]      [ *]      [ *]      [ *] 

Permitted Percentage Variance

     [ *]%      [ *]%      [ *]%      [ *]%      [ *]% 

If Dialysis Center submits a Rolling Forecast that contains a forecast for any month therein that is not in compliance with this Section 2.4.3, Amgen shall have the right, in its sole discretion, to either (a) accept such forecast for any month therein that is not in compliance with this Section; or (b) adjust such non-compliant forecasted quantity for any such month to increase or decrease the amount forecasted for such month by up to the minimum amount necessary to bring such forecasted quantity into compliance with this Section 2.4.3. Dialysis Center may, at any time for any good faith reason, request additional variances to the Permitted Percentage Variances and, in such event, the Parties shall work in good faith to accommodate such request; provided, however, that (i) in no event shall Amgen be liable for any resulting Supply Shortfall or Actual Supply Shortfall and (ii) Dialysis Center shall remain liable for any Forecast Shortfall that may occur. If in any Quarter during the Term, the Dialysis Center Purchasers have a Forecast Shortfall and the Parties have determined, after good faith discussions, that such Forecast Shortfall is the necessary result of a Material Label Change, then the Dialysis Center Purchasers shall not be liable for such Forecast Shortfall.

 

  2.4.4.

Good Faith Estimates. Each Rolling Forecast submitted by Dialysis Center shall represent good faith estimates of the Dialysis Center Purchasers’ actual anticipated purchases of EPOGEN for the treatment of dialysis patients in the

 

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Territory and reasonable inventory requirements for EPOGEN in the Territory during the relevant timeframes.

 

  2.4.5.

Available EPOGEN SKUs. The Available EPOGEN SKU Schedule attached as Schedule 3 hereto sets forth the “Available EPOGEN SKUs” as of the Term Start Date. Amgen may add Available EPOGEN SKUs to, or remove Available EPOGEN SKUs (with respect to all purchasers of EPOGEN for free-standing dialysis clinics) from, the Available EPOGEN SKUs Schedule upon at least [*] advance written notice to Dialysis Center; provided that Amgen may not remove any Available EPOGEN SKUs from the Available EPOGEN SKUs Schedule that accounted for [*] percent ([*]%) or more of the Qualified Gross Purchases of EPOGEN during the immediately preceding [*] without the prior written consent of Dialysis Center, which consent may be withheld by Dialysis Center in its sole discretion, unless there is an Available EPOGEN SKU that corresponds to the same dosage, size and potency of the deleted Available EPOGEN SKU; and provided further that, notwithstanding the foregoing, Amgen may immediately remove any Available EPOGEN SKU should Amgen determine, in its sole discretion, that the removal of any such Available EPOGEN SKU is for safety or quality or similar reasons. The Parties shall mutually agree upon (a) the first period for which any such new Available EPOGEN SKU may be ordered by the Dialysis Center Purchasers and (b) any permitted adjustments to the EPOGEN SKU mix contained in Dialysis Center’s then applicable Rolling Forecast to reflect any changes in the Available EPOGEN SKUs or as otherwise may be required due to any production shortfall applicable to all EPOGEN customers.

 

2.5.

Supply Commitment Shortfalls. Dialysis Center shall promptly notify Amgen in writing (the “Supply Shortfall Notice”) if a Dialysis Center Purchaser has not been able to purchase from the Authorized Wholesalers a quantity of EPOGEN in [*] for any Available EPOGEN SKU that meets the Minimum Forecast Commitment for any Quarter for any reason, including as a result of a Force Majeure Event related to Amgen (a “Supply Shortfall Quarter”), setting forth in such notice the quantity of EPOGEN in [*] by Available EPOGEN SKU representing such shortfall, including as a result of a Force Majeure Event related to Amgen (the “Supply Shortfall”). In the event of a Supply Shortfall, Amgen shall not intentionally discriminate against any of the Dialysis Center Purchasers in its allocation of the available quantities of an Available EPOGEN SKU subject to such Supply Shortfall by making its allocation decisions, in whole or in part, on the basis of the prices, Discounts, and/or other financial terms offered to the Dialysis Center Purchasers pursuant to the terms and conditions of this Agreement. In no event shall the inability to obtain a particular Available EPOGEN SKU in a Minimum Forecast Commitment be deemed a Supply Shortfall, if a Dialysis Center Purchaser can purchase (i) the same quantity of EPOGEN in [*] through other Available EPOGEN SKUs or (ii) Aranesp, other than with respect to use by physicians with privileges at a Dialysis Center Purchaser who have obtained approval through Dialysis Center’s formulary exception process to use a “short-acting” Alternative ESA instead of Aranesp. If the Authorized Wholesalers are actually unable to supply the Dialysis Center Purchasers with a quantity of (i) EPOGEN or (ii) Aranesp equal to the Supply Shortfall within the time period reasonably required by the Dialysis Center Purchasers as set forth in the Supply Shortfall Notice, which in no event will be less than five (5) business days after Amgen’s receipt of the applicable Supply Shortfall Notice, the Purchase Commitment shall be reduced by the quantity of any Supply Shortfall that actually occurs (the “Actual Supply Shortfall”).

 

  2.5.1.

In the event of an Actual Supply Shortfall, Dialysis Center shall use good faith efforts to procure any Alternative ESAs from a Third Party at the [*]. Dialysis

 

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Center shall deliver to Amgen a statement setting forth the aggregate [*] (i.e., the aggregate [*] less all applicable discounts, rebates, chargebacks and other price adjustments) actually paid by the Dialysis Center Purchasers to any such Third Party for that quantity of Alternative ESAs purchased by such Dialysis Center Purchasers during the Supply Shortfall Quarter solely as a substitute for the Actual Supply Shortfall (the “[*]”); provided that should Dialysis Center be subject to any confidentiality restrictions that Dialysis Center may have with any Third Party from which it procured Alternative ESAs, then the Parties agree to send such [*] to the Firm to be verified. Amgen shall pay to Dialysis Center an amount of cash equal to the difference, if any, between (a) the [*] and (b) the product of (i) (1) [*] in effect for the Supply Shortfall Quarter less (2) the Discounts per [*] of Available EPOGEN SKU earned by the Dialysis Center Purchasers in such Supply Shortfall Quarter multiplied by (ii) the Actual Supply Shortfall. Amgen shall also pay to Dialysis Center any incremental difference in the aggregate [*] of Aranesp purchased by Dialysis Center Purchasers as a result of the Supply Shortfall compared to the aggregate [*] of EPOGEN unless Amgen shall have notified Dialysis Center in advance that Dialysis Center Purchasers may purchase an Alternative ESA as opposed to Aranesp during the Actual Supply Shortfall.

 

  2.5.2.

Upon the completion of an Actual Supply Shortfall, the Purchase Commitment, with respect to the quantities of EPOGEN in [*] of the Available EPOGEN SKUs that constitute the Actual Supply Shortfall shall be suspended for a period of [*] days to allow the Dialysis Center Purchasers to transition back from any Alternative ESA’s used by the Dialysis Center Purchasers during such Actual Supply Shortfall back to such applicable Available EPOGEN SKU.

 

  2.5.3.

Provided that Amgen complies with its obligations under Section 2.5.1, then Amgen will not be in breach of Section 2.1 and the Supply Commitment as a result of the Actual Supply Shortfall.

 

2.6.

[*]. The Dialysis Center Purchasers shall purchase EPOGEN from an Authorized Wholesaler at the then-prevailing [*] (subject to any wholesaler markup, discount, services fees or other charges), and any Discounts shall be applied in accordance with the schedules and terms set forth in Exhibit A and this Agreement. Amgen reserves the right to change [*] at any time, by any amount, without notice. Amgen shall promptly notify Dialysis Center of any change to [*].

 

2.7.

Authorized Wholesalers. Prior to the Term Start Date, Dialysis Center shall select one or more Authorized Wholesalers from the Authorized Wholesaler list prepared by Amgen and set forth on Exhibit B (as such list may be amended from time to time as provided in this Agreement, the “Authorized Wholesaler List”), and only such selected Authorized Wholesalers shall be Authorized Wholesalers for purposes of this Agreement. From and after the Term Start Date, Dialysis Center shall have the right to change its selection of Authorized Wholesalers from the Authorized Wholesaler List with thirty (30) days prior written notice to Amgen. Dialysis Center may request Amgen to add wholesalers to the Authorized Wholesaler List, and Amgen, at its sole discretion, shall have the right to determine whether to approve of such addition to the Authorized Wholesaler List. Amgen shall have the right to add or remove wholesalers from the Authorized Wholesaler List set forth on Exhibit B in the exercise of its commercially reasonable discretion by thirty (30) days prior written notice to Dialysis Center, provided that for any removal (a) Amgen removes such Authorized Wholesaler with respect to providing EPOGEN to all purchasers of EPOGEN for free standing dialysis clinics, or (b) such Authorized Wholesaler requests Amgen to remove it as an Authorized Wholesaler for

 

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Dialysis Center Purchasers. In the event of any removal of an Authorized Wholesaler from the Authorized Wholesaler List by Amgen, Amgen shall work with Dialysis Center to transition the Dialysis Center Purchasers’ purchases of EPOGEN to an alternative Authorized Wholesaler, and if no alternative Authorized Wholesaler exists at such time, the Parties shall use reasonable efforts to establish a direct purchasing relationship in any interim period between the removal of the removed Authorized Wholesaler and the initiation of purchases from a new Authorized Wholesaler, if no Authorized Wholesaler exists at such time. Any such direct purchasing relationship shall be subject to credit qualification and the approval by Amgen of an application for direct ship account. If the Dialysis Center Purchasers purchase EPOGEN directly from Amgen as contemplated in this Section 2.7, all purchases of EPOGEN made from Amgen by such Dialysis Center Purchasers shall be deemed Qualified Gross Purchases of EPOGEN and eligible for the Discounts.

 

2.8.

Dialysis Center Purchasers

 

  2.8.1.

Designated Affiliates and Managed Centers. Only the Designated Affiliates listed on Exhibit C (as such list may be amended from time to time as provided in this Agreement, the “Designated Affiliates List”) and the Managed Centers set forth on Exhibit D (as such list may be amended from time to time as provided in this Agreement, the “Managed Centers List”) shall be Dialysis Center Purchasers for purposes of this Agreement. Dialysis Center shall promptly update and maintain the accuracy of the Designated Affiliates List and the Managed Centers List throughout the Term, but in no event later than thirty (30) days after the addition or removal of a Dialysis Center Purchaser pursuant to Section 2.8.2 or 2.8.3 below. Dialysis Center shall not acquire, divest, restructure, reorganize or reclassify its Affiliates or Managed Centers, or request any addition or removal of any Dialysis Center Purchaser, with the purpose or intent in whole or in part to avoid or eliminate its obligations or commitments, or the obligations and commitments of each of the Dialysis Center Purchasers set forth in this Agreement.

 

  2.8.2.

Addition of Dialysis Center Purchasers. After the Term Start Date, subject to Amgen’s reasonable consent under this Section 2.8.2, all new Affiliates and Managed Centers in the Territory shall be added to this Agreement and become Dialysis Center Purchasers. Dialysis Center shall provide prior written notice to Amgen of each new Affiliate and Managed Center in the Territory (each a “Notice of Added Dialysis Center Purchaser”), which notice shall include the proposed Added Dialysis Center Purchaser Transaction Date, plus any additional information regarding the proposed Dialysis Center Purchaser that Amgen shall reasonably request. Upon Amgen’s reasonable consent and subject to the terms and conditions of Section 2.2 with respect to the Purchase Commitment, the Designated Affiliates List and the Managed Centers List shall be amended to include such Affiliates or Managed Centers effective as of the later of (i) thirty (30) days from the date of Amgen’s receipt of a Notice of Added Dialysis Center Purchaser or (ii) the applicable Added Dialysis Center Purchaser Transaction Date (each such effective date, the “Added Dialysis Center Purchaser Effective Date”, and each of the Affiliates and Managed Centers added by such amendments, an “Added Dialysis Center Purchaser”). The Designated Affiliates List and the Managed Centers List shall be amended without further action required of the Parties to reflect additions made in accordance with this Section 2.8.2.

 

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  2.8.3.

Removal of Dialysis Center Purchasers. (A) Dialysis Center may remove Designated Affiliates from the Designated Affiliates List and Managed Centers from the Managed Center List only (i) upon the written consent of Amgen, which consent shall not be unreasonably withheld, conditioned, and/or delayed or (ii) upon thirty (30) days prior written notice to Amgen in the event such removal is a result of a (a) sale of all or substantially all of the assets or equity interests of a Designated Affiliate to a Third Party, whether by reorganization, merger, sales of assets, or sale of equity interests, (b) permanent closure of a Designated Affiliate facility or (c) termination of the relevant management agreement for a Managed Center that has ceased its management relationship with Dialysis Center and/or any Affiliate of Dialysis Center (each of the events described in this clause (ii), an “Authorized Removal Occurrence”). Dialysis Center shall provide Amgen written notice describing the nature of any requested removal, including the anticipated effective date of any Authorized Removal Occurrence, and such removal shall be effective thirty (30) days after Amgen has provided Dialysis Center with written consent to such removal or such earlier period as may be agreed to by Amgen or, in the event of an Authorized Removal Occurrence, the effective date of the Authorized Removal Occurrence.

(B) Amgen shall also have the right to remove any Designated Affiliates from the Designated Affiliates List and any Managed Centers from the Managed Centers List upon thirty (30) days (or such shorter /period as may be required by Law or any Governmental Authority) written notice to Dialysis Center (a) that such removal is required by order of a court or Governmental Authority or (b) in instances in which Amgen determines, in its reasonable discretion, that such removal is required (i) to comply with Law or (ii) as a result of any such Designated Affiliate’s or Managed Center’s negligence or willful misconduct in the use or administration of EPOGEN.

(C) The Designated Affiliates List and the Managed Centers List shall be amended without further action required of the Parties to reflect removals made in accordance with this Section 2.8.3.

 

  2.8.4.

Adjustments to Rolling Forecast. Following the addition or removal of an Affiliate to or from the Designated Affiliates List or a Managed Center to or from the Managed Centers List, the Parties shall mutually agree in good faith to implement any reasonable and necessary adjustments to the Rolling Forecast to account for such addition or removal of an Affiliate to or from the Designated Affiliates List or a Managed Center to or from the Managed Centers List; provided, that Amgen shall have no obligation under Section 2.5 for an Actual Supply Shortfall in the event that any increase to the quantities of each Available EPOGEN SKU set forth in such adjusted Rolling Forecast is in excess of the applicable Permitted Percentage Variances.

 

  2.8.5.

Dialysis Center Committed Purchasers List. The Dialysis Center Purchasers as of the Term Start Date shall constitute the initial list of “Dialysis Center Committed Purchasers” as listed on Exhibit E (as such list may be amended from time to time as provided in this Agreement, the “Dialysis Center Committed Purchasers List”). Each Added Dialysis Center Purchaser shall automatically be added to the Dialysis Center Committed Purchasers List as of the Added Dialysis Center Purchaser Effective Date unless Amgen shall have provided notice to the contrary prior to the Added Dialysis Center Purchaser Effective Date. Any Dialysis Center Purchaser removed from the Designated Affiliates List or the Managed Center List in accordance with Section 2.8.3 shall automatically be removed from the Dialysis

 

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Center Committed Purchaser List as of the effective date of such removal from the Designated Affiliates List or the Managed Center List. Amgen shall have the right in its sole discretion to add or remove any Dialysis Center Purchasers from the Dialysis Center Committed Purchasers List upon at least fifteen (15) days’ written notice to Dialysis Center, effective as of the first day of the Quarter after the expiration of the fifteen (15) day notice period; provided, that Amgen shall work together with Dialysis Center to agree as to which specific Dialysis Center Purchasers will be added or removed and, in the event, the Parties are unable to agree in a reasonable time, Amgen may in its discretion add or remove specific Dialysis Center Purchasers that are not disproportionate in their use of Alternative ESAs compared to all Dialysis Center Purchasers. For avoidance of doubt, any Dialysis Center Committed Purchaser that is removed from the Dialysis Center Committed Purchasers List but remains on the Designated Affiliates List or the Managed Center List shall still be considered a Dialysis Center Purchaser.

 

  2.8.6.

Access to Dialysis Center Facilities. Amgen covenants and agrees that neither it nor any of its employees and/or agents shall have the right to access to any Individually Identifiable Health Information while accessing any of the Dialysis Center Purchasers’. The Parties acknowledge and agree that (a) all of Dialysis Center’s applicable policies and procedures regarding visitors and any updates thereto (the “Policies and Procedures”) that will be in effect during the Term are and will be available for viewing by Amgen and its employees and/or agents during the Term at http://www.davita.com/about/vendor-policies and (b) Amgen and its employees and/or agents shall have [*] during [*] to the Dialysis Center Purchasers’ facilities for the purpose of promoting and providing [*] regarding [*] and shall abide by all the Policies and Procedures during the Term to the extent that such Policies and Procedures have not changed since the Term Start Date, other than as required by any applicable Law and/or generally accepted industry guidance covering vendor access to facilities, in a manner that would limit Amgen’s rights under this Section 2.8.6; provided, however, that, notwithstanding anything contained in the Policies and Procedures, Amgen’s employees and/or agents shall be permitted to utilize, without any pre-approval or review by Dialysis Center, any Amgen internally approved (i) [*] materials that have been submitted to the FDA, (ii) [*] materials, and (iii) [*] materials, provided, such [*] materials have been previously submitted to Dialysis Center’s Vice President of Clinical Management and Vendor Relations for approval and not objected to by Dialysis Center’s Vice President of Clinical Management and Vendor Relations within [*] business days of such submission; and provided, further, that Amgen shall provide Dialysis Center’s Vice President of Clinical Management and Vendor Relations with copies of all materials to be utilized at the Dialysis Center Purchaser’s facilities prior to their first use at any facility of the Dialysis Center Purchasers.

 

3. DISCOUNTS

 

3.1.

Earning, Calculating, Payment and Vesting of Discounts. All Discounts will be earned, calculated and vested as set forth in Exhibit A. For the purposes of calculating the Discounts hereunder, Qualified Gross Purchases of EPOGEN by any Dialysis Center Purchaser shall be deemed to be made on the date of invoice by an Authorized Wholesaler or Amgen pursuant to Section 2.7 to any such Dialysis Center Purchaser. The Discounts (other than invoice discounts) shall be paid in arrears by electronic funds transfer using information provided to Amgen by Dialysis Center as necessary to enable payment. All Discounts, excluding the Base Rate Rebate and the Base Invoice Discount, shall be conditioned upon material compliance with Section 2.8.6. Amgen Inc.

 

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hereby guarantees Amgen’s obligations to pay all Discounts earned by Dialysis Center hereunder.

 

3.2.

Verification and Audit. Discounts (including any qualification criteria for any Discounts) specified herein and/or any other amounts paid by one Party to the other Party pursuant to this Agreement are subject to verification and audit of the relevant purchase and other data (including the Data, the Self-Reported Data and the Compensation Data), as reasonably necessary to calculate any amounts payable hereunder. Dialysis Center Purchasers shall maintain their books and records in accordance with U.S. generally accepted accounting principles, consistently applied. To the extent either Amgen or Dialysis Center, in its reasonable discretion, determines that it is necessary to verify and confirm the calculation of: (a) any Discount described in this Agreement in order to audit and assure compliance with the terms of this Agreement and/or (b) any other amount that one Party must pay to the other Party under this Agreement, the requesting Party shall provide written notice of same to the other Party (an “Objection Notice”) setting forth in detail any and all items of disagreement related to such computation, statement, and/or amount that must be paid by one Party to the other Party. Amgen and Dialysis Center shall jointly engage (at the requesting Party’s sole cost and expense, subject to any reimbursement by the other Party as set forth below) and refer the items in dispute to a nationally recognized firm of independent, certified public accountants as to which Amgen and Dialysis Center mutually agree (the “Firm”), to resolve any disagreements. Amgen and Dialysis Center will direct the Firm to render a written determination within twenty (20) days of its retention, and Amgen and Dialysis Center and their respective employees and/or agents will cooperate with the Firm during its engagement. The Firm shall keep strictly confidential all data reviewed and information learned or obtained in connection with resolving any Objection Notice and shall report to the requesting Party only the conclusion of its review without the disclosure of any Confidential Information. All reports of the Firm shall be made available to both Parties simultaneously, promptly upon completion, and shall be deemed to conclusively and definitively resolve the related Objection Notice, which shall be reimbursed (if applicable) in accordance with this Section 3.2. Any such audit shall be conducted during normal business hours, and so as not to unreasonably interfere with the business of Amgen and/or any of the Dialysis Center Purchasers. In the event any such audit is requested by Amgen and shows that Dialysis Center Purchasers have submitted incorrect information resulting in Dialysis Center receiving in excess of [*] percent ([*]%) of the amount to which it was entitled in any Quarter, Dialysis Center shall reimburse Amgen for the reasonable costs of such audit; otherwise, Amgen shall be responsible for the costs of such audit. In the event any such audit is requested by Dialysis Center and shows that Dialysis Center Purchasers have submitted correct information but have been underpaid by more than [*] percent ([*]%) of the amount to which they were entitled in any Quarter, Amgen shall reimburse Dialysis Center for the reasonable costs of such audit; otherwise, Dialysis Center shall be responsible for the costs of such audit. The determination of the Firm will be conclusive and binding upon Amgen and Dialysis Center. Following any audit that shows any over or underpayment hereunder, the relevant Party shall, within sixty (60) days, make payment to the other Party for the difference between the amount paid hereunder and the amount actually payable hereunder based upon the results of such audit.

 

3.3.

Adjustments for Changes. In accordance with Section 2.8.2 and/or 2.8.3 above, in the event of an Affiliate’s addition to or deletion from the Designated Affiliates List or a Managed Center’s addition to or deletion from the Managed Centers List during any Quarter of the Term, Amgen shall adjust Qualified Gross Purchases of EPOGEN to account for such Affiliate’s addition to or deletion from the Designated Affiliates List or a

 

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Managed Center’s addition to or deletion from the Managed Centers List by adding or deleting such Designated Affiliates’ or Managed Centers’, as applicable, purchases to or from the relevant Quarter or comparison Quarter (or portion thereof).

 

3.4.

Treatment of Discounts and Rebates.

 

  3.4.1.

Dialysis Center agrees that Dialysis Center Purchasers shall properly disclose and account for all Discounts earned hereunder, in whatever form, in compliance with all applicable federal, state, and local Laws, including §1128B(b) of the Social Security Act, as amended and its implementing regulations. Dialysis Center agrees that, if required by such statutes or regulations, it (together with its Designated Affiliates) shall and it shall cause its Managed Centers to (i) claim the benefit of such Discount received in the fiscal year in which such Discount was earned or the year after, (ii) fully and accurately report the value of such Discount in any cost reports filed under Title XVIII or Title XIX of the Social Security Act, as amended or a state or local health care program, and (iii) provide, upon request by the U.S. Department of Health and Human Services or a state or local agency or any other federally funded state health care program, the information furnished to Dialysis Center Purchasers by Amgen concerning the amount or value of such Discount.

 

  3.4.2.

In order to assist Dialysis Center’s compliance with its obligations as set forth in Section 3.4.1 above, Amgen agrees that it will fully and accurately report all Discounts on the invoices or statements submitted to Dialysis Center and use reasonable efforts to inform Dialysis Center of its obligations to report all such Discounts to the extent specified by 42 C.F.R § 1001.952(h)(2)(ii)(A) or where the value of a Discount is not known at the time of sale, Amgen shall fully and accurately report the existence of the Discount program on the invoices or statements submitted to Dialysis Center and use reasonable efforts to inform Dialysis Center of its obligations to report all such Discounts to the extent specified by 42 C.F.R § 1001.952(h)(2)(ii)(B), and when the value of the Discounts become known, provide Dialysis Center with documentation of the calculation of the Discount identifying the specific goods or services purchased to which the Discount will be applied, in accordance with Section 3.5 below.

 

3.5.

Reports. Within ninety (90) days of the end of each Quarter, Amgen shall provide to Dialysis Center a statement of the Discounts earned hereunder with the itemization of EPOGEN purchases made in a particular Quarter, broken down for each Dialysis Center Purchaser and any other information that Dialysis Center may reasonably request that is reasonably available to Amgen and necessary for Dialysis Center to obtain in order to comply with its obligations hereunder. Dialysis Center agrees that it will provide such information to its Dialysis Center Purchasers in a timely manner in order to allow such Dialysis Center Purchasers to meet their reporting and other obligations hereunder and under applicable Law.

 

3.6.

Best Price Limitation. At any time following the repeal, enactment or modification of any Law, policy, program memorandum, or the interpretation thereof, including a decision by the Centers for Medicare & Medicaid Services, that affects the definition of “Best Price” (which, for purposes of this Agreement, shall mean the price reported in Amgen’s Best Price Submission under Title XIX of the Social Security Act) or the methodology by which Best Price must be calculated, Amgen shall have the right, in its sole discretion, to determine the extent to which any [*] to any Third Party due to such repeal, enactment, modification or decision may impact Amgen’s Best Price calculation under this Agreement alone or in combination with any other [*] in other agreements with Dialysis Center or any Third Party. In the event that Amgen determines reasonably and in good

 

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faith that the then-existing [*] under this Agreement establishes or would establish a new “Best Price,” Amgen shall have the right, in its sole discretion, upon the later of (a) the effective date of such repeal, enactment, modification or decision, or (b) notice to Dialysis Center, to [*] the Discounts offered under this Agreement [*], and shall promptly notify Dialysis Center of the [*]; provided that the [*] as adjusted by Amgen shall result in [*] available to Dialysis Center which would [*] the Best Price prior to the effective date of such repeal, enactment, modification or decision, calculated using the modified definition or methodology by which Best Price is to be calculated.

 

4. GOVERNANCE

 

4.1.

Business Representatives. The “Business Representatives” shall be comprised of: (i) in the case of Amgen, Amgen’s General Manager of the Nephrology Business Unit (the “Amgen Business Representative”); and (ii) in the case of Dialysis Center, the Chief Operating Officer of DaVita Inc. (the “Dialysis Center Business Representative”). Each Business Representative shall be entitled to appoint designees who have been identified to the other Business Representative in writing and have equivalent authority to the Party’s Business Representative or have been expressly given all requisite authority by the Party’s Business Representative.

 

4.2.

Responsibilities of Business Representatives. The Business Representatives shall be responsible for overseeing the Parties’ activities and conduct under this Agreement generally, and for ensuring an appropriate level of oversight. The Business Representatives shall meet in person, via teleconference or videoconference at such times as may be deemed necessary by the Parties).

 

5. PATIENT AND PRODUCT DATA

 

5.1.

Data Submission. Dialysis Center shall deliver all Data to Amgen (or to a data collection vendor specified by Amgen) in the format and manner provided in Exhibit A and subject to the provisions of this Section 5. To the extent Amgen requests that Dialysis Center deliver Data to a data collection vendor, Amgen agrees to cause any such data collection vendor to adhere to and be bound by a substantially similar confidentiality obligation as is applicable to Amgen under this Agreement, and Amgen shall be liable for any failure by any such data collection vendor to act in accordance with such requirements.

 

5.2.

HIPAA Compliance. Neither Party has the intent that Dialysis Center will provide Amgen (or any specified data collection vendor) any Data in violation of HIPAA. Accordingly, the Parties shall engage an appropriately qualified statistician, reasonably acceptable to each Party, who meets the requirements set forth in 45 C.F.R. § 164.514(b)(1) to review the Data and deliver a written certification that shall conclude that, subject to any conditions, requirements or assumptions set forth therein, each delivery of Data pursuant to this Agreement will meet the standards for “de-identification” under HIPAA (the “Certification”). In connection with the Certification, the Parties agree to use their commercially reasonable best efforts to facilitate the completion and delivery of such Certification to each Party in an expedited manner, and Amgen shall bear the pre-approved costs of such Certification. Notwithstanding anything in this Agreement to the contrary, in order to assure compliance, as determined by either Party in its reasonable discretion, with any existing Law relating to patient privacy of medical records, or at any time following the enactment of any Law relating to patient privacy of medical records that in any manner reforms, modifies, alters, restricts, or otherwise affects any of the Data received or to be received in connection with any of the Discounts contemplated under this Agreement, either Party may, upon thirty (30) days’ prior written notice, seek to amend this Agreement with respect to the affected Discount. Dialysis Center and

 

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Amgen shall meet and in good faith mutually agree to modify this Agreement to accommodate any such change in the Law, with the intent to, if possible, retain the essential terms of this Section 5 and the affected Discount and pricing structure of this Agreement.

 

5.3.

Case Identifier. Dialysis Center shall consistently use a unique alpha-numeric code (which shall not be derived from Individually Identifiable Health Information) as a “case identifier” to track the care rendered to each individual patient over time, and such case identifier shall be included in the Data provided to Amgen. The key or list matching patient identities to their unique case identifiers shall not be provided to Amgen.

 

5.4.

Data Use. Amgen and its Affiliates shall have the right to use Data (a) to support verification of the services under this Agreement, (b) for its [*] and [*], development of [*], running [*] analyses, overall analyses of how to improve treatment of patients on dialysis and creating tools by its marketing personnel, (c) in the aggregate for publications as part of a larger data set incorporating comparable clinical data received from other dialysis providers in the Territory and provided that no portion of such data shall be attributed to Dialysis Center or its Affiliates, and (d) for purposes of verifying the Dialysis Center Purchasers’ performance under this Agreement and the calculation of amounts payable hereunder, including verifying the Dialysis Center Purchasers’ Purchase Commitment performance under this Agreement and calculating or determining the Dialysis Center Purchasers’ eligibility to receive any Discount. Notwithstanding the foregoing, without Dialysis Center’s prior written consent (such consent not to be unreasonably conditioned, withheld or delayed): Amgen and its Affiliates shall not (i) disclose to Third Parties the Data provided by Dialysis Center hereunder except (1) in any publication referenced in clause (c) above, (2) pursuant to public health activities, (3) to agents of Amgen bound by obligations of confidentiality no less restrictive than those contained in Section 11.14 or (4) to other Third Parties as required by Law or regulation as determined in Amgen’s discretion; and (ii) sell or resell any such data or derivative works thereof to any Third Party.

 

5.5.

Clinical Research Studies. Dialysis Center and Amgen acknowledge that Dialysis Center, either directly or through DaVita Clinical Research, Inc., an Affiliate of Dialysis Center, may from time to time be engaged in research studies in which patients of the Dialysis Center Purchasers, may serve as clinical trial subjects (a “Research Study”). Notwithstanding any obligation of Dialysis Center in this Agreement to the contrary, including any requirement in Section 3.5 of Exhibit A, Dialysis Center shall not be required to submit Data for any patients of the Dialysis Center Purchasers that are participating in a Research Study (a “[*]”), but shall continue without limitation to be eligible for, and if earned receive, all Discounts granted pursuant to this Agreement, so long as (i) Dialysis Center notifies Amgen of the [*] whose Data will not be delivered by Dialysis Center to Amgen as otherwise required by this Agreement as a result of such patient being a [*], and (ii) the aggregate number of [*] whose Data is excluded by Dialysis Center does not exceed the [*]. For purposes of the foregoing, “[*]” means [*] percent ([*]%) of the aggregate number of persons receiving treatment from the Dialysis Center Purchasers in any calendar month.

 

6. OTHER DATA

 

6.1.

Compensation Data. Dialysis Center agrees that it shall provide the data, with respect to EPOGEN, set forth on Schedule 2 attached hereto (the “Compensation Data”) to Amgen in the electronic format set forth on Schedule 2 on a calendar [*] basis no later than the fourteenth (14th) day of the following calendar [*] following the [*] for which such Compensation Data is being provided. Amgen acknowledges, agrees and covenants

 

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that it shall only use the Compensation Data for sales force targeting and compensation. Dialysis Center and Amgen acknowledge and agree that the Compensation Data does not include and shall never include any Individually Identifiable Health Information of any patient of Dialysis Center Purchasers. Notwithstanding the foregoing, Amgen acknowledges and agrees that Dialysis Center shall only be required to deliver the Compensation Data to Amgen for as long as [*]. Amgen shall indemnify, defend and hold harmless Dialysis Center from and against any and all loss, damage and/or expense (including reasonable attorney’s fees) that it may suffer as a result of claims, demands, actions, proceedings, liabilities, costs or judgments, or threats thereof arising out Dialysis Center’s supply of the Compensation Data to Amgen.

 

6.2.

Self-Reported Purchase Data. Dialysis Center, on behalf of the Dialysis Center Purchasers, acknowledges, covenants and agrees that it shall submit full and complete Self-Reported Purchase Data for each Quarter to Amgen within forty-five (45) days of the end of each such Quarter through a Purchase Data Submission Form attached here to as Exhibit SR-1Exhibit SR-1 is subject to modification by mutual written agreement of the Parties. Dialysis Center on behalf of the Dialysis Center Purchasers shall submit Exhibit SR-1 in an Excel file format electronically by e-mail to [*] or in such other manner as may be specified by Amgen through written notification to Dialysis Center.

 

7.

JOINT PROJECTS

 

7.1.

Joint Projects. The Parties shall form a “Joint Project Committee” comprised of three (3) executives from each Party, one (1) of whom shall be a clinical executive, and shall be led by two (2) co-chairs, one (1) appointed by each of the Parties. During the Term, either Party may present to the Joint Project Committee one or more written proposals (a “Project Proposal”) for a project or projects to be undertaken jointly by the Parties related to the provision of Dialysis Services (a “Joint Project”), together with a draft project plan for the Joint Project (a “Project Plan”) which the Parties shall discuss in good faith. If the Parties agree in writing to undertake a Joint Project, the Parties shall jointly pursue such Joint Project in accordance with the Project Plan without any further approval action required by the Parties.

 

7.2.

Joint Project Committee.

 

  7.2.1.

Joint Project Committee Responsibilities. The Joint Project Committee shall be responsible for the following:

 

  a)

Reviewing and approving each new Project Proposal prior to adoption of any Joint Projects set forth in such new Project Proposal;

 

  b)

Reviewing and approving changes to the Project Plans for existing Joint Projects prior to adoption of such changes;

 

  c)

Providing for communication and discussion between the Parties to, as appropriate, coordinate and optimize the development activities of the Parties under each Joint Project;

 

  d)

Reviewing and monitoring the activities and progress of the Parties against the Joint Projects;

 

  e)

Communicating with the Business Representatives regarding all of the foregoing; and

 

  f)

Such other matters as are appropriate to make operational the terms of this Agreement in respect of Joint Projects and as the Parties shall agree in writing.

 

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  7.2.2.

Meetings. The Joint Project Committee shall meet in person, via teleconference or videoconference or otherwise, as frequently as deemed necessary by the Joint Project Committee. All Joint Project Committee meetings shall have at least one (1) member appointed by each Party in attendance.

 

  7.2.3.

Decision Making. The Joint Project Committee shall make decisions by a unanimous vote. The Parties shall use good faith, reasonable efforts to come to a complete agreement. In the event the Joint Project Committee fails to reach unanimity with respect to any matter, such matter shall be escalated to the Business Representatives.

 

8. WARRANTIES, REPRESENTATIONS AND COVENANTS

 

8.1.

Power and Authority. Each Party represents and warrants to the other that this Agreement: (a) has been duly authorized, executed, and delivered by it, (b) constitutes a valid, legal, and binding agreement enforceable against it in accordance with the terms contained herein, and (c) does not and shall not conflict with or violate any of its other contractual obligations, expressed or implied, to which it is a party or by which it may be bound.

 

8.2.

Compliance with Law and Regulation. Amgen and Amgen Inc. shall, and Dialysis Center shall, comply with all applicable Laws related to the performance of their respective obligations under this Agreement. Each Party represents and warrants that (which representations and warranties shall be ongoing representations and warranties during the Term): (i) it is not currently named on any of the following lists: (A) HHS/OIG List of Excluded Individuals/Entities, (B) GSA List of Parties Excluded from Federal Programs, or (C) OFAC “SDN and Blocked Individuals” and (ii) it shall promptly notify the other Party in the event it becomes named on any of the following lists: (x) HHS/OIG List of Excluded Individuals/Entities, (y) GSA List of Parties Excluded from Federal Programs, or (z) OFAC “SDN and Blocked Individuals”.

 

8.3.

Product. Amgen covenants and agrees that EPOGEN is not and will not be adulterated or misbranded within the meaning of the Federal Food, Drug and Cosmetic Act, as amended, or within the meaning of any applicable Law, or is or will be a product which may not be introduced in to interstate commerce. Amgen warrants that EPOGEN purchased pursuant to this Agreement (a) is manufactured, and up to the time of its receipt by Authorized Wholesalers is handled, stored, and transported in accordance with all applicable Laws, and meet all specifications for effectiveness and reliability as required by the United States Food and Drug Administration (the “FDA”), and (b) when used in accordance with the directions in its labeling is fit for the purposes and indications described in its labeling. Amgen warrants that the use of EPOGEN by Dialysis Center Purchasers shall not infringe upon any ownership rights of any other individual or entity or upon any patent, copyright, trademark or other intellectual property or proprietary right or trade secret of any individual or entity. Amgen agrees that as soon as practicable it will notify Dialysis Center of any material defect in EPOGEN delivered to any Dialysis Center Purchasers in accordance with applicable Law.

 

8.4.

Data. Dialysis Center represents and warrants to Amgen that: (a) the Data, the Compensation Data, and the Self-Reported Purchase Data that the Dialysis Center Purchasers deliver to Amgen pursuant to Section 5 and Section 6 shall be: (i) prepared and delivered in accordance with the provisions of Section 5, Section 6 and Exhibit A and (ii) as complete and accurate as is reasonably obtainable in view of the Dialysis Center Purchasers’ customary method of compilation and the nature and accuracy of the Dialysis Center Purchasers’ resources; (b) the Dialysis Center Purchasers shall not knowingly and intentionally misrepresent any of the Data, the Compensation Data,

 

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and/or the Self-Reported Purchase Data provided by the Dialysis Center Purchasers to Amgen; and (c) Dialysis Center shall promptly notify Amgen in the event it has actual knowledge that any of the Data, the Compensation Data, and/or the Self-Reported Purchase Data is not complete and/or accurate.

 

8.5.

Designated Affiliates List and Managed Centers List. Dialysis Center represents and warrants that the Designated Affiliates List and the Managed Centers List, as each of them is attached to this Agreement as of the Term Start Date (and as of any subsequent date that such lists are updated in accordance with the terms hereof) are complete and accurate lists of all Affiliates of Dialysis Center and Managed Centers of Dialysis Center providing Dialysis Services in the Territory as of the Term Start Date (and as of each such subsequent date).

 

8.6.

Adverse Claims. Each Party represents and warrants to the other Party that, as of the execution of this Agreement, such Party has no actual knowledge of any legal claim or right to be asserted against the other Party or its Affiliates related to the negotiation or execution of this Agreement.

 

8.7.

NO OTHER WARRANTIES. OTHER THAN THE WARRANTIES EXPRESSLY SET FORTH IN THIS AGREEMENT, NEITHER PARTY MAKES, AND EACH PARTY EXPRESSLY DISCLAIMS, ALL OTHER WARRANTIES, STATUTORY, EXPRESS, AND/OR IMPLIED, INCLUDING THOSE OF MERCHANTABILITY AND/OR FITNESS FOR A PARTICULAR PURPOSE. EACH PARTY HEREBY EXPRESSLY WAIVES ANY AND ALL OTHER WARRANTIES, STATUTORY, EXPRESS, AND/OR IMPLIED, INCLUDING THOSE OF MERCHANTABILITY AND/OR FITNESS FOR A PARTICULAR PURPOSE.

 

9.

DISPUTE RESOLUTION, INSURANCE and INDEMNITY

 

9.1.

Escalation of Disputes to Business Representatives. The Parties recognize that claims, disputes or controversies arising out of or relating to this Agreement (“Disputes”) may occur from time to time. It is the objective of the Parties to establish procedures to facilitate the resolution of Disputes arising under this Agreement in an expedient manner by mutual cooperation and, if possible, without resort to litigation.

In the event of any Dispute, and prior to either Party (a) commencing any action in a court of law or under any Governmental Authority, or (b) taking any action to terminate this Agreement as provided in Section 10, the Parties shall first undertake that the employees of each Party with relevant expertise and authority with respect to a Dispute shall meet to discuss such Dispute within five (5) business days of a Party receiving notice of a Dispute (except in the case where delay in resolving any such Dispute would be materially prejudicial to a Party, in which case the Dispute will be referred directly to the Business Representatives). In the event the Parties are unable to resolve any such Dispute within thirty (30) business days of the initial meeting between the Parties, it shall be referred to the Business Representatives, who shall negotiate with one another in good faith to reach a good faith resolution of the Dispute; provided, that the Parties shall use commercially reasonable best efforts to expedite the resolution of any Disputes which by their nature need to be made quickly by the Business Representatives. In the event the Dispute cannot be resolved by the Business Representatives within fifteen (15) business days of the initial meeting between the Business Representatives or such other period of time as is mutually agreed to by the Parties, then, upon the written demand of either Party, the Dispute shall be subject to arbitration, as provided in Section 9.2. Pending resolution of any Dispute, both Parties will continue their performance under this Agreement of all obligations that are not the subject of any such Dispute. If there is a Dispute relating to any amount owed by either Party to the other Party, the undisputed

 

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portion of such amount shall be paid to the other Party in accordance with the terms hereof, and the Parties shall first attempt to resolve the disputed balance in accordance with this Section 9.1.

 

9.2.

Arbitration.

 

  9.2.1.

Claims. Subject to Section 9.3 below, any Dispute that is not resolved under Section 9.1 within thirty (30) days after a Party’s initial written request for resolution, shall be resolved by final and binding arbitration administered by JAMS (the “Administrator”) in accordance with its Comprehensive Arbitration Rules and Procedures (the “Rules”), except to the extent any such Rule conflicts with the express provisions of this Section 9.2. (capitalized terms in this Section 9.2 used but not otherwise defined in this Agreement shall have the meanings provided in the Rules.) For Disputes valued at less than Five Million Dollars ($5,000,000), the Arbitration shall be conducted by one (1) neutral arbitrator (“Arbitrator”) selected in accordance with the Rules, provided that such Arbitrator shall not be a current or former employee or director, or a current stockholder, of either Party or any of their respective Affiliates. For Disputes valued at or more than Five Million Dollars ($5,000,000), the Arbitration shall be conducted by a panel of three (3) neutral Arbitrators selected in accordance with the Rules, provided that any such Arbitrator shall not be a current or former employee or director, or a current stockholder, of either Party or any of their respective Affiliates. The Arbitration shall be held in Los Angeles, California.

 

  9.2.2.

Discovery. Within forty-five (45) days after selection of the Arbitrator(s), the Arbitrator(s) shall conduct the Preliminary Conference. In addressing any of the subjects within the scope of the Preliminary Conference, the Arbitrator(s) shall take into account both the needs of the Parties for an understanding of any legitimate issue raised in the Arbitration and the desirability of making discovery efficient and cost-effective. In that regard, the Parties agree to the application of the E-Discovery procedures set forth in Rule 16.2(c) of JAMS’ Expedited Procedures; provided that the Parties agree that the time limitations identified in Rule 16.2 of JAMS’ Expedited Procedures shall not be binding and the Arbitrator(s) shall set time limitations for discovery and depositions that are reasonable and necessary in light of the issues and matters raised in the Preliminary Conference. In no event shall the time limitations set by the Arbitrator(s) for discovery and depositions be shorter than the time periods for discovery and depositions that are set forth in Rule 16.2 of JAMS’ Expedited Procedures.

 

  9.2.3.

Hearing; Decision. The hearing (“Hearing”) shall commence within a reasonable time after the discovery cutoff. The Arbitrator(s) shall require that each Party submit concise written statements of position and shall permit the submission of rebuttal statements, subject to reasonable limitations on the length of such statements to be established by the Arbitrator(s). The Arbitrator(s) shall also permit the submission of expert reports. The Arbitrator(s) shall render the award (“Award”) within thirty (30) days after the Arbitrator(s) declares the Hearing closed, and the Award shall include a written statement describing the essential findings and conclusions on which the Award is based, including the calculation of any damages awarded. The Arbitrator(s) will, in rendering his, her or their decision, apply the substantive law of the State of California, without giving effect to its principles of conflicts of law, and without giving effect to any rules or laws relating to arbitration. The Award rendered by the Arbitrator(s) shall be final, binding and non-appealable, and judgment may be entered upon it in any court of competent jurisdiction. However, the Parties agree that the JAMS Optional Arbitration Appeal Procedures

 

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(“Appeal Procedures”) shall apply to the Arbitration, at the request by either Party in accordance with such Appeal Procedures. If a Party appeals the Award rendered by the Arbitrator(s), the Award issued by the Appeal Panel (as defined in such Appeal Procedures) shall be final, binding and non-appealable, and judgment may be entered upon it in any court of competent jurisdiction.

 

  9.2.4.

Costs. Each Party shall bear its own attorney’s fees, costs, and disbursements arising out of the Arbitration, and shall pay an equal share of the fees and costs of the Arbitrator(s); provided, however, the Arbitrator(s) shall be authorized to determine whether a Party is the prevailing party, and if so, to award to that prevailing party reimbursement for any or all of its reasonable attorneys’ fees, costs and disbursements (including, for example, expert witness fees and expenses, photocopy charges, travel expenses, etc.), and/or the fees and costs of the Administrator and the Arbitrator(s).

 

  9.2.5.

Confidentiality. Each Party acknowledges and agrees that: (a) any discovery pursuant to this Section 9.2, (b) the Hearing, (c) any and all documents exchanged or delivered in connection with the Hearing, settlement negotiations, and/or settlement terms, including the statements of position, rebuttal statements, and expert reports, (d) settlement negotiations and/or settlement terms, and (e) the Award shall be treated as Confidential Information and subject to the terms and conditions of Section 11.14.

 

9.3.

Court Actions. Nothing contained in this Agreement shall deny either Party the right to seek injunctive or other equitable relief from a court of competent jurisdiction in the context of a bona fide emergency or prospective irreparable harm, and such an action may be filed and maintained notwithstanding any ongoing discussions between the Parties or any ongoing arbitration proceeding.

 

9.4.

Insurance. Each Party shall secure and maintain in full force and effect throughout the Term (and following termination, to the extent necessary to cover any claims arising from this Agreement) commercial general liability insurance and product liability (in the case of Amgen only) which include contractual liability with limits of no less than [*] dollars ($[*] USD); professional liability insurance (in the case of Dialysis Center only) with limits of no less than [*] dollars ($[*] USD), and workers’ compensation with statutory limits. Any limits on each of a Party’s insurance coverage shall not be construed to create any limit on such Party’s liability with respect to its obligations under this Agreement or otherwise. Each of the Parties shall have the right to satisfy its obligations under this Section 9.4 through self-insurance. Amgen Inc. hereby guarantees the performance of Amgen’s obligations as set forth in this Section 9.4.

 

9.5.

Indemnity.

 

  9.5.1.

By Amgen. Amgen agrees to indemnify, defend, and hold Dialysis Center, its officers, directors, agents and employees (collectively, the “Dialysis Center Indemnitees”) harmless from and against any and all loss, damage and/or expense (including reasonable attorney’s fees) that they may suffer as a result of Third Party claims, demands, actions, proceedings, liabilities, costs or judgments, or threats thereof (“Third Party Claim(s)”) arising out of (i) any defect in the design and/or manufacture of EPOGEN or the storage and/or transportation of EPOGEN in Amgen’s possession, including claims for property damage, loss of life, and/or bodily injury; and/or (ii) the breach by Amgen or Amgen Inc. of any of their respective warranties, representations, and/or covenants contained in this Agreement. Notwithstanding anything to the contrary contained herein, Amgen and Amgen Inc. shall not have any obligation to defend, indemnify, and/or hold the

 

Page 24 of 136


 

Dialysis Center Indemnitees harmless from any Third Party Claims arising out of the negligent acts and/or omissions and/or willful misconduct of the Dialysis Center Indemnitees. This indemnification shall survive the termination or expiration of this Agreement. Amgen Inc. hereby guarantees the performance of Amgen’s obligations as set forth in this Section 9.5.1.

 

  9.5.2.

By Dialysis Center. Dialysis Center agrees to indemnify, defend, and hold Amgen, its officers, directors, agents and employees (collectively, the “Amgen Indemnitees”) harmless from and against any and all Third Party Claims arising out of (i) any Dialysis Center Purchasers’ administration, promotion or use of EPOGEN purchased under this Agreement to its patients; (ii) any Dialysis Center Purchasers’ failure to store and/or transport any EPOGEN in its possession in accordance with any applicable Law and/or labeling information; and/or (iii) the breach by Dialysis Center of any of its warranties, representations, and/or covenants contained in this Agreement. For purposes of the foregoing, the “administration” of EPOGEN by Dialysis Center shall mean the dispensing and handling by Dialysis Center and its employees of EPOGEN and the actual administration of EPOGEN to patients by Dialysis Center and its employees, but shall exclude physician prescriptions of EPOGEN to patients. Notwithstanding anything to the contrary contained herein, Dialysis Center shall not have any obligation to defend, indemnify, and/or hold the Amgen Indemnitees harmless from any Third Party Claims arising out of the negligent acts and/or omissions and/or willful misconduct of the Amgen Indemnitees. This indemnification shall survive the termination or expiration of this Agreement.

 

9.6.

Procedure for Third Party Claims.

 

  9.6.1.

Notice. The Party receiving indemnification hereunder (the “Indemnified Party”) shall give the Party providing indemnification hereunder (the “Indemnifying Party”) written notice within fifteen (15) business days after the Indemnified Party receives notice of any Third Party Claim, subject to indemnification hereunder upon which such Indemnified Party intends to base a request for indemnification under Section 9.5.1 or Section 9.5.2. Failure to give any such notice shall not constitute a waiver of any right to indemnification or reduce in any way the indemnification available hereunder, except and only to the extent that as a result of such failure the Indemnifying Party demonstrates that it was directly and materially damaged as a result of such failure to give timely notice.

 

  9.6.2.

Control of Defense. The Indemnifying Party, at its expense, shall assume control of the defense and resolution of each Third Party Claim using legal counsel reasonably approved by the Indemnified Party and shall keep the Indemnified Party fully and timely informed of the progress of such defense and resolution. With respect to each Third Party Claim, the Indemnified Party shall have the right to retain independent legal counsel at its cost and monitor such Third Party Claim’s defense and resolution. In such a case, the Indemnifying Party and its legal counsel shall fully cooperate with the Indemnified Party and its legal counsel in providing such information as the Indemnified Party may reasonably request. Notwithstanding this Section 9.6.2, the Indemnifying Party shall not be entitled to control, but may participate in, and the Indemnified Party shall be entitled to have sole control over and select counsel to conduct, the defense or settlement of each Third Party Claim that: (i) seeks a temporary restraining order, a preliminary or permanent injunction, and/or specific performance against the Indemnified Party, (ii) involves criminal allegations against the Indemnified Party, (iii) if unsuccessful, would set a precedent that would materially interfere with

 

Page 25 of 136


 

and/or have a material adverse effect on the business and/or financial condition of the Indemnified Party, and/or (iv) imposes liability on the part of the Indemnified Party for which the Indemnified Party is not entitled to indemnification hereunder. In such an event, the Indemnifying Party will still have all of its obligations hereunder with respect to any such affected Third Party Claims; provided that the Indemnified Party will not settle any such affected Third Party Claims without the prior written consent of the Indemnifying Party, which consent will not be unreasonably withheld, conditioned, and/or delayed by the Indemnifying Party.

 

  9.6.3.

Representation. If both the Indemnifying Party and the Indemnified Party are named parties in any Third Party Claim and representation of both Parties by the same legal counsel would be inappropriate due to the actual or potential differing interests between them, then the Indemnified Party, at the Indemnifying Party’s expense, shall have the right to be represented by separate counsel of the Indemnified Party’s choosing.

 

  9.6.4.

Resolution. The Indemnifying Party shall not settle, compromise or resolve any Third Party Claim without the written consent of the Indemnified Party; provided that, the Indemnifying Party may, without such consent, enter into any such judgment, settlement, compromise or resolution that relates solely to the payment of money damages, involves a full release of the Indemnified Party and does not result in any admission of any fault of the Indemnified Party with respect to such Third Party Claim.

 

  9.6.5.

Payment. Any final judgment entered or settlement agreed upon in the manner provided in this Section 9.6, as applicable, shall be binding upon the Indemnifying Party and shall conclusively be deemed to be an obligation with respect to which the Indemnified Party is entitled to prompt indemnification hereunder, if applicable. Payment of all amounts owing by the Indemnifying Party under this Section 9.6, as applicable, shall be made promptly upon a final settlement between the Indemnifying Party and the Indemnified Party or upon a final adjudication determined by the Arbitrator(s) that an indemnification obligation is owed by the Indemnifying Party to the Indemnified Party.

 

10.

TERM AND TERMINATION

 

10.1.

Term. This Agreement shall come into effect as of the Term Start Date and shall expire on the earlier of the Term End Date, or the Termination Date.

 

10.2.

Termination for Cause. Amgen or Dialysis Center may terminate this Agreement only in the event of the following:

 

  10.2.1.

Breach of Purchase Commitment. The Parties acknowledge and agree that the Purchase Commitment is the principal value expected to be received by Amgen under this Agreement and it is the essential inducement for Amgen to enter into this Agreement, pursuant to which it has agreed, among other things, (a) to provide the Dialysis Center Purchasers for the duration of the Term the economic benefits of the Discounts provided for herein, (b) to make the Supply Commitment, which requires that Amgen commit facilities to the manufacture of EPOGEN at the expense of other Amgen uses and allocate significant resources to maintain its manufacturing capabilities and capacity at a commensurate level, (c) to assume the business risks and financial liability in respect of the representations, warranties and covenants made by it hereunder and (d) to forego potential other commercial opportunities in respect of its nephrology business. In the event that the Dialysis

 

Page 26 of 136


 

Center Committed Purchasers do not meet an Amgen ESAs Share of Sales of (i) at least [*] percent ([*]%) for [*] or more [*] during the Term with respect to which the Dialysis Center is required to pay the Alternative ESA Purchase Amount with respect to each of such [*] in any [*] period during the Term, or (ii) at least [*] percent ([*]%) in any [*], then Amgen shall be entitled to terminate this Agreement immediately upon written notice to Dialysis Center and, notwithstanding any other provision of this Agreement, thereupon either receive the “Liquidated Damages” defined below or exercise such other rights and remedies as may be allowed at law or in equity under applicable Law.

 

  10.2.2.

Termination for Failure to Supply. Dialysis Center may terminate this Agreement immediately upon written notice to Amgen in the event that Amgen has not been able to supply to Dialysis Center through one or more Authorized Wholesalers EPOGEN in [*] (or Aranesp subject to the terms of Section 2.5) equal to at least [*] percent ([*]%) of the Minimum Forecast Commitment (other than as a result of one or more Force Majeure Events) for [*].

 

  10.2.3.

Termination for Exclusion from Federal Health Care Program. Either Amgen or Dialysis Center may immediately terminate this Agreement upon written notice to the other Party in the event there is change in the other Party’s status which excludes it from participation in any “Federal health care program” (as defined under 42 U.S.C. § 1320a-7b(f)) (a “Debarred Party”), provided that no Party shall have the right to terminate this Agreement pursuant to this Section 10.2.3 if the Debarred Party can complete its obligations through, or otherwise transfer its obligations to, an Affiliate as permitted by applicable Law.

 

10.3.

Liquidated Damages. The Parties acknowledge that Amgen’s actual damages in the event of a termination by Amgen, pursuant to Section 10.2.1 or Section 10.2.3, would be difficult to ascertain, and that the payment of the Liquidated Damages represents the best estimate of the amount of such damages by the Parties at this time. The Parties further expressly acknowledge and agree that the Liquidated Damages are intended not as a penalty, but as full liquidated damages, in the event of Amgen’s termination of this Agreement pursuant to Section 10.2.1 or Section 10.2.3 and as compensation for Amgen’s losses and other expenses associated with this Agreement.

For purposes of this Agreement, “Liquidated Damages” means, in addition to any amounts owed to Amgen under this Agreement, including for breach of the Purchase Commitment under Section 2.1, an amount in cash equal to [*] percent ([*]%) of the [*] of Amgen’s projected [*] for each remaining Quarter (including any fractional Quarters) in the Term, with such [*] equal to A – B, grown Quarterly at a [*] percent ([*]%) annual rate and discounted on a Quarterly basis, at a rate equal to the average annual increase in [*] for EPOGEN on an [*] basis for all calendar years during the Term prior to the related [*] calculation, where:

 

   A =  

The average [*] for the [*] most recent Quarters prior to the Termination Date in which Dialysis Center satisfied the Purchase Commitment in full (or, if less than [*] such Quarters exist, then “A” shall equal the average of the sum of (i) [*] plus (ii) the [*], for the [*] most recent Quarters prior to the Termination Date); and

   B =  

The average aggregate [*] (other than the [*] Rebate, the [*] Rebate and the [*] Rebate) earned by Dialysis Center Purchasers during the [*] most recent Quarters prior to the Termination Date, regardless of whether Dialysis Center satisfied the Purchase Commitment in such Quarters.

 

Page 27 of 136


10.4.

Effect of Termination. Upon any termination or expiration of this Agreement, (a) any earned and vested Discounts shall be paid in accordance with the terms set forth in Exhibit A, (b) any Alternative ESA Purchase Amounts shall be paid pursuant to Section 2.1.1, (c) any payments by Amgen owing to Dialysis Center under Section 2.5.1 shall be paid, (d) any payment by Dialysis Center owing to Amgen under Section 2.4.2 shall be paid and (e) the Liquidated Damages pursuant to Section 10.3 shall be paid. All Discounts available to Dialysis Center in the particular Quarter in which such termination occurs shall be paid to Dialysis Center based on an achievement of the eligibility and vesting requirements set forth in Exhibit A.

 

10.5.

Survival. Any provision that, either expressly or by its nature is intended to survive this Agreement, shall survive any expiration or termination of this Agreement, including Sections 1, 3, 8, 9, 10, and 11.

 

11.

MISCELLANEOUS

 

11.1.

Amendment. Except as expressly set forth herein, no amendment of this Agreement shall be effective unless expressed in a writing signed by a duly authorized representative of each Party.

 

11.2.

Assignment. Neither Party shall have the right to assign or otherwise transfer this Agreement, or any of its rights and obligations hereunder, in whole or in part, without the other Party’s prior written consent, and any attempted assignment or transfer without such consent shall be void; provided, however, that Amgen may assign or otherwise transfer this Agreement and its rights and obligations hereunder to any of its Affiliates that is not in the business of providing Dialysis Services in the Territory. Notwithstanding the foregoing, each Party shall be obligated to assign and transfer this Agreement, without any required consent, to any Person to whom either such Party has transferred all or substantially all of its business relating to this Agreement, and the Parties agree that they shall take all reasonable and necessary actions in respect thereof including the execution and delivery of all appropriate instruments to effectuate such assignment and transfer of this Agreement; provided that any assignment and transfer of this Agreement by Amgen to any Person, a substantial portion of whose business consists of providing Dialysis Services in the Territory, shall require the prior written consent of Dialysis Center, which consent may be withheld by Dialysis Center in its sole and absolute discretion. This Agreement and the provisions hereof shall be binding upon, and inure to the benefit of, the Parties’ permitted successors and assigns.

 

11.3.

Modification of Law. If at any time following the Term Start Date, the enactment or modification of any Law occurs and, as a result, either Party’s performance of its obligations under this Agreement would not comply with such Law, either Party may, upon notice to the other Party, recommend an amendment to modify this Agreement to address those provisions of the Agreement that may not comply with such Law. The Parties agree to use their commercially reasonable best efforts to modify this Agreement as necessary to bring it into compliance with the Law if that can be done while retaining, in all material respects, the essential rights and benefits of each Party under this Agreement, including the Purchase Commitment, the Supply Commitment, the collection, exchange and use of the Data and the ability for Dialysis Center Purchasers to earn the Discounts that the Dialysis Center Purchasers are eligible to receive hereunder. Promptly following the delivery of such notice describing the Law at issue and the proposed modifications to bring this Agreement into compliance with such Law, Dialysis Center and Amgen shall meet and in good faith seek to mutually agree to amend this Agreement to accommodate any such Law in accordance with this Section 11.3.

 

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11.4.

Conflicting Provisions. To the extent that any provisions of Amgen’s general or customary policies and procedures or any terms of any purchase order conflict with or are in addition to the terms of this Agreement or any Exhibit or Schedule attached hereto, the terms of this Agreement and its Exhibits and Schedules shall govern.

 

11.5.

Construction. This Agreement shall be deemed to have been jointly drafted by the Parties, and no rule of strict construction shall apply against either Party. As used herein, the word “including” shall mean “including, without limitation.”

 

11.6.

Counterparts; Facsimile/PDF Signatures. This Agreement may be executed in one or more counterparts, each of which shall be considered an original. The Parties agree that facsimile or PDF transmission of original signatures shall constitute and be accepted as original signatures.

 

11.7.

Currency. All amounts herein are set forth in United States Dollars.

 

11.8.

Force Majeure. Except as provided in Section 2.1.1 or Section 2.5, neither Party will be liable for delays in performance or nonperformance of this Agreement or any covenant contained herein if such delay or nonperformance is a result of acts of God, acts of civil or military authority, acts of any Governmental Authority, civil disobedience or commotion, epidemics, war, terrorist acts, failure or default of public utilities or common carriers, destruction of production facilities or materials by fire, earthquake, storm or like catastrophe, inability to procure necessary raw materials in a commercially reasonable manner or default of suppliers or subcontractors or any events beyond the reasonable control and without the fault or negligence of a Party (all of the foregoing, a “Force Majeure Event”). Force Majeure Events shall not adversely affect Dialysis Center’s eligibility for any Discounts.

 

11.9.

Further Assurances. Each Party shall perform all further acts reasonably requested by the other to effectuate the purposes of this Agreement, including obtaining the Certifications under Section 5 or obtaining purchase data necessary from third parties to calculate any amounts payable pursuant to Exhibit A.

 

11.10.

Governing Law. This Agreement shall be governed by the laws of the State of California (without regard to its conflict of law rules) and, except as otherwise set forth in this Agreement, the Parties submit to the jurisdiction of the California courts, both state and federal.

 

11.11.

Merger/No Reliance. This Agreement, together with the Schedules, and the Exhibits constitutes the entire agreement, written or oral, of the Parties as of the Term Start Date concerning the subject matter hereof. The Parties acknowledge that, in making the determination to enter into this Agreement or otherwise, they have not relied, in whole or in part, on any promise, information, understanding, guarantees, discussions, representation, or warranty, expressed or implied, not contained specifically in this Agreement. Without limiting the generality of the foregoing, the Parties agree that neither Party makes or has made any representation or warranty with respect to any potential changes in the dialysis segment or the use or pricing of ESAs in dialysis, including as a result of the introduction of Alternative ESAs (including [*]) including the timing of such introduction(s), the pricing of such Alternative ESAs and their potential physician acceptance and impact on prescribing practices.

 

11.12.

No Partnership. The relationship between Amgen and Dialysis Center is that of independent contractors, and not a partnership or an agency, franchise or other relationship. Neither Party shall have the authority to bind the other.

 

11.13.

Notices. Any notice or other communication required or permitted hereunder (excluding purchase orders) shall be in writing and shall be deemed given or made five (5) days

 

Page 29 of 136


 

after deposit in the United States mail with proper postage for first-class registered or certified mail prepaid, return receipt requested, or when delivered personally or by facsimile (as shown by concurrent written transmission confirmation and confirmed by overnight mail), or one (1) day following traceable delivery to a nationally recognized overnight delivery service with instructions for overnight delivery, in each case addressed to the address set forth below, or at such designated address that either Party shall have furnished to the other in accordance with this Section 11.13:

 

  If to Amgen:   
     Amgen USA Inc.
     One Amgen Center Drive, [*]
     Thousand Oaks, CA 91320-1789
     Attn: Specialist, Contracts & Pricing – Nephrology Business Unit
     Fax: [*]
  with a copy to :   
     Amgen USA Inc.
     One Amgen Center Drive, [*]
     Thousand Oaks, CA 91320-1789
     Attn: General Counsel
     Fax: [*]
  If to Amgen Inc.:    Amgen Inc.
     One Amgen Center Drive, [*]
     Thousand Oaks, CA 91320-1789
     Attn: General Counsel
     Fax No.: [*]
  If to Dialysis Center:
     DaVita Inc.
     1350 Old Bayshore Highway, Suite 777
     Burlingame, California 94010
     Attn: Vice-President of Purchasing
     Fax No.: [*]
  with a copy to:   
     DaVita Inc.
     1551 Wewatta Street
     Denver, CO 80202
     Attn: Chief Legal Officer
     Fax No.: [*]

 

11.14.

Confidentiality. “Confidential Information” means any and all information provided by one Party and/or any of its Affiliates (including Managed Centers in the case of Dialysis Center) (the “Disclosing Party”) to the other Party and/or any of its Affiliates (including Managed Centers in the case of Dialysis Center) (the “Non-Disclosing Party”) which is identified in writing or orally as confidential by the Disclosing Party to the Non-Disclosing Party or given the nature of the information or circumstances surrounding its disclosure reasonably should be considered as confidential, whether in written, computerized, oral, tangible or intangible, and/or other form. Nothing in this Section 11.14 shall prohibit,

 

Page 30 of 136


 

Amgen from using the Data, the Compensation Data, and/or the Self-Reported Purchase Data as provided in Section 5 and Section 6.

 

  11.14.1.

Confidentiality Covenants. Except to the extent expressly authorized by this Agreement or otherwise agreed in writing by the Parties, the Non-Disclosing Party agrees that for the Term, and for a period of five (5) years following the Term, the Non-Disclosing Party will keep confidential and not publish or otherwise disclose to any Third Party or use for any purpose, other than in accordance with this Agreement, any Confidential Information, provided, however, that the Non-Disclosing Party may disclose any such Confidential Information to its directors, officers, employees, agents, consultants and advisors as necessary for the Non-Disclosing Party to carry out its rights and obligations under this Agreement on the condition that such directors, officers, employees, agents, consultants and advisors are bound by confidentiality provisions at least as restrictive as those contained in this Agreement. The confidentiality provisions contained in this Section 11.14 shall not apply to the extent that it can be established by the Non-Disclosing Party by competent proof that such Confidential Information:

 

  (a)

was generally available to the public or otherwise part of the public domain at the time of its disclosure to the Non-Disclosing Party by the Disclosing Party; or

 

  (b)

became generally available to the public or otherwise part of the public domain after its disclosure to the Non-Disclosing Party by the Disclosing Party and other than through any act or omission of the Non-Disclosing Party in breach of this Agreement; or

 

  (c)

was independently discovered or developed by the Non-Disclosing Party without the use of or reference to the Confidential Information belonging to the Disclosing Party.

 

  11.14.2.

Retention and Destruction of Confidential Information. At any time upon the written request of the Disclosing Party the Non-Disclosing Party shall promptly return to the Disclosing Party or destroy all Confidential Information. Notwithstanding the return or destruction of the Confidential Information to the Disclosing Party or such other party as designated by the Disclosing Party to the Non-Disclosing Party, the Non-Disclosing Party covenants and agrees that it will continue to abide by its obligations hereunder with respect to any and all Confidential Information.

 

  11.14.3.

Disclosures Required By Law. In the event that the Non-Disclosing Party and/or any of its directors, officers, employees, agents, consultants and advisors that have received any Confidential Information is required by Law (e.g., by oral questions, interrogatories, request for information or documents, subpoena, civil investigative demand, or similar process) to disclose any Confidential Information, the Non-Disclosing Party agrees to (and shall cause each of its directors, officers, employees, agents, consultants and advisors that have received any Confidential Information to) provide the Disclosing Party with immediate written notice of any such disclosure of Confidential Information that is required by Law in order to provide the Disclosing Party with an opportunity to seek a protective order or other similar order with respect to such Confidential Information. If disclosure of any Confidential Information is required by Law, the Non-Disclosing Party will (and will cause each of its directors, officers, employees, agents, consultants and advisors that have received any Confidential

 

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Information to) furnish only that portion of the Confidential Information which it is legally obligated to disclose by Law and consistent with the terms of any protective order or other similar order obtained by the Disclosing Party with respect to such Confidential Information required to be disclosed by Law.

 

  11.14.4.

Public Announcements; Authorized Disclosure. Neither Party shall make a public announcement or other public disclosure concerning this Agreement without the consent of the other Party, except that either Party may make such announcement or disclosure if it is required by applicable Law, reasonably necessary for any filings with any Governmental Authority or pursuant to the rules of any securities exchange or interdealer quotation system; provided, that the disclosing Party shall give reasonable prior advance notice of the proposed text of such announcement or disclosure to the other Party for its prior review and approval, which review and approval shall not be unreasonably conditioned, withheld or delayed. The proviso in the immediately preceding sentence shall not apply to Relevant Information included in any cost report filed under Title XVIII or Title XIX of the Social Security Act, or health care program of any Governmental Authority.

 

  11.14.5.

Confidential Terms. Notwithstanding the foregoing, each Party may disclose the terms of this Agreement in confidence under terms and conditions at least as restrictive as set forth herein on a need-to-know basis to its legal and financial advisors to the extent such disclosure shall be reasonably necessary in connection with such Party’s activities as expressly permitted by this Agreement.

 

  11.14.6.

Enforcement. Each Party agrees that money damages alone would not be an adequate remedy for any breach of the terms and conditions of this Section 11.14. Therefore, in the event of a breach or threatened breach of this Section 11.14, the non-breaching Party may, in addition to other rights and remedies existing in its favor, apply to any court of competent jurisdiction for specific performance and/or injunctive and/or other relief in order to enforce and/or prevent any violation of the provisions of this Section 11.14 by the breaching Party (without proving monetary damages and/or posting a bond and/or other security).

 

11.15.

Severability. Subject to the provisions of Section 11.3, if any one or more of the provisions of this Agreement is held to be invalid or unenforceable, the provisions shall be considered severed from this Agreement and shall not serve to invalidate any remaining provisions hereof.

 

11.16.

Waiver. No Party shall be deemed to have waived any right hereunder, unless such waiver is expressed in a writing signed by such Party.

 

11.17.

Open Records. To the extent required by §1861(v)(1)(I) of the Social Security Act, as amended, the Parties will allow the U.S. Department of Health and Human Services, the U.S. Comptroller General and their duly authorized representatives, access to this Agreement and all books, documents and records necessary to certify the nature and extent of costs incurred pursuant to it during the Term and for four (4) years following the last date any EPOGEN or services are furnished under it. If Amgen carries out the duties of this Agreement through a subcontract worth $10,000 or more over a 12-month period with a related organization, the subcontract shall also contain an access clause to permit access by the U.S. Department of Health and Human Services, the U.S. Comptroller General, and their duly authorized representatives to the related organization’s books and records.

 

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11.18.

Amgen’s ESA Risk Evaluation and Mitigation Strategy Program. Dialysis Center and its Designated Affiliates and Managed Centers shall reasonably cooperate and comply with Amgen in Amgen’s implementation of its ESA Risk Evaluation and Mitigation Strategy program as found at the FDA website: http://www.fda.gov/downloads/Drugs /DrugSafety/PostmarketDrugSafetyInformationforPatientsandProviders/UCM200105.pdf (“the FDA Website”) and which may be modified from time to time by the FDA (the “Amgen ESA Risk Evaluation Program”). Dialysis Center shall refer to the FDA Website for updates to the Amgen ESA Risk Evaluation Program.

 

11.19.

Recall. In the event the FDA initiates a mandatory recall or Amgen initiates a recall, field market withdrawal, stock recovery, or other similar action with respect to EPOGEN (a “Recall”), the Dialysis Center Purchasers shall cooperate with Amgen in implementing the Recall consistent with applicable Law, any industry guidance issued by the FDA, and the terms or procedures of the Recall, including reasonable cooperation with any Amgen designated Third Party vendors.

 

11.20.

Assumption of Risk. Each Party expressly accepts and assumes all risks that may arise out of or result from uncertainties or changes to the dialysis market including those resulting from the introduction of Alternative ESAs (including [*]), including the timing of such introduction(s), the pricing of such Alternative ESAs and their potential physician acceptance and impact on prescribing practices.

 

Page 33 of 136


The Parties have executed this Agreement by their designated representatives set forth below.

 

AMGEN USA INC.
By:  

/s/ Anthony C. Hooper

Name (print):  

Anthony C. Hooper

Title:  

EVP

Date:  

11/15/2011

DIALYSIS CENTER
By:  

/s/ Dennis Kogod

Name (print):  

Dennis Kogod

Title:  

Chief Operating Officer

Date:  

11/15/2011

 

 

Amgen Inc. with respect to certain provisions of this Agreement as set forth herein.

Amgen Inc.

 

By:  

/s/ Anthony C. Hooper

Name (print):  

Anthony C. Hooper

Title:  

EVP

Date:  

11/15/2011

 

Page 34 of 136


Exhibit A

Discount Terms and Conditions

 

1

DEFINITIONS. In addition to the defined terms set forth in Section 1 of this Agreement, the following terms, as used in this Exhibit A, shall have the meaning ascribed below.

[*] Rebate Definitions

 

  1.1

Amgen Dialysis Contract” shall mean, as of any determination date, a contract between Amgen or one of its Affiliates and a Qualified Customer in effect as of such date that provides for such Qualified Customer to purchase EPOGEN for its commercial use in providing Dialysis Services in the Territory.

 

  1.2

Qualified Customer” shall mean a Third Party commercial enterprise collectively with all of its Affiliates and/or any dialysis facility in which a Third Party commercial enterprise and/or any of its Affiliates has an ownership interest of less than fifty percent (50%) but for which the Third Party commercial enterprise and/or any of its Affiliates provides management services or administrative services in which it controls the selection or procurement of ESAs (a) who has entered into an Amgen Dialysis Contract and (b) who is not exempt from consideration in the calculation of Best Price as defined by the Social Security Act at section 1927(c)(1)(C), as amended, and as implemented by regulation (e.g., any hospital participating in 340B Drug Pricing Program, any qualified state pharmaceutical assistance program, or any purchaser under the Federal Supply Schedule would not be a “Qualified Customer” for purposes of this Agreement).

 

  1.3

[*]” shall mean for each [*] of EPOGEN purchased by a Qualified Customer in any Quarter under an Amgen Dialysis Contract, the [*] in effect on the date of purchase [*] all of the discounts and rebates per [*] of EPOGEN that, for such Quarter were actually earned by such Qualified Customer pursuant to the terms of such Amgen Dialysis Contract (regardless of the actual Quarter in which such discounts or rebates are actually paid to such Qualified Customer); provided, that if any such discounts and rebates once paid are subsequently returned, revised or withdrawn, including pursuant to any retroactive amendment of the Amgen Dialysis Contract or payment settlement (whether in such Quarter or any subsequent Quarter), the applicable “[*]” shall be based on the discounts, rebates and chargebacks taking into full account such returns, revisions or withdrawals.

[*] Rebate Definitions

 

  1.4 [*] Rebate” shall mean the rebate described in Section 3.3 of this Exhibit A.

 

  1.5 [*] Percentage” shall mean, at any date of determination, an amount equal to

((A – B) if > 0)

          C

Where

“A” equals [*]

“B” equals [*]

“C” equals [*] in effect at the time of purchase

For example, a determination of [*] Rebate Percentage would be as follows:

 

Page 35 of 136


[*] Rebate Percentage Illustration:

(([*] - [*]) if greater than zero)

÷

[*] in effect at the time of purchase

 

  1.6

“[*]” shall mean a trial comparing the [*] of patients receiving EPOGEN and the [*] in connection with the provision of Dialysis Services.

 

  1.7

[*] Price” shall mean the [*] of the [*] for the applicable Quarter as reported by the Centers for Medicare & Medicaid Services as mandated by the Patient Protection and Affordable Care Act, as amended and reconciled by the Healthcare and Education Reconciliation Act and implementing regulations and as adjusted to take into account the [*] agreed to by the Parties or the results of the [*], as applicable.

 

  1.8

[*]” shall mean a [*] product that has been approved by the FDA both as a [*] and as [*]. [*] shall have the meanings ascribed to such terms in the Public Health Service Act (Title 42 U.S. Code, Chapter 6A), as such terms may be further defined by the FDA.

 

Page 36 of 136


  1.9

[*]” shall mean for each [*] of EPOGEN purchased by a Dialysis Center Purchaser under this Agreement in any Quarter, the [*] in effect on the date of purchase less for such Quarter (i) the Discounts that Dialysis Center is eligible to earn under this Agreement during the applicable Quarter, including the [*] Rebate, the [*] Rebate, and the [*] Rebate, as applicable, and (ii) any other discount, rebate or other price adjustment received by a Dialysis Center Purchaser per [*] of EPOGEN which is included in the “Best Price” reported in Amgen’s Best Price Submission under Title XIX of the Social Security Act in respect of such EPOGEN purchase.

 

  1.10 [*]” shall mean, for any Quarter in which the [*] Rebate is applied, an amount equal to

(A * B) + A

Where

“A” equals the [*] Price during such Quarter

“B” equals [*]%

For example, a determination of [*] would be as follows:

[*] Illustration:

([*] Price * [*]%) + [*] Price

Dialysis Share of Sales Definitions

 

  1.11

Dialysis Market [*] Purchases of [*]” means, for any period, the aggregate [*] paid for purchases of [*] by all purchasers, including those by all Dialysis Center Purchasers, during such period for use in providing Dialysis Services, from any source measured using the prevailing [*] as set by the product manufacturer in effect at the time of purchase to be determined by Amgen based on DDD™ data provided by IMS or if IMS’ DDD™ data is unavailable, by reliable alternative means to be determined by Amgen in Amgen’s reasonable discretion, subject to verification by Amgen.

 

  1.12

“Dialysis Share of Sales” shall mean Dialysis Center Qualified [*] Purchases [*] during the Quarter divided by Dialysis Market [*] Purchases of [*] during the Quarter.

Dialysis Share of Sales Illustration:

Dialysis Center Qualified [*] Purchases of [*]

÷

Dialysis Market [*] Purchases of [*]

 

  1.13

Dialysis Share of Sales Requirement” shall mean, for any Quarter, that Dialysis Center had an aggregate Dialysis Share of Sales for any such Quarter and the immediately preceding Quarter that was equal to or greater than [*] percent ([*]%) in the aggregate for such two (2) Quarter period. It is not the intent of the Parties that a [*] of any Alternative ESA (on a [*] equivalent basis) that is significantly higher than the [*] for EPOGEN should negatively affect Dialysis Center’s attainment of the Dialysis Share of Sales Requirement. If at any time during a Quarter, an Alternative ESA is introduced with respect to the provision of Dialysis Services which has a [*] for such Alternative ESA to [*] as established by the manufacturer of such Alternative ESA that potentially is significantly greater than (on a [*] equivalent basis) the [*] for EPOGEN (a “[*] Event”), Dialysis Center shall deliver a written notice to Amgen

 

Page 37 of 136


 

indicating that there has been a [*] Event (a “[*] Event Notice”). Within thirty (30) days after Amgen’s receipt of a [*] Event Notice, the Parties shall meet and discuss in good faith any necessary changes, amendments, and/or adjustments to the calculation of the Dialysis Share of Sales Requirement to account for the impact of such [*] Event on the Parties.

 

  1.14

Dialysis Center Qualified [*] Purchases of [*]” means, for any period, the aggregate [*] paid for purchases of [*] by all Dialysis Center Purchasers during such period for use in providing Dialysis Services, from any source measured using the prevailing [*] as set by the product manufacturer in effect at the time of purchase to be determined by Amgen based on the DDD™ data provided by IMS or if IMS’ DDD™ data is unavailable, by reliable alternative means to be determined by Amgen in Amgen’s sole discretion, subject to verification by Amgen.

 

  1.15

[*] Event” has the meaning set forth in Section 1.13 of this Exhibit A.

 

  1.16

[*] Event Notice” has the meaning set forth in Section 1.13 of this Exhibit A.

[*] Share of Sales Definitions

 

  1.17

Dialysis Market [*] Purchases of [*] for [*] Rebate” means, for any period, the aggregate [*] paid for purchases of [*] by all purchasers, but excluding all Dialysis Center Purchasers, during such period for use in providing Dialysis Services, from any source measured using the prevailing [*] as set by the product manufacturer in effect at the time of purchase to be determined by Amgen based on data provided by a third-party reporting agency or if third-party reporting agency data is unavailable, by reliable alternative means to be determined by Amgen in Amgen’s sole reasonable discretion, subject to verification by the Parties.

 

  1.18

[*] Share of Sales” shall mean Qualified [*] Purchases of the [*] during the Quarter divided by Dialysis Market [*] Purchases of [*] for [*] Rebate during the Quarter.

[*] Share of Sales Illustration:

Qualified [*] Purchases of [*]

÷

Dialysis Market [*] Purchases of [*] for [*] Rebate

 

  1.19

Qualified [*] Purchases of [*]” means, for any period the aggregate [*] paid for purchases of the applicable [*] by all purchasers, but excluding all Dialysis Center Purchasers, during such period for use in providing Dialysis Services, from any source measured using the prevailing [*] as set by the product manufacturer in effect at the time of purchase to be determined by Amgen based on data provided by a third-party reporting agency or if third-party reporting agency data is unavailable, by some alternative means to be determined by Amgen in Amgen’s sole discretion, subject to verification by Amgen.

[*] Rebate Definitions

 

  1.20

[*]” shall mean the applicable [*] per [*] of EPOGEN as set forth in the [*] Table below.

 

Page 38 of 136


[*] Table

 

Calendar Year

   [*]  

2012

   $ [*

2013

   $ [*

2014

   $ [*

2015

   $ [*

2016

   $ [*

2017

   $ [*

2018

   $ [*

 

  1.21 [*] Rebate Percentage” shall mean, at any date of determination, an amount equal to

((A – B) if > 0)

C

Where

“A” equals [*]

“B” equals [*]

“C” equals [*] in effect at the time of purchase

For example, a determination of the [*] Rebate Percentage would be as follows:

[*] Rebate Percentage Illustration:

(([*] - [*]) if greater than zero)

÷

[*] in effect at the time of purchase

[*] Incentive Definitions

 

  1.22 [*]” shall mean the [*] incentive described in Section 3.5 of this Exhibit A.

 

  1.23

Other. The Parties acknowledge and agree that (i) the aggregate [*] paid for purchases of [*] by all purchasers for use in providing Dialysis Services in the Territory include purchases by [*] as well as other purchasers of ESAs for use in providing Dialysis Services, (ii) there may not be commercially available data comprising purchases of ESAs by all purchasers for use in providing Dialysis Services in the Territory that Dialysis Center could access in order to understand and track the Dialysis Share of Sales on an ongoing basis, (iii) there is commercially available data comprising purchases of ESAs by [*] in the Territory that Dialysis Center could access, (iv) the [*] purchases of ESAs by [*] in the Territory currently represents approximately [*] percent ([*]%) of [*] purchases of ESAs by all purchases for use in providing Dialysis Services in the Territory, (v) for the sole and limited purpose of determining whether Dialysis Center shall have met the Dialysis Share of Sales requirement under Sections 3.2.1 and 3.4.1 of this Exhibit A, the aggregate [*] paid for purchases of [*] by all purchasers for use in providing Dialysis Services in the Territory shall be calculated as [*] percent ([*]%) of the aggregate [*] purchases of ESAs by [*] in the Territory and (vi) for the sole and limited purpose of determining whether the [*] Share of Sales

 

Page 39 of 136


 

requirement under Section 3.3.1 and Section 3.3.2 of this Exhibit A has been met, (a) the aggregate [*] paid for purchases of [*] by all purchasers, but excluding all Dialysis Center Purchasers, for use in providing Dialysis Services in the Territory shall be calculated as [*] percent ([*]%) of the aggregate [*] purchases of ESAs by [*], but excluding all Dialysis Center Purchasers, in the Territory and (b) the aggregate [*] paid for purchases of the applicable [*] by all purchasers, but excluding all Dialysis Center Purchasers, for use in providing Dialysis Services in the Territory shall be calculated as [*] percent ([*]%) of the aggregate [*] purchases of the applicable [*] by [*], but excluding all Dialysis Center Purchasers, in the Territory.

 

2 PRODUCT INVOICE DISCOUNTS

 

  2.1

Base Invoice Discounts. Subject to the terms and conditions contained in the Agreement, Dialysis Center Purchasers shall be entitled to the Base Invoice Discount set forth in the following Base Invoice Discount Table, applied to [*] in effect at the time of purchase of EPOGEN by Dialysis Center Purchasers under the Agreement, exclusive of any wholesaler markup, discount, service fees or other charges:

Base Invoice Discount Table

 

PRODUCT

  

NDC

   INVOICE
DISCOUNT
 

EPOGEN

   All NDCs      [* ]% 

 

3 PRODUCT REBATES

 

  3.1

Base Rate Rebate. Dialysis Center shall earn a non-performance Base Rate Rebate for each Quarter during the Term in the manner described below in this Section 3.1.

 

  3.1.1

Base Rate Rebate Calculation. Amgen shall calculate the amount of Dialysis Center’s Base Rate Rebate by multiplying Dialysis Center’s Qualified Gross Purchases of EPOGEN during a Quarter by the applicable Base Rate Rebate Percentage for the calendar year in which such Quarter occurs, according to the Base Rate Rebate Percentage Table below.

 

Page 40 of 136


Base Rate Rebate Percentage Table

 

Calendar Year

   Base Rate
Rebate
Percentage
 

2012

     [* ]% 

2013

     [* ]% 

2014

     [* ]% 

2015

     [* ]% 

2016

     [* ]% 

2017

     [* ]% 

2018

     [* ]% 

 

  3.1.2

Payment of Base Rate Rebate. Amgen will pay the Base Rate Rebate within [*] days after the end of the corresponding Quarter, provided Amgen is in receipt of all Relevant Information in a form acceptable to Amgen.

 

  3.1.3

Vesting of Base Rate Rebate. The Base Rate Rebate for a given Quarter shall vest on the last day of such Quarter.

 

  3.2

[*] Rebate. Dialysis Center shall earn the [*] Rebate, if any, for each Quarter during the Term provided it meets the requirements described below in this Section 3.2.

 

  3.2.1

Eligibility for [*] Rebate. Dialysis Center shall be eligible to receive the [*] Rebate for any Quarter during the Term if each of the following shall have occurred in such Quarter: (a) Dialysis Center shall have met the Dialysis Share of Sales Requirement, (b) any Qualified Customer received a [*] under an Amgen Dialysis Contract that is lower than the [*] and (c) either (i) the aggregate net sales for all EPOGEN purchased by any such Qualified Customer who received a [*] under an Amgen Dialysis Contract that is lower than the [*] during such Quarter were greater than [*] percent ([*]%) of the aggregate net sales of EPOGEN to all purchasers in the Territory in such Quarter or (ii) the aggregate net sales for all EPOGEN purchased during such Quarter by all Qualified Customers in the aggregate who received a [*] under an Amgen Dialysis Contract that is lower than the [*] were greater than [*] percent ([*]%) of the aggregate net sales of EPOGEN to all purchasers in the Territory in such Quarter. Amgen’s calculation of the [*] Rebate shall not take into account any reallocation of discounts for purposes of any reports filed under Title XVIII or Title XIX of the Social Security Act, under any health care program of a Governmental Authority or pursuant to any other Law.

 

Page 41 of 136


  3.2.2

Calculation of [*] Rebate. Amgen shall calculate the amount of Dialysis Center’s [*] Rebate for any Quarter by taking the total of the [*] minus the [*], multiplied by the number of [*] of EPOGEN purchased by all Dialysis Center Purchasers at a [*] during such Quarter.

[*] Rebate Illustration:

([*] – [*])

x

Number of [*] of EPOGEN purchased at [*]

 

  3.2.3

Payment of [*] Rebate Amount. Amgen will pay the [*] Rebate within [*] days after the end of the corresponding Quarter, provided Amgen is in receipt of all Relevant Information in a form acceptable to Amgen.

 

  3.2.4

Vesting of [*] Rebate. The [*] Rebate for a given Quarter shall vest on the last day of such Quarter.

 

  3.3

[*] Rebate. Dialysis Center shall earn a [*] Rebate for each Quarter during the Term in the manner described below in this Section 3.3.

 

  3.3.1

Trigger Event for [*] Rebate. In the event that an [*] had an [*] Share of Sales of greater than [*] percent ([*]%) for [*] consecutive Quarters during the Term, the Parties shall work together in good faith to determine a [*] between the [*] and EPOGEN. In the event the Parties are not able to determine a mutually agreed upon [*] between the [*] and EPOGEN within thirty (30) days of the end of the applicable Quarter at which the [*] Rebate is at issue or such longer period of time as mutually agreed to by the Parties, the Parties shall work together in good faith to undertake a [*], which [*] shall be jointly funded by the Parties. If the Parties fail to agree on a design for the [*], the Parties shall jointly appoint a mutually agreeable Third Party to design and undertake the [*].

 

  3.3.2

Qualification Criteria. If for a Quarter during the Term, an [*] had an [*] Share of Sales of greater than [*] percent ([*]%) for such Quarter and the immediately prior Quarter, then Dialysis Center shall be entitled to the [*] Rebate for such Quarter, as calculated in Section 3.3.3 below.

 

  3.3.3

[*] Rebate Calculation. Amgen shall calculate the amount of Dialysis Center’s [*] Rebate by multiplying the Qualified Gross Purchases of EPOGEN during the applicable Quarters by the applicable [*] Rebate Percentage for such applicable Quarters.

 

  3.3.4

Payment of [*] Rebate. Amgen will pay the [*] Rebate within [*] days after the end of the corresponding Quarter, provided Amgen is in receipt of all Relevant Information in a form acceptable to Amgen and provided further, that in the event a final [*] for the applicable [*] has not been determined hereunder within thirty (30) days after the end of the applicable Quarter pursuant to Section 3.3.1 of this Exhibit A, such [*] Rebate will be paid within [*] days after the end of the Quarter in which a final [*] for the applicable [*] has been determined.

 

  3.3.5

Vesting of [*] Rebate. The [*] Rebate for a given Quarter shall vest on the last day of such Quarter.

 

Page 42 of 136


  3.4

[*] Rebate. Dialysis Center shall earn the [*] Rebate for each Quarter during the Term in the manner described below in this Section 3.4

 

  3.4.1

Qualification Criteria. If, for any Quarter during the Term, the [*] exceeds the [*] (“[*] Trigger Event”), then Dialysis Center Purchasers shall be entitled to the [*] Rebate as calculated in Section 3.4.2 below, provided that the Dialysis Share of Sales Requirement is met during such Quarter. Such [*] Rebate shall apply to all purchases of EPOGEN by Dialysis Center Purchasers during such Quarter from the date of the [*] Trigger Event until the date (if any) at which the [*] is equal to or greater than the [*].

 

  3.4.2

Calculation of [*] Rebate. Amgen shall calculate the amount of Dialysis Center’s [*] Rebate by multiplying the Qualified Gross Purchases of EPOGEN during the applicable Quarter by the [*] Rebate Percentage for such Quarter; provided, however, that in the event of an increase of [*] other than on the first day of a calendar year, then the [*] Rebate shall be reduced by an amount equal to the Qualified Gross Purchases of EPOGEN during such calendar year prior to the increase in [*] multiplied by the [*] minus the [*].

 

  3.4.3

Payment of [*] Rebate. Amgen will pay such [*] Rebate within [*] days after the end of the corresponding Quarter, provided Amgen is in receipt of all Relevant Information in a form reasonably acceptable to Amgen.

 

  3.4.4

Vesting of [*] Rebate. The [*] Rebate for a given Quarter shall vest on the last day of such Quarter.

 

  3.5

[*] Incentive. Dialysis Center shall earn the [*] for each Quarter during the Term provided all Dialysis Center Purchasers provide to Amgen the Data set forth in Schedule 1 and provided Dialysis Center meets the requirements described below in this Section 3.5.

 

  3.5.1

Submission of Data Requirement. Subject to the validity of a Certification as described in Section 5 of this Agreement, Dialysis Center Purchasers must provide to Amgen the Data in a machine readable format acceptable to Amgen (Excel; or text file that is tab delimited, comma delimited, colon delimited or space delimited including a line of column headers identifying the column contents and [*], if applicable). The Data files shall contain record counts for each file contained in the data submission; provided, however, that Dialysis Center shall be required to submit such test results only for those dialysis patients whose test results are actually determined by laboratories owned and operated by Dialysis Center.

 

  3.5.2

Calculation of [*]. Provided Dialysis Center has fulfilled all requirements described in this Section 3.5 of this Exhibit A, Dialysis Center shall be eligible to receive a [*] percent ([*]%) [*] payment. The [*] will be calculated as a percentage of the Qualified Gross Purchases of EPOGEN during each Quarter.

 

  3.5.3

Payment of [*]. The Data must be submitted, on a calendar monthly basis by the last day of the following calendar month (or the next business day if such last day is not a business day). If the Data is received after such timeframe for any month within a given Quarter, the total Qualified Gross Purchases of EPOGEN during such month will be excluded from the calculation of the [*] for that Quarter. Notwithstanding the foregoing, if Amgen receives all required Data from a minimum of [*] percent ([*]%) of all Dialysis Center Purchasers within the time frame referenced above for any calendar month within a given Quarter, the total Qualified Gross Purchases of EPOGEN during such calendar month, will be included in the calculation of the [*] for that Quarter; provided that for purposes of clarity, the [*] percent ([*]%) will not include Dialysis Center Purchasers that are acute facilities. Failure of Dialysis Center to qualify under this Section 3.5 of this

 

Page 43 of 136


 

Exhibit A during a particular Quarter shall not affect Dialysis Center’s eligibility to qualify during any other Quarter, nor shall Dialysis Center’s qualification during a particular Quarter automatically result in qualification during any other Quarter. If Amgen receives all required Data from less than [*] percent ([*]%) of Dialysis Center Purchasers for any calendar month within a given Quarter, no Qualified Gross Purchases of EPOGEN during such calendar month will be included in the calculation of the [*] for that Quarter; provided, however, that if such [*] percent ([*]%) threshold is not met in any month due to the inclusion of de novo facilities that have not yet treated patients and/or inactive facilities, Amgen shall exclude any such facilities identified by Amgen and Dialysis Center from such month when calculating Dialysis Center’s eligibility for the [*] at the end of each Quarter. However, if Amgen determines that any Dialysis Center Purchaser is consistently not submitting the required Data, Amgen and Dialysis Center will work collaboratively in resolving such inconsistencies. Amgen will use commercially reasonable efforts to notify Dialysis Center in writing, no later than fifteen (15) business days after the receipt and acceptance by Amgen of the Data of the identity of all Dialysis Center Purchasers, if any, which have failed to meet the Data submission requirements for that month. Amgen reserves the right, in its sole discretion, to exclude any Qualified Gross Purchases of EPOGEN of any Dialysis Center Purchaser that is consistently non-reporting from the calculation of the [*] for any relevant Quarter. Amgen will pay such [*] within [*] days after the end of the corresponding Quarter provided Amgen is in receipt of all Data in the form and in the time period described in Section 3.5.1 and this Section 3.5.3 of this Exhibit A. If the failure of Dialysis Center to deliver any of the Data is a result of a Certification not being valid due to Amgen’s failure to satisfy any conditions, requirements or assumptions set forth in such Certification applicable to Amgen, then the [*] shall still be available to Dialysis Center and payable by Amgen, in which case Dialysis Center shall deliver the Data to Amgen as soon as the Certification becomes valid. Upon a valid Certification being issued, Dialysis Center shall submit to Amgen all Data dating back to the date Dialysis Center stopped submitting the Data to Amgen within thirty (30) days.

 

  3.5.4 Vesting of [*]. The [*] for a given Quarter shall vest on the last day of such Quarter.

 

4 SUMMARY OF DISCOUNTS

Provided Dialysis Center has fulfilled all Discount requirements, the total discount opportunity is as set forth in the Summary of Discounts Table below.

Summary of Discounts Table

 

     2012     2013     2014     2015     2016     2017     2018  

Base Invoice Discount

     [* ]%      [* ]%      [* ]%      [* ]%      [* ]%      [* ]%      [* ]% 

Base Rate Rebate

     [* ]%      [* ]%      [* ]%      [* ]%      [* ]%      [* ]%      [* ]% 

[*] Rebate

     [* ]%      [* ]%      [* ]%      [* ]%      [* ]%      [* ]%      [* ]% 

Total Discount Opportunity

     [* ]%      [* ]%      [* ]%      [* ]%      [* ]%      [* ]%      [* ]% 

 

Page 44 of 136


Exhibit B

Authorized Wholesalers

The below represents a list of wholesalers authorized for participation under the attached Agreement. Any changes must be made in accordance with Section 2.7 of the Agreement. Only purchases from wholesalers set forth on this List (as may be modified pursuant to such Section 2.7) shall be eligible for the discounts and fees set forth in the Agreement. Notice(s) regarding pricing and membership alignment for the Agreement shall be sent to the wholesalers that Dialysis Center has designated for such notification below. In the absence of any such designation, Amgen shall send pricing and membership alignment notices for the Agreement to those Authorized Wholesalers as designated by Dialysis Center in its previously executed Agreement.

 

   American Medical Distributors, Div. of AmerisourceBergen Corporation

 

  
   American Medical Services, Div. of Henry Schein, Inc.

 

  
   AmerisourceBergen Corporation

 

  
   ASD Healthcare, Div. of AmerisourceBergen Specialty Group

 

  
   Bellco Drug Corporation, Div of AmerisourceBergen Corporation

 

  
   Besse Medical Supply, Div. of AmerisourceBergen Specialty Group

 

  
   Borschow Hospital and Medical Supplies, Inc., Div of Cardinal Health, Inc.

 

  
   Cardinal Health Inc.

 

  
   Cesar Castillo, Inc.

 

  
   CuraScript Specialty Distribution (Priority Healthcare Distribution)

 

  
   Dakota Drug Inc.

 

  
   Dik Drug Company

 

  
   DMS Pharmaceutical Group Inc.

 

  
   Drogueria Central, Inc.

 

  
   Florida Infusion Services, Inc.

 

  
   Frank W. Kerr Company

 

  
   General Injectables & Vaccines, Div. of Henry Schein, Inc.

 

  
   HD Smith Wholesale Drug Company

 

  
   Henry Schein, Inc.

 

  
   J.M. Blanco, Div of AmerisourceBergen Corporation

 

  
   Kinray, Inc.

 

  
   McKesson Corporation

 

  
  

McKesson Medical-Surgical Maine Inc., Div. of McKesson Medical-Surgical

 

  
  

McKesson Medical-Surgical Minnesota Supply Inc., Div. of McKesson Medical

 

  
  

Surgical

  

McKesson Medical-Surgical, Div. of McKesson Corporation

 

  
   McKesson Specialty Care Distribution Corporation, Div. of McKesson Corporation

 

  
   Metro Medical Supply Inc.

 

  
   Morris & Dickson Company LLC

 

  
   N.C. Mutual Wholesale Drug Company

 

  
   Oncology Supply, Div. of AmerisourceBergen Specialty Group

 

  
   Rochester Drug Corporation (RDC)

 

  
   Smith Drug Company

 

  
   Value Drug Company

 

  

 

Page 45 of 136


Exhibit C

Designated Affiliates List

 

Page 46 of 136


Exhibit C

Designated Affiliates List

 

Active
count

 

TYPE

 

CTR #

 

CENTER NAME

 

LEGAL NAME

 

ADDRESS

 

ADDRESS

 

CITY

 

STATE

 

ZIP

1   Affiliated   398   Los Angeles Dialysis Center   Los Angeles Dialysis Center (LADC)   3901 S WESTERN AVE     LOS ANGELES   CA   90062-1112
2   Affiliated   613   Garfield   Garfield Hemodialysis Center   118 HILLIARD AVE     MONTEREY PARK   CA   91754-1118
3   Affiliated   614   Lynwood   Kidney Dialysis Care Unit (Lynwood)   3600 E MARTIN LUTHER KING JR BLVD     LYNWOOD   CA   90262-2607
4   Affiliated   615   Lakewood Dialysis-CA   Lakewood Dialysis-CA   4611 SILVA ST     LAKEWOOD   CA   90712-2512
5   Affiliated   616   Valley Dialysis   Valley Dialysis   16149 HART ST     VAN NUYS   CA   91406-3906
6   Affiliated   617   Downey Dialysis   Downey Dialysis   8630 FLORENCE AVE   STE 1   DOWNEY   CA   90240-4017
7   Affiliated   618   Covina Dialysis   Covina Dialysis   1547 W GARVEY AVE N     WEST COVINA   CA   91790-2139
8   Affiliated   625   Four Corners Farmington   Four Corners Farmington   801 W BROADWAY     FARMINGTON   NM   87401-5650
9   Affiliated   626   Tuba City Dialysis   Tuba City Dialysis   500 EDGEWATER DR   PO BOX 291   TUBA CITY   AZ   86045-2905
10   Affiliated   627   Camelback Dialysis Center   Camelback Dialysis Center (fka Scottsdale Dialysis Center)   7321 E OSBORN DR     SCOTTSDALE   AZ   85251-6418
11   Affiliated   630   Westbank   Westbank Chronic Renal Center   3631 BEHRMAN PLACE     NEW ORLEANS   LA   70114
12   Affiliated   632   Fleur de Lis   Fleur de Lis Dialysis (fka Tri-Parish)   5555 BULLARD AVE     NEW ORLEANS   LA   70128-3450
13   Affiliated   637   Desert Mountain   Desert Mountain Dialysis   9220 E MOUNTAIN VIEW RD   STE 15   SCOTTSDALE   AZ   85258-5134
14   Affiliated   638   Chinle   Chinle Dialysis   US HWY 191   PO BOX 879   CHINLE   AZ   86503-0879
15   Affiliated   648   Central City   Central City Dialysis Center   1300 MURCHISON DR   STE 32   EL PASO   TX   79902-4840
16   Affiliated   651   Federal Way   Federal Way Community Dialysis Center   1015 S 348TH ST     FEDERAL WAY   WA   98003-7078
17   Affiliated   663   Beverly Hills   Beverly Hills Dialysis Center   50 N LA CIENEGA BLVD   3RD FLOOR, STE 3   BEVERLY HILLS   CA   90211-2205
18   Affiliated   667   Walnut Creek   Walnut Creek Dialysis Center   404 N WIGET LN     WALNUT CREEK   CA   94598-2408
19   Affiliated   672   Norwalk   Norwalk Dialysis Center   12375 E IMPERIAL HWY   STE D3   NORWALK   CA   90650-3129
20   Affiliated   673   El Monte   Greater El Monte Dialysis Center   1938 TYLER AVE   STE J-168   SOUTH EL MONTE   CA   91733-3623
21   Affiliated   676   Bayonet Point   Bayonet Point-Hudson Kidney   14144 NEPHRON LN     HUDSON   FL   34667-6504
22   Affiliated   677   New Port Richey   New Port Richey Kidney Center   7421 RIDGE RD     PORT RICHEY   FL   34668-6933
23   Affiliated   678   Hernando   Hernando Kidney Center, Inc   2985 LANDOVER BLVD     SPRING HILL   FL   34608-7258
24   Affiliated   681   Woodbridge   CDC Of Woodbridge   2751 KILLARNEY DR     WOODBRIDGE   VA   22192-4119
25   Affiliated   682   Manassas   CDC-Manassas Dialysis   10655 LOMOND DR   STE 11   MANASSAS   VA   20109-2877
26   Affiliated   683   Springfield   CDC-Springfield Dialysis   8350 TRAFORD LN   STE A   SPRINGFIELD   VA   22152-1671
27   Affiliated   684   Sterling   CDC-Sterling   46396 BENEDICT DR   STE 1   STERLING   VA   20164-6626
28   Affiliated   687   Alexandria   Springfield-Alexandria   5999 STEVENSON AVE   STE 1   ALEXANDRIA   VA   22304-3302
29   Affiliated   642   Statesboro   Nephrology Center of Statesboro fka Statesboro Dialysis   4B COLLEGE PLZ     STATESBORO   GA   30458-4928
30   Affiliated   643   Vidalia   Nephrology Center of Vidalia   1806 EDWINA DR     VIDALIA   GA   30474-8927
31   Affiliated   657   Papago Dialysis   Papago Dialysis Center (fka PD Central & Squaw Peak)   1401 N 24TH ST   STE 2   PHOENIX   AZ   85008-4638
32   Affiliated   658   Boca Raton   Boca Raton Artificial Kidney Center   998 NW 9TH CT     BOCA RATON   FL   33486-2214
33   Affiliated   644   Piedmont   Buckhead Dialysis   1575 NORTHSIDE DR NW   STE 365   ATLANTA   GA   30318-4210
34   Affiliated   311   Logan Square   Logan Square Dialysis Services   2659 N MILWAUKEE AVE   1ST FL   CHICAGO   IL   60647-1643
35   Affiliated   312   Lake County   Lake County Dialysis Services   918 S MILWAUKEE AVE     LIBERTYVILLE   IL   60048-3229
36   Affiliated   314   Lincoln Park   Lincoln Park Dialysis fka Lincoln Park Nephrology   3157 N LINCOLN AVE     CHICAGO   IL   60657-3111
37   Affiliated   318   Lincoln Pk-PD   Skyline Home Dialysis (fka Lincoln Park PD)   7009 W BELMONT AVE     CHICAGO   IL   60634-4533
38   Affiliated   670   West Palm Beach   Dialysis Associates of the Palm Beaches   2611 POINSETTIA AVE     WEST PALM BEACH   FL   33407-5919
39   Affiliated   693   Sunrise   Sunrise Dialysis Center   13039 HAWTHORNE BLVD     HAWTHORNE   CA   90250-4415
40   Affiliated   655   Kayenta   Kayenta Dialysis   PO BOX 217   US HWY 163 N   KAYENTA   AZ   86033-0217
41   Affiliated   321   Hyde Park   Emerald Dialysis (fka Hyde Park Kidney Center)   710 W 43RD ST     CHICAGO   IL   60609-3435
42   Affiliated   322   Olympia Fields   Olympia Fields Dialysis Center   4557B LINCOLN HWY   STE B   MATTESON   IL   60443-2318
43   Affiliated   351   CKD   Center for Kidney Disease at North Shore   1190 NW 95TH ST   STE 28   MIAMI   FL   33150-2065
44   Affiliated   352   Venture   Center for Kidney Disease at Venture   16855 NE 2ND AVE   STE 25   N MIAMI BEACH   FL   33162-1744
45   Affiliated   360   South Broward   South Broward Artifical Kidney   4401 HOLLYWOOD BLVD     HOLLYWOOD   FL   33021-6609
46   Affiliated   688   East End   East End Dialysis Center   2201 E MAIN ST   STE 1   RICHMOND   VA   23223-7071
47   Affiliated   354   Flamingo Park   Flamingo Park Kidney Cntr, Inc   901 E 10TH AVE   BAY 17   HIALEAH   FL   33010-3762
48   Affiliated   355   Interamerican   InterAmerican Dialysis Center   7815 CORAL WAY   STE 115   MIAMI   FL   33155-6541
49   Affiliated   356   Coral Gables Dialysis Center   Coral Gables Kidney Center (fka LeJeune)   3280 PONCE DE LEON BLVD     CORAL GABLES   FL   33134-7252

 

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50   Affiliated   370   Cielo Vista Dialysis   DaVita East Dialysis dba Cielo Vista Dialysis (fkaTotal Renal Care East Dialysis Center)   7200 GATEWAY BLVD E   STE B   EL PASO   TX   79915-1301
51   Affiliated   371   West Texas Dialysis   DaVita West Dialysis Center dba West Texas (fkaTotal Renal Care West Dialysis Center)   5595 ALAMEDA AVE B   STE B   EL PASO   TX   79905
52   Affiliated   656   Shiprock   Shiprock Dialysis   PO BOX 2156   US HWY 491 N   SHIPROCK   NM   87420-2156
53   Affiliated   202   Arden Hills   Arden Hills Dialysis Unit   3900 NORTHWOODS DR   STE 11   ARDEN HILLS   MN   55112-6911
54   Affiliated   203   Burnsville   Burnsville Dialysis Unit   501 E NICOLLET BLVD   STE 15   BURNSVILLE   MN   55337-6784
55   Affiliated   204   Coon Rapids   Coon Rapids Dialysis Unit   3960 COON RAPIDS BLVD NW   STE 39   COON RAPIDS   MN   55433-2598
56   Affiliated   205   Edina   Edina Dialysis Unit   6550 YORK AVE S   STE 1   EDINA   MN   55435-2332
57   Affiliated   206   Maplewood   Maplewood Dialysis Center   2785 WHITE BEAR AVE N   STE 21   MAPLEWOOD   MN   55109-1320
58   Affiliated   207   Minneapolis   Minneapolis Dialysis Unit   825 S EIGHTH ST   STE SL42   MINNEAPOLIS   MN   55404-1208
59   Affiliated   208   Minnetonka   Minnetonka Dialysis Unit   17809 HUTCHINS DR     MINNETONKA   MN   55345-4100
60   Affiliated   209   St. Paul Dialysis   St. Paul Dialysis Unit   555 PARK ST   STE 18   SAINT PAUL   MN   55103-2192
61   Affiliated   210   Special Needs   University Dialysis Unit Riverside (Minneapolis-Special Needs Dialysis)   1045 WESTGATE DR   STE 9   SAINT PAUL   MN   55114-1079
62   Affiliated   211   West St. Paul   West St. Paul Dialysis   1555 LIVINGSTON AVE     WEST ST PAUL   MN   55118-3411
63   Affiliated   213   Cass Lake   Cass Lake Dialysis Unit   602 GRANT UTLEY ST   PO BOX 757   CASS LAKE   MN   56633-0757
64   Affiliated   215   Faribault   Faribault Dialysis Unit   201 LYNDALE AVE S   STE F   FARIBAULT   MN   55021-5758
65   Affiliated   217   Marshall   Marshall Dialysis Unit   300 S BRUCE ST   AVERA MARSHALL REGIONAL MEDICAL CENTER   MARSHALL   MN   56258-1934
66   Affiliated   218   Montevideo   Montevideo Dialysis Center   824 N 11TH ST   MONTEVIDEO HOSPITAL   MONTEVIDEO   MN   56265-1629
67   Affiliated   220   Pine City   TRC-Pine City (fka-Pine City Dialysis Unit)   129 6TH AVE SE   LAKESIDE MEDICAL CENTER   PINE CITY   MN   55063-1913
68   Affiliated   222   Red Wing   Red Wing Dialysis Unit   3028 N SERVICE DR     RED WING   MN   55066-1921
69   Affiliated   223   Redwood Falls   Redwood Falls Dialysis Center   100 FALLWOOD RD     REDWOOD FALLS   MN   56283-1828
70   Affiliated   240   Mitchell   Mitchell Dialysis   525 N FOSTER   QUEEN OF PEACE HOSPITAL   MITCHELL   SD   57301-2966
71   Affiliated   242   Rosebud   Rosebud Dialysis   1 SOLDIER CREEK RD     ROSEBUD   SD   57570-0610
72   Affiliated   243   Sioux Falls   Sioux Falls Dialysis Community Unit   1325 S CLIFF AVE   STE 46   SIOUX FALLS   SD   57105-1016
73   Affiliated   250   St. Croix Falls   St. Croix Falls Dialysis   744 E LOUISIANA ST     SAINT CROIX FALLS   WI   54024-9501
74   Affiliated   260   Hayward   Hayward Dialysis Center   21615 HESPERIAN BLVD   STE F   HAYWARD   CA   94541-7026
75   Affiliated   262   Pleasanton   Pleasanton Dialysis Center (HEMO) (fka Dublin)   5720 STONERIDGE MALL RD   STE 16   PLEASANTON   CA   94588-2882
76   Affiliated   263   Union City   Union City Dialysis Center (aka TRC-Union City)   32930 ALVARADO NILES RD   STE 3   UNION CITY   CA   94587-8101
77   Affiliated   264   East Bay - PD   East Bay Peritoneal Dialysis Center   13939 E 14TH ST   STE 11   SAN LEANDRO   CA   94578-2613
78   Affiliated   383   Greer   Greer Kidney Center   211 VILLAGE DR     GREER   SC   29651-1238
79   Affiliated   382   Upstate   Upstate Dialysis Center   308 MILLS AVE     GREENVILLE   SC   29605-4022
80   Affiliated   390   Kenner   Kenner Regional Dialysis Center   200 W ESPLANADE AVE   STE 1   KENNER   LA   70065-2473
81   Affiliated   689   Downtown Dialysis   Downtown Dialysis Center   821 N EUTAW ST   STE 41   BALTIMORE   MD   21201-6304
82   Affiliated   331   Eaton Canyon   Eaton Canyon Dialysis   2551 E WASHINGTON BLVD     PASADENA   CA   91107-1446
83   Affiliated   190   Georgetown   Georgetown on the Potomac   3223 K ST NW   STE 11   WASHINGTON   DC   20007-4412
84   Affiliated   395   St. Mary   Newtown Dialysis Center (fka St. Mary Dialysis)   60 BLACKSMITH RD     NEWTOWN   PA   18940-1847
85   Affiliated   393   Bertha Sirk   Bertha Sirk Dialysis Center   5820 YORK RD   STE 1   BALTIMORE   MD   21212-3620
86   Affiliated   394   Greenspring   Greenspring Dialysis Center   4701 MOUNT HOPE DR   STE C   BALTIMORE   MD   21215-3246
87   Affiliated   378   Houston Kidney - NW   Northwest Kidney Center (Houston)   11029 NORTHWEST FWY     HOUSTON   TX   77092-7311
88   Affiliated   379   NorthStar Dialysis   NorthStar Dialysis Center (fka North Houston Kidney Center)   380 W LITTLE YORK RD     HOUSTON   TX   77076-1303
89   Affiliated   363   Port Charlotte   Port Charlotte Artificial Kidney Center   4300 KINGS HWY STE 406     PORT CHARLOTTE   FL   33980
90   Affiliated   364   Gulf Coast PD   Gulf Coast Dialysis   3300 TAMIAMI TRL   STE 11A   PORT CHARLOTTE   FL   33952-8054
91   Affiliated   649   Loma Vista   Loma Vista Dialysis Center Partnership   1382 LOMALAND DR   STE A   EL PASO   TX   79935-5204
92   Affiliated   332   Paramount   Paramount Dialysis Center   8319 ALONDRA BLVD     PARAMOUNT   CA   90723-4403
93   Affiliated   334   East LA   Doctors Dialysis of East LA (aka East Los Angeles Dialysis)   950 S EASTERN AVE     LOS ANGELES   CA   90022-4801
94   Affiliated   335   Montebello   Doctors Dialysis of Montebello   1721 W WHITTIER BLVD     MONTEBELLO   CA   90640-4004
95   Affiliated   361   Pine Island   Pine Island Kidney Center   1871 N PINE ISLAND RD     PLANTATION   FL   33322-5208
96   Affiliated   365   Complete   Complete Dialysis Care   7850 W SAMPLE RD     MARGATE   FL   33065-4710
97   Affiliated   122   Lone Star Dialysis   Lone Star Dialysis (fka Hobby Dialysis)   8560 MONROE RD     HOUSTON   TX   77061-4815
98   Affiliated   255   Forest Lake   Forest Lake Dialysis   1068 S LAKE ST   STE 11   FOREST LAKE   MN   55025-2633
99   Affiliated   690   USC Phase II   TRC/USC Dialysis Center   2310 ALCAZAR ST     LOS ANGELES   CA   90033-5327
100   Affiliated   396   TRC/Union Plaza Ctr   Union Plaza Dialysis Center   810 1ST ST NE   STE 1   WASHINGTON   DC   20002-4227
101   Affiliated   130   Mid-Columbia Kidney   Mid Columbia Kidney Center   6825 BURDEN BLVD   STE A   PASCO   WA   99301-9584
102   Affiliated   131   Mt. Adams Kidney Ctr   Mt. Adams Kidney Center   3220 PICARD PL     SUNNYSIDE   WA   98944-8400
103   Affiliated   650   Lakewood   Lakewood Community Dialysis Center   5919 LAKEWOOD TOWNE CENTER BLVD SW   STE A   LAKEWOOD   WA   98499-6513

 

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104   Affiliated   228   St. Paul Ramsey   St. Paul Capitol Dialysis   555 PARK ST   STE 23   SAINT PAUL   MN   55103-2193
105   Affiliated   229   River City Dialysis   River City Dialysis (fka Lakeview Dialysis)   1970 NORTHWESTERN AVE S     STILLWATER   MN   55082-6567
106   Affiliated   231   Woodbury   Woodbury Dialysis   1850 WEIR DR   STE 3   WOODBURY   MN   55125-2260
107   Affiliated   281   Alhambra   Alhambra Dialysis Center   1315 ALHAMBRA BLVD   STE 1   SACRAMENTO   CA   95816-5245
108   Affiliated   282   Antelope   Antelope Dialysis Center   6406 TUPELO DR   STE A   CITRUS HEIGHTS   CA   95621-1780
109   Affiliated   283   Chico   Chico Dialysis Center (aka Chico Clinic)   530 COHASSET RD     CHICO   CA   95926-2212
110   Affiliated   285   North Clinic   Manzanita Dialysis Center (aka North Clinic)   4005 MANZANITA AVE   STE 17   CARMICHAEL   CA   95608-1779
111   Affiliated   286   Placerville   Cameron Park Dialysis (fka Placerville)   3311 COACH LN   STE C   CAMERON PARK   CA   95682
112   Affiliated   288   South Sacramento   South Sacramento Dialysis Center   7000 FRANKLIN BLVD   STE 88   SACRAMENTO   CA   95823-1838
113   Affiliated   289   Redding   Redding Dialysis Center   1876 PARK MARINA DR     REDDING   CA   96001-0913
114   Affiliated   291   Yuba City   Yuba City Dialysis Center   1525 PLUMAS CT   STE A   YUBA CITY   CA   95991-2971
115   Affiliated   292   University Clinic   University Dialysis Center   777 CAMPUS COMMONS RD   STE 1   SACRAMENTO   CA   95825-8344
116   Affiliated   372   Mesa Vista   Mesa Vista Dialysis Center (El Paso)   2400 N OREGON ST   STE C   EL PASO   TX   79902-3135
117   Affiliated   694   Hollywood   Hollywood Dialysis Center   5108 W SUNSET BLVD     LOS ANGELES   CA   90027-5708
118   Affiliated   697   UCLA Harbor   TRC/Harbor-UCLA MFI Total Renal Dialysis Center   21602 S VERMONT AVE     TORRANCE   CA   90502-1940
119   Affiliated   325   Brighton   Brighton Dialysis (fka Michigan Kidney Center of Brighton)   7960 GRAND RIVER RD   STE 21   BRIGHTON   MI   48114-7336
120   Affiliated   326   Macomb   Macomb Kidney Center (fka Macomb Dialysis)   28295 SCHOENHERR RD   STE A   WARREN   MI   48088-4300
121   Affiliated   327   North Oakland   North Oakland Dialysis   450 N TELEGRAPH RD   STE 6   PONTIAC   MI   48341-1037
122   Affiliated   328   Novi   Novi Dialysis   47250 W 10 MILE RD     NOVI   MI   48374-2932
123   Affiliated   329   Southfield   Cornerstone Dialysis (fka Southfield)   23857 GREENFIELD RD     SOUTHFIELD   MI   48075-3122
124   Affiliated   319   Children’s Mem’l Hosp.   TRC Children’s Dialysis Center aka Children’s Chicago/Children’s Memorial Hospital   2611 N HALSTED ST     CHICAGO   IL   60614-2301
125   Affiliated   151   New Center   New Center Dialysis   3011 W GRAND BLVD   STE 65   DETROIT   MI   48202-3012
126   Affiliated   2003   Whittier   Whittier Dialysis Center (fka Whittier Hills)   10055 WHITTWOOD DR     WHITTIER   CA   90603-2313
127   Affiliated   357   Miami Lakes   Miami Lakes Artificial Kidney Center (ALTHIN)   14600 NW 60TH AVE     MIAMI LAKES   FL   33014-2811
128   Affiliated   571   Anson County   Dialysis Care of Anson County   923 E CASWELL ST     WADESBORO   NC   28170-2305
129   Affiliated   573   Edgecomb County   Dialysis Care of Edgecomb County   3206 WESTERN BLVD     TARBORO   NC   27886-1828
130   Affiliated   574   Franklin County   Dialysis Care of Franklin County   1706 NC HWY 39 N     LOUISBURG   NC   27549-8329
131   Affiliated   575   Hoke County   Dialysis Care of Hoke County   403 S MAIN ST     RAEFORD   NC   28376-3222
132   Affiliated   576   Martin County   Dialysis Care of Martin County   100 MEDICAL DR     WILLIAMSTON   NC   27892-2156
133   Affiliated   578   Montgomery County   Dialysis Care of Montgomery County (aka Montgomery)   323 W MAIN ST     BISCOE   NC   27209-9528
134   Affiliated   579   Moore County   Dialysis Care of Moore County (aka Pinehurst)   16 REGIONAL DR     PINEHURST   NC   28374-8850
135   Affiliated   580   Richmond County   Dialysis Care of Richmond County   771 CHERAW RD     HAMLET   NC   28345-7158
136   Affiliated   581   Rockingham County   Dialysis Care of Rockingham County   251 W KINGS HWY     EDEN   NC   27288-5009
137   Affiliated   582   Rowan County   Dialysis Care of Rowan County   111 DORSETT DR     SALISBURY   NC   28144-2278
138   Affiliated   583   Rutherford County   Dialysis Care of Rutherford County   226 COMMERCIAL ST     FOREST CITY   NC   28043-2851
139   Affiliated   399   Monterey Park   Monterey Park Dialysis Center   2560 CORPORATE PL   STE 1-11 BLDG D   MONTEREY PARK   CA   91754-7612
140   Affiliated   183   Mason Dixon   Mason-Dixon Baltimore County   9635-A LIBERTY RD   STE 1   RANDALLSTOWN   MD   21133-2436
141   Affiliated   184   Carrol County   Carroll County Dialysis Facility   412 MALCOLM DR   STE 31   WESTMINSTER   MD   21157-6167
142   Affiliated   167   South Brooklyn   South Brooklyn Nephrology Center   3915 AVENUE V   STE 14   BROOKLYN   NY   11234-5150
143   Affiliated   843   Phenix City   Phenix City Dialysis Center   1900 OPELIKA RD     PHENIX CITY   AL   36867-3640
144   Affiliated   876   Brea   Brea Dialysis Center   595 TAMARACK AVE   STE A   BREA   CA   92821-3125
145   Affiliated   878   Hemet   Hemet Dialysis Center   3050 W FLORIDA AVE     HEMET   CA   92545-3619
146   Affiliated   883   Temecula   Temecula Dialysis Center   40945 COUNTY CENTER DR   STE G   TEMECULA   CA   92591-6006
147   Affiliated   880   Riverside   Riverside Dialysis Center   4361 LATHAM ST   STE 1   RIVERSIDE   CA   92501-1767
148   Affiliated   870   Napa   Napa Dialysis Center   3900 BEL AIRE PLZ   STE C   NAPA   CA   94558-2823
149   Affiliated   875   Santa Ana   Santa Ana Dialysis Center   1820 E DEERE AVE     SANTA ANA   CA   92705-5721
150   Affiliated   879   Valley View Dialysis Center   Valley View Dialysis Center (aka Morneo Valley)   26900 CACTUS AVE     MORENO VALLEY   CA   92555-3912
151   Affiliated   884   Orange   Mainplace Dialysis Center (fka Orange Dialysis Center)   972 W TOWN AND COUNTRY RD     ORANGE   CA   92868-4714
152   Affiliated   882   San Bernadino   Mountain Vista Dialysis Center (fka San Bernadino Dailysis Center (Mountain Vista))   4041 NORTH UNIVERSITY PKWY     SAN BERNARDINO   CA   92407-1823
153   Affiliated   871   Lakeport   Lakeport Dialysis Center   804 11TH ST   STE 2   LAKEPORT   CA   95453-4102
154   Affiliated   873   Vacaville   Vacaville Dialysis Center   941 MERCHANT ST     VACAVILLE   CA   95688-5315
155   Affiliated   877   Corona   Corona Dialysis Center   1820 FULLERTON AVE   STE 18   CORONA   CA   92881-3147
156   Affiliated   872   Fairfield   Fairfield Dialysis Center   4660 CENTRAL WAY     FAIRFIELD   CA   94534-1803
157   Affiliated   902   Westminster   Westminster Dialysis Center (Federal Heights)   9053 HARLAN ST   STE 9   WESTMINSTER   CO   80031-2908

 

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158   Affiliated   901   Aurora   Aurora Dialysis Center   1411 S POTOMAC ST   AMC II STE 1   AURORA   CO   80012-4536
159   Affiliated   900   Denver   Denver Dialysis Center   2900 DOWNING ST   STE C   DENVER   CO   80205-4699
160   Affiliated   903   Littleton   Littleton Dialysis Center   209 W COUNTY LINE RD     LITTLETON   CO   80129-1901
161   Affiliated   904   South Denver   South Denver Dialysis Center   850 E HARVARD AVE   STE 6   DENVER   CO   80210-5030
162   Affiliated   946   Lee Street Dialysis   Lee Street Dialysis (fka Grant Park Dialysis Center)   5155 LEE ST NE     WASHINGTON   DC   20019-4051
163   Affiliated   868   Leesburg   Leesburg Dialysis Center   801 E DIXIE AVE   STE 18A   LEESBURG   FL   34748-7699
164   Affiliated   866   Panama City   Panama City Dialysis Center   615 HIGHWAY 231     PANAMA CITY   FL   32405-4704
165   Affiliated   867   Marianna   Marianna Dialysis Center   2930 OPTIMIST DR     MARIANNA   FL   32448-7703
166   Affiliated   864   Venice   Venice Dialysis Center   816 PINEBROOK RD     VENICE   FL   34285-7103
167   Affiliated   827   Buena Vista   Buena Vista Dialysis Center   349 GENEVA RD     BUENA VISTA   GA   31803-1701
168   Affiliated   828   Decatur   Decatur Dialysis Center   1987 CANDLER RD     DECATUR   GA   30032-4212
169   Affiliated   825   Moultrie   Moultrie Dialysis Center   2419 S MAIN ST     MOULTRIE   GA   31768-6531
170   Affiliated   820   SW Atlanta   Southwest Atlanta Dialysis Center   3620 MARTIN LUTHER KING DR SW     ATLANTA   GA   30331-3711
171   Affiliated   818   Griffin   Griffin Dialysis Center   731 S 8TH ST     GRIFFIN   GA   30224-4818
172   Affiliated   826   Columbus   Columbus Dialysis Center   6228 BRADLEY PARK DR   STE B   COLUMBUS   GA   31904-3604
173   Affiliated   829   East Macon   East Macon Dialysis Center   165 EMERY HWY   STE 11   MACON   GA   31217-3666
174   Affiliated   817   Jonesboro   Jonesboro Dialysis Center   129 KING ST     JONESBORO   GA   30236-3656
175   Affiliated   824   Milledgeville   Milledgeville Dialysis Center   400 S WAYNE ST     MILLEDGEVILLE   GA   31061-3446
176   Affiliated   823   Fort Valley   Fort Valley Dialysis Center   557 BLUEBIRD BLVD     FORT VALLEY   GA   31030-5083
177   Affiliated   821   Midtown   Linden Dialysis (fka Midtown-Atlanta)   121 LINDEN AVE NE     ATLANTA   GA   30308-2432
178   Affiliated   953   E. St. Louis   Sauget Dialysis (fka East St. Louis Dialysis Center)   2061 GOOSE LAKE RD     SAUGET   IL   62206-2822
179   Affiliated   952   Granite City   Granite City Dialysis Center   9 AMERICAN VLG     GRANITE CITY   IL   62040-3706
180   Affiliated   937   Batesville   Batesville Dialysis Center Aka Renal Treatment Centers-Batesville   232 STATE ROAD 129 S     BATESVILLE   IN   47006-7694
181   Affiliated   938   Lawrenceburg   Lawrenceburg Dialysis Center   721 RUDOLPH WAY     GREENDALE   IN   47025-8378
182   Affiliated   939   Madison   Madison Dialysis Center   220 CLIFTY DR   UNIT K   MADISON   IN   47250-1669
183   Affiliated   836   Newton   Renal Treatment Center-Newton aka-Newton Dialysis Center   1223 WASHINGTON RD     NEWTON   KS   67114-4855
184   Affiliated   837   Derby   Renal Treatment Center-Derby aka Derby Dialysis Center   250 W RED POWELL DR     DERBY   KS   67037-2626
185   Affiliated   834   Winfield   Renal Treatment Center-Winfield aka, Winfield Dialysis Center   1315 E 4TH AVE     WINFIELD   KS   67156-2457
186   Affiliated   830   Wichita   Wichita Dialysis Center   909 N TOPEKA ST     WICHITA   KS   67214-3620
187   Affiliated   833   Garden City   Renal Treatment Center-Garden City Aka-Garden City Dialysis Center   401 N MAIN ST     GARDEN CITY   KS   67846-5429
188   Affiliated   831   E. Wichita   East Wichita Dialysis Center   320 N HILLSIDE ST     WICHITA   KS   67214-4918
189   Affiliated   832   Independance   Independence Dialysis Center   801 W MYRTLE ST     INDEPENDENCE   KS   67301-3239
190   Affiliated   835   Parson, KS   Parsons Dialysis Center   1902 S US HWY 59   BLDG B   PARSONS   KS   67357-4948
191   Affiliated   814   Wheaton   Wheaton Dialysis Center   11941 GEORGIA AVE     WHEATON   MD   20902
192   Affiliated   812   Rockville   Rockville Dialysis Center   14915 BROSCHART RD   STE 1   ROCKVILLE   MD   20850-3367
193   Affiliated   815   Owing Mills   Owings Mills Dialysis Center (fka-Renal Treatment Center-Owings Mills)   10 CROSSROADS DR   STE 11   OWINGS MILLS   MD   21117-5463
194   Affiliated   811   Berlin   Berlin Dialysis Center   314 FRANKLIN AVE   STE 36   BERLIN   MD   21811-1238
195   Affiliated   810   Easton   Easton Dialysis Center   402 MARVEL CT     EASTON   MD   21601-4052
196   Affiliated   813   Chestertown   Chestertown Dialysis Center (fka Renal Treatment Centers-Chestertown)   100 BROWN ST     CHESTERTOWN   MD   21620
197   Affiliated   951   Hope Again   Hope Again Dialysis Center- fka Kennett Dialysis Center   1207 STATE ROUTE VV     KENNETT   MO   63857-3823
198   Affiliated   950   Poplar Bluff   Bluff City Dialysis Center   2400 LUCY LEE PKWY   STE E   POPLAR BLUFF   MO   63901-2429
199   Affiliated   949   Crystal City   Crystal City Dialysis Center   960 SO TRUMAN BLVD     CRYSTAL CITY   MO   63019-1329
200   Affiliated   947   St. Louis   St. Louis Dialysis Center (fka Renal Treatment Center-St. Louis)   2610 CLARK AVE     SAINT LOUIS   MO   63103-2502
201   Affiliated   944   Burlington   Burlington Dialysis   873 HEATHER RD     BURLINGTON   NC   27215-6288
202   Affiliated   838   Scottsbluff   Scottsbluff Dialysis Center   3812 AVENUE B     SCOTTSBLUFF   NE   69361-4780
203   Affiliated   802   Bridgewater   Bridgewater Dialysis Center (fka Renal Treatment Center-Bridgewater)   2121 US HWY 22     BOUND BROOK   NJ   08805-1546
204   Affiliated   845   West Las Vegas   Las Vegas Dialysis Center   150 S VALLEY VIEW BLVD     LAS VEGAS   NV   89107
205   Affiliated   846   North Las Vegas   North Las Vegas Dialysis Center   2300 MCDANIEL ST     NORTH LAS VEGAS   NV   89030-6318
206   Affiliated   940   Cincinnati   Eastgate Dialysis (fka Cincinnati)   4435 AICHOLTZ RD     CINCINNATI   OH   45245-1690
207   Affiliated   885   Tulsa   Tulsa Dialysis   4436 S HARVARD AVE     TULSA   OK   74135-2605
208   Affiliated   897   NW Bethany   Northwest Bethany Dialysis Center   7800 NW 23RD ST   STE A   BETHANY   OK   73008-4948
209   Affiliated   890   Duncan   Duncan Dialysis Center   2645 W ELK AVE     DUNCAN   OK   73533-1572
210   Affiliated   893   Shawnee   Shawnee Dialysis Center   4409 N KICKAPOO AVE   STE 113   SHAWNEE   OK   74804-1224
211   Affiliated   895   Stillwater   Stillwater Dialysis Center   406 E HALL OF FAME AVE   STE 3   STILLWATER   OK   74075-5447

 

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212   Affiliated   955   Midwest City   Midwest City Dialysis Center   7221 E RENO AVE     MIDWEST CITY   OK   73110-4474
213   Affiliated   886   Broken Arrow   Broken Arrow Dialysis Center   1700 N 9TH ST     BROKEN ARROW   OK   74012
214   Affiliated   888   Tahlequah   Tahlequah Dialysis Center   1373 E BOONE ST     TAHLEQUAH   OK   74464-3330
215   Affiliated   899   Edmund   Edmond Dialysis   50 S BAUMANN AVE     EDMOND   OK   73034-5676
216   Affiliated   889   Altus   Altus Dialysis Center   205 S PARK LN   STE 13   ALTUS   OK   73521-5756
217   Affiliated   896   Elk City   Elk City Dialysis Center   1601 W 2ND ST     ELK CITY   OK   73644-4427
218   Affiliated   887   Claremore   Claremore Dialysis Center   202 E BLUE STARR DR     CLAREMORE   OK   74017-4223
219   Affiliated   891   Norman   Norman Dialysis Center   1818 W LINDSEY ST   STE 14 BLDG B   NORMAN   OK   73069-4159
220   Affiliated   862   Pocono   Pocono Dialysis Center   100 PLAZA CT   STE B   EAST STROUDSBURG   PA   18301-8258
221   Affiliated   861   Palmerton   Palmerton Dialysis Center   185 DELAWARE AVE   STE C   PALMERTON   PA   18071-1716
222   Affiliated   860   Jennersville   Jennersville Dialysis Center   1011 W BALTIMORE PIKE     WEST GROVE   PA   19390-9446
223   Affiliated   858   Lewistown   Lewistown Dialysis Center   611 ELECTRIC AVE     LEWISTOWN   PA   17044-1128
224   Affiliated   854   Lemoyne   Camp Hill Dialysis Center (fka Lemoyne Dialysis Center (York Hospital Acutes))   425 N 21ST ST   LOWER LEVEL   CAMP HILL   PA   17011-2223
225   Affiliated   856   Upland   Upland Dialysis Center   1 MEDICAL CENTER BLVD   STE 12   CHESTER   PA   19013-3902
226   Affiliated   848   South Philadelphia   So. Philadelphia Dialysis Center   109 DICKINSON ST     PHILADELPHIA   PA   19147-6107
227   Affiliated   857   Exton   Exton Dialysis Center   710 SPRINGDALE DR     EXTON   PA   19341-2828
228   Affiliated   847   Northeast Philadelphia   NE Philadelphia Dialysis Center   518 KNORR ST     PHILADELPHIA   PA   19111-4604
229   Affiliated   934   Longview   Longview Dialysis Center   425 N FREDONIA ST     LONGVIEW   TX   75601-6464
230   Affiliated   935   Marshall-RTC   Marshall Dialysis Center   1301 S WASHINGTON AVE     MARSHALL   TX   75670-6215
231   Affiliated   933   Conroe   Conroe Dialysis Center   500 MEDICAL CENTER BLVD   STE 175   CONROE   TX   77304-2899
232   Affiliated   928   San Marcos   Hill Country Dialysis Center Of San Marcos   1820 PETER GARZA DR     SAN MARCOS   TX   78666-7407
233   Affiliated   923   Sherman   Sherman Dialysis Center   205 W LAMBERTH RD     SHERMAN   TX   75092-2659
234   Affiliated   932   Tomball   Tomball Dialysis Center   27720A TOMBALL PKWY     TOMBALL   TX   77375-
235   Affiliated   919   Cleveland   Cleveland Dialysis Center   600 E HOUSTON   STE 63   CLEVELAND   TX   77327-4689
236   Affiliated   921   Livingston   Livingston Dialysis Center   209 W PARK     LIVINGSTON   TX   77351-7020
237   Affiliated   920   Kingwood   Kingwood Dialysis Center   2300 GREEN OAK DR   STE 5   KINGWOOD   TX   77339-2053
238   Affiliated   930   North Houston   North Houston Dialysis Center   129 LITTLE YORK RD     HOUSTON   TX   77076-1020
239   Affiliated   926   Omni   Omni Dialysis Center (fka Hamilton Dialysis Center)   9350 KIRBY DR   STE 11   HOUSTON   TX   77054-2528
240   Affiliated   925   Victoria   Victoria Dialysis Center   1405 VICTORIA STATION DR     VICTORIA   TX   77901-3092
241   Affiliated   922   Lufkin   Lufkin Dialysis Center   700 S JOHN REDDITT DR     LUFKIN   TX   75904-3145
242   Affiliated   927   Gonzales   Gonzales Dialysis Center   1406 N SARAH DEWITT DR     GONZALES   TX   78629-2702
243   Affiliated   924   Denison   Denison Dialysis Center   1220 REBA MCENTIRE LANE     DENISON   TX   75020-9057
244   Affiliated   918   South San Antonio   South San Antonio Dialysis Center   1313 SE MILITARY DR   STE 111   SAN ANTONIO   TX   78214-2850
245   Affiliated   913   Austin   Waterloo Dialysis Center (fka Austin Dialysis Center)   5310 BURNET RD   UNIT 122   AUSTIN   TX   78756-2003
246   Affiliated   916   S. Austin   El Milagro Dialysis Unit (fka South Austin Dialysis Center)   2800 S INTERSTATE HWY 35   STE 12   AUSTIN   TX   78704-5700
247   Affiliated   929   SW San Antonio   Southwest San Antonio Dialysis Center   7515 BARLITE BLVD     SAN ANTONIO   TX   78224-1311
248   Affiliated   936   Bedford   HEB Dialysis Center (Bedford)   1401 BROWN TRL   STE A   BEDFORD   TX   76022-6416
249   Affiliated   917   TRC Med Cntr   Med-Center Dialysis, fka Plaza Dialysis Center & Houston Kidney Center #376   5610 ALMEDA RD     HOUSTON   TX   77004-7515
250   Affiliated   908   Chesapeake   Chesapeake Dialysis Center   1400 CROSSWAYS BLVD   CROSSWAYS II STE 16   CHESAPEAKE   VA   23320-2839
251   Affiliated   912   Hopewell   Hopewell Dialysis Center   301 W BROADWAY AVE     HOPEWELL   VA   23860-2645
252   Affiliated   911   Newport News   Newport News Dialysis Center   711 79TH ST     NEWPORT NEWS   VA   23605-2767
253   Affiliated   907   Norfolk   Norfolk Dialysis Center   962 NORFOLK SQ     NORFOLK   VA   23502-3235
254   Affiliated   909   Virginia Beach   Virginia Beach Dialysis Center   740 INDEPENDENCE CIR     VIRGINIA BEACH   VA   23455-6438
255   Affiliated   171   Palmer   Palmer Dialysis Center   30 COMMUNITY DR     EASTON   PA   18045-2658
256   Affiliated   589   Burgaw   SEDC (NC II) Burgaw Dialysis Center   704 S DICKERSON ST   PO BOX 1391   BURGAW   NC   28425-4904
257   Affiliated   590   Elizabethtown   SEDC (NC II) Elizabethtown Dialysis Center   101 DIALYSIS DR     ELIZABETHTOWN   NC   28337-9048
258   Affiliated   591   Jacksonville   SEDC (NC II) Jacksonville Dialysis Center   14 OFFICE PARK DR     JACKSONVILLE   NC   28546-7325
259   Affiliated   592   Kenansville   SEDC (NC II) Kenansville Dialysis Center   305 BEASLEY ST     KENANSVILLE   NC   28349-8798
260   Affiliated   593   Shallotte   SEDC (NC II) Shallotte Dialysis Center   4770 SHALLOTTE AVE     SHALLOTTE   NC   28470-6596
261   Affiliated   594   Whiteville   SEDC (NC II) Whiteville Dialysis Center   608 PECAN LN     WHITEVILLE   NC   28472-2949
262   Affiliated   595   Wilmington   SEDC (NC II) Wilmington Dialysis Center   2215 YAUPON DR     WILMINGTON   NC   28401-7334
263   Affiliated   175   Deerfield   Deerfield Beach Artificial Kidney Center   1983 W HILLSBORO BLVD     DEERFIELD BEACH   FL   33442-1418
264   Affiliated   176   Pampano Beach   Pompano Beach Artificial Kidney Center   600 SW 3RD ST   STE 11   POMPANO BEACH   FL   33060-6936
265   Affiliated   177   Tamarack   Tamarac Artificial Kidney Center   7140 W MCNAB RD     TAMARAC   FL   33321-5306

 

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266   Affiliated   168   Atlantic AKC   Atlantic Artificial Kidney Center   6 INDUSTRIAL WAY W   STE B   EATONTOWN   NJ   07724-2258
267   Affiliated   587   Rowan/Kannapolis   Dialysis Care of Kannapolis   1607 N MAIN ST     KANNAPOLIS   NC   28081-2317
268   Affiliated   654   Cortez   Cortez Dialysis   610 E MAIN ST   STE C   CORTEZ   CO   81321-3308
269   Affiliated   142   West Bountiful 4/6/98   West Bountiful Dialysis   724 W 500 S   STE 3   WEST BOUNTIFUL   UT   84087-1471
270   Affiliated   187   Meherrin   Meherrin Dialysis Center   201A WEAVER AVE     EMPORIA   VA   23847-1248
271   Affiliated   436   Montclair   Montclair Dialysis Center   5050 PALO VERDE ST   STE 1   MONTCLAIR   CA   91763-2329
272   Affiliated   259   Pipestone   Pipestone Dialysis   916 4TH AVE SW     PIPESTONE   MN   56164-1054
273   Affiliated   236   Washington   Washington Dialysis Center   154 WASHINGTON PLZ     WASHINGTON   GA   30673-2074
274   Affiliated   235   Elberton   Elberton Dialysis Center   894 ELBERT ST     ELBERTON   GA   30635-2628
275   Affiliated   174   Gulf Breeze   Gulf Breeze Dialysis Center   1519 MAIN ST     DUNEDIN   FL   34698-4650
276   Affiliated   526   Asheville   Asheville Kidney Center   1600 CENTRE PARK DR     ASHEVILLE   NC   28805-6206
277   Affiliated   528   Sylva   Sylva Dialysis Center   655 ASHEVILLE HWY     SYLVA   NC   28779-2747
278   Affiliated   527   Hendersonville   Hendersonville Dialysis Center   500 BEVERLY HANKS CTR   HWY 25 N   HENDERSONVILLE   NC   28792
279   Affiliated   389   Memorial   Memorial Dialysis   4427 S ROBERTSON ST     NEW ORLEANS   LA   70115-6308
280   Affiliated   127   Warner Robbins   Dialysis Center of Middle Georgia-Warner Robins   509 N HOUSTON RD     WARNER ROBINS   GA   31093-8844
281   Affiliated   126   Macon - Middle Georgia   Dialysis Center of Middle Georgia-Macon   747 2ND ST     MACON   GA   31201-6835
282   Affiliated   344   Oakland PD   Oakland Peritoneal Dialysis Center (Piedmont PD)   5352 CLAREMONT AVE     OAKLAND   CA   94618
283   Affiliated   384   Fairfax   Fairfax Dialysis Center   8501 ARLINGTON BLVD   STE 1   FAIRFAX   VA   22031-4625
284   Affiliated   374   Houston SW   Houston Kidney Center Southwest   11111 BROOKLET DR   STE 1 BLDG 1   HOUSTON   TX   77099-3555
285   Affiliated   545   Pikes Peak   Pikes Peak Dialysis Center   2002 LELARAY ST   STE 13   COLORADO SPRINGS   CO   80909-2804
286   Affiliated   546   Printers Place   Printers Place Dialysis   2802 INTERNATIONAL CIR     COLORADO SPRINGS   CO   80910-3127
287   Affiliated   541   Lakewood Colorado   Lakewood Dialysis Center   1750 PIERCE ST     LAKEWOOD   CO   80214-1434
288   Affiliated   543   Boulder   Boulder Dialysis Center   2880 FOLSOM ST   STE 11   BOULDER   CO   80304-3769
289   Affiliated   542   Thornton   Thornton Dialysis Center   8800 FOX DR     THORNTON   CO   80260-6880
290   Affiliated   544   Arvada   Arvada Dialysis Center   9950 W 80TH AVE   STE 25   ARVADA   CO   80005-3914
291   Affiliated   173   Ft. Lauderdale   CDC South-Ft Lauderdale Renal Associates   6264 N FEDERAL HWY     FORT LAUDERDALE   FL   33308-1904
292   Affiliated   380   Houston Cypress Station   Houston Kidney Center Cypress Station   221 FM 1960 RD W   STE H   HOUSTON   TX   77090-3537
293   Affiliated   169   Erie County   Cleve Hill Dialysis Center (Fka Cleve Hill Limited Partnership-Erie Dialysis &ECMC Dialysis Center At Cleve Hill )   1461 KENSINGTON AVE     BUFFALO   NY   14215-1436
294   Affiliated   430   UCLA Pediatrics   Century City Dialysis (fka UCLA, DaVita Westwood UCLA)   10630 SANTA MONICA BLVD     LOS ANGELES   CA   90025-4837
295   Affiliated   501   Bronx   Bronx Dialysis Center   1615 EASTCHESTER RD     BRONX   NY   10461-2603
296   Affiliated   502   Catskill   Catskill Dialysis Center   139 FORESTBURGH RD     MONTICELLO   NY   12701-2364
297   Affiliated   505   Riverdale   Riverdale Dialysis Center   170 W 233RD ST     BRONX   NY   10463-5639
298   Affiliated   506   South Bronx   South Bronx Dialysis Center   1940 WEBSTER AVE     BRONX   NY   10457-4261
299   Affiliated   507   Stanten Island   Richmond Kidney Center (Staten Island)   1366 VICTORY BLVD     STATEN ISLAND   NY   10301-3907
300   Affiliated   238   McDonough   McDonough Dialysis Center   114 DUNN ST     MCDONOUGH   GA   30253-2347
301   Affiliated   192   Milford   Delaware Valley Dialysis Center (fka Milford)   102 DAVITA DR     MILFORD   PA   18337-9390
302   Affiliated   191   Honesdale   Honesdale Dialysis Center-NE Regional   RR 6 BOX 6636   STOURBRIDGE MALL   HONESDALE   PA   18431-9649
303   Affiliated   247   Memorial   Memorial Dialysis Center   11621 KATY FWY     HOUSTON   TX   77079-1801
304   Affiliated   246   Katy Dialysis Center   Grand Parkway Dialysis Center   403 W GRAND PKWY S   STE T   KATY   TX   77494-8358
305   Affiliated   245   Cyfair Dialysis Center   Cyfair Dialysis Center   9110 JONES RD   STE 11   HOUSTON   TX   77065-4489
306   Affiliated   165   Port Chester   Port Chester Dialysis and Renal Center   38 BULKLEY AVE     PORT CHESTER   NY   10573-3902
307   Affiliated   193   Franklin Dialysis   Franklin Dialysis Center   150 SOUTH INDEPENDENCE WEST   11 PUBLIC LEDGER BLDG   PHILADELPHIA   PA   19106-3413
308   Affiliated   156   Grand Blanc   Grand Blanc Dialysis Center   3625 GENESYS PKWY     GRAND BLANC   MI   48439-8070
309   Affiliated   397   Oxford Court   Oxford Court Dialysis   930 TOWN CENTER DR   STE G1   LANGHORNE   PA   19047-4260
310   Affiliated   348   Antioch   Antioch Dialysis   3100 DELTA FAIR BLVD     ANTIOCH   CA   94509-4001
311   Affiliated   401   North Palm Beach   North Palm Beach Dialysis Center   2841 PGA BLVD     PALM BEACH GARDENS   FL   33410-2910
312   Affiliated   277   Lodi   Lodi Dialysis Center   1610 W KETTLEMAN LN   STE D   LODI   CA   95242-4210
313   Affiliated   438   United   United Dialysis Center   3111 LONG BEACH BLVD     LONG BEACH   CA   90807-5015
314   Affiliated   437   Premier   Premier Dialysis Center   7612 ATLANTIC AVE     CUDAHY   CA   90201-5020
315   Affiliated   349   Salinas   Salinas Dialysis Center   955 BLANCO CIR   STE C   SALINAS   CA   93901-4452
316   Affiliated   428   Lowry I   Lowry Dialysis Center   7465 E 1ST AVE   STE A   DENVER   CO   80230-6877
317   Affiliated   154   Ypsilanti   Ypsilanti Dialysis   2766 WASHTENAW RD     YPSILANTI   MI   48197-1506
318   Affiliated   237   Eastpoint   East Point Dialysis   2669 CHURCH ST     EAST POINT   GA   30344-3115
319   Affiliated   520   Celia Dill   Celia Dill Dialysis Center   667 STONELEIGH AVE   STE 123 BARNS OFFICE CENTER   CARMEL   NY   10512-2454

 

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320   Affiliated   248   Elmbrook   Brookriver Dialysis   8101 BROOKRIVER DR     DALLAS   TX   75247-4003
321   Affiliated   402   Ocala East   OCALA Regional Kidney Center-East   2870 SE 1ST AVE     OCALA   FL   34471-0406
322   Affiliated   403   Ocala West   OCALA Regional Kidney Center-West   9401 SW HWY 200   BLDG 6   OCALA   FL   34481-9612
323   Affiliated   404   Ocala South   OCALA Regional Kidney Center-South   13940 N US HWY 441   BLDG 4   LADY LAKE   FL   32159-8908
324   Affiliated   417   Delta Sierra Dialysis   Delta-Sierra Dialysis Center   555 W BENJAMIN HOLT DR   STE 2   STOCKTON   CA   95207-3839
325   Affiliated   552   Olympic View   Olympic View Dialysis Center   125 16TH AVE E CSB   5TH FL   SEATTLE   WA   98112
326   Affiliated   148   Pratt   Pratt Dialysis Center   203 WATSON ST   STE 11   PRATT   KS   67124-3092
327   Affiliated   196   Buffalo   Renal Care of Buffalo   550 ORCHARD PARK RD     WEST SENECA   NY   14224-2646
328   Affiliated   555   Woodland   Woodland Dialysis Center   912 WOODLAND DR   STE B   ELIZABETHTOWN   KY   42701-2795
329   Affiliated   556   Taylor   Taylor County Dialysis Center   101 KINGSWOOD DR     CAMPBELLSVILLE   KY   42718-9634
330   Affiliated   491   Gary   Comprehensive Renal Care (CRC)-Gary   4802 BROADWAY     GARY   IN   46408-4509
331   Affiliated   492   Hammond   Comprehensive Renal Care (CRC)-Hammond   222 DOUGLAS ST     HAMMOND   IN   46320-1960
332   Affiliated   493   Valparaiso   Comprehensive Renal Care (CRC)-Valparaiso   606 E LINCOLNWAY     VALPARAISO   IN   46383-5728
333   Affiliated   494   Michigan City   Comprehensive Renal Care (CRC)-Michigan City   9836 WEST 400 NORTH     MICHIGAN CITY   IN   46360-2910
334   Affiliated   495   Munster   Comprehensive Renal Care (CRC)-Munster   9100 CALUMET AVE     MUNSTER   IN   46321-1737
335   Affiliated   497   South County-Deaconess   South County Dialysis (Deaconess)   4145 UNION RD     SAINT LOUIS   MO   63129-1064
336   Affiliated   266   South Hayward   South Hayward Dialysis Center   254 JACKSON ST     HAYWARD   CA   94544-1907
337   Affiliated   164   Dyker Heights   Dyker Heights Dialysis Center   1435 86TH ST     BROOKLYN   NY   11228-3435
338   Affiliated   152   Clarkston   Clarkston Dialysis Center   6770 DIXIE HWY   STE 25   CLARKSTON   MI   48346-2089
339   Affiliated   534   Hudson Valley   Hudson Valley Dialysis Center   155 WHITE PLAINS RD     TARRYTOWN   NY   10591-5523
340   Affiliated   971   Central Tulsa   Central Tulsa Dialysis Center   1124 S SAINT LOUIS AVE     TULSA   OK   74120-5413
341   Affiliated   972   Okmulgee   Okmulgee Dialysis Center   201 SO DELAWARE AVE     OKMULGEE   OK   74447-5528
342   Affiliated   974   Muskogee   Muskogee Community Dialysis   2316 W SHAWNEE ST     MUSKOGEE   OK   74401-2228
343   Affiliated   975   Miami-Oklahoma   Tri-State Dialysis Center (fka Miami Dialysis Center (OK))   2510 N MAIN ST     MIAMI   OK   74354-1602
344   Affiliated   977   Stilwell   Stilwell Dialysis Center   80851 HWY 59     STILWELL   OK   74960
345   Affiliated   496   East Chicago   Comprehensive Renal Care (CRC)-East Chicago   4320 FIR ST   UNIT 44   EAST CHICAGO   IN   46312-3078
346   Affiliated   549   Bright Dialysis   Bright Dialysis (fka Fort Pierce Artificial Kidney Center, TRC of Fort Pierce-AKC)   1801 S 23RD ST   STE 1   FORT PIERCE   FL   34950-4830
347   Affiliated   153   Detroit   Detroit Dialysis Center (Eastern Market, Brewery Park Development)   2674 E JEFFERSON AVE     DETROIT   MI   48207-4129
348   Affiliated   166   White Plains   White Plains Dialysis Center   200 HAMILTON AVE   STE 13B   WHITE PLAINS   NY   10601-1859
349   Affiliated   337   Crescent Heights   Crescent Heights Dialysis Center   8151 BEVERLY BLVD     LOS ANGELES   CA   90048-4514
350   Affiliated   547   Pahrump Dialysis   Pahrump Dialysis Center   330 S LOLA LN   STE 1   PAHRUMP   NV   89048-0884
351   Affiliated   598   Cherokee Dialysis Center   Cherokee Dialysis Center   53 ECHOTA CHURCH RD     CHEROKEE   NC   28719-9702
352   Affiliated   444   Utah Valley   Utah Valley Dialysis Center   1055 N 500 W   STE 221   PROVO   UT   84604-3305
353   Affiliated   439   Washington Plaza   Washington Plaza Dialysis Center   516 E WASHINGTON BLVD   # 522   LOS ANGELES   CA   90015-3723
354   Affiliated   539   Commerce City   Commerce City Dialysis Center   6320 HOLLY ST     COMMERCE CITY   CO   80022-3325
355   Affiliated   251   Bloomington Dialysis   Bloomington Dialysis Unit of TRC (fka Richfield)   8591 LYNDALE AVE S     BLOOMINGTON   MN   55420-2237
356   Affiliated   133   Kent Community Dialysis   Kent Dialysis Center   21501 84TH AVE S     KENT   WA   98032-1960
357   Affiliated   278   Florin Dialyis   Florin Dialysis Center   7000 STOCKTON BLVD     SACRAMENTO   CA   95823-2312
358   Affiliated   540   South Las Vegas Dialysis   South Las Vegas Dialysis Center (Palms)   2250 S RANCHO DR   STE 115   LAS VEGAS   NV   89102-4456
359   Affiliated   538   Longmont Dialysis   Longmont Dialysis Center   1715 IRON HORSE DR   STE 17   LONGMONT   CO   80501-9617
360   Affiliated   500   Great Bridge   Great Bridge Dialysis (fka Chesapeake II)   745 BATTLEFIELD BLVD N   STE 1   CHESAPEAKE   VA   23320-0305
361   Affiliated   569   Weaverville Dialysis   Weaverville Dialysis Facility   329 MERRIMON AVE     WEAVERVILLE   NC   28787-9253
362   Affiliated   427   Lakewood Crossing   Lakewood Crossing Dialysis   1057 S WADSWORTH BLVD   STE 1   LAKEWOOD   CO   80226-4361
363   Affiliated   155   Jackson   Jackson Dialysis Center   234 W LOUIS GLICK HWY     JACKSON   MI   49201-1326
364   Affiliated   429   Englewood   Englewood Dialysis Center   3247 S LINCOLN ST     ENGLEWOOD   CO   80113-2505
365   Affiliated   387   Harford Road Dialysis   Harford Road Dialysis Center   5800 HARFORD RD     BALTIMORE   MD   21214-1847
366   Affiliated   179   Arcadia   Arcadia Dialysis Center   1341 E OAK ST     ARCADIA   FL   34266-8902
367   Affiliated   388   Richmond Community   Richmond Community Hospital Dialysis (fkaTRC @ Richmond Community/Richmond II)   1510 N 28TH ST   STE 11   RICHMOND   VA   23223-5311
368   Affiliated   119   Henderson   Henderson Dialysis Center   1002 US HWY 79 N     HENDERSON   TX   75652-6008
369   Affiliated   253   Augusta   Nephrology Center of South Augusta   1631 GORDON HWY STE 1B     AUGUSTA   GA   30906
370   Affiliated   510   Boston Post Road   Boston Post Road Dialysis Center fka Co Op City Dialysis   4026 BOSTON RD     BRONX   NY   10475-1122
371   Affiliated   512   Peekskill   Peekskill Cortlandt Dialysis Center   2050 E MAIN ST   STE 15   CORTLANDT MANOR   NY   10567-2502
372   Affiliated   513   Queens   Queens Dialysis Center   11801 GUY R BREWER BLVD     JAMAICA   NY   11434-2101
373   Affiliated   517   Soundview   Soundview Dialysis Center   1622 BRUCKNER BLVD   STE 24   BRONX   NY   10473-4553

 

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374   Affiliated   516   Port Washington   Port Washington Dialysis Center   50 SEAVIEW BLVD     PORT WASHINGTON   NY   11050-4615
375   Affiliated   515   Lynbrook   Lynbrook Dialysis Center   147 SCRANTON AVE     LYNBROOK   NY   11563-2808
376   Affiliated   518   Yonkers Dialysis Center   Yonkers Dialysis   575 YONKERS AVE     YONKERS   NY   10704-2601
377   Affiliated   537   IHS - Queens Village   Queens Village Dialysis Center   22202 HEMPSTEAD AVE   STE 17   QUEENS VILLAGE   NY   11429-2123
378   Affiliated   536   Coney Island - IHS   Sheepshead Bay Renal Care Center (fka Coney Island)   26 BRIGHTON 11TH ST     BROOKLYN   NY   11235-5304
379   Affiliated   521   Garden City I.H.S   Garden City Dialysis Center   1100 STEWART AVE   STE 2   GARDEN CITY   NY   11530-4839
380   Affiliated   267   Kenneth Hahn- I.R.A   Kenneth Hahn Plaza Dialysis Center (Willowbrook)   11854 S WILMINGTON AVE     LOS ANGELES   CA   90059-3016
381   Affiliated   279   North Highland   North Highlands Dialysis Center   4986 WATT AVE   STE F   NORTH HIGHLANDS   CA   95660-5182
382   Affiliated   294   TRC Orangevale   Orangevale Dialysis Center   9267 GREENBACK LN   STE A2   ORANGEVALE   CA   95662-4864
383   Affiliated   554   Forest Park Dialysis Center   Forest Park Dialysis Center   380 FOREST PKWY   STE C   FOREST PARK   GA   30297-2107
384   Affiliated   446   Grant Park Nursing Home Dialysis   Grant Park Dialysis (fka Grants Park Nursing Home)   5000 NANNIE HELEN BURROUGHS AVE NE     WASHINGTON   DC   20019-5506
385   Affiliated   455   Fourth Street Dialysis   Fourth Street Dialysis   3101 N 4TH ST   STE B   LONGVIEW   TX   75605-5146
386   Affiliated   274   Bay Breeze   Bay Breeze Dialysis   11465 ULMERTON RD     LARGO   FL   33778-1602
387   Affiliated   416   Hopi   Hopi Dialysis Center- fka First Mesa   PO BOX 964   HWY 264   POLACCA   AZ   86042
388   Affiliated   178   Orlando Dialysis   Orlando Dialysis   14050 TOWN LOOP BLVD   STE 14A   ORLANDO   FL   32837-6190
389   Affiliated   170   Celebration Dialysis   Celebration Dialysis   1154 CELEBRATION BLVD     CELEBRATION   FL   34747-4605
390   Affiliated   1500   Mt. Dora Dialysis   Mt. Dora Dialysis   2735 W OLD US HIGHWAY 441     MOUNT DORA   FL   32757-3526
391   Affiliated   1501   Lake Dialysis   Lake Dialysis   221 N 1ST ST     LEESBURG   FL   34748-5150
392   Affiliated   146   Puyallup Community Dialysis   Puyallup Dialysis Center   716 SOUTH HILL PARK DR   STE C   PUYALLUP   WA   98373-1445
393   Affiliated   562   Towson Dialysis   Dulaney Towson Dialysis Center   113 WEST RD   STE 21   TOWSON   MD   21204-2318
394   Affiliated   188   Purcellville   Purcellville Dialysis Center   280 N HATCHER AVE     PURCELLVILLE   VA   20132-3193
395   Affiliated   476   Iris City   Iris City Dialysis (aka Griffin)   521 N EXPRESSWAY   STE 159   GRIFFIN   GA   30223-2073
396   Affiliated   1521   Slidell Kidney Care   Slidell Kidney Care   1150 ROBERT BLVD   STE 24   SLIDELL   LA   70458-2005
397   Affiliated   385   Rivertowne Dialysis   Rivertowne Dialysis (fka Oxon Hill Dialysis)   6192 OXON HILL RD   1ST FL   OXON HILL   MD   20745-3114
398   Affiliated   477   Pearland Dialysis   Pearland Dialysis   6516 BROADWAY ST   STE 122   PEARLAND   TX   77581-7879
399   Affiliated   419   East Aurora Dialysis   East Aurora Dialysis (aka Aurora II)   482 S CHAMBERS RD     AURORA   CO   80017-2092
400   Affiliated   1507   Merrillville Dialysis   CRC-Merrillville Dialysis Center   9223 TAFT ST     MERRILLVILLE   IN   46410-6911
401   Affiliated   563   Bricktown Dialysis   Bricktown Dialysis Center   525 JACK MARTIN BLVD   FL 2   BRICK   NJ   08724-7735
402   Affiliated   423   Sapulpa   Sapulpa Dialysis (fka Jenks-Sapulpa)   9647 RIDGEVIEW ST     TULSA   OK   74131-6205
403   Affiliated   1526   Ellijay Dialysis   Ellijay Dialysis   449 INDUSTRIAL BLVD   STE 24   ELLIJAY   GA   30540-6724
404   Affiliated   1527   Gainesville Dialysis   Gainesville Dialysis   2545 FLINTRIDGE RD   STE 13   GAINESVILLE   GA   30501-7428
405   Affiliated   1528   Newnan Dialysis   Newnan Dialysis   1565 E HWY 34   STE 13   NEWNAN   GA   30265
406   Affiliated   405   Ocala Regional Kidney Center - North   OCALA North Dialysis Center   2620 W HWY 316     CITRA   FL   32113-3555
407   Affiliated   1516   Pin Oak Dialysis   Pin Oak Dialysis Center (aka Katy II)   1302 PIN OAK RD     KATY   TX   77494-6848
408   Affiliated   1523   Imperial Care Dialysis   Imperial Care Dialysis Center   4345 E IMPERIAL HWY     LYNWOOD   CA   90262-2318
409   Affiliated   1533   St. Louis Park Dialysis   St. Louis Park Dialysis Center   3505 LOUISIANA AVE S     ST LOUIS PARK   MN   55426-4121
410   Affiliated   1517   Minneapolis NE Dialysis   Minneapolis NE Dialysis   1049 10TH AVE SE     MINNEAPOLIS   MN   55414-1312
411   Affiliated   298   Flushing Dialysis   Flushing Dialysis Center   3469 PIERSON PL   STE A   FLUSHING   MI   48433-2413
412   Affiliated   1535   Dialysis Systems of Covington   Dialysis Systems of Covington   210 GREENBRIAR BLVD     COVINGTON   LA   70433-7235
413   Affiliated   1536   Dialysis Systems of Hammond   Dialysis Systems of Hammond   15799 PROFESSIONAL PLZ     HAMMOND   LA   70403-1452
414   Affiliated   433   Soledad Dialysis   Soledad Dialysis Center   901 LOS COCHES DR     SOLEDAD   CA   93960-2995
415   Affiliated   443   Lake Elsinore Dialysis   Lake Elsinore Dialysis   32291 MISSION TRL   BLDG S   LAKE ELSINORE   CA   92530
416   Affiliated   1511   Clinton Dialysis Center   Clinton Dialysis Center   150 S 31ST ST     CLINTON   OK   73601-9118
417   Affiliated   456   Bakers Ferry   Bakers Ferry Dialysis   3645 BAKERS FERRY RD SW     ATLANTA   GA   30331-3712
418   Affiliated   1509   Hermiston   Hermiston Community Dialysis Center   1155 W LINDA AVE     HERMISTON   OR   97838-9601
419   Affiliated   1539   Yakima   Yakima Dialysis Center   1221 N 16TH AVE     YAKIMA   WA   98902-1347
420   Affiliated   409   Madison   Madison Dialysis Center   302 HIGHWAY ST     MADISON   NC   27025-1672
421   Affiliated   1508   Swannanoa Dialysis   Swannanoa Dialysis Center (fka Black Mountain, NC)   2305 US HIGHWAY 70     SWANNANOA   NC   28778-8207
422   Affiliated   2009   NE Wichita Dialysis   NE Wichita Dialysis Center   2630 N WEBB RD   STE 1 BLDG 1   WICHITA   KS   67226-8174
423   Affiliated   2005   Chadbourn Dialysis   Chadbourn Dialysis Center (fkaColumbus County)   210 STRAWBERRY BLVD     CHADBOURN   NC   28431-1418
424   Affiliated   1506   Western Home Dialysis   Mile High Home Dialysis PD (fka Western Home)   1750 PIERCE ST   STE A   LAKEWOOD   CO   80214-1434
425   Affiliated   2019   Tustin Dialysis   Tustin Dialysis (aka Santa Ana)   2090 N TUSTIN AVE   STE 1   SANTA ANA   CA   92705-7869
426   Affiliated   182   Appomatox   Appomattox Dialysis (Petersburg)   15 W OLD ST     PETERSBURG   VA   23803-3221
427   Affiliated   2002   Maryville Dialysis   Maryville Dialysis   2130 VADALABENE DR     MARYVILLE   IL   62062-5632

 

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428   Affiliated   2001   Mission Hills   Mission Hills Dialysis (aka Cristo Rey)   2700 N STANTON ST     EL PASO   TX   79902-2500
429   Affiliated   125   Moncrief   Moncrief Dialysis Partners   800 W 34TH ST   STE 11   AUSTIN   TX   78705-1144
430   Affiliated   295   Southfield West Dialysis   Southfield West Dialysis   21900 MELROSE AVE   STE 4   SOUTHFIELD   MI   48075-7967
431   Affiliated   525   Neptune Dialysis   Neptune Dialysis Center   2180 BRADLEY AVE     NEPTUNE   NJ   07753-4427
432   Affiliated   2014   Portsmouth Dialysis   Portsmouth Dialysis Center   2000 HIGH ST     PORTSMOUTH   VA   23704-3012
433   Affiliated   2016   Tokay Dialysis   Tokay Dialysis Center (fka East Lodi, CA)   312 S FAIRMONT AVE   STE A   LODI   CA   95240-3840
434   Affiliated   1504   Mt. Pocono Dialysis   Mt. Pocono Dialysis   100 COMMUNITY DR   STE 16   TOBYHANNA   PA   18466-8986
435   Affiliated   1544   Greater Portsmouth   Greater Portsmouth (aka Bon View Dialysis & Mid Town Hampton Road Dialysis)   3516 QUEEN ST     PORTSMOUTH   VA   23707-3238
436   Affiliated   1545   Peninsula Dialysis   Peninsula Dialysis Center (aka Immaculate Dialysis)   716 DENBIGH BLVD   STE D1 AND D2   NEWPORT NEWS   VA   23608-4414
437   Affiliated   1540   Saginaw Dialysis   Saginaw Dialysis   1527 E GENESEE AVE     SAGINAW   MI   48607-1755
438   Affiliated   1560   Churchview Dialysis   Churchview Dialysis   5970 CHURCHVIEW DR     ROCKFORD   IL   61107-2574
439   Affiliated   1562   Freeport Dialysis   Freeport Dialysis   1028 S KUNKLE BLVD     FREEPORT   IL   61032-6914
440   Affiliated   1563   Rockford Dialysis   Rockford Dialysis   3339 N ROCKTON AVE     ROCKFORD   IL   61103-2839
441   Affiliated   1564   Whiteside Dialysis   Whiteside Dialysis   2600 N LOCUST   STE D   STERLING   IL   61081-4602
442   Affiliated   2021   Pikesville Dialysis   Pikesville Dialysis   1500 REISTERSTOWN RD   STE 22   PIKESVILLE   MD   21208-3836
443   Affiliated   2000   Waynesville Dialysis   Waynesville Dialysis Center (fka Haywood, NC)   11 PARK TERRACE DR     CLYDE   NC   28721-7445
444   Affiliated   296   Davison Dialysis   Davison Dialysis   1011 S STATE RD     DAVISON   MI   48423-1903
445   Affiliated   1557   Flint Dialysis   Flint Dialysis Center   2 HURLEY PLZ   STE 115   FLINT   MI   48503-5904
446   Affiliated   1558   Hallwood Dialysis   Hallwood Dialysis Center   4929 CLIO RD   STE B   FLINT   MI   48504-1886
447   Affiliated   1559   Park Plaza Dialysis   Park Plaza Dialysis   G1075 N BALLENGER HWY     FLINT   MI   48504-4431
448   Affiliated   1518   Rosemead Springs Dialysis   Rosemead Springs Dialysis Center   3212 ROSEMEAD BLVD     EL MONTE   CA   91731-2807
449   Affiliated   2022   Scottsdale Dialysis   Scottsdale Dialysis Center   4725 N SCOTTSDALE RD   STE 1   SCOTTSDALE   AZ   85251-7621
450   Affiliated   1570   Washington Parish Dialysis   Washington Parish Dialysis   724 WASHINGTON ST     FRANKLINTON   LA   70438-1790
451   Affiliated   2027   Brookhollow Dialysis   Brookhollow Dialysis   4918 W 34TH ST     HOUSTON   TX   77092-6606
452   Affiliated   2017   Creekside   Creekside Dialysis Center (fka So. Vacaville, CA)   141 PARKER ST     VACAVILLE   CA   95688-3921
453   Affiliated   529   Middletown   Middletown Dialysis Center (fka-Red Bank)   500 STATE ROUTE 35   UNION SQUARE PLAZA   RED BANK   NJ   07701-5038
454   Affiliated   1541   Southwest Ohio Dialysis   Southwest Ohio Dialysis (Xenia-SWORC)   215 S ALLISON AVE     XENIA   OH   45385-3694
455   Affiliated   369   Oak Park   Oak Park Dialysis Center   13481 W 10 MILE RD     OAK PARK   MI   48237-4633
456   Affiliated   2042   Eden Prairie   Eden Prairie Dialysis   14852 SCENIC HEIGHTS RD   STE 255 BLDG B   EDEN PRAIRIE   MN   55344-2320
457   Affiliated   1530   Owensboro Dialysis   Owensboro Dialysis Center   1930 E PARRISH AVE     OWENSBORO   KY   42303-1443
458   Affiliated   1531   Tell City Dialysis   CRC-Tell City Dialysis Center   1602 MAIN ST     TELL CITY   IN   47586-1310
459   Affiliated   1576   Crestwood Dialysis   Crestwood Dialysis (fka Health Research Group-St. Louis (HRG))   9901 WATSON RD   STE 125   SAINT LOUIS   MO   63126-1855
460   Affiliated   2004   Copperfield Dialysis   Copperfield Dialysis (fka Cabarrus County-NC, and Concord)   1030 VINEHAVEN DR     CONCORD   NC   28025-2438
461   Affiliated   1572   Grand Island Dialysis   Grand Island Dialysis   603 S WEBB RD     GRAND ISLAND   NE   68803-5141
462   Affiliated   1573   Harlan Dialysis   Harlan Dialysis   1213 GARFIELD AVE     HARLAN   IA   51537-2057
463   Affiliated   1574   Shenandoah Dialysis   Shenandoah Dialysis   300 PERSHING AVE     SHENANDOAH   IA   51601-2355
464   Affiliated   2053   Germantown Dialysis   Germantown Dialysis   20111 CENTURY BLVD   STE C   GERMANTOWN   MD   20874-9165
465   Affiliated   2051   Lamplighter Dialysis   Lamplighter Dialysis   12654 LAMPLIGHTER SQUARE     ST LOUIS   MO   63128
466   Affiliated   1578   Kidney Care of Largo   Kidney Care of Largo   1300 MERCANTILE LN   STE 194   UPPER MARLBORO   MD   20774
467   Affiliated   1579   Kidney Care of Laurel   Kidney Care of Laurel   14631 LAUREL BOWIE ROAD   UNITS 1-15   LAUREL   MD   20707
468   Affiliated   2024   Durant Dialysis   Durant Dialysis Center   411 WESTSIDE DR     DURANT   OK   74701-2932
469   Affiliated   2038   Palm Brook Dialysis   Palm Brook Dialysis Center   14664 N DEL WEBB BLVD     SUN CITY   AZ   85351-2137
470   Affiliated   2043   Cambridge Dialysis   Cambridge Dialysis Center   300 BYRN ST     CAMBRIDGE   MD   21613-1908
471   Affiliated   2059   Reston Dialysis Center   Reston Dialysis Center   1875 CAMPUS COMMONS DR   STE 11   RESTON   VA   20191-1564
472   Affiliated   2040   Franconia Dialysis   Franconia Dialysis Centre   5695 KING CENTRE DRIVE     ALEXANDRIA   VA   22315-5744
473   Affiliated   2041   Eagan Dialysis   Eagan Dialysis Unit   2750 BLUE WATER RD   SUITE 3   EAGAN   MN   55121-1400
474   Affiliated   1594   Central Des Moines Dialysis   Central Des Moines Dialysis   1215 PLEASANT ST   STE 16   DES MOINES   IA   50309-1409
475   Affiliated   1595   West Des Moines Dialysis   West Des Moines Dialysis   6800 LAKE DR   STE 185   WEST DES MOINES   IA   50266-2544
476   Affiliated   1596   Creston Dialysis   Creston Dialysis   1700 W TOWNLINE ST     CRESTON   IA   50801-1054
477   Affiliated   1597   Atlantic Dialysis   Atlantic Dialysis   1500 E 10TH ST     ATLANTIC   IA   50022-1935
478   Affiliated   1598   Newton Dialysis   Newton Dialysis   204 N 4TH AVE E   STE 134   NEWTON   IA   50208-3135
479   Affiliated   2046   Dialysis of Des Moines   Riverpoint Dialysis Unit   501 SW 7TH ST   STE B   DES MOINES   IA   50309-4538
480   Affiliated   2060   Bellevue Dialysis   Bellevue Dialysis Center   3535 FACTORIA BLVD SE   STE 15   BELLEVUE   WA   98006-1293
481   Affiliated   414   Somerset Dialysis   Somerset Dialysis Center   240 CHURCHILL AVE     SOMERSET   NJ   08873-3451

 

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482   Affiliated   2031   East Ft. Lauderdale Dialysis   East Ft. Lauderdale Dialysis Center (fka No. Broward)   1301 S ANDREWS AVE   STE 11   FT LAUDERDALE   FL   33316-1823
483   Affiliated   1593   Spring Branch Dialysis   Spring Branch Dialysis   1425 BLALOCK   STE 1   HOUSTON   TX   77055-4446
484   Affiliated   1599   Battle Creek Dialysis   Battle Creek Dialysis   220 E GOODALE AVE     BATTLE CREEK   MI   49037-2728
485   Affiliated   2025   Hampton Avenue Dialysis   Hampton Avenue Dialysis-MO (Forest Park)   1425 HAMPTON AVE     SAINT LOUIS   MO   63139-3115
486   Affiliated   1605   Bogalusa Kidney Care   Bogalusa Kidney Care   2108 SOUTH AVE F     BOGALUSA   LA   70427
487   Affiliated   2055   Bardstown Dialysis   Bardstown Dialysis Center   210 W JOHN FITCH AVE     BARDSTOWN   KY   40004-1115
488   Affiliated   2050   Southern Pines   Southern Pines Dialysis Center   209 WINDSTAR PL     SOUTHERN PINES   NC   28387-7086
489   Affiliated   2030   Montclare Dialysis   Montclare Dialysis Center (aka Belmont Ave)   7009 W BELMONT AVE     CHICAGO   IL   60634-4533
490   Affiliated   2048   Southern Hills   Southern Hills Dialysis Center   9280 W SUNSET RD   STE 11   LAS VEGAS   NV   89148-4861
491   Affiliated   2068   Kilgore Dialysis   Kilgore Dialysis Center   209 HWY 42 NORTH     KILGORE   TX   75662-5019
492   Affiliated   2067   Brighton Dialysis   Brighton Dialysis   4700 E BROMLEY LN   STE 13   BRIGHTON   CO   80601-7821
493   Affiliated   2023   Union Gap   Union Gap Dialysis (aka Yakima)   1236 AHTANUM RIDGE DR   AHTANUM RIDGE BUSINESS PARK   UNION GAP   WA   98903-1813
494   Affiliated   2039   Dallas North Dialysis   Dallas North Dialysis Center (aka Greenville)   11886 GREENVILLE AVE   STE 1B   DALLAS   TX   75243-9743
495   Affiliated   2061   Grovepark Dialysis   Grovepark Dialysis Center (fka Jackson Dialysis)   794 MCDONOUGH RD     JACKSON   GA   30233-1572
496   Affiliated   1583   Eastern Kentucky Dialysis   Eastern Kentucky Dialysis   167 WEDDINGTON BRANCH RD     PIKEVILLE   KY   41501-3204
497   Affiliated   1584   Paintsville Dialysis   Paintsville Dialysis   4750 S KY ROUTE 321     HAGERHILL   KY   41222
498   Affiliated   1582   West Virginia Dialysis   West Virginia Dialysis   300 PROSPERITY LANE   STE 15   LOGAN   WV   25601-3494
499   Affiliated   2049   Reidsville Dialysis   Reidsville Dialysis   1307 FREEWAY DR     REIDSVILLE   NC   27320-7104
500   Affiliated   2034   Elk Grove Dialysis   Elk Grove Dialysis   9281 OFFICE PARK CIR   STE 15   ELK GROVE   CA   95758-8069
501   Affiliated   2035   Weston Dialysis   Weston Dialysis Center (fka Cleveland Clinic )   2685 EXECUTIVE PARK DR   STE 1   WESTON   FL   33331-3651
502   Affiliated   1600   McCook Dialysis   McCook Dialysis Center   801 W C ST     MCCOOK   NE   69001-3591
503   Affiliated   1601   Hastings Dialysis   Hastings Dialysis Center   1900 N SAINT JOSEPH AVE     HASTINGS   NE   68901-2652
504   Affiliated   1602   Capital City Dialysis   Capital City Dialysis   307 N 46TH ST     LINCOLN   NE   68503-3714
505   Affiliated   1616   Renal Care of Bowie   Renal Care of Bowie   4861 TELSA DRIVE   STES G-H   BOWIE   MD   20715-4318
506   Affiliated   1617   Renal Care of Takoma Park   Takoma Park Dialysis (fka Renal Care of Takoma Park)   1502 UNIVERSITY BLVD E     HYATTSVILLE   MD   20783
507   Affiliated   1618   Renal Care of Lanham   Renal Care of Lanham   8855 ANNAPOLIS RD   STE 2   LANHAM   MD   20706-2942
508   Affiliated   1619   Parma Dialysis   Parma Dialysis Center   6735 AMES RD     CLEVELAND   OH   44129-5601
509   Affiliated   1620   Middleburg Heights Dialysis   Middleburg Hts. Dialysis   7360 ENGLE RD     MIDDLEBURG HTS   OH   44130
510   Affiliated   1621   Rocky River Dialysis   Rocky River Dialysis   20220 CENTER RIDGE RD   STE 5   ROCKY RIVER   OH   44116-3567
511   Affiliated   1606   Diamond Valley Dialysis   Diamond Valley Dialysis   1030 E FLORIDA AVE     HEMET   CA   92543-4511
512   Affiliated   1607   Murrieta Dialysis   Murrieta Dialysis   25100 HANCOCK AVE   STE 11   MURRIETA   CA   92562-5973
513   Affiliated   2057   South Chico Dialysis   South Chico Dialysis Center   2345 FOREST AVE     CHICO   CA   95928-7641
514   Affiliated   2099   Dixon Kidney Center   Dixon Kidney Center   1131 N GALENA AVE     DIXON   IL   61021-1015
515   Affiliated   1640   Grand Rapids   PDI-Grand Rapids   801 CHERRY ST SE     GRAND RAPIDS   MI   49506-1440
516   Affiliated   1641   Grand Rapids East   PDI-Grand Rapids East   1230 EKHART ST NE     GRAND RAPIDS   MI   49503-1372
517   Affiliated   1642   Grand Haven   PDI-Grand Haven   16964 ROBBINS RD     GRAND HAVEN   MI   49417-2796
518   Affiliated   1644   Highland Park   PDI-Highland Park   64 VICTOR ST     HIGHLAND PARK   MI   48203-3128
519   Affiliated   1645   Cadieux   PDI-Cadieux   6150 CADIEUX ROAD     DETROIT   MI   48224-2006
520   Affiliated   1646   Montgomery   PDI-Montgomery   1001 FOREST AVE     MONTGOMERY   AL   36106-1181
521   Affiliated   1647   East Montgomery   PDI-East Montgomery   6890 WINTON BLOUNT BLVD     MONTGOMERY   AL   36117-3516
522   Affiliated   1648   Prattville   PDI-Prattville   1815 GLYNWOOD DR     PRATTVILLE   AL   36066-5584
523   Affiliated   1649   Elmore   PDI-Elmore   125 HOSPITAL DR     WETUMPKA   AL   36092-1626
524   Affiliated   1650   Fitchburg   PDI-Fitchburg   551 ELECTRIC AVE     FITCHBURG   MA   01420-5371
525   Affiliated   1652   Rocky Hill   PDI-Rocky Hill   30 WATERCHASE DR     ROCKY HILL   CT   06067-2110
526   Affiliated   1653   Middlesex   PDI-Middlesex Dialysis Center   100 MAIN ST   STE A   MIDDLETOWN   CT   06457-3477
527   Affiliated   1655   Johnstown   PDI-Johnstown   344 BUDFIELD ST     JOHNSTOWN   PA   15904-3214
528   Affiliated   1656   Ebensburg   PDI-Ebensburg   236 JAMESWAY RD     EBENSBURG   PA   15931-4207
529   Affiliated   1657   Walnut Tower   PDI-Walnut Tower   834 WALNUT ST     PHILADELPHIA   PA   19107-5109
530   Affiliated   1659   Lancaster   PDI-Lancaster   1412 E KING ST     LANCASTER   PA   17602-3240
531   Affiliated   1660   Ephrata   PDI-Ephrata   67 W CHURCH ST     STEVENS   PA   17578-9203
532   Affiliated   2083   Pinecrest Dialysis   Pinecrest Dialysis (aka North Marshall-TX)   913 E PINECREST DR     MARSHALL   TX   75670-7309
533   Affiliated   551   Westwood Dialysis   Westwood Dialysis Center (aka West Seattle)   2615 SW TRENTON ST     SEATTLE   WA   98126-3745
534   Affiliated   2107   Louisville Dialysis   Louisville Dialysis   8037 DIXIE HWY     LOUISVILLE   KY   40258-1344
535   Affiliated   2018   Fair Oaks Dialysis   Fair Oaks Dialysis Center (fka Chantilly & Centreville)   3955 PENDER DR   ONE PENDER BUSINESS PARK   FAIRFAX   VA   22030-6091

 

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536   Affiliated   421   Oak Cliff   Oak Cliff Dialysis   2000 S LLEWELLYN AVE     DALLAS   TX   75224-1804
537   Affiliated   2126   Gilmer Dialysis   Gilmer Dialysis Center   519 N WOOD ST     GILMER   TX   75644-1746
538   Affiliated   1608   Chicago Heights Dialysis   Chicago Heights Dialysis   177 W JOE ORR RD   STE B   CHICAGO HEIGHTS   IL   60411-1733
539   Affiliated   1623   East Georgia Dialysis   East Georgia Dialysis   450 GEORGIA AVE   STE A   STATESBORO   GA   30458-5590
540   Affiliated   1639   Northlake Dialysis   Northlake Dialysis   1350 MONTREAL RD   STE 2   TUCKER   GA   30084-8144
541   Affiliated   1680   Down River Dialysis   Downriver Kidney Center   5600 ALLEN RD     ALLEN PARK   MI   48101-2604
542   Affiliated   2063   Belcaro   Belcaro Dialysis Center   755 S COLORADO BLVD     DENVER   CO   80246-8005
543   Affiliated   2076   Sherwood Dialysis Center   Sherwood Dialysis Center   21035 SW PACIFIC HWY     SHERWOOD   OR   97140-8062
544   Affiliated   2054   Lonetree Dialysis   Lonetree Dialysis Center (aka Skyridge)   9777 MOUNT PYRAMID CT   STE 14   ENGLEWOOD   CO   80112-6017
545   Affiliated   2078   River Park Dialysis   River Park Dialysis (aka Conroe)   2010 S LOOP 336 W   STE 2   CONROE   TX   77304-3313
546   Affiliated   2058   Northshore Dialysis   Northshore Kidney Center (fka Slidell II)   106 MEDICAL CENTER DR     SLIDELL   LA   70461-5575
547   Affiliated   2036   Marysville Dialysis   Marysville Dialysis Center   1015 8TH ST     MARYSVILLE   CA   95901-5271
548   Affiliated   2070   West Georgia Dialysis   West Georgia Dialysis   1216 STARK AVE     COLUMBUS   GA   31906-2500
549   Affiliated   2102   East Dearborn Dialysis   Westland Dialysis (aka Canton)   36588 FORD RD     WESTLAND   MI   48185-3769
550   Affiliated   2045   Downtown Houston Dialysis   Downtown Houston Dialysis Center   2207 CRAWFORD ST     HOUSTON   TX   77002-8915
551   Affiliated   2066   Concord Dialysis   Concord Dialysis Center   2300 STANWELL DR   STE C   CONCORD   CA   94520-4841
552   Affiliated   2087   Pendleton Dialysis   Pendleton Dialysis (aka Clemson, Tri-County)   7703 HIGHWAY 76     PENDLETON   SC   29670-1818
553   Affiliated   2106   New Albany Dialysis   New Albany Dialysis   2669 CHARLESTON RD     NEW ALBANY   IN   47150-2573
554   Affiliated   1585   Whitesburg Dialysis   Whitesburg Dialysis   222 HOSPITAL RD   STE D   WHITESBURG   KY   41858-7627
555   Affiliated   2047   Jacinto Dialysis   Jacinto Dialysis Center (aka East Houston)   11515 MARKET STREET RD     HOUSTON   TX   77029-2305
556   Affiliated   2088   Transmountain Dialysis   Transmountain Dialysis (aka Northeast El Paso, Rushfair)   5255 WOODROW BEAN   STE B18   EL PASO   TX   79924-3832
557   Affiliated   2029   Southcrest Dialysis   Southcrest Dialysis (aka South Creek)   9001 S 101ST EAST AVE   STE 11   TULSA   OK   74133-5799
558   Affiliated   2071   Lake Hearn   Lake Hearn Dialysis (aka Dunwoody, Roswell, Northside)   1150 LAKE HEARN DR NE   STE 1   ATLANTA   GA   30342-1566
559   Affiliated   2118   Mt. Greenwood   Mt. Greenwood Dialysis   3401 W 111TH ST     CHICAGO   IL   60655-3329
560   Affiliated   2086   Citrus Valley Dialysis Center   Citrus Valley Dialysis (aka San Bernadino II)   894 HARDT STREET     SAN BERNARDINO   CA   92408-2854
561   Affiliated   2095   McDowell County Dialysis   McDowell County Dialysis Center   100 SPAULDING RD   STE 2   MARION   NC   28752-5116
562   Affiliated   2115   Leigh Dialysis Center   Leigh Dialysis Center (aka Leigh-Kempville-VA)   420 N CENTER DR   STE 128   NORFOLK   VA   23502-4019
563   Affiliated   2120   Dialysis of Lithonia   Dialysis of Lithonia   2485 PARK CENTRAL BLVD     DECATUR   GA   30035-3902
564   Affiliated   2114   Embassy Lake Artificial Kidney Center   Embassy Lake Artificial Kidney Center (fka Davie & South Broward AKC)   11011 SHERIDAN ST   STE 38   HOLLYWOOD   FL   33026-1505
565   Affiliated   2056   Sun City Dialysis   Sun City Dialysis (akaTexas Tech II)   600 NEWMAN ST     EL PASO   TX   79902-5543
566   Affiliated   1651   PDI Worcester   PDI-Worcester Dialysis   19 GLENNIE ST   STE A   WORCESTER   MA   01605-3918
567   Affiliated   2130   Davenport Dialysis Center   Davenport Dialysis Center (aka Haines City II)   45597 HIGHWAY 27   RIDGEVIEW PLAZA   DAVENPORT   FL   33897-4519
568   Affiliated   2081   Cinema Dialysis   Cinema Dialysis (aka OKC South)   3909 S WESTERN AVE     OKLAHOMA CITY   OK   73109-3405
569   Affiliated   2037   Greenwood Dialysis Center   Greenwood Dialysis Center (North Tulsa)   1345 N LANSING AVE     TULSA   OK   74106-5911
570   Affiliated   1712   TRC Alamosa Diakysis   Alamosa Dialysis   612 DEL SOL DR     ALAMOSA   CO   81101-8548
571   Affiliated   1682   South Austin   South Austin Dialysis   6114 S 1ST ST     AUSTIN   TX   78745-4008
572   Affiliated   2109   Durango Dialysis Center   Durango Dialysis Center   72 SUTTLE STREET   STE D   DURANGO   CO   81303-6829
573   Affiliated   1700   Bolivar Dialysis   Bolivar Dialysis   515 PECAN DR     BOLIVAR   TN   38008-1611
574   Affiliated   1701   Brownsville Dialysis   Brownsville Dialysis   380 N DUPREE AVE     BROWNSVILLE   TN   38012-2332
575   Affiliated   1702   Camden Dialysis   Camden Dialysis   168 W MAIN ST   STE A   CAMDEN   TN   38320-1767
576   Affiliated   1703   Collierville Dialysis   Collierville Dialysis   791 W POPLAR AVE     COLLIERVILLE   TN   38017-2543
577   Affiliated   1705   Galleria Dialysis   Galleria Dialysis   9160 HIGHWAY 64     LAKELAND   TN   38002-4766
578   Affiliated   1706   Humboldt Dialysis   Humboldt Dialysis   2214 OSBORNE ST     HUMBOLDT   TN   38343-3044
579   Affiliated   1707   Stonegate Dialysis   North Jackson Dialysis (fka Stonegate)   217 STERLING FARM DR     JACKSON   TN   38305-5727
580   Affiliated   1708   Lexington Dialysis   Lexington Dialysis   317 W CHURCH ST     LEXINGTON   TN   38351-2096
581   Affiliated   1709   Pickwick Dialysis   Pickwick Dialysis   121 PICKWICK ST     SAVANNAH   TN   38372-1953
582   Affiliated   1710   Selmber Dialysis   Selmer Dialysis   251 OAKGROVE RD     SELMER   TN   38375-1881
583   Affiliated   1713   Childs Dialysis   Childs Dialysis   101 MAIN ST     CHILDS   PA   18407-2614
584   Affiliated   1714   Dunmore Dialysis   Dunmore Dialysis   1212 O'NEIL HWY     DUNMORE   PA   18512-1717
585   Affiliated   1716   Old Forge Dialysis   Old Forge Dialysis   325 S MAIN ST     OLD FORGE   PA   18518-1677
586   Affiliated   1717   Scranton Dialysis   Scranton Dialysis   475 MORGAN HWY     SCRANTON   PA   18508-2605
587   Affiliated   1718   Tunkhannock Dialysis   Tunkhannock Dialysis   5950 SR 6     TUNKHANNOCK   PA   18657-7905
588   Affiliated   1725   East Evansville Dialysis   East Evansville Dialysis   1312 PROFESSIONAL BLVD     EVANSVILLE   IN   47714-8007
589   Affiliated   1726   North Evansville Dialysis   North Evansville Dialysis   1151 W BUENA VISTA RD     EVANSVILLE   IN   47710-3334

 

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590   Affiliated   1728   Jasper Dialysis   Jasper Dialysis   721 W 13TH ST   STE 15   JASPER   IN   47546-1856
591   Affiliated   1729   Daviess County Dialysis   Daviess County Dialysis   310 NE 14TH ST     WASHINGTON   IN   47501-2137
592   Affiliated   1730   Gardenside Dialysis   Gardenside Dialysis   70 N GARDENMILE RD     HENDERSON   KY   42420-5529
593   Affiliated   1732   PD Evansville Dialysis   East Evansville Dialysis PD   1312 PROFESSIONAL BLVD     EVANSVILLE   IN   47714-8007
594   Affiliated   2098   Meridian Dialysis Center   Meridian Dialysis Center (aka Bayshore)   201 W FAIRMONT PKWY   STE A   LA PORTE   TX   77571-6303
595   Affiliated   2100   Sycamore Dialysis   Sycamore Dialysis (aka DeKalb)   2200 GATEWAY DR     SYCAMORE   IL   60178-3113
596   Affiliated   2104   Ballenger Pointe Dialysis   Ballenger Pointe Dialysis (aka West Flint)   2262 S BALLENGER HWY     FLINT   MI   48503-3447
597   Affiliated   2139   Leitchfield Dialysis   Leitchfield Dialysis   912 WALLACE AVE   STE 16   LEITCHFIELD   KY   42754-2405
598   Affiliated   2097   Roxbury Dialysis Center   Roxbury Dialysis   622 ROXBURY RD     ROCKFORD   IL   61107-5089
599   Affiliated   2148   LaGrange Dialysis   La Grange Dialysis   240 PARKER DR     LA GRANGE   KY   40031-1200
600   Affiliated   2132   Des Moines East   East Des Moines Dialysis (aka Des Moines II)   1301 PENNSYLVANIA AVE   STE 28   DES MOINES   IA   50316-2365
601   Affiliated   2119   Lake Villa Dialysis   Lake Villa Dialysis   37809 N IL ROUTE 59     LAKE VILLA   IL   60046-7332
602   Affiliated   159   Seneca Dialysis   Seneca County Dialysis   65 SAINT FRANCIS AVE     TIFFIN   OH   44883-3413
603   Affiliated   407   Perry   Perry Dialysis Center   1027 KEITH DR     PERRY   GA   31069-2948
604   Affiliated   661   Wilshire   Wilshire Dialysis   1212 WILSHIRE BLVD     LOS ANGELES   CA   90017-1902
605   Affiliated   692   University Park   University Park Dialysis Center   3986 S FIGUEROA ST     LOS ANGELES   CA   90037-1222
606   Affiliated   1720   Metro East Dialysis   Metro East Dialysis   5105 W MAIN ST     BELLEVILLE   IL   62226-4728
607   Affiliated   2196   Ocala Regional Kidney Centers   Ocala Regional Kidney Centers Home Dialysis Division PD   2860 SE 1ST AVE     OCALA   FL   34471-0406
608   Affiliated   2133   Little Village Dialysis   Little Village Dialysis (Chicago)   2335 W CERMAK RD     CHICAGO   IL   60608-3811
609   Affiliated   2112   Crossroads   Crossroads Dialysis (aka Fullerton Dialysis)   3214 YORBA LINDA BLVD     FULLERTON   CA   92831-1707
610   Affiliated   1727   Vincennes Dialysis   Vincennes Dialysis   700 WILLOW ST     VINCENNES   IN   47591-1028
611   Affiliated   1723   Spring Dialysis   Spring Dialysis   607 TIMBERDALE LN   STE 1   HOUSTON   TX   77090-3043
612   Affiliated   2190   River Center   Rivercenter Dialysis (aka Central San Antonio)   1123 N MAIN AVE   STE 15   SAN ANTONIO   TX   78212-4738
613   Affiliated   2193   Southcross Dialysis Center   Southcross Dialysis (aka SouthEast San Antonio)   4602 E SOUTHCROSS BLVD     SAN ANTONIO   TX   78222-4911
614   Affiliated   2125   Bonham Dialysis   Bonham Dialysis   201 W 5TH ST     BONHAM   TX   75418-4302
615   Affiliated   2192   Northwest Medical Center Dialysis   NW Medical Center Dialysis (aka NorthWest San Antonio)   5284 MEDICAL DR   STE 1   SAN ANTONIO   TX   78229-4849
616   Affiliated   2124   Ontario Dialysis   Ontario Dialysis (aka Dr. Handoko)   1950 S GROVE AVE   STE 11-15   ONTARIO   CA   91761-5693
617   Affiliated   1750   Chipley Community Dialysis   Chipley Dialysis   877 3RD ST   STE 2   CHIPLEY   FL   32428-1855
618   Affiliated   1751   North Ikaloosa   North Okaloosa Dialysis   320 REDSTONE AVE W     CRESTVIEW   FL   32536-6433
619   Affiliated   1752   West Florida Dialysis   West Florida Dialysis   8333 N DAVIS HWY   1ST FLOOR ATTN DIALYSIS ROOM   PENSACOLA   FL   32514-6049
620   Affiliated   1753   Santa Rosa Dialysis   Santa Rosa Dialysis   5819 HIGHWAY 90     MILTON   FL   32583-1763
621   Affiliated   1755   Atmore Dialysis   Atmore Dialysis Center   807 E CRAIG ST     ATMORE   AL   36502-3017
622   Affiliated   1756   South Baldwin Dialysis   South Baldwin Dialysis Center   150 W PEACHTREE AVE     FOLEY   AL   36535-2244
623   Affiliated   1731   Olney Dialysis   Olney Dialysis Center (aka Good Samaritan Hospital)   117 N BOONE ST     OLNEY   IL   62450-2109
624   Affiliated   2156   Lancaster Dialysis   Lancaster Dialysis   2424 W PLEASANT RUN RD     LANCASTER   TX   75146-4005
625   Affiliated   2136   Columbia Dialysis   RTC-Columbia Dialysis (MO)   1701 E BROADWAY   STE G12   COLUMBIA   MO   65201-8029
626   Affiliated   2194   Las Palmas Dialysis Center   Las Palmas Dialysis Center (aka West San Antonio)   803 CASTROVILLE RD   STE 415   SAN ANTONIO   TX   78237-3148
627   Affiliated   2116   South Shore Dialysis Center   South Shore Dialysis (aka Horizon)   212 GULF FWY S   STE G3   LEAGUE CITY   TX   77573-3957
628   Affiliated   2191   Marymount Dilaysis Center   Marymont Dialysis (aka NorthEast San Antonio)   2391 NE LOOP 410   STE 211   SAN ANTONIO   TX   78217-5675
629   Affiliated   1744   Fox River Dialysis   Fox River Dialysis   1910 RIVERSIDE DR     GREEN BAY   WI   54301-2319
630   Affiliated   1745   Titletown Dialysis   Titletown Dialysis   120 SIEGLER ST     GREEN BAY   WI   54303-2636
631   Affiliated   1746   Northwoods Dialysis   Green Bay Northwood Dialysis   W 7305 ELM AVENUE     SHAWANO   WI   54166-1024
632   Affiliated   1758   North Charleston Dialysis   North Charleston Dialysis   5900 RIVERS AVE   STE E   NORTH CHARLESTON   SC   29406
633   Affiliated   1759   Charleston County Dialysis   Faber Place Dialysis   3801 FABER PLACE DR     NORTH CHARLESTON   SC   29405-8533
634   Affiliated   1760   Goose Creek Dialysis   Goose Creek Dialysis   109 GREENLAND DR     GOOSE CREEK   SC   29445-5354
635   Affiliated   2501   Bridgeport Dialysis   Bridgeport Dialysis   900 MADISON AVE   STE 221   BRIDGEPORT   CT   06606-5534
636   Affiliated   2503   Greater Waterbury Dialysis   Greater Waterbury Dialysis   209 HIGHLAND AVE     WATERBURY   CT   06708-3026
637   Affiliated   2506   Shelton Dialysis   Shelton Dialysis   750 BRIDGEPORT AVE     SHELTON   CT   06484-4734
638   Affiliated   2508   Yuma Dialysis   Yuma Dialysis   2130 W 24TH ST     YUMA   AZ   85364-6122
639   Affiliated   2509   Pittsburgh Dialysis   Pittsburgh Dialysis   4312 PENN AVE     PITTSBURGH   PA   15224-1310
640   Affiliated   2510   Elizabeth Dialysis   Elizabeth Dialysis   201 MCKEESPORT RD     ELIZABETH   PA   15037-1623
641   Affiliated   2511   Brandon East Dialysis   Brandon East Dialysis   114 E BRANDON BLVD     BRANDON   FL   33511-5219
642   Affiliated   2513   North Rolling Road Dialysis   North Rolling Road Dialysis   1108 N ROLLING RD     BALTIMORE   MD   21228-3826
643   Affiliated   2521   Memphis South Dialysis   Memphis South Dialysis   1205 MARLIN RD     MEMPHIS   TN   38116-5812

 

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644   Affiliated   2524   Hartford Dialysis   Hartford Dialysis   675 TOWER AVE   RENAL UNIT 2ND FL   HARTFORD   CT   6112
645   Affiliated   2538   New Orleans Uptown Dialysis   New Orleans Uptown Dialysis   1401 FOUCHER ST   4TH FLOOR DIALYSIS   NEW ORLEANS   LA   70115-3515
646   Affiliated   2540   Omaha West Dialysis   Omaha West Dialysis   13014 W DODGE RD     OMAHA   NE   68154-2148
647   Affiliated   2541   White Memorial Dialysis   East Los Angeles Plaza Dialysis (fka White Memorial)   1700 E CESAR E CHAVEZ AVE   STE L 1   LOS ANGELES   CA   90033-2424
648   Affiliated   2542   Imperial Dialysis   Imperial Dialysis   2738 W IMPERIAL HWY     INGLEWOOD   CA   90303-3111
649   Affiliated   2546   North Hollywood Dialysis   North Hollywood Dialysis   12126 VICTORY BLVD     NORTH HOLLYWOOD   CA   91606-3205
650   Affiliated   2555   Mountain View Dialysis   Mountain View Dialysis   2881 BUSINESS PARK CT   STE 13   LAS VEGAS   NV   89128-9019
651   Affiliated   2560   San Juan Capistrano South Dialysis   San Juan Capistrano South Dialysis   31736 RANCHO VIEJO RD   STE B   SAN JUAN CAPISTRANO   CA   92675-2783
652   Affiliated   2564   Mission Viejo Dialysis   Mission Viejo Dialysis   27640 MARGUERITE PKWY     MISSION VIEJO   CA   92692-3604
653   Affiliated   2568   HI-Desert Dialysis   HI-Desert Dialysis   58457 29 PALMS HWY   STE 12   YUCCA VALLEY   CA   92284-5879
654   Affiliated   2571   Banning Dialysis   Banning Dialysis   6090 W RAMSEY ST     BANNING   CA   92220-3052
655   Affiliated   2601   Rainbow City Dialysis   Rainbow City Dialysis   2800 RAINBOW DR     RAINBOW CITY   AL   35906-5811
656   Affiliated   2604   Gadsden Dialysis   Gadsden Dialysis   409 S 1ST ST     GADSDEN   AL   35901-5358
657   Affiliated   2605   Chateau Dialysis   Chateau Dialysis   720 VILLAGE RD     KENNER   LA   70065-2751
658   Affiliated   2606   Donaldsonville Dialysis   Donaldsonville Dialysis   101 PLIMSOL DR     DONALDSONVILLE   LA   70346-4357
659   Affiliated   2609   Dothan Dialysis   Dothan Dialysis   216 GRACELAND DR     DOTHAN   AL   36305-7346
660   Affiliated   2614   Birmingham East Dialysis   Birmingham East Dialysis   1105 E PARK DR     BIRMINGHAM   AL   35235-2560
661   Affiliated   2615   Tuscaloosa Dialysis   Tuscaloosa Dialysis   805 OLD MILL ST     TUSCALOOSA   AL   35401-7132
662   Affiliated   2616   Demopolis Dialysis   Demopolis Dialysis   511 S CEDAR AVE     DEMOPOLIS   AL   36732-2235
663   Affiliated   2623   Singing River Dialysis   Singing River Dialysis   4907 TELEPHONE RD     PASCAGOULA   MS   39567-1823
664   Affiliated   2624   Ocean Springs Dialysis   Ocean Springs Dialysis   13150 PONCE DE LEON DR     OCEAN SPRINGS   MS   39564-2460
665   Affiliated   2625   Lucedale Dialysis   Lucedale Dialysis   652 MANILA ST     LUCEDALE   MS   39452-5962
666   Affiliated   2707   Holmdel Dialysis   Holmdel Dialysis   668 N BEERS ST     HOLMDEL   NJ   07733-1526
667   Affiliated   2855   Alameda County Dialysis   Alameda County Dialysis   10700 MACARTHUR BLVD   STE 14   OAKLAND   CA   94605-5260
668   Affiliated   2908   Elizabeth City Dialysis   Elizabeth City Dialysis   1840 W CITY DR     ELIZABETH CITY   NC   27909-9632
669   Affiliated   2914   Cookeville Dialysis   Cookeville Dialysis   140 W 7TH ST     COOKEVILLE   TN   38501-1726
670   Affiliated   3001   Inglewood Dialysis   Inglewood Dialysis   125 E ARBOR VITAE ST     INGLEWOOD   CA   90301-3839
671   Affiliated   3002   Rome Dialysis   Rome Dialysis   15 JOHN MADDOX DR NW     ROME   GA   30165-1413
672   Affiliated   3004   Pomona Dialysis   Pomona Dialysis   2111 N GAREY AVE     POMONA   CA   91767-2328
673   Affiliated   3005   Oak Street Dialysis   Oak Street Dialysis (fka Valdosta)   2704 N OAK ST   BLDG H   VALDOSTA   GA   31602-1723
674   Affiliated   3006   Channelview Dialysis   Channelview Dialysis   777 SHELDON RD   STE C   CHANNELVIEW   TX   77530-3509
675   Affiliated   3007   Sagemont Dialysis   Sagemont Dialysis   10851 SCARSDALE BLVD   STE 2   HOUSTON   TX   77089-5738
676   Affiliated   3008   San Jacinto Dialysis   San Jacinto Dialysis   11430 EAST FWY   STE 33   HOUSTON   TX   77029-1959
677   Affiliated   3009   Victor Valley Dialysis   Victor Valley Dialysis   16049 KAMANA RD     APPLE VALLEY   CA   92307-1331
678   Affiliated   3010   Delran Dialysis   Delran Dialysis   8008 ROUTE 130     DELRAN   NJ   08075-1869
679   Affiliated   3011   Central Houston Dialysis   Central Houston Dialysis   610 S WAYSIDE DR   UNIT B   HOUSTON   TX   77011-4605
680   Affiliated   3012   Southern Lane Dialysis   Southern Lane Dialysis   1840 SOUTHERN LN     DECATUR   GA   30033-4033
681   Affiliated   3013   Northumberland Dialysis   Northumberland Dialysis   103 W STATE ROUTE 61     MOUNT CARMEL   PA   17851-2539
682   Affiliated   3014   Pryor Dialysis   Pryor Dialysis   309 E GRAHAM AVE     PRYOR   OK   74361-2434
683   Affiliated   3015   Oklahoma City South Dialysis   Oklahoma City South Dialysis   5730 S MAY AVE     OKLAHOMA CITY   OK   73119-5604
684   Affiliated   3016   Abington Dialysis   Abington Dialysis   3940A COMMERCE AVE     WILLOW GROVE   PA   19090-1705
685   Affiliated   3017   Memphis Central Dialysis   Memphis Central Dialysis   889 LINDEN AVE     MEMPHIS   TN   38126-2412
686   Affiliated   3018   Memphis East Dialysis   Memphis East Dialysis   50 HUMPHREYS CTR   STE 42   MEMPHIS   TN   38120-2372
687   Affiliated   3019   Clarksville Dialysis   Clarksville Dialysis   231 HILLCREST DR     CLARKSVILLE   TN   37043-5093
688   Affiliated   3020   Miami Campus Dialysis   Miami Campus Dialysis   1500 NW 12TH AVE   STE 16   MIAMI   FL   33136-1028
689   Affiliated   3021   Orlando Dialysis   Orlando Dialysis   116 STURTEVANT ST     ORLANDO   FL   32806-2021
690   Affiliated   3024   Durham Dialysis   Durham Dialysis   601 FAYETTEVILLE ST     DURHAM   NC   27701-3910
691   Affiliated   3025   Candler County Dialysis   Candler County Dialysis   325 CEDAR ST     METTER   GA   30439-4043
692   Affiliated   3027   Kerrville Dialysis   Kerrville Dialysis   515 GRANADA PL     KERRVILLE   TX   78028-5992
693   Affiliated   3028   Floresville Dialysis   Floresville Dialysis   543 10TH ST     FLORESVILLE   TX   78114-3107
694   Affiliated   3029   Pearsall Dialysis   Pearsall Dialysis   1305 N OAK ST     PEARSALL   TX   78061-3414
695   Affiliated   3030   Nogales Dialysis   Nogales Dialysis   1231 W TARGET RANGE RD     NOGALES   AZ   85621-2417
696   Affiliated   3032   Wilson Dialysis   Wilson Dialysis   1605 MEDICAL PARK DR W     WILSON   NC   27893-2799
697   Affiliated   3033   Goldsboro Dialysis   Goldsboro Dialysis   2609 HOSPITAL RD     GOLDSBORO   NC   27534-9424

 

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698   Affiliated   3034   Roxboro Dialysis   Roxboro Dialysis   718 RIDGE RD     ROXBORO   NC   27573-4508
699   Affiliated   3035   Boston Dialysis   Boston Dialysis   660 HARRISON AVE     BOSTON   MA   02118-2304
700   Affiliated   3037   Jesup Dialysis   Jesup Dialysis   301 PEACHTREE ST     JESUP   GA   31545-0245
701   Affiliated   3038   Sheffield Dialysis   Sheffield Dialysis   1120 S JACKSON HWY   ST 17   SHEFFIELD   AL   35660-5777
702   Affiliated   3039   Berkeley Dialysis   Berkeley Dialysis   2920 TELEGRAPH AVE     BERKELEY   CA   94705-2031
703   Affiliated   3040   Douglas Dialysis   Douglas Dialysis   190 WESTSIDE DR   STE A   DOUGLAS   GA   31533-3534
704   Affiliated   3041   Hopkinsville Dialysis   Hopkinsville Dialysis   1914 S VIRGINIA ST     HOPKINSVILLE   KY   42240-3610
705   Affiliated   3042   Roxborough Dialysis   Roxborough Dialysis   5003 UMBRIA ST     PHILADELPHIA   PA   19128-4301
706   Affiliated   3043   New Haven Dialysis   New Haven Dialysis   100 CHURCH ST S   STE C   NEW HAVEN   CT   06519-1703
707   Affiliated   3044   Ocoee Dialysis   Ocoee Dialysis   11140 W COLONIAL DR   STE 5   OCOEE   FL   34761-3300
708   Affiliated   3045   Waverly Dialysis   Waverly Dialysis   407 E BALTIMORE PIKE     MORTON   PA   19070-1042
709   Affiliated   3046   Sells Dialysis   Sells Dialysis   PO BOX 3030   HWY 86 MILEPOST 113   SELLS   AZ   85634-3030
710   Affiliated   3047   Sierra Vista Dialysis   Sierra Vista Dialysis   629 N HIGHWAY 90   STE 6   SIERRA VISTA   AZ   85635-2257
711   Affiliated   3048   Callaghan Road Dialysis   San Antonio West Dialysis (fka Callaghan Road)   4530 CALLAGHAN RD     SAN ANTONIO   TX   78228
712   Affiliated   3049   Houston Dialysis   Houston Dialysis   7543 SOUTH FWY     HOUSTON   TX   77021-5928
713   Affiliated   3050   South Yuma Dialysis   South Yuma Dialysis   7179 E 31ST PLACE     YUMA   AZ   85365-8392
714   Affiliated   3052   Cherry Hill Dialysis   Cherry Hill Dialysis   1030 KINGS HWY N   STE 1   CHERRY HILL   NJ   08034-1907
715   Affiliated   3055   Escondido Dialysis   Escondido Dialysis   203 E 2ND AVE     ESCONDIDO   CA   92025-4212
716   Affiliated   3056   Brookline Dialysis   Brookline Dialysis   322 WASHINGTON ST     BROOKLINE   MA   02445-6850
717   Affiliated   3057   Reliant Dialysis   Reliant Dialysis   1335 LA CONCHA LN     HOUSTON   TX   77054-1809
718   Affiliated   3058   Fullerton Dialysis   Fullerton Dialysis   238 ORANGEFAIR MALL     FULLERTON   CA   92832-3037
719   Affiliated   3059   Huntington Beach Dialysis   Huntington Beach Dialysis   16892 BOLSA CHICA ST   STE 1   HUNTINGTON BEACH   CA   92649-3571
720   Affiliated   3060   Eastlake Dialysis   Eastlake Dialysis (fka South Dekalb)   1757 CANDLER RD     DECATUR   GA   30032-3276
721   Affiliated   3061   Mt. Olive Dialysis   Mt. Olive Dialysis   105 MICHAEL MARTIN RD     MOUNT OLIVE   NC   28365-1112
722   Affiliated   3062   Southwest San Antonio Dialysis   Southwest San Antonio Dialysis   1620 SOMERSET RD     SAN ANTONIO   TX   78211-3021
723   Affiliated   3064   North Loop East Dialysis   North Loop East Dialysis   7139 NORTH LOOP E     HOUSTON   TX   77028-5903
724   Affiliated   3065   Katy Cinco Ranch Dialysis   Katy Cinco Ranch Dialysis   1265 ROCK CANYON DR     KATY   TX   77450-3831
725   Affiliated   3067   Palm Springs Dialysis   Palm Springs Dialysis   1061 N INDIAN CANYON DR     PALM SPRINGS   CA   92262-4854
726   Affiliated   3069   Muskegon Dialysis   Muskegon Dialysis   1277 MERCY DR     MUSKEGON   MI   49444-4605
727   Affiliated   3070   Loomis Road Dialysis   Loomis Road Dialysis   4120 W LOOMIS RD     GREENFIELD   WI   53221-2052
728   Affiliated   3071   Ludington Dialysis   Ludington Dialysis   5 N ATKINSON DR   STE 11   LUDINGTON   MI   49431-2918
729   Affiliated   3073   Walterboro Dialysis   Walterboro Dialysis   302 RUBY ST     WALTERBORO   SC   29488-2758
730   Affiliated   3074   K Street   K Street Dialysis (fka GWU N Street Dialysis)   2131 K ST NW     WASHINGTON   DC   20037-1898
731   Affiliated   3075   GWU Southeast Dialysis   GWU Southeast Dialysis   3857A PENNSYLVANIA AVE SE     WASHINGTON   DC   20020-1309
732   Affiliated   3076   Lakeside Dialysis   Lakeside Dialysis   10401 HOSPITAL DR   STE G2   CLINTON   MD   20735-3113
733   Affiliated   3077   Summit Dialysis   Summit Dialysis   1139 SPRUCE DR     MOUNTAINSIDE   NJ   07092-2221
734   Affiliated   3078   Aiken Dialysis   Aiken Dialysis   775 MEDICAL PARK DR     AIKEN   SC   29801-6306
735   Affiliated   3092   Ozark Dialysis   Ozark Dialysis   214 HOSPITAL AVE     OZARK   AL   36360-2038
736   Affiliated   3094   Wylds Road Dialysis   Wylds Road Dialysis (fka Augusta South)   1815 WYLDS RD     AUGUSTA   GA   30909-4430
737   Affiliated   3104   Douglasville Dialysis   Douglasville Dialysis   3899 LONGVIEW DR     DOUGLASVILLE   GA   30135-1373
738   Affiliated   3106   Brunswick Dialysis   Brunswick Dialysis   53 SCRANTON CONNECTOR     BRUNSWICK   GA   31525-1862
739   Affiliated   3109   Benicia Dialysis   Benicia Dialysis   560 1ST ST   STE 13 BLDG D   BENICIA   CA   94510-3295
740   Affiliated   3111   Atlanta Dialysis   Atlanta Dialysis   567 NORTH AVE NE   STE 2   ATLANTA   GA   30308-2719
741   Affiliated   3115   Rolla Dialysis   Rolla Dialysis   1503 E 10TH ST     ROLLA   MO   65401-3696
742   Affiliated   3119   East Atlanta Dialysis   East Atlanta Dialysis   1308 MORELAND AVE SE     ATLANTA   GA   30316-3224
743   Affiliated   3120   Brunswick South Dialysis   Brunswick South Dialysis   2930 SPRINGDALE RD     BRUNSWICK   GA   31520
744   Affiliated   3121   Thomaston Dialysis   Thomaston Dialysis   1065 US HIGHWAY 19 NORTH     THOMASTON   GA   30286-2233
745   Affiliated   3128   Piedmont Dialysis   Piedmont Dialysis   105 COLLIER RD NW   STE B   ATLANTA   GA   30309-1730
746   Affiliated   3130   Athens West Dialysis   Athens West Dialysis   2047 PRINCE AVE   STE A   ATHENS   GA   30606-6033
747   Affiliated   3131   Florence Dialysis   Florence Dialysis   422 E DR HICKS BLVD   STE B   FLORENCE   AL   35630-5763
748   Affiliated   3138   Atwater Dialysis   Atwater Dialysis   1201 COMMERCE AVE     ATWATER   CA   95301
749   Affiliated   3143   North Merced Dialysis   Merced Dialysis   3150 G ST   STE A   MERCED   CA   95340-1346
750   Affiliated   3169   Wisconsin Avenue Dialysis   Wisconsin Avenue Dialysis   3801 W WISCONSIN AVE     MILWAUKEE   WI   53208-3155
751   Affiliated   3171   River Center Dialysis   River Center Dialysis   117 N JEFFERSON ST     MILWAUKEE   WI   53202-6160

 

Page 60 of 136


752   Affiliated   3175   South Fulton Dialysis   South Fulton Dialysis   2685 METROPOLITAN PKWY SW   STE F   ATLANTA   GA   30315-7926
753   Affiliated   3201   Heartland Dialysis   Heartland Dialysis   925 NE 8TH ST     OKLAHOMA CITY   OK   73104-5800
754   Affiliated   3202   Hospital Hill Dialysis   Hospital Hill Dialysis   2250 HOLMES ST     KANSAS CITY   MO   64108-2639
755   Affiliated   3203   Tucson South Dialysis   Tucson South Dialysis   3662 S 16TH AVE     TUCSON   AZ   85713-6001
756   Affiliated   3204   Greene County Dialysis   Greene County Dialysis (AL)   544 US HIGHWAY 43     EUTAW   AL   35462-4017
757   Affiliated   3205   Fayette Dialysis   Fayette Dialysis   2450 TEMPLE AVE N     FAYETTE   AL   35555-1160
758   Affiliated   3206   Tuscaloosa University Dialysis   Tuscaloosa University Dialysis   220 15TH STREET     TUSCALOOSA   AL   35401
759   Affiliated   3207   Goldsboro South Dialysis   Goldsboro South Dialysis   1704 WAYNE MEMORIAL DR     GOLDSBORO   NC   27534-2240
760   Affiliated   3208   Orlando North Dialysis   Orlando North Dialysis   5135 ADANSON ST   STE 7   ORLANDO   FL   32804-1338
761   Affiliated   3209   UT Southwestern-Dallas Dialysis   UT Southwestern-Dallas Dialysis   204 E AIRPORT FREEWAY     IRVING   TX   75062
762   Affiliated   3210   San Diego South Dialysis   San Diego South Dialysis   995 GATEWAY CENTER WAY   STE 11   SAN DIEGO   CA   92102-4550
763   Affiliated   3211   Santa Monica Dialysis   Santa Monica Dialysis   1260 15TH ST   STE 12   SANTA MONICA   CA   90404-1136
764   Affiliated   3212   Airport Dialysis   Airport Dialysis   4632 W CENTURY BLVD     INGLEWOOD   CA   90304-1456
765   Affiliated   3220   Plantation Dialysis   Plantation Dialysis   7061 CYPRESS RD   STE 13   PLANTATION   FL   33317-2243
766   Affiliated   3224   Laurens County Dialysis   Laurens County Dialysis   2400 BELLEVUE RD   STE 8   DUBLIN   GA   31021-2856
767   Affiliated   3225   Ford Factory Square Dialysis   Ford Factory Square Dialysis   567 NORTH AVE NE   STE 1   ATLANTA   GA   30308-2719
768   Affiliated   3226   North Fulton Dialysis   North Fulton Dialysis   1250 NORTHMEADOW PKWY   STE 12   ROSWELL   GA   30076-4914
769   Affiliated   3228   Freehold Dialysis   Freehold Dialysis   300 CRAIG RD     MANALAPAN   NJ   07726-8742
770   Affiliated   3229   Neptune Dialysis   Neptune Route 66 Dialysis   3297 STATE ROUTE 66     NEPTUNE   NJ   07753-2762
771   Affiliated   3231   East Orange Dialysis   East Orange Dialysis   90 WASHINGTON ST   BSMT   EAST ORANGE   NJ   07017-1050
772   Affiliated   3234   UT Southwestern-Oakcliff Dialysis   UT Southwestern-Oakcliff Dialysis   610 WYNNEWOOD DR     DALLAS   TX   75224
773   Affiliated   3236   Atlanta West Dialysis   Atlanta West Dialysis   2538 MARTIN LUTHER KING JR DR SW     ATLANTA   GA   30311-1779
774   Affiliated   3237   Columbia University Dialysis Center   Columbia University Dialysis Center   60 HAVEN AVE     NEW YORK   NY   10032-2604
775   Affiliated   3238   Northeast Cambridge Dialysis   Northeast Cambridge Dialysis   799 CONCORD AVE     CAMBRIDGE   MA   02138-1048
776   Affiliated   3239   New Bedford Dialysis   New Bedford Dialysis   524 UNION ST     NEW BEDFORD   MA   02740-3546
777   Affiliated   3242   Weymouth Dialysis   Weymouth Dialysis   330 LIBBEY INDUSTRIAL PARK   STE 9   WEYMOUTH   MA   02189-3122
778   Affiliated   3243   Woburn Dialysis   Woburn Dialysis   23 WARREN AVE     WOBURN   MA   01801-7906
779   Affiliated   3248   Bryan Dialysis   College Station Dialysis (fka Bryan Dialysis)   701 UNIVERSITY DR E   STE 41   COLLEGE STATION   TX   77840-1866
780   Affiliated   3249   Brenham Dialysis   Brenham Dialysis   2815 HIGHWAY 36 SO     BRENHAM   TX   77833
781   Affiliated   3250   Huntsville Dialysis   Huntsville Dialysis   521 IH 45S   STE 2   HUNTSVILLE   TX   77340-5651
782   Affiliated   3252   Utica Avenue Dialysis Center   Utica Avenue Dialysis Center   1305 UTICA AVE     BROOKLYN   NY   11203-5911
783   Affiliated   3254   New London Dialysis   New London Dialysis   5 SHAWS COVE   STE 1   NEW LONDON   CT   06320-4974
784   Affiliated   3258   Baxley Dialysis   Baxley Dialysis   539 FAIR ST     BAXLEY   GA   31513-0112
785   Affiliated   3261   Pascua Yaqui Tribe Dialysis   Pascua Yaqui Tribe Dialysis   7490 S CAMINO DE OESTE     TUCSON   AZ   85746-9308
786   Affiliated   3262   JHHS North Bond Street Dialysis   JHHS North Bond Street Dialysis   409 N CAROLINE ST     BALTIMORE   MD   21231-1003
787   Affiliated   3263   Syosset Kidney Center   Syosset Kidney Center   1 LOCUST LN     SYOSSET   NY   11791-4834
788   Affiliated   3264   Freeport Kidney Center   Freeport Kidney Center   267 W MERRICK RD     FREEPORT   NY   11520-3346
789   Affiliated   3265   Huntington Station Dialysis Center   HAKC-Huntington   256 BROADWAY     HUNTINGTON STATION   NY   11746-1403
790   Affiliated   3266   Medford Kidney Center   Medford Kidney Center   1725 N OCEAN AVE     MEDFORD   NY   11763-2649
791   Affiliated   3267   Blue Ash Dialysis   Blue Ash Dialysis   10600 MCKINLEY RD     CINCINNATI   OH   45242-3716
792   Affiliated   3269   Mt. Auburn Dialysis   Mt. Auburn Dialysis   2109 READING RD     CINCINNATI   OH   45202-1417
793   Affiliated   3272   Charlottesville Dialysis   Charlottesville Dialysis   1460 PANTOPS MOUNTAIN PLACE     CHARLOTTESVILLE   VA   22911
794   Affiliated   3273   Alexandria Dialysis   Alexandria Dialysis   5150 DUKE ST     ALEXANDRIA   VA   22304-2906
795   Affiliated   3275   Sebastian Dialysis   Sebastian Dialysis   1424 US HWY 1   STE C   SEBASTIAN   FL   32958-1619
796   Affiliated   3276   Crestview Hills Dialysis   Crestview Hills Dialysis   400 CENTERVIEW BLVD     CRESTVIEW HILLS   KY   41017-3478
797   Affiliated   3278   Washington Square Dialysis   Washington Square Dialysis   1112 WASHINGTON SQ     WASHINGTON   MO   63090-5336
798   Affiliated   3279   Florissant Dialysis   Florissant Dialysis   11687 W FLORISSANT AVE     FLORISSANT   MO   63033-6711
799   Affiliated   3282   Ithaca Dialysis Center   Ithaca Dialysis Center   201 DATES DR   STE 26   ITHACA   NY   14850-1345
800   Affiliated   3289   Fairfield Dialysis   Fairfield Dialysis   1210 HICKS BLVD     FAIRFIELD   OH   45014-1921
801   Affiliated   3290   Fairfield Home Training Dialysis   Fairfield Home Training Dialysis   1210 HICKS BLVD     FAIRFIELD   OH   45014-1921
802   Affiliated   3291   South Hill Dialysis   South Hill Dialysis   525 ALEXANDRIA PIKE   STE 12   SOUTHGATE   KY   41071-3243
803   Affiliated   3292   Silver Spring Dialysis   Silver Spring Dialysis   8412 GEORGIA AVE     SILVER SPRING   MD   20910-4406
804   Affiliated   3295   Philadelphia PMC Dialysis   Philadelphia PMC Dialysis   51 N 39TH ST     PHILADELPHIA   PA   19104-2640
805   Affiliated   3298   Tulare Dialysis   Tulare Dialysis   545 E TULARE AVE     TULARE   CA   93274-4220

 

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806   Affiliated   3300   Visalia Dialysis   Visalia Dialysis   5429 W CYPRESS AVE     VISALIA   CA   93277-8341
807   Affiliated   3310   Falls Road Dialysis   Falls Road Dialysis   10753 FALLS RD   STE 115   LUTHERVILLE   MD   21093-4572
808   Affiliated   3312   Malden Dialysis   Wellington Circle Dialysis Center (fka Malden)   10 CABOT RD   STE 13B   MEDFORD   MA   02155-5173
809   Affiliated   3313   Salem Northeast Dialysis   Salem Northeast Dialysis (MA)   10 COLONIAL RD   STE 25   SALEM   MA   01970-2947
810   Affiliated   3314   Lexington   Lexington Prison Unit (OK)   15151 STATE HWY 39 E   PO BOX 26   LEXINGTON   OK   73051-0260
811   Affiliated   3315   Macon County Dialysis   Macon County Dialysis   1090 W MCKINLEY AVE     DECATUR   IL   62526-3208
812   Affiliated   3316   Effingham Dialysis   Effingham Dialysis   904 MEDICAL PARK DR   STE 1   EFFINGHAM   IL   62401-2193
813   Affiliated   3317   Jacksonville Dialysis   Jacksonville Dialysis   1515 W WALNUT ST     JACKSONVILLE   IL   62650-1150
814   Affiliated   3318   Litchfield Dialysis   Litchfield Dialysis   915 ST FRANCES WAY     LITCHFIELD   IL   62056-1775
815   Affiliated   3319   Mattoon Dialysis   Mattoon Dialysis   6051 DEVELOPMENT DR     CHARLESTON   IL   61920-9467
816   Affiliated   3320   Springfield Central Dialysis   Springfield Central Dialysis   932 N RUTLEDGE ST     SPRINGFIELD   IL   62702-3721
817   Affiliated   3321   Taylorville Dialysis   Taylorville Dialysis   901 W SPRESSER ST     TAYLORVILLE   IL   62568-1831
818   Affiliated   3322   Lincoln Dialysis   Lincoln Dialysis   2100 WEST FIFTH     LINCOLN   IL   62656-9115
819   Affiliated   3323   J. B. Zachary Dialysis Center   J. B. Zachary Dialysis Center   333 CASSELL DR   STE 23   BALTIMORE   MD   21224-6815
820   Affiliated   3324   Whitesquare Dialysis   Whitesquare Dialysis   1 NASHUA CT STE E     BALTIMORE   MD   21221
821   Affiliated   3325   25th Street Dialysis   25th Street Dialysis   920 E 25TH ST     BALTIMORE   MD   21218-5503
822   Affiliated   3326   Perth Amboy Dialysis   Perth Amboy Dialysis   530 NEW BRUNSWICK AVE     PERTH AMBOY   NJ   08861-3654
823   Affiliated   3327   Old Bridge Dialysis   Old Bridge Dialysis   3 HOSPITAL PLZ   STE 11   OLD BRIDGE   NJ   08857-3084
824   Affiliated   3328   Pear Tree Dialysis   Pear Tree Dialysis (fka Ukiah)   126 N ORCHARD AVE     UKIAH   CA   95482-4502
825   Affiliated   3334   Hubbard Road Dialysis   Hubbard Road Dialysis   1963 HUBBARD RD     MADISON   OH   44057-2105
826   Affiliated   3335   St. Charles Dialysis   St. Charles Dialysis   2125 BLUESTONE DR     SAINT CHARLES   MO   63303-6704
827   Affiliated   3336   Bel Air Dialysis   Bel Air Dialysis   2225 OLD EMMORTON RD   STE 15   BEL AIR   MD   21015-6122
828   Affiliated   3339   Cedarburg Dialysis   Cedarburg Dialysis   N 54 W 6135 MILL ST     CEDARBURG   WI   53012-2021
829   Affiliated   3340   Western Hills Dialysis   Western Hills Dialysis   3267 WESTBOURNE DR     CINCINNATI   OH   45248-5130
830   Affiliated   3341   Winton Road Dialysis   Winton Road Dialysis   6550 WINTON RD     CINCINNATI   OH   45224-1327
831   Affiliated   3342   Stamford Dialysis   Stamford Dialysis   30 COMMERCE RD     STAMFORD   CT   06902-4550
832   Affiliated   3343   Boaz Dialysis   Boaz Dialysis   16 CENTRAL HENDERSON RD     BOAZ   AL   35957-5922
833   Affiliated   3344   Guernsey County Dialysis   Guernsey County Dialysis   1300 CLARK ST     CAMBRIDGE   OH   43725-8875
834   Affiliated   3345   Marietta Dialysis   Marietta Dialysis   1019 PIKE ST     MARIETTA   OH   45750-3500
835   Affiliated   3346   Zanesville Dialysis   Zanesville Dialysis   3120 NEWARK RD     ZANESVILLE   OH   43701-9659
836   Affiliated   3351   Orlando East Dialysis   Orlando East Dialysis   1160 S SEMORAN BLVD   STE C   ORLANDO   FL   32807-1461
837   Affiliated   3352   Norwich Dialysis   Norwich Dialysis   113 SALEM TPKE     NORWICH   CT   06360-6484
838   Affiliated   3354   Columbus Dialysis   Columbus Dialysis   3830 OLENTANGY RIVER RD     COLUMBUS   OH   43214-5404
839   Affiliated   3362   Pasadena Dialysis   Pasadena Dialysis   8894 FORT SMALLWOOD RD   STE 12   PASADENA   MD   21122-7608
840   Affiliated   3369   Baltimore Geriatric & Rehab Dialysis Center   Baltimore Geriatric & Rehab Dialysis Center   4940 EASTERN AVE   FLOOR 5   BALTIMORE   MD   21224-2735
841   Affiliated   3373   Frederick Dialysis   Frederick Dialysis   140 THOMAS JOHNSON DR   STE 1   FREDERICK   MD   21702-4475
842   Affiliated   3376   Fayetteville Dialysis   Fayetteville Dialysis   1279 HIGHWAY 54 W   STE 11   FAYETTEVILLE   GA   30214-4551
843   Affiliated   3377   Birmingham Central Dialysis   Birmingham Central Dialysis   728 RICHARD ARRINGTON JR BLVD S     BIRMINGHAM   AL   35233-2106
844   Affiliated   3379   Birmingham North Dialysis   Birmingham North Dialysis   1917 32ND AVE N     BIRMINGHAM   AL   35207-3333
845   Affiliated   3380   Bessemer Dialysis   Bessemer Dialysis   901 W LAKE MALL     BESSEMER   AL   35020
846   Affiliated   3382   Ensley Dialysis   Ensley Dialysis   2630 AVENUE E     BIRMINGHAM   AL   35218-2163
847   Affiliated   3383   Sylacauga Dialysis   Sylacauga Dialysis   331 JAMES PAYTON BLVD     SYLACAUGA   AL   35150
848   Affiliated   3385   Branford Dialysis   Branford Dialysis   249 W MAIN ST     BRANFORD   CT   06405-4048
849   Affiliated   3386   Shrewsbury Dialysis   Shrewsbury Dialysis   7435 WATSON RD   STE 119   SAINT LOUIS   MO   63119-4472
850   Affiliated   3389   Milford Dialysis   Milford Dialysis   470 BRIDGEPORT AVE     MILFORD   CT   06460-4167
851   Affiliated   3414   Cedartown Dialysis   Cedartown Dialysis   325 WEST AVE     CEDARTOWN   GA   30125-3439
852   Affiliated   3416   Brookfield Dialysis   Brookfield Dialysis   19395 W CAPITOL DR   BLDG C   BROOKFIELD   WI   53045-2736
853   Affiliated   3417   Henrico County Dialysis   Henrico County Dialysis   5270 CHAMBERLAYNE RD     RICHMOND   VA   23227-2950
854   Affiliated   3418   St. Louis West Dialysis   St. Louis West Dialysis   400 N LINDBERGH BLVD     SAINT LOUIS   MO   63141-7814
855   Affiliated   3420   Springfield Montvale Dialysis   Springfield Montvale Dialysis   2930 MONTVALE DR   STE A   SPRINGFIELD   IL   62704-5376
856   Affiliated   3422   South Norwalk Dialysis   South Norwalk Dialysis   31 STEVENS ST     NORWALK   CT   06850-3805
857   Affiliated   3425   Decatur East Wood Dialysis   Decatur East Wood Dialysis   794 E WOOD ST     DECATUR   IL   62523-1155
858   Affiliated   3426   Schaeffer Drive Dialysis   Schaeffer Drive Dialysis   18100 SCHAEFER HWY     DETROIT   MI   48235-2600
859   Affiliated   3427   Redford Dialysis   Redford Dialysis   22711 GRAND RIVER AVE     DETROIT   MI   48219-3113

 

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860   Affiliated   3428   Kresge Dialysis   Kresge Dialysis   4145 CASS AVE     DETROIT   MI   48201-1707
861   Affiliated   3429   Motor City Dialysis   Motor City Dialysis   4727 SAINT ANTOINE ST   STE 11   DETROIT   MI   48201-1461
862   Affiliated   3431   Whitebridge Dialysis   Whitebridge Dialysis   103 WHITE BRIDGE PIKE   STE 6   NASHVILLE   TN   37209-4539
863   Affiliated   3432   Columbia Dialysis   Columbia Dialysis (TN)   1705 GROVE ST     COLUMBIA   TN   38401-3517
864   Affiliated   3433   Murfreesboro Dialysis   Murfreesboro Dialysis   1346 DOW ST     MURFREESBORO   TN   37130-2470
865   Affiliated   3434   Lawrenceburg Dialysis   Lawrenceburg Dialysis (TN)   2022 N LOCUST AVE     LAWRENCEBURG   TN   38464-2336
866   Affiliated   3436   Sumner Dialysis   Sumner Dialysis   300 STEAM PLANT RD   STE 27   GALLATIN   TN   37066-3019
867   Affiliated   3437   Cumberland Dialysis   Cumberland Dialysis   312 HOSPITAL DR   STE 5   MADISON   TN   37115-5037
868   Affiliated   3438   Williamson County Dialysis   Williamson County Dialysis   3983 CAROTHERS PKWY   STE E-4   FRANKLIN   TN   37067-5936
869   Affiliated   3441   Cumming Dialysis   Cumming Dialysis   911 MARKET PLACE BLVD   STE 3   CUMMING   GA   30041-7938
870   Affiliated   3443   Silverton Dialysis   Silverton Dialysis   6929 SILVERTON AVE     CINCINNATI   OH   45236-3701
871   Affiliated   3445   Atlanta South Dialysis   Atlanta South Dialysis   3158 EAST MAIN ST   STE A   EAST POINT   GA   30344-4800
872   Affiliated   3447   St. Petersburg Dialysis   St. Petersburg Dialysis   1117 ARLINGTON AVE N     ST PETERSBURG   FL   33705-1521
873   Affiliated   3449   Alton Dialysis   Alton Dialysis   3511 COLLEGE AVE     ALTON   IL   62002-5009
874   Affiliated   3451   Edison Dialysis   Edison Dialysis   29 MERIDIAN RD     EDISON   NJ   08820-2823
875   Affiliated   3452   Dundalk Dialysis   Dundalk Dialysis   14 COMMERCE ST     DUNDALK   MD   21222-4307
876   Affiliated   3454   Columbus East Dialysis   Columbus East Dialysis   299 OUTERBELT ST     COLUMBUS   OH   43213-1529
877   Affiliated   3455   Dallas East Dialysis   Dallas East Dialysis   3312 N BUCKNER BLVD   STE 213   DALLAS   TX   75228-5642
878   Affiliated   3456   San Ysidro Dialysis   San Ysidro Dialysis   1445 30TH ST   STE A   SAN DIEGO   CA   92154-3496
879   Affiliated   3457   Olathe Dialysis   Olathe Dialysis   732 W FRONTIER LN     OLATHE   KS   66061-7202
880   Affiliated   3459   Orange City Dialysis   Orange City Dialysis   242 TREEMONT DR   BLDG II   ORANGE CITY   FL   32763-7945
881   Affiliated   3460   Miami East Dialysis   Miami East Dialysis   1250 NW 7TH ST   STE 16   MIAMI   FL   33125-3744
882   Affiliated   3462   Temple Terrace Dialysis   Temple Terrace Dialysis   11306 N 53RD ST     TEMPLE TERRACE   FL   33617-2214
883   Affiliated   3463   Midlothian Dialysis   Midlothian Dialysis   14281 MIDLOTHIAN TPKE   BLDG B   MIDLOTHIAN   VA   23113-6560
884   Affiliated   3464   Christian County Dialysis   Christian County Dialysis   200 BURLEY AVE     HOPKINSVILLE   KY   42240-8725
885   Affiliated   3465   St. Louis West PD Dialysis   St. Louis West PD Dialysis   450 N LINDBERGH BLVD   STE 1C   CREVE COEUR   MO   63141-7858
886   Affiliated   3467   Atlanta Midtown Dialysis   Atlanta Midtown Dialysis PD   418 DECATUR ST SE   STE A   ATLANTA   GA   30312-1801
887   Affiliated   3468   Silverton Home Training Dialysis   Silverton Home Training Dialysis   6929 SILVERTON AVE     CINCINNATI   OH   45236-3701
888   Affiliated   3472   Philadelphia 42nd Street Dialysis   Philadelphia 42nd Street Dialysis   4126 WALNUT ST     PHILADELPHIA   PA   19104-3511
889   Affiliated   3473   Radnor Dialysis   Radnor Dialysis   250 KING OF PRUSSIA RD     RADNOR   PA   19087-5220
890   Affiliated   3475   St. Louis Dialysis   St. Louis Dialysis   324 DE BALIVIERE AVE     SAINT LOUIS   MO   63112-1804
891   Affiliated   3477   Elkins Park Dialysis   Wyncote Dialysis (fka Elkins Park)   1000 EASTON RD   STE 25   WYNCOTE   PA   19095-2934
892   Affiliated   3478   Mainland Dialysis   Mainland Dialysis   2600 GULF FWY     LA MARQUE   TX   77568-4922
893   Affiliated   3479   Island Dialysis   Island Dialysis   5920 BROADWAY ST     GALVESTON   TX   77551-4305
894   Affiliated   3481   Orlando Home Training Dialysis   Orlando Home Training Dialysis   116 STURTEVANT ST   STE 2   ORLANDO   FL   32806-2021
895   Affiliated   3482   Mechanicsville Dialysis   Mechanicsville Dialysis   8191 ATLEE RD     MECHANICSVILLE   VA   23116-1807
896   Affiliated   3484   San Diego East Dialysis   San Diego East Dialysis   292 EUCLID AVE   STE 1   SAN DIEGO   CA   92114-3629
897   Affiliated   3485   Russellville Dialysis   Russellville Dialysis   14897 HIGHWAY 43     RUSSELLVILLE   AL   35653-1954
898   Affiliated   3486   Encinitas Dialysis   Encinitas Dialysis   332 SANTA FE DR   STE 1   ENCINITAS   CA   92024-5143
899   Affiliated   3491   Rushville Dialysis   Rushville Dialysis   112 SULLIVAN DRIVE     RUSHVILLE   IL   62681-1293
900   Affiliated   3493   Plainfield Dialysis   Plainfield Dialysis   1200 RANDOLPH RD   MUHLENBURG CAMPUS   PLAINFIELD   NJ   07060-3361
901   Affiliated   3494   Parkersburg Dialysis   Parkersburg Dialysis   1824 MURDOCH AVE   STE 44   PARKERSBURG   WV   26101-3230
902   Affiliated   3497   Tucson South Central Dialysis   Tucson South Central Dialysis   2024 E IRVINGTON RD   STE 7   TUCSON   AZ   85714-1825
903   Affiliated   3499   Hazelwood Dialysis   Hazelwood Dialysis   637 DUNN RD     HAZELWOOD   MO   63042-1755
904   Affiliated   3503   Durham West Dialysis   Durham West Dialysis   4307 WESTERN PARK PL     DURHAM   NC   27705-1204
905   Affiliated   3504   Liberty Dialysis   Liberty Dialysis   2525 GLEN HENDREN DR     LIBERTY   MO   64068-9625
906   Affiliated   3506   Chino Dialysis   Chino Dialysis   4445 RIVERSIDE DR     CHINO   CA   91710-3961
907   Affiliated   3507   Greenview Dialysis   Greenview Dialysis   18544 W 8 MILE RD     SOUTHFIELD   MI   48075-4194
908   Affiliated   3508   Perry Dialysis   Perry Dialysis   118 W MAIN ST     PERRY   FL   32347-2656
909   Affiliated   3511   Ashtabula Dialysis   Ashtabula Dialysis   1614 W 19TH ST     ASHTABULA   OH   44004-3036
910   Affiliated   3513   Northland Dialysis   Northland Dialysis   2750 CLAY EDWARDS DR   STE 1   N KANSAS CITY   MO   64116-3257
911   Affiliated   3516   Lake St. Louis Dialysis   Lake St. Louis Dialysis   200 BREVCO PLZ   STE 21   LAKE SAINT LOUIS   MO   63367-2950
912   Affiliated   3517   Wyandotte West Dialysis   Wyandotte West Dialysis   8919 PARALLEL PKWY   STE 121   KANSAS CITY   KS   66112-1655
913   Affiliated   3518   Huntingdon Valley Dialysis   Temp CLSD-Huntingdon Valley Dialysis   769 HUNTINGDON PIKE   STE 18   HUNTINGDON VALLEY   PA   19006-8362

 

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914   Affiliated   3519   Glendale Dialysis   Glendale Dialysis   1000 E PALMER AVE     GLENDALE   CA   91205-3532
915   Affiliated   3520   Toledo Dialysis   Toledo Dialysis   1614 S BYRNE RD     TOLEDO   OH   43614-3464
916   Affiliated   3523   Cameron Dialysis   Cameron Dialysis   1003 W 4TH ST     CAMERON   MO   64429-1466
917   Affiliated   3524   Omaha Central Dialysis   Omaha Central Dialysis   144 S 40TH ST     OMAHA   NE   68131-3004
918   Affiliated   3525   Chillicothe Dialysis   Chillicothe Dialysis   588 E BUSINESS 36     CHILLICOTHE   MO   64601-3721
919   Affiliated   4210   Council Bluffs Dialysis   Council Bluffs Dialysis Center   300 W BROADWAY   STE 15   COUNCIL BLUFFS   IA   51503-9077
920   Affiliated   3528   DeRidder Dialysis   DeRidder Dialysis   239 E 1ST ST     DERIDDER   LA   70634-4105
921   Affiliated   3530   Dodge County Dialysis   Dodge County Dialysis   1949 E 23RD AVE S     FREMONT   NE   68025-2452
922   Affiliated   3533   Omaha North Dialysis   Omaha North Dialysis   6572 AMES AVE     OMAHA   NE   68104-1931
923   Affiliated   3534   Omaha South Dialysis   Omaha South Dialysis   3427 L ST   STE 16   OMAHA   NE   68107-2577
924   Affiliated   3535   Lake Charles Southwest Dialysis   Lake Charles Southwest Dialysis   300 W 18th ST     LAKE CHARLES   LA   70601-7342
925   Affiliated   3536   St. Joseph Dialysis   St. Joseph Dialysis   5514 CORPORATE DR   STE 1   SAINT JOSEPH   MO   64507-7752
926   Affiliated   3537   Sulphur Dialysis   Sulphur Dialysis   944 BEGLIS PKWY     SULPHUR   LA   70663-5102
927   Affiliated   3539   Tipton County Dialysis   Tipton County Dialysis   107 TENNESSEE AVE     COVINGTON   TN   38019-3902
928   Affiliated   3540   Dyersburg Dialysis   Dyersburg Dialysis   1575 PARR AVE     DYERSBURG   TN   38024-3151
929   Affiliated   3544   Effingham North Dialysis   Effingham North Dialysis   301 N PINE ST     SPRINGFIELD   GA   31329-3076
930   Affiliated   3545   Westminster South Dialysis   Westminster South Dialysis   14014 MAGNOLIA ST.     WESTMINSTER   CA   92683-4736
931   Affiliated   3546   Williams Street Dialysis   Williams Street Dialysis   2812 WILLIAMS ST     SAVANNAH   GA   31404-4134
932   Affiliated   3547   DeRenne Dialysis   DeRenne Dialysis   5303 MONTGOMERY ST     SAVANNAH   GA   31405-5138
933   Affiliated   3548   Abercorn Dialysis   Abercorn Dialysis   11706 MERCY BLVD   STE 9   SAVANNAH   GA   31419-1751
934   Affiliated   3551   Fort Myers North Dialysis   Fort Myers North Dialysis   16101 N CLEVELAND AVE     N FT MYERS   FL   33903-2148
935   Affiliated   3552   Butler County Dialysis   Butler County Dialysis   3497 S DIXIE HWY     FRANKLIN   OH   45005-5717
936   Affiliated   3556   Willingboro   Willingboro Dialysis   230 VAN SCIVER PKWY     WILLINGBORO   NJ   08046-1131
937   Affiliated   3557   McKeesport West Dialysis   McKeesport West Dialysis   101 9TH ST     MCKEESPORT   PA   15132-3953
938   Affiliated   3559   College Dialysis   College Dialysis   6535 UNIVERSITY AVE     SAN DIEGO   CA   92115-5810
939   Affiliated   3560   Montezuma Dialysis   Montezuma Dialysis   114 DEVAUGHN AVE     MONTEZUMA   GA   31063-1708
940   Affiliated   3561   Romulus Dialysis   Romulus Dialysis   31470 ECORSE RD     ROMULUS   MI   48174-1963
941   Affiliated   3564   Wrightsville Dialysis   Wrightsville Dialysis   2240 W ELM ST     WRIGHTSVILLE   GA   31096-2016
942   Affiliated   3565   Tower Dialysis   Tower Dialysis   8635 W 3RD ST   STE 56W   LOS ANGELES   CA   90048-6110
943   Affiliated   3566   Columbus Downtown Dialysis   Columbus Downtown Dialysis   415 E MOUND ST     COLUMBUS   OH   43215-5512
944   Affiliated   3568   Charlotte East Dialysis   Charlotte East Dialysis   3204 N SHARON AMITY RD     CHARLOTTE   NC   28205-6541
945   Affiliated   3569   Carmel Mountain Dialysis   Carmel Mountain Dialysis   9850 CARMEL MOUNTAIN RD     SAN DIEGO   CA   92129-2892
946   Affiliated   3571   Lenexa Dialysis   Lenexa Dialysis   8630 HALSEY ST     LENEXA   KS   66215-2880
947   Affiliated   3577   Nashua Dialysis   Nashua Dialysis   38 TYLER ST   STE 1   NASHUA   NH   03060-2912
948   Affiliated   3580   Illini Renal Dialysis   Illini Renal Dialysis   507 E UNIVERSITY AVE     CHAMPAIGN   IL   61820-3828
949   Affiliated   3586   Loring Heights Dialysis   Loring Heights Dialysis   1575 NORTHSIDE DR NW   STE 45   ATLANTA   GA   30318-4211
950   Affiliated   3588   Forest Hills Dialysis   Forest Hills Dialysis   2693 FOREST HILLS RD SW     WILSON   NC   27893-8611
951   Affiliated   3589   St. Peters Dialysis   St. Peters Dialysis   300 FIRST EXECUTIVE AVE   STE A   SAINT PETERS   MO   63376-1655
952   Affiliated   3591   Platte Woods Dialysis   Platte Woods Dialysis   7667 NW PRAIRIE VIEW RD     KANSAS CITY   MO   64151-1544
953   Affiliated   3593   Fresno North Dialysis   Fresno Palm Bluffs Dialysis (fka Fresno North)   770 W PINEDALE AVE     FRESNO   CA   93711-5744
954   Affiliated   3594   Middlesex County Dialysis   Burlington Regional Dialysis (fka Middlesex County)   31 MALL RD   STE 1B   BURLINGTON   MA   01803-4138
955   Affiliated   3596   Clearfield Dialysis   Clearfield Dialysis   1033 TURNPIKE AVE   STE 1   CLEARFIELD   PA   16830-3061
956   Affiliated   3597   Papillion Dialysis   Papillion Dialysis   1502 S WASHINGTON ST   STE 1   PAPILLION   NE   68046-3136
957   Affiliated   3598   Birmingham Home Training Dialysis   Birmingham Home Training Dialysis   2101 7TH AVE S     BIRMINGHAM   AL   35233-3105
958   Affiliated   3603   Bayou Dialysis   Magnolia Dialysis   210 E SPILLMAN ST     GONZALES   LA   70737-4604
959   Affiliated   3609   Radford Dialysis   Radford Dialysis   600 E MAIN ST   STE F   RADFORD   VA   24141-1826
960   Affiliated   3610   Eufaula Dialysis   Eufaula Dialysis   220 S ORANGE AVE     EUFAULA   AL   36027-1612
961   Affiliated   3612   Coshocton Dialysis   Coshocton Dialysis   1404 CHESTNUT ST EAST     COSHOCTON   OH   43812-1401
962   Affiliated   3614   Costa Mesa Dialysis   Costa Mesa Dialysis   1590 SCENIC AVE     COSTA MESA   CA   92626-1400
963   Affiliated   3615   Little Rock Dialysis   Central Little Rock Dialysis   5800 W 10TH ST   STE 51   LITTLE ROCK   AR   72204-1760
964   Affiliated   3619   Northport Dialysis   Northport Dialysis   2401 HOSPITAL DR     NORTHPORT   AL   35476-3392
965   Affiliated   3632   Pageland Dialysis   Pageland Dialysis   505A S PEARL ST     PAGELAND   SC   29728-2222
966   Affiliated   3633   Bakersfield South Dialysis   White Lane Dialysis (fka Bakersfield South)   7701 WHITE LN   STE D   BAKERSFIELD   CA   93309-0201
967   Affiliated   3634   Newaygo County Dialysis   Newaygo County Dialysis   1317 W MAIN ST     FREMONT   MI   49412-1478

 

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968   Affiliated   3636   Cedar Lane Dialysis   Cedar Lane Dialysis   6334 CEDAR LN   STE 11   COLUMBIA   MD   21044-3898
969   Affiliated   3639   Torrington Dialysis   Torrington Dialysis   780 LITCHFIELD ST   STE 1   TORRINGTON   CT   06790-6268
970   Affiliated   3642   Janesville Dialysis   Janesville Dialysis   1305 WOODMAN RD     JANESVILLE   WI   53545-1068
971   Affiliated   3643   Bloomfield Dialysis   Bloomfield Dialysis   29 GRIFFIN RD S     BLOOMFIELD   CT   06002-1351
972   Affiliated   3645   Anthem Village Dialysis   Anthem Village Dialysis   2530 ANTHEM VILLAGE DR     HENDERSON   NV   89052-5548
973   Affiliated   3646   Glen Burnie Dialysis   Glen Burnie Dialysis   120 LANGLEY RD N     GLEN BURNIE   MD   21060-6578
974   Affiliated   3655   Melbourne Dialysis   Melbourne Dialysis   2235 S BABCOCK ST     MELBOURNE   FL   32901-5305
975   Affiliated   3656   St. Petersburg South Dialysis   St. Petersburg South Dialysis   2850 34TH ST S     ST PETERSBURG   FL   33711-3817
976   Affiliated   3663   Belpre Dialysis   Belpre Dialysis   2906 WASHINGTON BLVD     BELPRE   OH   45714-1848
977   Affiliated   3666   Stockton Home Training Dialysis   Stockton Home Training Dialysis   545 E CLEVELAND ST   STE A   STOCKTON   CA   95204-5535
978   Affiliated   3670   Rock Prairie Road Dialysis   Rock Prairie Road Dialysis   1605 ROCK PRAIRIE RD   STE 11   COLLEGE STATION   TX   77845-8358
979   Affiliated   3675   Market Street   Market Street Dialysis   3701 MARKET ST   STE 1   PHILADELPHIA   PA   19104-5503
980   Affiliated   3677   Northwood   Northwood Dialysis (aka Toledo East)   611 LEMOYNE RD     NORTHWOOD   OH   43619-1811
981   Affiliated   3701   Tyson’s Corner Dialysis   Tyson’s Corner Dialysis   8391 OLD COURTHOUSE RD   STE 16   VIENNA   VA   22182-3819
982   Affiliated   3704   Southern Maryland Dialysis   Southern Maryland Dialysis   9211 STUART LN   4TH FL   CLINTON   MD   20735-2712
983   Affiliated   3707   Brentwood Dialysis   Brentwood Dialysis   1231 BRENTWOOD RD NE     WASHINGTON   DC   20018-1019
984   Affiliated   3708   Amelia Dialysis   Amelia Dialysis   15151 PATRICK HENRY HWY     AMELIA COURT HOUSE   VA   23002-4700
985   Affiliated   3714   Eighth Street Dialysis   Eighth Street Dialysis   300 8TH ST NE     WASHINGTON   DC   20002-6108
986   Affiliated   3715   Chester Dialysis   Chester Dialysis   10360 IRONBRIDGE RD     CHESTER   VA   23831-1425
987   Affiliated   3716   Howard County Dialysis   Howard County Dialysis   5999 HARPERS FARM RD   STE 11E   COLUMBIA   MD   21044-3023
988   Affiliated   3717   Catonsville Dialysis   Catonsville Dialysis   1581 SULPHUR SPRING RD   STE 112   BALTIMORE   MD   21227
989   Affiliated   3718   Mercy Dialysis   Mercy Dialysis   315 N CALVERT ST   STE 3   BALTIMORE   MD   21202-3611
990   Affiliated   3719   Harbor Park Dialysis   Harbor Park Dialysis   111 CHERRY HILL RD     BALTIMORE   MD   21225-1392
991   Affiliated   3732   Dabney Dialysis   Three Chopt Dialysis (fka Dabney)   8813 THREE CHOPT RD     RICHMOND   VA   23229
992   Affiliated   3733   Hioaks Dialysis   Hioaks Dialysis   671 HIOAKS RD   STE A   RICHMOND   VA   23225-4072
993   Affiliated   3757   Arlington Dialysis   Arlington Dialysis   4805 1st ST N     ARLINGTON   VA   22203
994   Affiliated   3759   Landover Dialysis   Landover Dialysis   1200 MERCANTILE LN   STE 15   UPPER MARLBORO   MD   20774-5389
995   Affiliated   3761   Staunton Dialysis   Staunton Dialysis   29 IDLEWOOD BLVD     STAUNTON   VA   24401-9355
996   Affiliated   3762   Covington Dialysis   Covington Dialysis   2504 VALLEY RIDGE RD     COVINGTON   VA   24426-6339
997   Affiliated   3763   Culpeper Dialysis   Culpeper Dialysis   430 SOUTHRIDGE PARKWAY     CULPEPER   VA   22701-3791
998   Affiliated   3764   Greenbrier Dialysis   Greenbrier Dialysis   129 SENECA TRL     LEWISBURG   WV   24901-1564
999   Affiliated   3765   Harrisonburg Dialysis   Harrisonburg Dialysis   871 CANTRELL AVE   STE 1   HARRISONBURG   VA   22801-4323
1000   Affiliated   3766   Lexington Dialysis   Lexington Dialysis   756 N LEE HWY     LEXINGTON   VA   24450-3724
1001   Affiliated   3802   Manteca Dialysis   Manteca Dialysis   1156 S MAIN ST     MANTECA   CA   95337-9505
1002   Affiliated   3804   Roseburg/Mercy Dialysis   Roseburg/Mercy Dialysis   2599 NW EDENBOWER BLVD     ROSEBURG   OR   97471-6220
1003   Affiliated   3805   Daly City Dialysis   Daly City Dialysis   1498 SOUTHGATE AVE   STE 11   DALY CITY   CA   94015-4015
1004   Affiliated   3806   Vallejo Dialysis   Vallejo Dialysis   121 HOSPITAL DR     VALLEJO   CA   94589-2562
1005   Affiliated   3812   Salem Dialysis   Salem Dialysis (OR)   3550 LIBERTY RD S   STE 1   SALEM   OR   97302-5700
1006   Affiliated   3817   Fresno Dialysis   Fresno Dialysis   1111 E WARNER AVE     FRESNO   CA   93710-4030
1007   Affiliated   3818   Oakland Dialysis   Oakland Dialysis   5354 CLAREMONT AVE     OAKLAND   CA   94618-1035
1008   Affiliated   3820   Bakersfield Dialysis   Bakersfield Brimhall Dialysis (fka California Ave.)   8501 BRIMHALL RD   BLDG 5   BAKERSFIELD   CA   93311-2252
1009   Affiliated   3821   Northeast Bakersfield Dialysis   Northeast Dialysis (fka NE Bakersfield)   3761 MALL VIEW RD     BAKERSFIELD   CA   93306-3048
1010   Affiliated   3830   San Francisco Dialysis   San Francisco Dialysis   1499 WEBSTER ST     SAN FRANCISCO   CA   94115-3705
1011   Affiliated   3831   Hanford Dialysis   Hanford Dialysis   402 W 8TH ST     HANFORD   CA   93230-4536
1012   Affiliated   3840   San Pablo Dialysis   San Pablo Dialysis   14020 SAN PABLO AVE     SAN PABLO   CA   94806-3604
1013   Affiliated   3847   Chinatown Dialysis   Chinatown Dialysis   636 CLAY ST     SAN FRANCISCO   CA   94111-2502
1014   Affiliated   3849   El Cerrito Dialysis   El Cerrito Dialysis   10690 SAN PABLO AVE     EL CERRITO   CA   94530-2620
1015   Affiliated   3857   Tracy Dialysis   Tracy Dialysis   425 W BEVERLY PL   STE A   TRACY   CA   95376-3086
1016   Affiliated   3858   Salem North Dialysis   Salem North Dialysis (OR)   1220 LIBERTY ST NE     SALEM   OR   97301-7330
1017   Affiliated   3860   Auburn Dialysis   Auburn Dialysis   3126 PROFESSIONAL DR   STE 1   AUBURN   CA   95603-2411
1018   Affiliated   3861   Grass Valley Dialysis   Grass Valley Dialysis   360 CROWN POINT CIRCLE   STE 21   GRASS VALLEY   CA   95945-2543
1019   Affiliated   3901   Santee Dialysis   Santee Dialysis   228 BRADFORD BLVD     SANTEE   SC   29142-8677
1020   Affiliated   3903   Upland Dialysis   Upland Dialysis   600 N 13TH AVE     UPLAND   CA   91786-4957
1021   Affiliated   3906   Vance County Dialysis   Vance County Dialysis   854 S BECKFORD DR     HENDERSON   NC   27536-3487

 

Page 65 of 136


1022   Affiliated   3907   Edenton Dialysis   Edenton Dialysis   703 LUKE ST     EDENTON   NC   27932-9694
1023   Affiliated   3909   Ahoskie Dialysis   Ahoskie Dialysis   129 HERTFORD COUNTY HIGH RD     AHOSKIE   NC   27910-8131
1024   Affiliated   3914   Allendale County Dialysis   Allendale County Dialysis   202 HAMPTON AVE N     FAIRFAX   SC   29827-4510
1025   Affiliated   3916   North Orangeburg Dialysis   North Orangeburg Dialysis   124 FIRE TOWER RD     ORANGEBURG   SC   29118-1443
1026   Affiliated   3917   South Orangeburg Dialysis   South Orangeburg Dialysis   1080 SUMMERS AVE     ORANGEBURG   SC   29115-4920
1027   Affiliated   3931   Greenwood Dialysis   Greenwood Dialysis   109 OVERLAND DR     GREENWOOD   SC   29646-4053
1028   Affiliated   3933   Union County Dialysis   Union County Dialysis   701 E ROOSEVELT BLVD   STE 4   MONROE   NC   28112-4107
1029   Affiliated   3934   South Charlotte Dialysis   South Charlotte Dialysis   6450 BANNINGTON RD     CHARLOTTE   NC   28226-1327
1030   Affiliated   3935   Lancaster SC Dialysis   Lancaster SC Dialysis   980 N WOODLAND DR   STE 1   LANCASTER   SC   29720-1964
1031   Affiliated   3952   Central Bamberg Dialysis   Central Bamberg Dialysis   67 SUNSET DR     BAMBERG   SC   29003-1181
1032   Affiliated   4001   West Tallahassee Dialysis   West Tallahassee Dialysis   2645 W TENNESSEE ST     TALLAHASSEE   FL   32304-2547
1033   Affiliated   4002   Daytona South Dialysis   Daytona South Dialysis   1801 S NOVA RD   STE 36   SOUTH DAYTONA   FL   32119-1775
1034   Affiliated   4003   Daytona Beach Dialysis   Daytona Beach Dialysis   578 HEALTH BLVD     DAYTONA BEACH   FL   32114-1492
1035   Affiliated   4004   West Tampa Dialysis   West Tampa Dialysis   4515 GEORGE RD   STE 3   TAMPA   FL   33634-7300
1036   Affiliated   4005   Fontana Dialysis   Fontana Dialysis   17590 FOOTHILL BLVD     FONTANA   CA   92335-8416
1037   Affiliated   4007   Fort Myers Dialysis   Fort Myers Dialysis   4220 EXECUTIVE CIRCLE   STE 38   FORT MYERS   FL   33916-7993
1038   Affiliated   4009   Lehigh Acres Dialysis   Lehigh Acres Dialysis   2719 4TH ST W     LEHIGH ACRES   FL   33971-1942
1039   Affiliated   4010   Los Banos Dialysis   Los Banos Dialysis   222 I ST     LOS BANOS   CA   93635-4132
1040   Affiliated   4013   Kissimmee Dialysis   Kissimmee Dialysis   802 N JOHN YOUNG PKWY     KISSIMMEE   FL   34741-4912
1041   Affiliated   4014   New Smyrna Beach Dialysis   New Smyrna Beach Dialysis   110 S ORANGE ST     NEW SMYRNA BEACH   FL   32168-7153
1042   Affiliated   4017   Lake Wales Dialysis   Lake Wales Dialysis   1125 BRYN MAWR AVE     LAKE WALES   FL   33853-4333
1043   Affiliated   4018   Dearborn Dialysis   Dearborn Dialysis   1185 MONROE ST     DEARBORN   MI   48124-2814
1044   Affiliated   4020   Greater Miami Dialysis   Greater Miami Dialysis   160 NW 176TH ST   STE 1   MIAMI   FL   33169-5023
1045   Affiliated   4021   Burbank Dialysis   Burbank Dialysis   1211 N SAN FERNANDO BLVD     BURBANK   CA   91504-4234
1046   Affiliated   4024   Lakeland Dialysis   Lakeland Dialysis   515 E BELLA VISTA ST     LAKELAND   FL   33805-3005
1047   Affiliated   4025   Burlington North Dialysis   Burlington North Dialysis   1164 E ROUTE 130     BURLINGTON   NJ   08016-2954
1048   Affiliated   4026   Delano Dialysis   Delano Dialysis   905 MAIN ST     DELANO   CA   93215-1729
1049   Affiliated   4027   Erie Dialysis   Erie Dialysis   350 E BAYFRONT PKWY   STE A   ERIE   PA   16507-2410
1050   Affiliated   4028   Homestead Dialysis   Homestead Dialysis   207 W 7TH AVE     W HOMESTEAD   PA   15120-1002
1051   Affiliated   4029   Plant City Dialysis   Plant City Dialysis   1211 W REYNOLDS ST     PLANT CITY   FL   33563-4321
1052   Affiliated   4030   Winter Haven Dialysis   Winter Haven Dialysis   1625 UNITY WAY NW     WINTER HAVEN   FL   33881
1053   Affiliated   4032   Charlotte Dialysis   Charlotte Dialysis   2321 W MOREHEAD ST   STE 12   CHARLOTTE   NC   28208-5145
1054   Affiliated   4034   McKeesport Dialysis   McKeesport Dialysis   2001 LINCOLN WAY   OAK PARK MALL   MCKEESPORT   PA   15131-2419
1055   Affiliated   4035   Broward Dialysis   Broward Dialysis   1500 N FEDERAL HWY   STE 1   FT LAUDERDALE   FL   33304-5600
1056   Affiliated   4036   Athens Dialysis   Athens Dialysis   15953 ATHENS LIMESTONE DR     ATHENS   AL   35613-2214
1057   Affiliated   4038   Bradenton Dialysis   Bradenton Dialysis   3501 CORTEZ RD W   STE 14   BRADENTON   FL   34210-3104
1058   Affiliated   4039   Deland Dialysis   Deland Dialysis   350 E NEW YORK AVE     DELAND   FL   32724-5510
1059   Affiliated   4040   Boynton/North Delray Dialysis   Boynton/North Delray Dialysis   2655 W ATLANTIC AVE     DELRAY BEACH   FL   33445-4400
1060   Affiliated   4041   Lake Worth Dialysis   Lake Worth Dialysis   2459 S CONGRESS AVE   STE 1   PALM SPRINGS   FL   33406-7616
1061   Affiliated   4042   Palm Coast Dialysis   Palm Coast Dialysis   13 KINGSWOOD DR   STE A   PALM COAST   FL   32137-4614
1062   Affiliated   4043   Fort Myers South Dialysis   Fort Myers South Dialysis   8570 GRANITE CT     FORT MYERS   FL   33908-4102
1063   Affiliated   4044   Woodburn Dialysis   Woodburn Dialysis   1840 NEWBERG HWY   STE 14   WOODBURN   OR   97071-3187
1064   Affiliated   4045   Four Freedoms   Four Freedoms Dialysis (fka Range Street)   289 SW RANGE AVE   STE A   MADISON   FL   32340-2351
1065   Affiliated   4046   West Philadelphia Dialysis   West Philadelphia Dialysis   7609 LINDBERGH BLVD     PHILADELPHIA   PA   19153-2301
1066   Affiliated   4048   Tucson West Dialysis   Tucson West Dialysis   1780 W ANKLAM RD     TUCSON   AZ   85745-2632
1067   Affiliated   4049   Tucson East Dialysis   Tucson East Dialysis   6420 E BROADWAY BLVD   STE C3   TUCSON   AZ   85710-3512
1068   Affiliated   4053   Tallahassee South Dialysis   Tallahassee South Dialysis   2410 S ADAMS ST     TALLAHASSEE   FL   32301-6325
1069   Affiliated   4054   Selma Dialysis   Selma Dialysis   2711 CINEMA WAY   STE 111   SELMA   CA   93662-2662
1070   Affiliated   4055   Hinesville Dialysis   Hinesville Dialysis   522 ELMA G MILES PKWY     HINESVILLE   GA   31313-4021
1071   Affiliated   4056   Los Angeles Downtown Dialysis   Los Angeles Downtown Dialysis   2021 S FLOWER ST     LOS ANGELES   CA   90007-1342
1072   Affiliated   4057   Anaheim Dialysis   Anaheim Dialysis   1107 W LA PALMA AVE     ANAHEIM   CA   92801-2804
1073   Affiliated   4058   Martinsville Dialysis   Martinsville Dialysis   33 BRIDGE ST S     MARTINSVILLE   VA   24112-6214
1074   Affiliated   4060   Jefferson Dialysis   Jefferson Dialysis   14 CLAIRTON BLVD     PITTSBURGH   PA   15236-3911
1075   Affiliated   4061   Saddleback Dialysis   Saddleback Dialysis   23141 PLAZA POINTE DR     LAGUNA HILLS   CA   92653-1425

 

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1076

  Affiliated   4064   Sun City Center Dialysis   Sun City Center Dialysis   783 CORTARO DR     RUSKIN   FL   33573-6812
1077   Affiliated   4065   Paris Dialysis   Paris Dialysis   32 STEUBENVILLE PK     PARIS   PA   15021
1078   Affiliated   4066   Central Tampa Dialysis   Central Tampa Dialysis   4204 N MACDILL AVE   SOUTH BLDG   TAMPA   FL   33607-6342
1079   Affiliated   4068   Zephyrhills Dialysis   Zephyrhills Dialysis   6610 STADIUM DR     ZEPHYRHILLS   FL   33542-7510
1080   Affiliated   4069   Bartow Dialysis   Bartow Dialysis   1190 E CHURCH ST     BARTOW   FL   33830-4117
1081   Affiliated   4070   Ormond Beach Dialysis   Ormond Beach Dialysis   495 S NOVA RD   STE 19   ORMOND BEACH   FL   32174-8444
1082   Affiliated   4071   Lakeland South Dialysis   Lakeland South Dialysis   5050 S FLORIDA AVE     LAKELAND   FL   33813-2501
1083   Affiliated   4072   St. Mary’s Dialysis   St. Mary’s Dialysis   2714 OSBORNE RD     ST MARY’S   GA   31558-4049
1084   Affiliated   4073   Miami North Dialysis   Miami North Dialysis   860 NE 125TH ST     NORTH MIAMI   FL   33161-5743
1085   Affiliated   4074   Naples Dialysis   Naples Dialysis   661 9TH ST N     NAPLES   FL   34102-8132
1086   Affiliated   4075   Bonita Springs Dialysis   Bonita Springs Dialysis   9134 BONITA BEACH RD SE     BONITA SPRINGS   FL   34135-4281
1087   Affiliated   4076   Orlando Southwest Dialysis   Orlando Southwest Dialysis   6925 LAKE ELLENOR DR   STE 65   ORLANDO   FL   32809-4670
1088   Affiliated   4088   Quincy Dialysis   Quincy Dialysis   878 STRONG RD     QUINCY   FL   32351-5243
1089   Affiliated   4089   Tallahassee Dialysis   Tallahassee Dialysis   1607 PHYSICIANS DR     TALLAHASSEE   FL   32308-4620
1090   Affiliated   4095   South Beach Dialysis   South Beach Dialysis   4701 N MERIDIAN AVE     MIAMI BEACH   FL   33140-2910
1091   Affiliated   4124   Americus Dialysis   Americus Dialysis   227 N LEE ST     AMERICUS   GA   31709-3525
1092   Affiliated   4204   Corry Dialysis   Corry Dialysis   300 YORK ST     CORRY   PA   16407-1420
1093   Affiliated   4208   Elizabethtown Dialysis   Elizabethtown Dialysis   844 N HANOVER ST     ELIZABETHTOWN   PA   17022-1303
1094   Affiliated   4209   Lumberton Dialysis   Lumberton Dialysis   668 MAIN ST     LUMBERTON   NJ   08048-5016
1095   Affiliated   4211   Cobbs Creek Dialysis   Cobbs Creek Dialysis   1700 S 60TH ST     PHILADELPHIA   PA   19142-1404
1096   Affiliated   4214   Westland Dialysis   Garden West Dialysis (fka Westland)   5715 N VENOY RD     WESTLAND   MI   48185-2830
1097   Affiliated   4215   Meadville Dialysis   Meadville Dialysis   19050 PARK AVENUE PLZ     MEADVILLE   PA   16335-4012
1098   Affiliated   4217   Bradford Dialysis   Bradford Dialysis   665 E MAIN ST     BRADFORD   PA   16701-1869
1099   Affiliated   4219   Southgate Dialysis   Southgate Dialysis   14752 NORTHLINE RD     SOUTHGATE   MI   48195-2467
1100   Affiliated   4223   Waynesburg Dialysis   Waynesburg Dialysis   248 ELM DR     WAYNESBURG   PA   15370-8269
1101   Affiliated   4224   Selinsgrove Dialysis   Selinsgrove Dialysis   1030 N SUSQUEHANNA TRAIL     SELINSGROVE   PA   17870-7767
1102   Affiliated   2153   Arlington Dialysis   Arlington Dialysis   1250 E PIONEER PKWY   STE 7   ARLINGTON   TX   76010-6423
1103   Affiliated   2154   Grapevine Dialysis   Grapevine Dialysis   1600 W NORTHWEST HWY   STE 1   GRAPEVINE   TX   76051-8131
1104   Affiliated   1740   Willow Dialysis   Willow Dialysis   1675 ALEX DR     WILMINGTON   OH   45177-2446
1105   Affiliated   1767   New Braunfels Dialysis   New Braunfels Dialysis   900 LOOP 337     NEW BRAUNFELS   TX   78130-3555
1106   Affiliated   2080   Chickasha Dialysis   Chickasha Dialysis   228 S 29TH ST     CHICKASHA   OK   73018-2502
1107   Affiliated   2184   Sugarloaf   Sugarloaf Dialysis (fka Lawrenceville)   1705 BELLE MEADE CT   STE 11   LAWRENCEVILLE   GA   30043-5895
1108   Affiliated   2166   Buford Dialysis   Buford Dialysis   1550 BUFORD HWY   STE 1E   BUFORD   GA   30518-3666
1109   Affiliated   1749   St. Louis Park PD   St. Louis Park Dialysis Center PD   3505 LOUISIANA AVE S     ST LOUIS PARK   MN   55426-4121
1110   Affiliated   1769   Front Royal Dialysis   Front Royal Dialysis   1077D N SHENANDOAH AVE     FRONT ROYAL   VA   22630-3546
1111   Affiliated   1770   Winchester Dialysis   Winchester Dialysis   2301 VALOR DR     WINCHESTER   VA   22601-6111
1112   Affiliated   2200   New Hope Dialysis   New Hope Dialysis (aka Minneapolis, Golden Valley)   5640 INTERNATIONAL PKWY     NEW HOPE   MN   55428-3047
1113   Affiliated   2175   Richfield Dialysis   Richfield Dialysis   6601 LYNDALE AVE S   STE 15   RICHFIELD   MN   55423-2490
1114   Affiliated   2162   Fairborne Dialysis   Fairborn Dialysis   3070 PRESIDENTIAL DR   STE A   FAIRBORN   OH   45324-6273
1115   Affiliated   1694   Benton Dialysis   Benton Dialysis   1151 ROUTE 14 W     BENTON   IL   62812-1500
1116   Affiliated   1695   Centralia Dialysis   Centralia Dialysis   1231 STATE ROUTE 161     CENTRALIA   IL   62801-6739
1117   Affiliated   1696   Marion Dialysis   Marion Dialysis   324 S 4TH ST     MARION   IL   62959-1241
1118   Affiliated   1697   Mount Vernon Dialysis   Mount Vernon Dialysis   1800 JEFFERSON AVE     MOUNT VERNON   IL   62864-4300
1119   Affiliated   2121   Bayou City Dialysis   Bayou City Dialysis (fka Hanson)   10655 EASTEX FWY     HOUSTON   TX   77093-4323
1120   Affiliated   2117   Metarie Dialysis Center   Metairie Dialysis   7100 AIRLINE DR     METAIRIE   LA   70003-5950
1121   Affiliated   1784   Stony Creek Dialysis   Stony Creek Dialysis   9115 S CICERO AVE     OAK LAWN   IL   60453-1895
1122   Affiliated   1785   Beverly Dialysis   Beverly Dialysis   8109 SOUTH WESTERN AVE     CHICAGO   IL   60620-5939
1123   Affiliated   2089   Summit Dialysis   Summit Dialysis Center   3150 POLK ST     HOUSTON   TX   77003-4631
1124   Affiliated   2212   Upper Valley Dialysis   Upper Valley Dialysis (fka West El Paso)   7933 N MESA ST   STE H   EL PASO   TX   79932-1699
1125   Affiliated   2134   Dallas County   Perry Dialysis (fka Dallas County)   610 10TH ST   STE L1   PERRY   IA   50220-2221
1126   Affiliated   1813   Nampa Dialysis Center   Nampa Dialysis   846 PARKCENTRE WAY     NAMPA   ID   83651-1790
1127   Affiliated   1814   Table Rock Dialysis   Table Rock Dialysis   5610 W GAGE ST   STE B   BOISE   ID   83706
1128   Affiliated   1815   Twin Falls Dialysis   Twin Falls Dialysis   1840 CANYON CREST DR     TWIN FALLS   ID   83301-3007
1129   Affiliated   1816   Burley Dialysis Center   Burley Dialysis   741 N OVERLAND AVE     BURLEY   ID   83318-3440

 

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1130   Affiliated   1817   Gate City Dialysis Center   Gate City Dialysis   2001 BENCH RD     POCATELLO   ID   83201-2033
1131   Affiliated   1818   Four Rivers Dialysis   Four Rivers Dialysis   515 EAST LN     ONTARIO   OR   97914-3953
1132   Affiliated   2231   River Parishes   River Parishes Dialysis (aka La Place)   2880 W AIRLINE HWY     LA PLACE   LA   70068-2922
1133   Affiliated   2177   South Lincoln   South Lincoln Dialysis   3401 PLANTATION DR   STE 14   LINCOLN   NE   68516-4712
1134   Affiliated   2105   Rochester Hills   Rochester Hills Dialysis (aka Sterling Heights)   1886 W AUBURN RD   STE 1   ROCHESTER HILLS   MI   48309-3865
1135   Affiliated   2101   Willowbrook Dialysis   Willowbrook Dialysis   12120 JONES RD   STE G   HOUSTON   TX   77070-5280
1136   Affiliated   2195   Springhurst Dialysis   Springhurst Dialysis (aka Louisville)   10201 CHAMPION FARMS DR     LOUISVILLE   KY   40241-6150
1137   Affiliated   2012   Magnolia West   Magnolia West Dialysis (aka Riverside II)   11161 MAGNOLIA AVE     RIVERSIDE   CA   92505-3605
1138   Affiliated   2206   Garrisonville Dialysis   Garrisonville Dialysis   70 DOC STONE RD   STE 11   STAFFORD   VA   22556-4628
1139   Affiliated   2152   Strongsville Dialysis   Strongsville Dialysis   17792 PEARL RD     STRONGSVILLE   OH   44136-6909
1140   Affiliated   984   Summerlin Dialysis   Summerlin Dialysis Center, LV   653 N TOWN CENTER DR   STE 7 BLDG 2   LAS VEGAS   NV   89144-0503
1141   Affiliated   2127   Red Bluff Dialysis   Red Bluff Dialysis Center   2455 SISTER MARY COLUMBA DR     RED BLUFF   CA   96080-4364
1142   Affiliated   1638   Cobb Dialysis   Cobb Dialysis   3865 MEDICAL PARK DR     AUSTELL   GA   30106-1109
1143   Affiliated   1693   Paulding Dialysis   Paulding Dialysis   4019 JOHNS RD     DALLAS   GA   30132-3420
1144   Affiliated   1839   Sweetwater Dialysis   Sweetwater Dialysis   7117 S SWEETWATER RD     LITHIA SPRINGS   GA   30122-2446
1145   Affiliated   3671   Charlottesville North   Charlottesville North Dialysis   1800 TIMBERWOOD BLVD   STE C   CHARLOTTESVILLE   VA   22911-7544
1146   Affiliated   2186   Southern Crescent   Southern Crescent Dialysis Center (fka Riverdale)   275 UPPER RIVERDALE RD SW   STE B   RIVERDALE   GA   30274-2556
1147   Affiliated   2169   Meridian Park   Meridian Park Dialysis Center (fka Lake Oswego)   19255 SW 65TH AVE   STE 1   TUALATIN   OR   97062-9712
1148   Affiliated   1812   Treasure Valley Dialysis   Treasure Valley Dialysis   3525 E LOUISE ST   STE 155   MERIDIAN   ID   83642-6303
1149   Affiliated   3637   White Oak   White Oak Dialysis (Chronic)   5520 CHEVIOT RD   STE B   CINCINNATI   OH   45247-7069
1150   Affiliated   1786   Ash Tree   Ash Tree Dialysis   2666 N GROVE INDUSTRIAL DR     FRESNO   CA   93727-1552
1151   Affiliated   2242   Madera Dialysis   Almond Wood Dialysis (fka Madera)   501 E ALMOND AVE     MADERA   CA   93637-5661
1152   Affiliated   2209   Carrollton   Carrollton Dialysis   1544 VALWOOD PKWY   STE 114   CARROLLTON   TX   75006-8425
1153   Affiliated   2202   Edna Dialysis   Edna Dialysis   1008 N WELLS ST     EDNA   TX   77957-2153
1154   Affiliated   2208   Bear Creek Dialysis   Bear Creek Dialysis (fka Clay Road)   4978 HIGHWAY 6 N   STE I   HOUSTON   TX   77084-5282
1155   Affiliated   1820   Windham Dialysis   Windham Dialysis   375 TUCKIE RD   STE C   NORTH WINDHAM   CT   06256-1345
1156   Affiliated   1819   Vernon Dialysis   Vernon Dialysis   460 HARTFORD TPKE STE C     VERNON ROCKVILLE   CT   6066
1157   Affiliated   2092   Fountain Dialysis   Fountain Dialysis (aka Security)   6910 BANDLEY DR     FOUNTAIN   CO   80817-2617
1158   Affiliated   1846   Grand Junction   Grand Junction Dialysis Center   710 WELLINGTON AVE   STE 2   GRAND JUNCTION   CO   81501-6100
1159   Affiliated   2183   Fort Mill   Fort Mill Dialysis   1975 CAROLINA PLACE DR     FORT MILL   SC   29708-6922
1160   Affiliated   2215   Mrytle Beach   JV-Myrtle Beach Dialysis   3919 MAYFAIR ST     MYRTLE BEACH   SC   29577-5773
1161   Affiliated   2032   Oakwood   Oakwood Dialysis Center   148 HECTOR AVE     GRETNA   LA   70056-2531
1162   Affiliated   2168   SP Hillsboro   Hillsboro Dialysis   2500 NW 229TH AVE   STE 3 BLDG E   HILLSBORO   OR   97124-7516
1163   Affiliated   2269   Kettering   Kettering Dialysis   5721 BIGGER RD     KETTERING   OH   45440-2752
1164   Affiliated   2246   Mansfield   Mansfield Dialysis Center (aka Dallas)   987 N WALNUT CREEK DR   STE 11   MANSFIELD   TX   76063-8016
1165   Affiliated   2290   Cottage Grove   Cottage Grove Dialysis   8800 E POINT DOUGLAS RD S   STE 1   COTTAGE GROVE   MN   55016-4160
1166   Affiliated   2257   Scott County Dialysis   Scott County Dialysis   7456 S PARK DR     SAVAGE   MN   55378
1167   Affiliated   1773   Virginia Beach   Camelot Dialysis Center   1800 CAMELOT DR   STE 1   VIRGINIA BEACH   VA   23454-2440
1168   Affiliated   1627   Amelia Island   Amelia Island Dialysis   1525 LIME ST   STE 12   FERNANDINA BEACH   FL   32034-3015
1169   Affiliated   2179   Laurel Manor at the Villages   Laurel Manor Dialysis Center at the Villages   1950 LAUREL MANOR DR   STE 19   LADY LAKE   FL   32162-5603
1170   Affiliated   2160   East Deerborn   East Dearborn Dialysis   13200 W WARREN AVE     DEARBORN   MI   48126-2410
1171   Affiliated   1661   North Houston   PDI-North Houston   7115 NORTH LOOP E     HOUSTON   TX   77028-5948
1172   Affiliated   1663   South Houston   PDI-South Houston   5989 SOUTH LOOP E     HOUSTON   TX   77033-1017
1173   Affiliated   1856   Ralph McGill Dialysis Center   Ralph McGill Dialysis   418 DECATUR ST SE     ATLANTA   GA   30312-1801
1174   Affiliated   2144   Chelsea   Chelsea Dialysis   1620 COMMERCE PARK DR   STE 2   CHELSEA   MI   48118-2136
1175   Affiliated   2214   Smokey Mountain   Smoky Mountain Dialysis   1611 ANDREWS RD     MURPHY   NC   28906-5100
1176   Affiliated   3680   Miami Gardens   Miami Gardens Dialysis   3363 NW 167TH ST     MIAMI GARDENS   FL   33056-4254
1177   Affiliated   2222   Deerbrook   Deerbrook Dialysis   9660 FM 1960 BYPASS RD W     HUMBLE   TX   77338-4039
1178   Affiliated   2227   Downtown Dallas   DaVita Downtown Dallas Dialysis Center (fka Grove)   3515 SWISS AVE   STE A   DALLAS   TX   75204-6223
1179   Affiliated   2197   Henderson   Siena Henderson Dialysis Center   2865 SIENNA HEIGHTS DR   STE 141   HENDERSON   NV   89052-4168
1180   Affiliated   2292   Wyandotte   Wyandotte Central Dialysis   3737 STATE AVE     KANSAS CITY   KS   66102-3830
1181   Affiliated   2235   Westview   Westview Dialysis   3749 COMMERCIAL DR   LAFAYETTE PLACE SHOPPING CENTER   INDIANAPOLIS   IN   46222-1676
1182   Affiliated   2286   Garland   Garland Dialysis   776 E CENTERVILLE RD     GARLAND   TX   75041-4640
1183   Affiliated   2333   Aberdeen   Aberdeen Dialysis   780 W BEL AIR AVE     ABERDEEN   MD   21001-2236

 

Page 68 of 136


1184   Affiliated   2259   Mountain Park   Mountain Park Dialysis   5235 MEMORIAL DR     STONE MOUNTAIN   GA   30083-3112
1185   Affiliated   2229   Downtown San Antonio   Downtown San Antonio Dialysis (Brooklyn St)   615 E QUINCY ST     SAN ANTONIO   TX   78215-1600
1186   Affiliated   2237   Medlock Bridge   Medlock Bridge Dialysis (aka Duluth)   10680 MEDLOCK BRIDGE RD   STE 13   DULUTH   GA   30097-8420
1187   Affiliated   2234   Greene County Dialysis   Greene County Dialysis Center (NC)   1025 KINGOLD BLVD     SNOW HILL   NC   28580-1616
1188   Affiliated   2243   West Broadway Dialysis   West Broadway Dialysis   720 W BROADWAY     LOUISVILLE   KY   40202-2240
1189   Affiliated   2072   St. Pauls Dialysis   St. Pauls Dialysis (aka Robeson County)   564 W MCLEAN ST     SAINT PAULS   NC   28384-1421
1190   Affiliated   2123   Carquinez Dialyis   Carquinez Dialysis (fka SW Vallejo)   125 CORPORATE PL   STE C   VALLEJO   CA   94590-6968
1191   Affiliated   2159   DaVita East   DaVita East Dialysis Clinic (fka La Bamba)   11989 PELLICANO DR     EL PASO   TX   79936-6287
1192   Affiliated   2187   Natomas   Natomas Dialysis   30 GOLDEN LAND CT   BLDG G   SACRAMENTO   CA   95834-2420
1193   Affiliated   2228   Tennesse Valley   Tennessee Valley Dialysis Center (aka Johnson City)   107 WOODLAWN DR   STE 2   JOHNSON CITY   TN   37604-6287
1194   Affiliated   2174   Turfway Dialysis   Turfway Dialysis (fka Florence)   11 SPIRAL DR   STE 15   FLORENCE   KY   41042-1394
1195   Affiliated   2291   Leavenworth   Leavenworth Dialysis   501 OAK ST     LEAVENWORTH   KS   66048-2646
1196   Affiliated   2270   Franklin Dialysis   Franklin Dialysis (IN)   1140 W JEFFERSON ST   STE A   FRANKLIN   IN   46131-2101
1197   Affiliated   2011   Norco   Norco Dialysis (fka Corona II)   1901 TOWN AND COUNTRY DR   STE 1   NORCO   CA   92860-3611
1198   Affiliated   2240   Andover   Andover Dialysis   488 S MAIN ST     ANDOVER   OH   44003-9602
1199   Affiliated   1863   Little Rock   Jacksonville Central Dialysis Center   400 T P WHITE DR     JACKSONVILLE   AR   72076-3287
1200   Affiliated   1864   North Little Rock Dialysis   North Little Rock Center   4505 E MCCAIN BLVD     NORTH LITTLE ROCK   AR   72117-2902
1201   Affiliated   2233   Anadarko   Anadarko Dialysis   412 SE 11TH STREET     ANADARKO   OK   73005-4442
1202   Affiliated   2331   Desert Springs   Desert Springs Dialysis   2110 E FLAMINGO RD   STE 18   LAS VEGAS   NV   89119-5191
1203   Affiliated   2213   Livingston   Vancouver Dialysis Center   9120 NE VANCOUVER MALL DR   STE 16   VANCOUVER   WA   98662-9401
1204   Affiliated   2300   Vancouver   Livingston TN Dialysis   308 OAK ST     LIVINGSTON   TN   38570-1729
1205   Affiliated   2225   Fenton Dialysis   Fenton Dialysis   17420 SILVER PKWY     FENTON   MI   48430-4429
1206   Affiliated   2332   Cold Spring   Cold Springs Dialysis   430 CROSS ROADS BLVD     COLD SPRING   KY   41076-2341
1207   Affiliated   2094   Yucaipa   Yucaipa Dialysis   33487 YUCAIPA BLVD     YUCAIPA   CA   92399-2064
1208   Affiliated   1900   Florida Renal Center   Florida Renal Center   3500 NW 7TH ST     MIAMI   FL   33125-4016
1209   Affiliated   2140   Harbor UCLA   Long Beach Harbor Dialysis (aka UCLA)   1075 E PACIFIC COAST HWY     LONG BEACH   CA   90806-5089
1210   Affiliated   2210   Seaton Drive   Seton Drive Dialysis (fka Greensprings II)   4800 SETON DR     BALTIMORE   MD   21215-3210
1211   Affiliated   1865   South Valley   South Valley Dialysis   17815 VENTURA BLVD   STE 1   ENCINO   CA   91316-3600
1212   Affiliated   2305   West Pensacola   West Pensacola Dialysis   598 N FAIRFIELD DR   STE 1   PENSACOLA   FL   32506-4320
1213   Affiliated   2073   Mar Vista   Mar Vista Dialysis Center (UCLA-Santa Monica)   2020 SANTA MONICA BLVD   STE 1   SANTA MONICA   CA   90404-2139
1214   Affiliated   2082   Riddle Dialysis   Riddle Dialysis   100 GRANITE DR   STE 16   MEDIA   PA   19063-5134
1215   Affiliated   2346   Uptown   Minneapolis Uptown Dialysis   3601 LYNDALE AVE S     MINNEAPOLIS   MN   55409-1103
1216   Affiliated   1907   Lake Griffith East Dialysis   Lake Griffin East Dialysis   401 E NORTH BLVD     LEESBURG   FL   34748-5256
1217   Affiliated   2170   West Linn   West Linn Dialysis   19056 WILLAMETTE DR     WEST LINN   OR   97068-1715
1218   Affiliated   2330   Cape Coral South Dialysis   Cape Coral South Dialysis   3046 DEL PRADO BLVD S   STE 4A   CAPE CORAL   FL   33904-7232
1219   Affiliated   2241   Ceres   Ceres Dialysis Center   1768 MITCHELL RD   STE 38   CERES   CA   95307-2156
1220   Affiliated   1862   Shaker Square   Shaker Square Dialysis   12800 SHAKER BLVD   STE 1   CLEVELAND   OH   44120-2004
1221   Affiliated   1906   St. Cloud Dialysis   St. Cloud Dialysis   4750 OLD CANOE CREEK RD     SAINT CLOUD   FL   34769-1430
1222   Affiliated   1915   Turlock Dialysis Center   Turlock Dialysis Center   50 W SYRACUSE AVE     TURLOCK   CA   95380-3143
1223   Affiliated   2268   Haymarket   Haymarket Dialysis (fka Gainesville)   14664 GAP WAY     GAINESVILLE   VA   20155-1683
1224   Affiliated   2272   Hackettstown   Hackettstown Dialysis   657 WILLOW GROVE ST   WEST WING MEDICAL PLAZA STE 22   HACKETTSTOWN   NJ   07840-1713
1225   Affiliated   2274   Regency   Regency Dialysis Center (fka Jacksonville)   9535 REGENCY SQUARE BLVD N     JACKSONVILLE   FL   32225-8128
1226   Affiliated   2149   Williamsburg   Williamsburg Dialysis (fka Yorktown)   500 SENTARA CIR   STE 13   WILLIAMSBURG   VA   23188-5727
1227   Affiliated   2141   Commerce Township   Commerce Township Dialysis   120 W COMMERCE RD     COMMERCE TOWNSHIP   MI   48382-3915
1228   Affiliated   2147   Kankakee   Kankakee County Dialysis   581 WILLIAM R LATHAM SR DR   STE 14   BOURBONNAIS   IL   60914-2439
1229   Affiliated   2283   Sandusky   Sandusky Dialysis Center   795 BARDSHAR RD     SANDUSKY   OH   44870-1505
1230   Affiliated   2252   Ionia   Ionia Dialysis   2622 HEARTLAND BLVD     IONIA   MI   48846-8757
1231   Affiliated   2289   Indian River   Indian River Dialysis Center   2150 45TH ST   UNIT 12   VERO BEACH   FL   32967-6281
1232   Affiliated   2360   North Henry   North Henry Dialysis (fka Stockbridge)   5627 N HENRY BLVD   STE I1   STOCKBRIDGE   GA   30281-3244
1233   Affiliated   2077   Tacoma Dialysis   Tacoma Dialysis Center   3401 S 19TH ST     TACOMA   WA   98405-1909
1234   Affiliated   1908   Hileah Kidney Center I   Hialeah Artificial Kidney Center   2750 W 68TH ST   STE 27   HIALEAH   FL   33016-5450
1235   Affiliated   2315   St. Francis   Charter Colony Dialysis Center (fka St. Francis Dialysis)   2312 COLONY CROSSING PL     MIDLOTHIAN   VA   23112-4280
1236   Affiliated   2138   Bellflower   Bellflower Dialysis Center (aka Widerhorn)   15736 WOODRUFF AVE     BELLFLOWER   CA   90706-4018
1237   Affiliated   2301   Smyrna   Smyrna Dialysis   537 STONECREST PKWY     SMYRNA   TN   37167-6884

 

Page 69 of 136


1238   Affiliated   2122   Clearlake   Clearlake Dialysis   14400 OLYMPIC DR     CLEARLAKE   CA   95422-8809
1239   Affiliated   1853   Dialysis Center of Erie   Dialysis Center of Erie   1641 SASSAFRAS ST     ERIE   PA   16502-1858
1240   Affiliated   1854   Warren Dialysis   Warren Dialysis   2 W CRESCENT PARK     WARREN   PA   16365-2111
1241   Affiliated   2322   Maysville   Maysville Dialysis   489 TUCKER DR     MAYSVILLE   KY   41056-9111
1242   Affiliated   2429   Fridley   East River Road Dialysis (fka Fridley Dialysis Unit)   5301 E RIVER RD   STE 117   FRIDLEY   MN   55421-3778
1243   Affiliated   2189   West Sacramento   West Sacramento Dialysis   3450 INDUSTRIAL BLVD   STE 1   WEST SACRAMENTO   CA   95691-5003
1244   Affiliated   2293   Anderson   Anderson Dialysis Center   7502 STATE RD   STE 116   CINCINNATI   OH   45255
1245   Affiliated   2383   North County   North St. Louis County Dialysis   13119 NEW HALLS FERRY RD     FLORISSANT   MO   63033-3228
1246   Affiliated   2439   Fargo   Fargo Dialysis Center   4474 23RD AVE S   STE M   FARGO   ND   58104-8795
1247   Affiliated   2008   Eastchester   Eastchester Road Dialysis Center (Bronx II)   1515 JARRETT PL     BRONX   NY   10461-2606
1248   Affiliated   2224   Fallon   Fallon Dialysis   1103 NEW RIVER PKWY     FALLON   NV   89406-6899
1249   Affiliated   2279   Clarksville North   Clarksville North Dialysis   3071 CLAY LEWIS RD     CLARKSVILLE   TN   37040-5141
1250   Affiliated   2308   Eaton   Eaton Dialysis   105 E WASHINGTON JACKSON RD     EATON   OH   45320-9789
1251   Affiliated   2447   Wallace   Wallace Dialysis   5650 S NC 41 HWY     WALLACE   NC   28466-6094
1252   Affiliated   2288   Central Kalazmazoo   Kalamazoo Central Dialysis   535 S BURDICK ST   STE 11   KALAMAZOO   MI   49007-5261
1253   Affiliated   2287   West Kalamazoo   Kalamazoo West Dialysis   1040 N 10TH ST     KALAMAZOO   MI   49009-6149
1254   Affiliated   1921   Bakersfield   Bakersfield Dialysis Center   5143 OFFICE PARK DR     BAKERSFIELD   CA   93309-0660
1255   Affiliated   1930   Antelope Valley Dialysis   Antelope Valley Dialysis   1759 W AVENUE J   STE 12   LANCASTER   CA   93534-2703
1256   Affiliated   1931   Indian Wells Valley Dialysis   Indian Wells Valley Dialysis   212 S RICHMOND RD     RIDGECREST   CA   93555-4434
1257   Affiliated   1932   Palmdale Regional Dialysis   Palmdale Regional   1643 E PALMDALE BLVD     PALMDALE   CA   93550-4847
1258   Affiliated   2185   South Star / Adamsville   Southstar Adamsville Dialysis (fka Cascade)   3651 BAKERS FERRY RD SW     ATLANTA   GA   30331-3712
1259   Affiliated   2314   Union City   Union City Dialysis   6851 SHANNON PKWY   STE 2   UNION CITY   GA   30291-2049
1260   Affiliated   2345   Waterbury   Waterbury Dialysis Center   150 MATTATUCK HEIGHTS RD     WATERBURY   CT   06705-3893
1261   Affiliated   2421   Butler Farm   Butler Farm Dialysis (Hope II)   501 BUTLER FARM RD     HAMPTON   VA   23666-1777
1262   Affiliated   2337   Blue Mtn Kidney Center   Blue Mountain Kidney Center (aka Wild Horse, Pendleton)   72556 COYOTE RD     PENDLETON   OR   97801-1002
1263   Affiliated   2249   Talladega   Talladega Dialysis   726 BATTLE ST E   STE A   TALLADEGA   AL   35160-2583
1264   Affiliated   2281   Athens East   Athens East Dialysis   2026 S MILLEDGE AVE   STE A2   ATHENS   GA   30605-6480
1265   Affiliated   2412   Mayland   Mayland Dialysis Center (aka Spruce Pine)   575 ALTAPASS HWY     SPRUCE PINE   NC   28777-3012
1266   Affiliated   2236   Salem   Salem Dialysis Center (IN)   1201 N JIM DAY RD   STE 13   SALEM   IN   47167-7219
1267   Affiliated   2239   Lake Cliff   Lake Cliff Dialysis Center   805 N BECKLEY AVE     DALLAS   TX   75203-1612
1268   Affiliated   2363   DVA Mid Cities Dialysis   Mid Cities Dialysis Center   117 E HARWOOD RD     HURST   TX   76054-3043
1269   Affiliated   2362   Boerne   Boerne Dialysis Center   1369 S MAIN ST   STE 11   BOERNE   TX   78006-2860
1270   Affiliated   2318   Columbus West   Columbus West Dialysis   1395 GEORGESVILLE RD     COLUMBUS   OH   43228-3611
1271   Affiliated   2306   Point Place   Point Place Dialysis   4747 SUDER AVE   STE 17   TOLEDO   OH   43611-2869
1272   Affiliated   2350   Delhi Dialysis   Delhi Dialysis   5040 DELHI AVE     CINCINNATI   OH   45238-5388
1273   Affiliated   2253   Pataskala   Pataskala Dialysis Center   642 E BROAD ST     PATASKALA   OH   43062-7627
1274   Affiliated   2384   Eastland   Eastland Dialysis (fka Independence)   19101 E VALLEY VIEW PKWY   STE E   INDEPENDENCE   MO   64055-6907
1275   Affiliated   2254   Wauseon   Wauseon Dialysis Center   721 S SHOOP AVE     WAUSEON   OH   43567-1729
1276   Affiliated   2327   Lebanon Dialysis   Lebanon Dialysis Center (Chronic Only)   918B COLUMBUS AVE     LEBANON   OH   45036-
1277   Affiliated   2460   Horton   Horton Dialysis   1901 EUCLID AVE     HORTON   KS   66439-1238
1278   Affiliated   2280   Lone Peak Dialysis   Lone Peak Dialysis   1175 E 50 S   STE 111   AMERICAN FORK   UT   84003-2845
1279   Affiliated   2347   Mena   Mena Dialysis Center   1200 CRESTWOOD CIR     MENA   AR   71953-5516
1280   Affiliated   1941   FAYETTEVILLE DIALYSIS   Fayetteville Dialysis   509 E MILLSAP RD   STE 111   FAYETTEVILLE   AR   72703-4862
1281   Affiliated   1942   BENTONVILLE DIALYSIS   Bentonville Dialysis   1104 SE 30TH ST     BENTONVILLE   AR   72712-4290
1282   Affiliated   1943   SILOAM SPRINGS DIALYSIS   Siloam Springs Dialysis   500 S MOUNT OLIVE ST   STE 17   SILOAM SPRINGS   AR   72761-3602
1283   Affiliated   1944   SPRINGDALE DIALYSIS   Springdale Dialysis   708 QUANDT AVE     SPRINGDALE   AR   72764-5309
1284   Affiliated   2273   Grosse Pointe   Grosse Pointe Dialysis   18000 E WARREN AVE   STE 1   DETROIT   MI   48224-1336
1285   Affiliated   2448   Indy South Dialysis   Indy South Dialysis   972 EMERSON PKWY   STE E   GREENWOOD   IN   46143-6202
1286   Affiliated   2358   Greensburg Dialysis   Greensburg Dialysis   1531 N COMMERCE EAST DR   STE 6   GREENSBURG   IN   47240-3259
1287   Affiliated   2319   Grove City   Grove City Dialysis   4155 KELNOR DR     GROVE CITY   OH   43123-2960
1288   Affiliated   2338   West Beach   West Beach Dialysis Center   16201 PANAMA CITY BEACH HWY   STE 12   PANAMA CITY BEACH   FL   32413-5301
1289   Affiliated   2371   Birmingham   Center Point Dialysis (aka Birmingham Center)   2337 1ST ST NE     CENTER POINT   AL   35215-3619
1290   Affiliated   2445   Eureka   Eureka Dialysis Center   419 MERAMEC BLVD     EUREKA   MO   63025-3906
1291   Affiliated   2313   Tifton   Tifton Dialysis   624 LOVE AVE     TIFTON   GA   31794-4406

 

Page 70 of 136


1292   Affiliated   2146   Woodlands   The Woodlands Dialysis   9301 PINECROFT DR   STE 13   SHENANDOAH   TX   77380-3178
1293   Affiliated   2266   Exerter   Exeter Dialysis   1116 W VISALIA RD   STE 16   EXETER   CA   93221-1482
1294   Affiliated   2396   Wayne County   Wayne County Dialysis (fka Fairfield)   303 NW 11TH ST   STE 1   FAIRFIELD   IL   62837-1203
1295   Affiliated   2415   Cordele Dialysis   Cordele Dialysis   1013 E 16TH AVE     CORDELE   GA   31015-1539
1296   Affiliated   2304   Winter Park   Winter Park Dialysis (aka Orlando)   3727 N GOLDENROD RD   STE 11   WINTER PARK   FL   32792-8611
1297   Affiliated   2449   Carmel   Carmel Dialysis   180 E CARMEL DR     CARMEL   IN   46032-2633
1298   Affiliated   2298   Corydon   Corydon Dialysis   1937 OLD HWY 135 NW     CORYDON   IN   47112-2013
1299   Affiliated   2382   Memphis Southeast   Memphis Southeast Dialysis (aka Midtown)   1805 MORIAH WOODS BLVD   STE 11   MEMPHIS   TN   38117-7119
1300   Affiliated   2399   Rim Country   Rim Country Dialysis   809 W LONGHORN RD     PAYSON   AZ   85541-4280
1301   Affiliated   2201   Cedar Park   Cedar Park Dialysis (fka North Austin)   1720 E WHITESTONE BLVD     CEDAR PARK   TX   78613-7640
1302   Affiliated   2368   Ellensburg   Ellensburg Dialysis   2101 W DOLARWAY RD   STE 1   ELLENSBURG   WA   98926-9310
1303   Affiliated   2260   Santa Fe Springs   Santa Fe Springs Dialysis   11147 WASHINGTON BLVD     WHITTIER   CA   90606-3007
1304   Affiliated   1950   Snapfinger Dialysis   Snapfinger Dialysis   5255 SNAPFINGER PARK DR   STE 115   DECATUR   GA   30035-4066
1305   Affiliated   1951   East Dekalb Dialysis   East DeKalb Dialysis   2801 CANDLER RD   STE 23   DECATUR   GA   30034-1429
1306   Affiliated   2258   Meadows East   Meadows East Dialysis   2529 SIX MILE LN     LOUISVILLE   KY   40220-2934
1307   Affiliated   2226   First Colony   First Colony Dialysis (aka Sugarland, Great Woods)   1447 HIGHWAY 6   STE 14   SUGAR LAND   TX   77478-5094
1308   Affiliated   1612   Coastal Kidney Center   Coastal Kidney Center   510 N MACARTHUR AVE     PANAMA CITY   FL   32401-3636
1309   Affiliated   2211   Clinton Township   Clinton Township Dailysis   15918 19 MILE RD   STE 11   CLINTON TOWNSHIP   MI   48038-1101
1310   Affiliated   2207   West Brook   Westbrook Dialysis (fka Palm Brook II)   13907 W CAMINO DEL SOL   STE 13   SUN CITY WEST   AZ   85375-4405
1311   Affiliated   1954   Johnson County   Johnson County Dialysis   10453 W 84TH TER     LENEXA   KS   66214-1641
1312   Affiliated   1956   Wyandotte County   Wyandotte County Dialysis   5001 STATE AVE     KANSAS CITY   KS   66102-3459
1313   Affiliated   2479   Maple Grove   Maple Grove Dialysis Unit   15655 GROVE CIR N     MAPLE GROVE   MN   55369-4489
1314   Affiliated   4336   East End   East End-Pittsburgh Dialysis (fka Wilkinsburg)   7714 PENN AVE PARK PLAZA     PITTSBURGH   PA   15221
1315   Affiliated   2493   Westminster II - North Metro   North Metro Dialysis Center (aka Denver, Westminster II)   12365 HURON ST   STE 5   WESTMINSTER   CO   80234-3498
1316   Affiliated   1960   Vidalia   Vidalia First Street Dialysis   906 E 1ST ST     VIDALIA   GA   30474-4207
1317   Affiliated   2357   Highland Park   Highland Park Dialysis   1559 W 7TH ST     SAINT PAUL   MN   55102-4238
1318   Affiliated   2367   Centennial Parkway   Centennial Dialysis Center   8775 DEER SPRINGS WAY     LAS VEGAS   NV   89149-0416
1319   Affiliated   2250   Lord Baltimore   Northwest Dialysis Center (aka Lord Baltimore, N. Rolling Road II, Owings Mills II)   2245 ROLLING RUN DR   STE 1   WINDSOR MILL   MD   21244-1858
1320   Affiliated   3944   North Charlotte   North Charlotte Dialysis   6620 OLD STATESVILLE RD     CHARLOTTE   NC   28269
1321   Affiliated   2410   Sun Ray Dialysis   Sun Ray Dialysis Unit (fka East St. Paul)   1758 OLD HUDSON RD   STE 1   SAINT PAUL   MN   55106-6161
1322   Affiliated   2425   Vandalia   Vandalia Dialysis   301 MATTES AVE     VANDALIA   IL   62471-2061
1323   Affiliated   2428   Westwood Hills   Westwood Hills Dialysis (fka Minneapolis, Excelsior)   7525 WAYZATA BLVD     SAINT LOUIS PARK   MN   55426-1621
1324   Affiliated   4305   Amery   Amery Dialysis   970 ELDEN AVE     AMERY   WI   54001-1448
1325   Affiliated   2434   Wadsworth   Wadsworth Dialysis   195 WADSWORTH RD   STE 32   WADSWORTH   OH   44281-9504
1326   Affiliated   2419   Dublin   Dublin Dialysis   6770 PERIMETER DR     DUBLIN   OH   43016-8063
1327   Affiliated   4314   Weber Valley   Weber Valley Dialysis (fka Ogden)   1920 W 250TH N     MARRIOTT-SLATERVILLE   UT   84404-9233
1328   Affiliated   2343   West Elk Grove   West Elk Grove Dialysis   2208 KAUSEN DR   STE 1   ELK GROVE   CA   95758-7174
1329   Affiliated   2355   Bedford Park   Bedford Park Dialysis Center   3119 WEBSTER AVE   1ST FLR   BRONX   NY   10467-4905
1330   Affiliated   1747   Cuero Lakeview Dialysis   Cuero Lakeview Dialysis   1105 E BROADWAY ST     CUERO   TX   77954
1331   Affiliated   1961   Madisonville Dialysis   Madisonville Dialysis Center   255 E NORTH ST     MADISONVILLE   KY   42431
1332   Affiliated   2467   Crescent City   Crescent City Dialysis Center   3909 BIENVILLE ST   STE B   NEW ORLEANS   LA   70119-5152
1333   Affiliated   4318   Callowhill   Callowhill Dialysis Center   313 CALLOWHILL ST     PHILADELPHIA   PA   19123-4103
1334   Affiliated   2406   Oak Creek   Oak Creek Dialysis (fka South Milwaukee)   8201 S HOWELL AVE   STE 6   OAK CREEK   WI   53154-8336
1335   Affiliated   4395   Leesburg Virginia   Leesburg Virginia Dialysis   224D CORNWALL ST NW   STE 1   LEESBURG   VA   20176-2700
1336   Affiliated   2386   Joy of Dixon   Joy of Dixon Dialysis Center   1640 N LINCOLN ST     DIXON   CA   95620-9255
1337   Affiliated   2137   Long Beach JV -Bixby Knolls   Bixby Knolls Dialysis (fka Long Beach)   3744 LONG BEACH BLVD     LONG BEACH   CA   90807-3310
1338   Affiliated   1790   Alliance Community Dialysis   Alliance Community Dialysis   270 E STATE ST   STE 11   ALLIANCE   OH   44601-4309
1339   Affiliated   1791   Belden Community Dialysis   Belden Community Dialysis   4685 FULTON DR NW     CANTON   OH   44718-2379
1340   Affiliated   1792   Mercy Canton Dialysis   Mercy Canton Dialysis   1320 MERCY DR NW     CANTON   OH   44708-2614
1341   Affiliated   2294   Marrero   Marrero Dialysis   1908 JUTLAND DR     HARVEY   LA   70058-2359
1342   Affiliated   2351   Miramar   Miramar Kidney Center   2501 DYKES RD   STE 2   MIRAMAR   FL   33027-4217
1343   Affiliated   2418   Chesterton   Chesterton Dialysis   711 PLAZA DR   STE 6   CHESTERTON   IN   46304-5506
1344   Affiliated   4368   St. John   St. John Dialysis   10033 WICKER AVE   STE 6   SAINT JOHN   IN   46373-8777
1345   Affiliated   2256   Princeton   Princeton Dialysis   2227 SHERMAN DR     PRINCETON   IN   47670-1062

 

Page 71 of 136


1346   Affiliated   4332   Black Rock   Black Rock Dialysis (aka Faifield)   427 STILLSON RD     FAIRFIELD   CT   06824-3153
1347   Affiliated   2422   Williamstown   Williamstown Dialysis (fka Dry Ridge)   103 BARNES RD   STE A   WILLIAMSTOWN   KY   41097-9468
1348   Affiliated   4376   Renaissance   Renaissance Dialysis   1840 DARBY DR     FLORENCE   AL   35630-2623
1349   Affiliated   4360   Portage   Portage Dialysis   5823 US HIGHWAY 6     PORTAGE   IN   46368-4851
1350   Affiliated   2393   Opelika   Opelika Dialysis Center   2340 PEPPERELL PKWY     OPELIKA   AL   36801-6240
1351   Affiliated   2435   Urbana   Urbana Dialysis Center   1880 E US HIGHWAY 36     URBANA   OH   43078-9600
1352   Affiliated   1913   Port Lavaca Dialysis   Port Lavaca Dialysis   1300 N VIRGINIA ST   STE 12   PORT LAVACA   TX   77979-2512
1353   Affiliated   2276   Cornerhouse Dialysis   Cornerhouse Dialysis Center (aka Santa Clara)   2005 NAGLEE AVE     SAN JOSE   CA   95128-4801
1354   Affiliated   2167   Snellville   Snellville Dialysis   2135 MAIN ST E   STE 13   SNELLVILLE   GA   30078-6424
1355   Affiliated   4334   Bloomfield   Bloomfield-Pittsburgh Dialysis   5171 LIBERTY AVE   STE C   PITTSBURGH   PA   15224-2254
1356   Affiliated   2489   Pennsauken   Pennsauken Dialysis   7024 KAIGHNS AVE     PENNSAUKEN   NJ   08109-4417
1357   Affiliated   2433   Logan   Logan Dialysis   12880 GREY ST     LOGAN   OH   43138-9638
1358   Affiliated   2454   Forest Fair   Forest Fair Dialysis (fka Forest Park)   1145 KEMPER MEADOW DR     CINCINNATI   OH   45240-4118
1359   Affiliated   4307   Knoxville   Knoxville Central Dialysis   9141 CROSS PARK DR   STE 12   KNOXVILLE   TN   37923-4557
1360   Affiliated   4338   Kennestone   Kennestone Dialysis (aka Cobb II)   200 COBB PKWY N   STE 318 BLDG 3   MARIETTA   GA   30062-3558
1361   Affiliated   4343   Wiregrass Kidney Center   Wiregrass Kidney Center (fka Ross Circle)   1450 ROSS CLARK CIR     DOTHAN   AL   36301-4765
1362   Affiliated   2432   Memphis Downtown   Memphis Downtown Dialysis   2076 UNION AVE     MEMPHIS   TN   38104-4138
1363   Affiliated   3953   Marshville   Marshville Dialysis Center   7260 E MARSHVILLE BLVD     MARSHVILLE   NC   28103-1191
1364   Affiliated   4356   Shamrock   Shamrock Dialysis   1016 CLAXTON DAIRY RD   STE 1A   DUBLIN   GA   31021-7971
1365   Affiliated   4367   North Colorado Springs   North Colorado Springs Dialysis   6071 E WOODMEN RD   STE 1   COLORADO SPRINGS   CO   80923-2610
1366   Affiliated   2466   Oakes   Oakes Dialysis   413 S 7TH ST     OAKES   ND   58474-1920
1367   Affiliated   1976   Pinnacle Dialysis of Boca Raton   Pinnacle Dialysis of Boca Raton   2900 N MILITARY TRL   STE 195   BOCA RATON   FL   33431-6308
1368   Affiliated   1980   Cedar Valley Dialysis   Cedar Valley Dialysis   1661 W RIDGEWAY AVE     WATERLOO   IA   50701-4541
1369   Affiliated   1981   West Union Dialysis   West Union Dialysis   405 HIGHWAY 150 N     WEST UNION   IA   52175-1003
1370   Affiliated   2161   Rockside   Rockside Dialysis (aka Independence, Parma II)   4801 ACORN DR     INDEPENDENCE   OH   44131-2566
1371   Affiliated   2263   Sunset   Sunset Dialysis Center (fka Sunrise II)   3071 GOLD CANAL DR     RANCHO CORDOVA   CA   95670-6129
1372   Affiliated   2442   Yosemite Street   Yosemite Street Dialysis   1650 W YOSEMITE AVE     MANTECA   CA   95337-5193
1373   Affiliated   2335   Jedburg   Jedburg Dialysis   2897 W 5TH NORTH ST     SUMMERVILLE   SC   29483-9674
1374   Affiliated   2441   Parker Dialysis   Parker Dialysis   10371 S PARK GLENN WAY   STE 18   PARKER   CO   80138-3885
1375   Affiliated   2296   Northgate   Northgate Dialysis Center (aka San Rafael-Terra)   650 LAS GALLINAS AVE     SAN RAFAEL   CA   94903-3620
1376   Affiliated   2271   The Nevada Center   The Nevada Dialysis Center (fka Warm Springs, Green Valley)   1510 W WARM SPRINGS RD   STE 1   HENDERSON   NV   89014-3586
1377   Affiliated   2091   Aventura   Aventura Kidney Center   22 SW 11TH ST   FLOOR 2   HALLANDALE BEACH   FL   33009-7038
1378   Affiliated   2408   US Grant Dialysis   US Grant Dialysis (fka Georgetown, Brown County)   458 HOME ST     GEORGETOWN   OH   45121-1408
1379   Affiliated   4400   Arbor Place   Arbor Place Dialysis   9559 HIGHWAY 5   STE 1   DOUGLASVILLE   GA   30135-1573
1380   Affiliated   4389   South Jacksonville   Jacksonville South Dialysis Center   14965 OLD SAINT AUGUSTINE RD   UNIT 114   JACKSONVILLE   FL   32258-9481
1381   Affiliated   2385   Somerville   Somerville Dialysis   12475 US HIGHWAY 64     SOMERVILLE   TN   38068-6029
1382   Affiliated   4321   District Heights   District Heights Dialysis (aka Pennsylvania Ave)   5701 SILVER HILL RD     DISTRICT HEIGHTS   MD   20747-1102
1383   Affiliated   2414   Edwardsville   Edwardsville Dialysis   235 S BUCHANAN ST     EDWARDSVILLE   IL   62025-2108
1384   Affiliated   2361   Broad St   South Broad Street Dialysis (aka S. Philadelphia II)   1172 S BROAD ST     PHILADELPHIA   PA   19146-3142
1385   Affiliated   2342   Las Vegas Pedidatrics   Las Vegas Pediatrics Dialysis (fka UMC Peds, DaVita Peds)   7271 W SAHARA AVE   STE 12   LAS VEGAS   NV   89117-2862
1386   Affiliated   1990   Apopka Dialysis   Apopka Dialysis   640 EXECUTIVE PARK CT     APOPKA   FL   32703-6075
1387   Affiliated   1991   Cassellberry Dialysis   Casselberry Dialysis   4970 S US HWY 17/92     CASSELBERRY   FL   32707-3888
1388   Affiliated   1992   Central Orlando Dialysis   Central Orlando Dialysis   2548 N ORANGE BLOSSOM TRL   STE 4   ORLANDO   FL   32804-4863
1389   Affiliated   1993   Sanford Dialysis   Sanford Dialysis   1701 W 1ST ST     SANFORD   FL   32771-1605
1390   Affiliated   1994   Winter Park Hemo Dialysis   Winter Park Hemo Dialysis   4100 METRIC DR   STE 3   WINTER PARK   FL   32792-6832
1391   Affiliated   2173   Graham   Graham Dialysis Center   10219 196TH ST CT E   STE C   GRAHAM   WA   98338-7792
1392   Affiliated   2316   Batavia   Batavia Dialysis   4000 GOLDEN AGE DR     BATAVIA   OH   45103-1913
1393   Affiliated   1967   Klamath Falls   Klamath Falls Dialysis   2230 N ELDORADO AVE     KLAMATH FALLS   OR   97601-6418
1394   Affiliated   2336   Longs   Longs Dialysis (fka Conway)   90 CLOVERLEAF DR   STE 36   LONGS   SC   29568-9262
1395   Affiliated   2452   Pooler   Pooler Dialysis   54 TRADERS WAY     POOLER   GA   31322-
1396   Affiliated   4380   Ohio Pike Dialysis   Ohio Pike Dialysis (aka Amelia)   1761 STATE ROUTE 125     AMELIA   OH   45102-2039
1397   Affiliated   2285   Canyon Springs   Canyon Springs Dialysis (aka Moreno Valley)   22555 ALESSANDRO BLVD     MORENO VALLEY   CA   92553-8533
1398   Affiliated   4306   Williamson   South Williamson Dialysis   204 APPALACHIAN PLAZA     SOUTH WILLIAMSON   KY   41503-9404
1399   Affiliated   4402   Gulf Shores   Gulf Shores Dialysis Center   3947 GULF SHORES PKWY   UNIT 15   GULF SHORES   AL   36542-2737

 

Page 72 of 136


1400   Affiliated   2496   Las Vegas Multi-Care Five Star   Five Star Dialysis Center (fka Las Vegas Multi-Care)   2400 TECH CENTER CT     LAS VEGAS   NV   89128-0804
1401   Affiliated   4358   North Vernon   North Vernon Dialysis   2340 N STATE HWY 7     NORTH VERNON   IN   47265-7183
1402   Affiliated   4316   Olympia   Olympia Dialysis Center   335 COOPER POINT RD NW   STE 15   OLYMPIA   WA   98502-4436
1403   Affiliated   4335   Monroeville   Monroeville Dialysis   2690 MONROEVILLE BLVD     MONROEVILLE   PA   15146-2302
1404   Affiliated   2317   East Galbraith   East Galbraith Dialysis   3877 E GALBRAITH RD   BLDG C   CINCINNATI   OH   45236-1500
1405   Affiliated   2261   San Marcos   San Marcos Dialysis Center   2135 MONTIEL RD   BLDG B   SAN MARCOS   CA   92069-3511
1406   Affiliated   4408   Winter Garden   Winter Garden Dialysis   1222 WINTER GARDEN VINELAND RD   BLDG 3 STE 1   WINTER GARDEN   FL   34787
1407   Affiliated   1926   Bremer County Dialysis   Relo-Bremer County Dialysis (5022-Cedar Valley Waverly Dialysis)   220 10th ST SW     WAVERLY   IA   50677-2930
1408   Affiliated   1927   Black Hawk Dialysis   Black Hawk Dialysis (Waterloo)   3421 W 9TH ST     WATERLOO   IA   50702-5401
1409   Affiliated   2218   Downey Landing   Downey Landing Dialysis Center (aka Downey-Kaiser)   11611 BELLFLOWER BLVD     DOWNEY   CA   90241-5408
1410   Affiliated   2427   Tucson Central   Tucson Central Dialysis   2901 E GRANT RD     TUCSON   AZ   85716-2717
1411   Affiliated   4377   Hamburg   Hamburg Dialysis (fka Lexington)   1745 ALYSHEBA WAY     LEXINGTON   KY   40509-9013
1412   Affiliated   2150   Midtown Norfolk   Midtowne Norfolk Dialysis (aka Ghent II)   2201 COLONIAL AVE     NORFOLK   VA   23517-1928
1413   Affiliated   2394   Yonkers II   Yonkers East Dialysis Center   5 ODELL PLZ   STE 131   YONKERS   NY   10701-1406
1414   Affiliated   2364   Caldwell   Caldwell Dialysis Center   821 S SMEED PKWY     CALDWELL   ID   83605-5130
1415   Affiliated   2278   Hesperia   Hesperia Dialysis Center   14135 MAIN ST   UNIT 51   HESPERIA   CA   92345-8097
1416   Affiliated   2339   Sealy   Sealy Dialysis   2242 CHAMPIONSHIP DR     SEALY   TX   77474-8026
1417   Affiliated   2438   Hearne   Hearne Dialysis Center   106 CEDAR ST     HEARNE   TX   77859-2523
1418   Affiliated   1998   Stockton Kidney Center   Stockton Kidney Center   1523 E MARCH LN   STE 2   STOCKTON   CA   95210-5607
1419   Affiliated   5525   University of South Florida   USF Dialysis   10770 N 46TH ST STE A100     TAMPA   FL   33617-3465
1420   Affiliated   4424   Westborough   Westborough Dialysis Center (fka South San Francisco, Daly City)   925 EL CAMINO REAL     SOUTH SAN FRANCISCO   CA   94080-3203
1421   Affiliated   4359   Rush County   Rush County Dialysis   1400 N CHERRY ST     RUSHVILLE   IN   46173-1097
1422   Affiliated   4339   Defuniak Springs   Defuniak Springs Dialysis   1045 US HWY 331 S   DEFUNIAK SHOPPING PLAZA   DEFUNIAK SPRINGS   FL   32435-3375
1423   Affiliated   2181   Foster city   Foster City Dialysis (fka Belmont)   1261 E HILLSDALE BLVD   STE 2   FOSTER CITY   CA   94404-1236
1424   Affiliated   4427   Red Bank   Redbank Village Dialysis (Cincinnati)   3960 RED BANK RD   STE 16   CINCINNATI   OH   45227-3421
1425   Affiliated   4448   Southport   Southport Dialysis Center   1513 N HOWE ST   STE 15   SOUTHPORT   NC   28461-2770
1426   Affiliated   4446   Orlando Park   Orlando Park Dialysis   5397 W COLONIAL DR   STE 12   ORLANDO   FL   32808-7647
1427   Affiliated   4431   Harrisburg   Harrisburg Dialysis Center (aka Concord)   3310 PERRY ST     CONCORD   NC   28027-3901
1428   Affiliated   2352   Waycross   Satilla River Dialysis   308 CARSWELL AVE     WAYCROSS   GA   31501-4762
1429   Affiliated   4455   Timberlake   Timberlake Dialysis (Kansas City)   12110 HOLMES RD     KANSAS CITY   MO   64145-1707
1430   Affiliated   4447   Dexter   Dexter Dialysis   2010 N OUTER RD     DEXTER   MO   63841
1431   Affiliated   4426   Norwood   Norwood Dialysis (Cincinnati)   2300 WALL ST     CINCINNATI   OH   45212-2781
1432   Affiliated   4420   Peachtree City   Peachtree City Dialysis   2830 W HWY 54   BLDG 1 STE J AND K   PEACHTREE CITY   GA   30269-1026
1433   Affiliated   5516   Rogue Valley   Rogue Valley Dialysis   760 GOLF VIEW DR   UNIT 1   MEDFORD   OR   97504-9685
1434   Affiliated   5517   Redwood Dialysis   Redwood Dialysis   201 SW L ST     GRANTS PASS   OR   97526-2913
1435   Affiliated   4410   Tucker   Tucker Dialysis   4434 HUGH HOWELL RD     TUCKER   GA   30084-4905
1436   Affiliated   4386   Shepherdsville   Shepherdsville Dialysis Center   150 BROOKS WAY   STE 15   BROOKS   KY   40109-6105
1437   Affiliated   4399   Muscle Shoals   Muscle Shoals Dialysis   712 STATE ST     MUSCLE SHOALS   AL   35661-2940
1438   Affiliated   2463   Tel Huron   Tel-Huron Dialysis (fka Waterford)   225 SUMMIT DR     WATERFORD   MI   48328-3364
1439   Affiliated   2481   Cherry Valley   Cherry Valley Dialysis (aka Newark)   1627 W MAIN ST     NEWARK   OH   43055-1345
1440   Affiliated   2437   Taylor   Taylor Dialysis   3100 W 2ND ST     TAYLOR   TX   76574
1441   Affiliated   4430   Forrest City   Forrest City Dialysis   1501 N WASHINGTON ST     FORREST CITY   AR   72335-2152
1442   Affiliated   4309   Kaufman   Kaufman Dialysis   2851 MILLENNIUM DR     KAUFMAN   TX   75142-8865
1443   Affiliated   4348   Artesia   Artesia Dialysis   702 N 13TH ST     ARTESIA   NM   88210-1166
1444   Affiliated   2381   North Hills   North Hills Dialysis   7927 BOULEVARD 26     NORTH RICHLAND HILLS   TX   76180-7103
1445   Affiliated   4428   Millington   Millington Dialysis   8510 WILKINSVILLE RD   STE 121   MILLINGTON   TN   38053-1537
1446   Affiliated   5519   Adams County   Adams County Dialysis   436 N 10TH ST     QUINCY   IL   62301-4152
1447   Affiliated   5518   Hannibal   Hannibal Dialysis   3140 PALMYRA ROAD     HANNIBAL   MO   63401-2204
1448   Affiliated   5520   Pittsfield   Pittsfield Dialysis   640 W WASHINGTON ST     PITTSFIELD   IL   62363-1350
1449   Affiliated   4463   Villa of Waterbury   Villa of Waterbury (fka Kissker Microcenter)   929 WATERBURY FALLS DR     O’FALLON   MO   63368-2202
1450   Affiliated   2465   Washington DC Nursing Facility   Washington DC Nursing Facility   2425 25TH ST SE     WASHINGTON   DC   20020-3408
1451   Affiliated   4325   Moscow   Moscow Dialysis Center   212 RODEO DR   STE 11   MOSCOW   ID   83843-9798
1452   Affiliated   2402   Chinook Kidney Center   Chinook Kidney Center (aka Richland)   1315 AARON DR   BLDG C1   RICHLAND   WA   99352-4678
1453   Affiliated   4416   River’s Edge   Rivers Edge Dialysis (aka Athens)   1006 E STATE ST   STE B   ATHENS   OH   45701-2121

 

Page 73 of 136


1454   Affiliated   5530   North Glendale Dialysis   North Glendale Dialysis   1505 WILSON TER STE 190     GLENDALE   CA   91206-4015
1455   Affiliated   4373   Everett   Everett Dialysis Center (fka Snohomish 2)   8130 EVERGREEN WAY     EVERETT   WA   98203-6419
1456   Affiliated   2069   Harbourview   Harbour View Dialysis (aka Churchland, Suffolk)   1039 CHAMPIONS WAY   BLDG 4   SUFFOLK   VA   23435-3761
1457   Affiliated   4357   Capelville   Capelville Dialysis Center   7008 E SHELBY DR     MEMPHIS   TN   38125-3416
1458   Affiliated   4485   San Leandro   San Leandro Dialysis (Bayfair Mall)   15555 E 14TH   STE 52   SAN LEANDRO   CA   94578-1900
1459   Affiliated   4317   Mill Creek   Mill Creek Dialysis Center (Snohomish/Everett)   18001 BOTHELL EVERETT HWY   STE 112   BOTHELL   WA   98012-1661
1460   Affiliated   2470   Seaview   Seaview Dialysis Center   101 18TH ST SE     LONG BEACH   WA   98631
1461   Affiliated   2461   East Tampa   East Tampa Dialysis (Ybor City)   1701 E 9TH AVE     YBOR CITY   FL   33605-3801
1462   Affiliated   5522   Detroit Road Dialysis   Detroit Road Dialysis   7901 DETROIT AVE     CLEVELAND   OH   44102-2828
1463   Affiliated   5523   St V Quadrangle Dialysis   St V Quadrangle Dialysis   2302 COMMUNITY COLLEGE AVE     CLEVELAND   OH   44115-3117
1464   Affiliated   5524   Westshore Dialysis   Westshore Dialysis   29000 CENTER RIDGE RD     WESTLAKE   OH   44145-5293
1465   Affiliated   2468   Magnolia Dialysis Center Texas   Magnolia Dialysis Center   17649 FM 1488 RD     MAGNOLIA   TX   77354-5235
1466   Affiliated   4471   Highland County   Highland County Dialysis (Hillsboro)   120 ROBERTS LN   STE 4   HILLSBORO   OH   45133-7608
1467   Affiliated   4313   Rockwall   Rockwall Dialysis   2455 RIDGE RD   STE 11   ROCKWALL   TX   75087-5530
1468   Affiliated   4354   Great Northern   Villa of Great Northern (fka North Olmsted)   22710 FAIRVIEW CENTER DR   STE 1   FAIRVIEW PARK   OH   44126-3607
1469   Affiliated   2440   Ridgeland   Ridgeland Dialysis   112 WEATHERSBY ST     RIDGELAND   SC   29936-9514
1470   Affiliated   2334   Livermore   Livermore Dialysis   3201 DOOLAN RD   STE 175   LIVERMORE   CA   94551-9605
1471   Affiliated   2265   Westlake Daly city   Westlake Daly City Dialysis (fka Colma)   2201 JUNIPERO SERRA BLVD   STE 175   DALY CITY   CA   94014-1908
1472   Affiliated   4488   12th Street Covington   12th Street Covington Dialysis   1500 JAMES SIMPSON JR WAY   STE 11   COVINGTON   KY   41011
1473   Affiliated   4384   Bourbon County   Bourbon County Dialysis (fka Paris)   213 LETTON DR   PARIS TOWNE SQUARE   PARIS   KY   40361-2251
1474   Affiliated   2499   Calverton   Calverton Dialysis   4780 CORRIDOR PL   STE C   BELTSVILLE   MD   20705-1165
1475   Affiliated   2199   Aborn   Aborn Dialysis (fka East San Jose)   3162 S WHITE RD   STE 1   SAN JOSE   CA   95148-4019
1476   Affiliated   4438   Clermont   Clermont County Dialysis (Milford,Goshen)   5901 MONTCLAIR BLVD   STE 1   MILFORD   OH   45150-2547
1477   Affiliated   4365   Rita Ranch   Rita Ranch Dialysis (aka Tucson East II)   7355 S HOUGHTON RD   STE 11   TUCSON   AZ   85747-9379
1478   Affiliated   4333   Wake Forest   Wake Forest Dialysis Center   11001 INGLESIDE PL     RALEIGH   NC   27614-8577
1479   Affiliated   4472   Colonial Springs   Colonial Springs Dialysis (fka Powder Springs)   2840 EAST WEST CONNECTOR   STE 35   AUSTELL   GA   30106-6813
1480   Affiliated   2474   Central Dallas   DaVita Central Dallas Dialysis   9500 N CENTRAL EXPY     DALLAS   TX   75231-5002
1481   Affiliated   2188   Sanger   Sanger Sequoia Dialysis   2517 JENSEN AVE   BLDG B   SANGER   CA   93657-2251
1482   Affiliated   4421   Conyers   Conyers Dialysis   1501 MILSTEAD RD NE     CONYERS   GA   30012-3838
1483   Affiliated   4337   Duncanville   Duncanville Dialysis (Cedar Hill)   270 E HIGHWAY 67   STE 1   DUNCANVILLE   TX   75137-4428
1484   Affiliated   4417   Gateway   Gateway Dialysis (Ft.Myers)   5705 LEE BLVD     LEHIGH ACRES   FL   33971-6342
1485   Affiliated   4487   Derry   Derry Dialysis   1 ACTION BLVD   STE 2   LONDONDERRY   NH   03053-3428
1486   Affiliated   4461   Villa of Wentzville Microcenter   Villa of Wentzville (Microcenter)   1126 W PEARCE BLVD   STE 116 & 118   WENTZVILLE   MO   63385-1053
1487   Affiliated   1925   Buchanan County Dialysis   Buchanan County Dialysis (Independence)   1600 1ST ST E     INDEPENDENCE   IA   50644-3155
1488   Affiliated   2450   Hoosier Hills   Hoosier Hills Dialysis   143 S KINGSTON DR     BLOOMINGTON   IN   47408-6342
1489   Affiliated   4492   Palm Breeze   Palm Breeze Dialysis (fka North Port)   14942 TAMIAMI TRL   STE E   NORTH PORT   FL   34287-2705
1490   Affiliated   4362   Big Oaks   Big Oaks Dialysis   5623 W TOUHY AVE     NILES   IL   60714-4019
1491   Affiliated   4407   Pinellas West Shore   Pinellas West Shore Dialysis   3451 66TH ST N   STE A   ST PETERSBURG   FL   33710-1568
1492   Affiliated   2267   Plano   Plano Dialysis   481 SHILOH RD   STE 1   PLANO   TX   75074-7231
1493   Affiliated   4350   Fairview   Villa of Fairview Park (fka Fairview Park Dialysis)   19050 LORAIN RD     FAIRVIEW PARK   OH   44126-1915
1494   Affiliated   2380   Ave Marisa   Ave Maria Dialysis (fka Immokalee)   5340 USEPPA DR     AVE MARIA   FL   34142-5051
1495   Affiliated   5037   Warminster   Franklin Commons Dialysis (fka Warminster)   720 JOHNSVILLE BLVD   STE 8   WARMINSTER   PA   18974-3546
1496   Affiliated   2446   Ripley   Ripley Dialysis Center   854 HWY 51 S     RIPLEY   TN   38063-5536
1497   Affiliated   5538   St Charles / Riverbend   River Bend Dialysis (St. Charles Parish)   1057 PAUL MAILLARD RD   ST B135   LULING   LA   70070-4349
1498   Affiliated   5570   Midwest Springfield   Midwest Springfield Dialysis   2200 N LIMESTONE ST STE 104     SPRINGFIELD   OH   45503-2692
1499   Affiliated   5571   Midwest Fairborn   Midwest Fairborn Dialysis   1266 N BROAD ST     FAIRBORN   OH   45324-5549
1500   Affiliated   5572   Midwest Urbana   Midwest Urbana Dialysis   1430 E US HIGHWAY 36     URBANA   OH   43078-9112
1501   Affiliated   5531   Camarillo   Camarillo Dialysis   2438 N PONDEROSA DR STE C101     CAMARILLO   CA   93010-2465
1502   Affiliated   5532   Thousand Oaks   Thousand Oaks Dialysis   375 ROLLING OAKS DR STE 100     THOUSAND OAKS   CA   91361-1024
1503   Affiliated   5533   Simi Valley   Simi Valley Dialysis   2950 SYCAMORE DR STE 100     SIMI VALLEY   CA   93065-1210
1504   Affiliated   5534   Santa Paula   Santa Paula Dialysis   253 MARCH ST     SANTA PAULA   CA   93060-2511
1505   Affiliated   5548   Ventura   Ventura Dialysis   2705 LOMA VISTA RD STE 101     VENTURA   CA   93003-1596
1506   Affiliated   4468   Villa of St. John   Villa of St John (Crossing Microcenter-MO)   9030 SAINT CHARLES ROCK RD     SAINT LOUIS   MO   63114-4246
1507   Affiliated   4372   Whidbey Island   Whidbey Island Dialysis Center   32650 STATE RD 20   BLDG E STE 18   OAK HARBOR   WA   98277-2641

 

Page 74 of 136


1508   Affiliated   4437   Baytown   Baytown Dialysis   4665 GARTH RD   STE 9   BAYTOWN   TX   77521-2261
1509   Affiliated   2475   Highland Ranch   Highland Ranch Dialysis Center   7223 CHURCH ST STE A14     HIGHLAND   CA   92346-6837
1510   Affiliated   4474   Tiptonville   Tiptonville Dialysis   795 HAMRA ST     TIPTONVILLE   TN   38079-1663
1511   Affiliated   1902   Carabello   Carabello Dialysis Center   757 E WASHINGTON BLVD     LOS ANGELES   CA   90021-3016
1512   Affiliated   5573   Palmetto   Palmetto Dialysis   317 PROFESSIONAL PARK RD     CLINTON   SC   29325-7625
1513   Affiliated   5574   Greer South   Greer South Dialysis   3254 BRUSHY CREEK RD     GREER   SC   29650-1000
1514   Affiliated   5575   Greenville West End   Greenville West End Dialysis   605 S ACADEMY ST     GREENVILLE   SC   29601-2407
1515   Affiliated   5576   Fountain Inn   Fountain Inn Dialysis   298 CHAPMAN RD     FOUNTAIN INN   SC   29644-6129
1516   Affiliated   5558   Sellersville   Sellersville Dialysis   1112 OLD BETHLEHEM PIKE     SELLERSVILLE   PA   18960-1423
1517   Affiliated   5564   Humbolt Ridge   Humboldt Ridge Dialysis   2211 N HUMBOLDT BLVD     MILWAUKEE   WI   53212-3507
1518   Affiliated   5565   West Appleton   West Appleton Dialysis   10130 W APPLETON AVE   STE 5   MILWAUKEE   WI   53225-2579
1519   Affiliated   5566   Bay Shore   Bay Shore Dialysis   5650 N GREEN BAY AVE   STE 15   GLENDALE   WI   53209-4449
1520   Affiliated   5567   South Ridge   South Ridge Dialysis   4848 S 76TH ST   STE 1   GREENFIELD   WI   53220-4361
1521   Affiliated   5568   Bluemound   Bluemound Dialysis   601 N 99TH ST   STE 1   MILWAUKEE   WI   53226-4362
1522   Affiliated   4385   Versailles   Versailles Dialysis   480 LEXINGTON RD     VERSAILLES   KY   40383-1918
1523   Affiliated   5035   Magnolia Oaks   Magnolia Oaks Dialysis (aka Hinesville)   2377 HWY 196 W     HINESVILLE   GA   31313-8036
1524   Affiliated   4489   Mesa County   Mesa County Dialysis (Grand Junction)   561 25 RD   STE D   GRAND JUNCTION   CO   81505-1303
1525   Affiliated   297   West Bloomfield   West Bloomfield Dialysis   6010 W MAPLE RD   STE 215   WEST BLOOMFIELD   MI   48322-4406
1526   Affiliated   5550   Crystal Springs Dialysis   Crystal Springs Dialysis   720 COG CIRCLE     CRYSTAL LAKE   IL   60014-7301
1527   Affiliated   5551   Cobblestone Dialysis   Cobblestone Dialysis   934 CENTER ST   STE A   ELGIN   IL   60120-2125
1528   Affiliated   5586   Oak Springs Dialysis   Oak Springs Dialysis   764 LOCUST AVE     WASHINGTON   PA   15301-2756
1529   Affiliated   5010   Maple Valley Plaza   Maple Valley Plaza Dialysis (Farmington)   649 MAPLE VALLEY DR     FARMINGTON   MO   63640-1993
1530   Affiliated   4433   Floyd Curl   Floyd Curl Dialysis (San Antonio)   9238 FLOYD CURL DR   STE 12   SAN ANTONIO   TX   78240-1691
1531   Affiliated   2387   Mission Valley   Mission Valley Dialysis (aka McAllen)   1203 ST CLAIRE BLVD 9B     MISSION   TX   78572-6601
1532   Affiliated   2180   Silver Lake   Silver Lake Dialysis   2723 W TEMPLE ST     LOS ANGELES   CA   90026-4723
1533   Affiliated   5578   Lake Park Dialysis   Lake Park Dialysis   1531 E HYDE PARK BLVD     CHICAGO   IL   60615-3039
1534   Affiliated   5579   Stoney Island Dialysis   Stony Island Dialysis   8725 S STONY ISLAND AVE     CHICAGO   IL   60617-2709
1535   Affiliated   5580   Woodlawn Dialysis   Woodlawn Dialysis   1164 E 55TH ST     CHICAGO   IL   60615-5115
1536   Affiliated   4440   Jefferson Ave   Jefferson Avenue Dialysis (aka Village Parkway, Hampton)   11234 JEFFERSON AVE     NEWPORT NEWS   VA   23601-2207
1537   Affiliated   4381   Robinson   Robinson Dialysis   1215 N ALLEN ST   STE B   ROBINSON   IL   62454-1100
1538   Affiliated   4320   Gateway Plaza   Gateway Plaza Dialysis (aka Willowbrook)   1580 W ROSECRANS AVE     COMPTON   CA   90222-3700
1539   Affiliated   4329   Pasadena Foothills   Pasadena Foothills Dialysis (fka Arcadia)   3722 E COLORADO BLVD     PASADENA   CA   91107-3803
1540   Affiliated   914   Live Oak Dialysis   Live Oak Dialysis (fka San Antonio)   6700 RANDOLPH BLVD   STE 11   LIVE OAK   TX   78233-4222
1541   Affiliated   5031   Frackville   Frackville Dialysis (aka JV_Pottsville)   801 SCHUYLKILL MALL     FRACKVILLE   PA   17931-2524
1542   Affiliated   5038   Castor   Cottman Kidney Center (Castor, NE Philadelphia)   7198 CASTOR AVE     PHILADELPHIA   PA   19149-1105
1543   Affiliated   4351   Villa of North Ridgevelle   Villa of North Ridgeville   35143 CENTER RIDGE RD     NORTH RIDGEVILLE   OH   44039-3089
1544   Affiliated   5503   Thorn Run Dialysis   Thorn Run Dialysis   1136 THORN RUN RD   STE J1   MOON TOWNSHIP   PA   15108
1545   Affiliated   5504   Allegheny Valley   Allegheny Valley Dialysis   1620 PACIFIC AVE   HEIGHTS PLAZA SHOPPING CENTER   NATRONA HEIGHTS   PA   15065-2101
1546   Affiliated   5506   Northside   Northside Dialysis (fka Allegheny General)   320 E NORTH AVE   4TH FL, SOUTH TOWER   PITTSBURGH   PA   15212-4756
1547   Affiliated   5507   Somerset   Somerset County Dialysis   229 S KIMBERLY AVE   STE 1   SOMERSET   PA   15501-2022
1548   Affiliated   4493   Carthage   Carthage Dialysis   165 SAVANNAH GARDENS DR     CARTHAGE   NC   28327
1549   Affiliated   2464   Riverwood Dialysis   Riverwood Dialysis (fka Nine Mile, Tree City & Southfield)   24467 W 10 MILE RD     SOUTHFIELD   MI   48033-2931
1550   Affiliated   4415   Burton   Burton Dialysis (fka Flint Northeast)   4015 DAVISON RD     BURTON   MI   48509-1401
1551   Affiliated   4490   Black Canyon   Black Canyon Dialysis (Montrose)   3421 S RIO GRANDE AVE   UNIT D   MONTROSE   CO   81401-4840
1552   Affiliated   4394   Memphis Midtown   Memphis Midtown Dialysis   3430 SUMMER AVE     MEMPHIS   TN   38122-3610
1553   Affiliated   5539   Stonecrest Dialysis   Stonecrest Dialysis   1302 E STATE ST     ROCKFORD   IL   61104-2228
1554   Affiliated   4412   West Plano   West Plano Dialysis   5036 TENNYSON PKWY     PLANO   TX   75024-3002
1555   Affiliated   2217   Redwood City   Redwood City Dialysis (fka Palo Alto)   1000 MARSHALL ST     REDWOOD CITY   CA   94063-2027
1556   Affiliated   1592   State Fair   State Fair Dialysis   19800 WOODWARD AVE     DETROIT   MI   48203-5102
1557   Affiliated   5589   ADC of Ft Lauderdale   Advanced Dialysis Center of Fort Lauderdale   911 E OAKLAND PARK BLVD     OAKLAND PARK   FL   33334-2725
1558   Affiliated   5008   Dover   Dover Community Dialysis (New Philadelphia)   899 E IRON AVE     DOVER   OH   44622-2097
1559   Affiliated   5045   McMinnville   McMinnville Dialysis   200 NE NORTON LN     MCMINNVILLE   OR   97128-8470
1560   Affiliated   5007   Sparta   Sparta Dialysis   150 SAM WALTON DR   STE 8   SPARTA   TN   38583-8818
1561   Affiliated   4409   Kendall   Kendall Kidney Center (fka Dadeland)   8364 MILLS DR   STE 174   MIAMI   FL   33183-4806

 

Page 75 of 136


1562   Affiliated   4397   Abbeville   Abbeville Dialysis   904 W GREENWOOD ST     ABBEVILLE   SC   29620
1563   Affiliated   2453   Delta View   Delta View Dialysis   1150 E LELAND RD     PITTSBURG   CA   94565-5319
1564   Affiliated   5013   Wolf River   Wolf River Dialysis (Germantown)   7990 TRINITY PL   STE 11   CORDOVA   TN   38018-7731
1565   Affiliated   5601   San Luis Obispo Dialysis   San Luis Obispo Dialysis   1043 MARSH ST     SAN LUIS OBISPO   CA   93401-3629
1566   Affiliated   5602   Templeton Dialysis   Templeton Dialysis   1310 LAS TABLAS RD   STE 11   TEMPLETON   CA   93465-9746
1567   Affiliated   5603   Pismo Beach Dialysis   Pismo Beach Dialysis   320 JAMES WAY   STE 11   PISMO BEACH   CA   93449-2813
1568   Affiliated   5583   Lincoln Way Dialysis   Lincoln Way Dialysis   1303 LINCOLN WAY STE A     WHITE OAK   PA   15131-1603
1569   Affiliated   5023   Grundy Center   Grundy Center Dialysis   101 E J AVENUE     GRUNDY CENTER   IA   50638-2031
1570   Affiliated   3862   Pickens County   Pickens County Dialysis   289 WILLIAM E HILL DR.   STE A   CARROLLTON   AL   35447
1571   Affiliated   5032   Willow Grove   Willow Grove Dialysis (Abington-Maplewood)   1849 DAVISVILLE RD     WILLOW GROVE   PA   19090-4111
1572   Affiliated   2255   Amherst   Amherst Dialysis (Lorain County)   3200 COOPER FOSTER PRK RD W     LORAIN   OH   44053-3654
1573   Affiliated   2220   South Fort Worth   South Fort Worth Dialysis   6260 SOUTHWEST BLVD     BENBROOK   TX   76109-6906
1574   Affiliated   5521   Jerseyville Dialysis   Jerseyville Dialysis   917 S STATE ST     JERSEYVILLE   IL   62052-2344
1575   Affiliated   5605   Independence County Dialysis   Independence County Dialysis   1700 HARRISON ST   STE F   BATESVILLE   AR   72501-7315
1576   Affiliated   5606   Jackson County Dialysis   Jackson County Dialysis   1912 MCLAIN ST   PRATT SQUARE   NEWPORT   AR   72112-3659
1577   Affiliated   5607   Searcy Dialysis   Searcy Dialysis   3208 LANGLEY DR     SEARCY   AR   72143-6020
1578   Affiliated   5608   Springhill Dialysis   Springhill Dialysis   3401 SPRINGHILL DR   STE 19   NORTH LITTLE ROCK   AR   72117-2925
1579   Affiliated   5609   Pulaski County Dialysis   Pulaski County Dialysis   202 JOHN HARDEN DR     JACKSONVILLE   AR   72076-3775
1580   Affiliated   5610   Little Rock Midtown Dialysis   Little Rock Midtown Dialysis   2 LILE CT   STE 12A   LITTLE ROCK   AR   72205-6241
1581   Affiliated   5611   Saline County Dialysis   Saline County Dialysis   1200 N MAIN ST   STE 2   BENTON   AR   72015-3341
1582   Affiliated   5612   Conway Dialysis   Conway Dialysis   2445 CHRISTINA LANE     CONWAY   AR   72034
1583   Affiliated   5614   Valley Baptist Harlingen Dialysis   Valley Baptist-Harlingen Dialysis   2220 HAINE DR STE 40     HARLINGEN   TX   78550-8584
1584   Affiliated   5615   Valley Baptist Raymondville Dialysis   Valley Baptist-Raymondville Dialysis   894 FM 3168     RAYMONDVILLE   TX   78580-4519
1585   Affiliated   2455   Hawaiian Gardens   Hawaiian Gardens Dialysis   12191 226TH ST     HAWAIIAN GARDENS   CA   90716-1510
1586   Affiliated   2310   Huntington park   Huntington Park Dialysis   5942 RUGBY AVE     HUNTINGTON PARK   CA   90255-2803
1587   Affiliated   2462   Poinciana   Poinciana Dialysis   1002 CYPRESS PKWY     KISSIMMEE   FL   34758-3328
1588   Affiliated   5005   Southtowns   Southtowns Dialysis (Hamburg)   4910 CAMP RD   STE 1   HAMBURG   NY   14075-2617
1589   Affiliated   5635   Parma Heights Dialysis   Parma Heights Dialysis   9050 N CHURCH DR     PARMA HEIGHTS   OH   44130-4701
1590   Affiliated   5636   Hillard Dialysis   Hilliard Dialysis   19133 HILLIARD BLVD     ROCKY RIVER   OH   44116-2907
1591   Affiliated   5546   Pacific Dialysis   Pacific Dialysis   2351 CLAY ST   FL 4   SAN FRANCISCO   CA   94115-1931
1592   Affiliated   5547   Davies Dialysis   Davies Dialysis   45 CASTRO ST   SOUTH TOWER 2ND FL   SAN FRANCISCO   CA   94114-1032
1593   Affiliated   4486   Newburgh   Newburgh Dialysis   4311 HIGHWAY 261   STE A   NEWBURGH   IN   47630-2653
1594   Affiliated   5052   Enterprise   Enterprise Dialysis (fka Geneva)   6002 BOLL WEEVIL CIRCLE     ENTERPRISE   AL   36330-9420
1595   Affiliated   4387   State Line   State Line Dialysis   2049 E SHELBY DR     MEMPHIS   TN   38116-7639
1596   Affiliated   5108   Cape Coral North   Cape Coral North Dialysis   1315 SE 8TH TERRACE     CAPE CORAL   FL   33990-3213
1597   Affiliated   5044   Willard Ave   Willard Avenue Dialysis (Newington)   445E WILLARD AVE     NEWINGTON   CT   06111-2318
1598   Affiliated   4363   West Lawn   West Lawn Dialysis (aka Midway)   7000 S PULASKI RD     CHICAGO   IL   60629-5842
1599   Affiliated   4353   Villa of Lakewood   Villa of Lakewood (Northcoast)   14050 MADISON AVE     LAKEWOOD   OH   44107-4530
1600   Affiliated   5054   North Carrolton   North Carrollton Dialysis (Parkview)   195 PARKWOOD CIRCLE     CARROLLTON   GA   30117-8756
1601   Affiliated   5620   Sikeston Jaycee Regional Dialysis   Sikeston Jaycee Regional Dialysis   135 PLAZA DR STE 101     SIKESTON   MO   63801-5148
1602   Affiliated   2244   Radcliff   Radcliff Dialysis   180 E LINCOLN TRAIL BLVD     RADCLIFF   KY   40160-1254
1603   Affiliated   4452   McAfee   McAfee Dialysis (Candler Road Decatur)   1987 CANDLER RD   STE C   DECATUR   GA   30032-4212
1604   Affiliated   5036   Avon   Avon Dialysis (Indy West)   9210 ROCKVILLE RD   STE D   INDIANAPOLIS   IN   46234-2669
1605   Affiliated   2485   Anaheim West   Anaheim West Dialysis   1821 W LINCOLN AVE     ANAHEIM   CA   92801-6731
1606   Affiliated   5043   Port Saint Joe   Port Saint Joe Dialysis   3871 HIGHWAY 98 E   STE 11   PORT ST. JOE   FL   32456-5318
1607   Affiliated   5056   Hayward Mission Hills   Hayward Mission Hills Dialysis   1661 INDUSTRIAL PKWY W     HAYWARD   CA   94544-7046
1608   Affiliated   2472   Cypress Woods Northwest   Cypress Woods Northwest Dialysis (aka NW Houston)   20320 NORTHWEST FWY   STE 1   HOUSTON   TX   77065-
1609   Affiliated   5641   Willow Creek Dialysis   Willow Creek Dialysis   1139 WARWICK WAY     RACINE   WI   53406-5661
1610   Affiliated   5642   Harbor View Dialysis   Harbor View Dialysis   818 6TH ST     RACINE   WI   53403-1176
1611   Affiliated   4451   Red River   Red River Dialysis (fka Shreveport South)   9205 LINWOOD AVE     SHREVEPORT   LA   71106-7006
1612   Affiliated   2392   South Dade Kidney Center   South Dade Kidney Center (Coral Reef)   11040 SW 184TH ST     CUTLER BAY   FL   33157-6602
1613   Affiliated   5604   Niagara Falls Memorial Dialysis   Niagara Falls Memorial Dialysis (was NF Kidney Care Center)   621 10TH ST     NIAGARA FALLS   NY   14301-1813
1614   Affiliated   5617   Silverado Dialysis   Silverado Dialysis   1100 TRANCAS ST   STE 266 AND 267   NAPA   CA   94558-2921
1615   Affiliated   5621   Prairie River Dialysis   Prairie River Dialysis   601 S CENTER AVE     MERRILL   WI   54452-3404

 

Page 76 of 136


1616   Affiliated   5622   Stevens Point Dialysis   Stevens Point Dialysis   900 ILLINOIS AVE   5th FLR   STEVENS POINT   WI   54481-2885
1617   Affiliated   5623   Grand Seasons Dialysis   Grand Seasons Dialysis   190 GRAND SEASONS DR     WAUPACA   WI   54981-8219
1618   Affiliated   5624   Wausau Dialysis   Wausau Dialysis   2600 STEWART AVE   STE 144   WAUSAU   WI   54401-1403
1619   Affiliated   5625   Pine Crest Dialysis   Pine Crest Dialysis   232 S COURTNEY ST   STE 2   RHINELANDER   WI   54501-3319
1620   Affiliated   5626   Meadow Lane Dialysis   Meadow Lane Dialysis   1120 PINE ST     STANLEY   WI   54768-1297
1621   Affiliated   5627   Wisconsin Rapids Dialysis   Wisconsin Rapids Dialysis   1041B HILL ST     WISCONSIN RAPIDS   WI   54494-5221
1622   Affiliated   5628   Marshfield Dialysis   Marshfield Dialysis   123 NORTHRIDGE ST     MARSHFIELD   WI   54449-8341
1623   Affiliated   5629   Northern Star Dialysis   Northern Star Dialysis   311 ELM ST     WOODRUFF   WI   54568-9190
1624   Affiliated   5632   Ames Mary Greeley Dialysis   Ames Mary Greeley Dialysis   2322 E 13TH ST     AMES   IA   50010-5669
1625   Affiliated   5633   Marshalltown Mary Greeley Dialysis   Marshalltown Mary Greeley Dialysis   3120 S 2ND ST     MARSHALLTOWN   IA   50158-4614
1626   Affiliated   5634   Iowa Falls Mary Greeley Dialysis   Iowa Falls Mary Greeley Dialysis   701 WASHINGTON AVE     IOWA FALLS   IA   50126-2100
1627   Affiliated   5649   Dialysis Center of Hutchinson   Dialysis Center of Hutchinson   1901 N WALDRON ST     HUTCHINSON   KS   67502-1129
1628   Affiliated   5650   Amarillo Dialysis   Amarillo Dialysis   8604 S COULTER ST     AMARILLO   TX   79119-7379
1629   Affiliated   4495   Sagemeadow   Sagemeadow Dialysis (Houston)   10923 SCARSDALE BLVD     HOUSTON   TX   77089-6024
1630   Affiliated   5009   McKinney   McKinney Dialysis   4717 MEDICAL CENTER DR     MCKINNEY   TX   75069-1870
1631   Affiliated   4499   Scottsburg   Scottsburg Dialysis   1619 W MCCLAIN AVE     SCOTTSBURG   IN   47170-1161
1632   Affiliated   2108   Snake River   Snake River Dialysis Center (fka Blackfoot)   1491 PARKWAY DR     BLACKFOOT   ID   83221-1667
1633   Affiliated   5034   Southpoint   Southpoint Dialysis (aka Durham South)   415 W NC HWY 54     DURHAM   NC   27713-7516
1634   Affiliated   5643   Burlingame Dialysis   Burlingame Dialysis   1720 EL CAMINO REAL   STE 12   BURLINGAME   CA   94010-3225
1635   Affiliated   5644   Mills Dialysis   Mills Dialysis   100 S SAN MATEO DR     SAN MATEO   CA   94401-3805
1636   Affiliated   5646   Stuebenville   Steubenville Dialysis   4000 JOHNSON RD     STEUBENVILLE   OH   43952-2300
1637   Affiliated   5656   Premiere Kidney Center of Newark   Premiere Kidney Center of Newark   65 SOUTH TERRACE AVE     NEWARK   OH   43055-1355
1638   Affiliated   5029   Calvine   Calvine Dialysis (Sacramento)   8243 E STOCKTON BLVD   STE 1   SACRAMENTO   CA   95828-8200
1639   Affiliated   4445   Durham Corners dialysis   Durham Corners Dialysis (South Plainfield)   241 DURHAM AVE     SOUTH PLAINFIELD   NJ   07080-2504
1640   Affiliated   4475   Mt Morris   Mt Morris Dialysis (aka North Flint)   6141 N. SAGINAW RD     MOUNT MORRIS   MI   48458-2403
1641   Affiliated   2176   Grandview   Grandview Dialysis   13812 S US HIGHWAY 71     GRANDVIEW   MO   64030-3685
1642   Affiliated   4450   Lemoore   Lemoore Dialysis   1345 W BUSH ST     LEMOORE   CA   93245-3303
1643   Affiliated   5663   Middlebrook Dialysis   Middlebrook Dialysis   12401 MIDDLEBROOK RD   STE 16   GERMANTOWN   MD   20874-1523
1644   Affiliated   5664   Catoctin Dialysis   Catoctin Dialysis   405 W 7TH ST     FREDERICK   MD   21701-4505
1645   Affiliated   5648   Central New York Dialysis Center   Central New York Dialysis Center   910 ERIE BLVD E     SYRACUSE   NY   13210-1060
1646   Affiliated   5014   South Jackson   South Jackson Dialysis   46 HARTS BRIDGE RD     JACKSON   TN   38301-7512
1647   Affiliated   2344   Los Alamitos   Los Alamitos Dialysis   4141 KATELLA AVE     LOS ALAMITOS   CA   90720-3406
1648   Affiliated   5048   Robbinsdale   Robbinsdale Dialysis   3461 W BROADWAY AVE     ROBBINSDALE   MN   55422-2955
1649   Affiliated   5557   Oxnard   Oxnard Dialysis   1900 OUTLET CENTER DR     OXNARD   CA   93036-0677
1650   Affiliated   4429   Marked Tree   DNVO-Marked Tree-AR   216 HESTER PARKER DR     MARKED TREE   AR   72365-2023
1651   Affiliated   5669   Louisa Dialysis   Louisa Dialysis   2145 HWY 2565     LOUISA   KY   41230
1652   Affiliated   5670   Point Pleasant Dialysis   Point Pleasant Dialysis   3683 OHIO RIVER DR     POINT PLEASANT   WV   25550
1653   Affiliated   6802   Marion   Renal Care of Marion (P150)   2921 HWY 77   SUITE #8   MARION   AR   72364-2368
1654   Affiliated   6803   Osceola   Osceola Dialysis (P151)   1420 W KEISER AVE     OSCEOLA   AR   72370-2800
1655   Affiliated   6805   Cottonwood   Cottonwood Dialysis (P153)   203 S CANDY LANE     COTTONWOOD   AZ   86326-8115
1656   Affiliated   6808   Prescott   Prescott Dialysis (P157)   980 WILLOW CREEK RD.   SUITE 11   PRESCOTT   AZ   86301-1619
1657   Affiliated   6811   Naples   Collier County Dialysis (P160)   6625 HILLWAY CIRCLE     NAPLES   FL   34112
1658   Affiliated   6813   Catersville   Cartersville Renal Center (P162)   203 S TENNESSEE ST     CARTERSVILLE   GA   30120
1659   Affiliated   6816   Arlington Heights Renal Center   Arlington Heights Renal Center (P165)   17 W GOLF RD     ARLINGTON HEIGHTS   IL   60006
1660   Affiliated   6817   Hazel Crest Renal Center   Hazel Crest Renal Center (P166)   3470 W 183RD ST     HAZEL CREST   IL   60429
1661   Affiliated   6818   Loop Renal Center   Loop Renal Center (P167)   1101 S CANAL ST   11TH FLR   CHICAGO   IL   60607
1662   Affiliated   6819   Markham Renal Center   Markham Renal Center (P168)   3053 W 159TH ST     MARKHAM   IL   60426
1663   Affiliated   6821   South Holland Renal Center   South Holland Renal Center (P170)   16136 S PARK AVE.     SOUTH HOLLAND   IL   60473
1664   Affiliated   6822   Waukegan Renal Center   Waukegan Renal Center (P171)   1616 GRAND AVE.   STE. C   WAUKEGAN   IL   60085
1665   Affiliated   6936   Waukegan Home Renal Center   Waukegan Home Training (P172)   1616 GRAND AVE   STE F   WAUKEGAN   IL   60085
1666   Affiliated   6825   Baton Rouge   East Baton Rouge Dialysis (P174)   1333 ONEAL LANE     BATON ROUGE   LA   70816
1667   Affiliated   6826   Houma Renal Center   Houma Dialysis (P175)   108 PICONE RD     HOUMA   LA   70363
1668   Affiliated   6827   Amesbury   Amesbury Renal Center (P177)   24 MORRILL PLACE     AMESBURY   MA   1913
1669   Affiliated   6828   North Andover   North Andover Renal Center (P178)   201 SUTTON ST     NORTH ANDOVER   MA   1845

 

Page 77 of 136


1670   Affiliated   6829   Canton   Canton Renal Center (P179)   620 E PEACE ST     CANTON   MS   39046-4729
1671   Affiliated   6830   Hazelhurst   Hazlehurst Dialysis (P180)   201 N HALEY ST     HAZLEHURST   MS   39083
1672   Affiliated   6831   Jackson North   Jackson North Dialysis (P181)   571 BEASLEY RD   SUITE B   JACKSON   MS   39206-3042
1673   Affiliated   6832   Jackson South   Jackson South Dialysis (P182)   2460 TERRY RD   SUITE 27-J   JACKSON   MS   39204-5767
1674   Affiliated   6833   Jackson Southwest   Jackson Southwest Dialysis (P183)   1828 RAYMOND RD     JACKSON   MS   39204-4126
1675   Affiliated   6834   Lexington   Renal Care of Lexington (P184)   22579 DEPOT STREET     LEXINGTON   MS   39095
1676   Affiliated   6835   Munroe Falls   Munroe Falls Dialysis (P185)   265 N MAIN ST     MUNROE FALLS   OH   44262
1677   Affiliated   6836   Summit   Summit Renal Center (P186)   73 MASSILLON ROAD     AKRON   OH   44312
1678   Affiliated   6837   White Ponds   White Ponds Dialysis (P187)   534 WHITE POND DRIVE   SUITE A   AKRON   OH   44320
1679   Affiliated   6838   Philadelphia   Memphis Street Renal Center (P189)   3310 24 MEMPHIS ST     PHILADELPHIA   PA   19134-4510
1680   Affiliated   6839   Memphis Central Renal Center   Renal Care of Central Memphis (P190)   1331 UNION AVE.   SUITE 11   MEMPHIS   TN   38104-7559
1681   Affiliated   6840   Memphis Graceland Renal Center   Memphis Graceland Renal Center (P191)   4180 AUBURN RD     MEMPHIS   TN   38116-6202
1682   Affiliated   6841   Memphis Midtown Renal Center   Renal Care of Midtown Memphis (P192)   1166 MONROE AVE.     MEMPHIS   TN   38104-6614
1683   Affiliated   6842   Memphis North Renal Center   Renal Care of Memphis North (P193)   4913 RALEIGH COMMON DR.   SUITE 1   MEMPHIS   TN   38128-2485
1684   Affiliated   6844   Whitehaven Renal Center   Whitehaven Renal Center (P195)   3420 ELVIS PRESLEY BLVD.     MEMPHIS   TN   38116-3260
1685   Affiliated   6846   Edinburg   Edinburg Renal Center (P197)   4302 S SUGAR RD   STE 15   EDINBURG   TX   78539-9140
1686   Affiliated   6847   Mcallen   Dialysis Care of McAllen (P198)   411 LINDBERG AVE     MCALLEN   TX   78501-2921
1687   Affiliated   6848   Weslaco   Weslaco Renal Center (P199)   910 SOUTH UTAH     WESLACO   TX   78596-4270
1688   Affiliated   6849   Marlton Dialysis Center   Marlton Dialysis (P200)   769 E ROUTE 70     MARLTON   NJ   08053-2341
1689   Affiliated   6850   Lawrenceville Renal Center   Lawrenceville Renal Center (P201)   1840 PRINCETON AVE     LAWRENCEVILLE   NJ   8648
1690   Affiliated   6851   Austell Renal Center   Austell Renal Center (P202)   3642 MARATHON CIRCLE     AUSTELL   GA   30106- 6821
1691   Affiliated   6852   Bartlett Renal Center   Bartlett Renal Center (P203_P290_P8203)   2920 COVINGTON PIKE     MEMPHIS   TN   38128-6007
1692   Affiliated   6854   Beaverton Dialysis Center   Beaverton Dialysis Center (P206)   15050 SW KOLL PARKWAY   SUITE J   BEAVERTON   OR   97006-6002
1693   Affiliated   6858   Walker County Dialysis   Walker County Dialysis (P212)   589 HIGHWAY 78W     JASPER   AL   35501
1694   Affiliated   6861   Lakewood   Manatee County Dialysis (P215)   8470 COOPER CREEK BVLD     UNIVERSITY PARK   FL   34201
1695   Affiliated   6862   Canton   Northwest Georgia Dialysis (P216)   260 HOSPITAL RD     CANTON   GA   30114
1696   Affiliated   6863   Buffulo Grove Renal Center   Buffalo Grove Dialysis (P218)   1291 W DUNDEE RD     BUFFALO GROVE   IL   60089
1697   Affiliated   6864   Evanston Renal Center   Evanston Renal Center (P219)   1715 CENTRAL ST     EVANSTON   IL   60201
1698   Affiliated   6865   Schaumburg Renal Center   Schaumburg Renal Center (P220)   1156 S. ROSELLE ROAD     SCHAUMBURG   IL   60193
1699   Affiliated   6937   Schaumburg Home Renal Center   Schaumburg Home Training (P270)   17 W GOLF RD     ARLINGTON HEIGHTS   IL   60005
1700   Affiliated   6866   Blue River Valley   Blue River Valley Renal Center (P222)   2309 S MILLER STREET   SUITE 1   SHELBYVILLE   IN   46176-9350
1701   Affiliated   6867   Central Fort Wayne   Central Fort Wayne Dialysis (P223)   1940 BLUFTON RD     FORT WAYNE   IN   46809-1307
1702   Affiliated   6869   Huntington   Renal Care of Huntington (P225)   3040 WEST PARK DRIVE     HUNTINGTON   IN   46750-8956
1703   Affiliated   6870   Lake Avenue Dialysis Renal Center   Lake Avenue Dialysis (P226)   3525 LAKE AVE   STE 4   FORT WAYNE   IN   46805-5545
1704   Affiliated   6871   Marion County   Marion County Dialysis (P229)   3834 S EMERSON AVE   BLDG B   INDIANAPOLIS   IN   46203-5902
1705   Affiliated   6873   Quad Counties Dialysis   Quad Counties Dialysis (P232)   528 NORTH GRANDSTAFF     AUBURN   IN   46706-1660
1706   Affiliated   6875   South Anthony   South Anthony Dialysis (P234)   7017 SOUTH ANTHONY BLVD.     FORT WAYNE   IN   46816-2016
1707   Affiliated   6876   Brandon   Brandon Renal Center (P235)   101 CHRISTIAN DR     BRANDON   MS   39042-2678
1708   Affiliated   6877   Carthage   Renal Care of Carthage (P236)   312 ELLIS STREET     CARTHAGE   MS   39051
1709   Affiliated   6878   Las Cruces Renal Center   Las Cruces Renal Center (P237)   3961 E LOHMAN AVE   STE 29   LAS CRUCES   NM   88011-8272
1710   Affiliated   6879   Northeast Portland   Northeast Portland Renal Center (P240)   703 NE HANCOCK ST     PORTLAND   OR   97212-3955
1711   Affiliated   6880   Oregon Kidney Center   Dialysis Care of Portland (P241)   5318 NE IRVING     PORTLAND   OR   97213
1712   Affiliated   6881   Sunnyside   Sunnyside Renal Center (P242)   6902 SE LAKE ROAD   SUITE 1   MILWAUKIE   OR   97267-2148
1713   Affiliated   6882   Willamette Valley   Williamette Valley Renal Center (P243)   1510 DIVISION STREET   SUITE 9   OREGON CITY   OR   97045-1572
1714   Affiliated   6883   Northern Philadelphia   Northern Philadelphia Dialysis (P244)   5933 N BROAD ST     PHILADELPHIA   PA   19141
1715   Affiliated   6884   North Providence Renal Center   North Providence Renal Center (P246)   1635 MINERAL SPRING AVE     NORTH PROVIDENCE   RI   02904-4025
1716   Affiliated   6889   Alice Renal Center   Alice Renal Center (P252)   2345 ALICE REGIONAL BLVD.     ALICE   TX   78332-7291
1717   Affiliated   6890   Beeville Renal Center   Beeville Renal Center (P253)   1905 NW FRONTAGE     BEEVILLE   TX   78102-2954
1718   Affiliated   6891   Brownsville   Brownsville Renal Center (P254)   2945 CENTRAL BLVD     BROWNSVILLE   TX   78520-8958
1719   Affiliated   6892   Corpus Christi Renal Center   Corpus Christi Dialysis (P255)   2733 SWANTNER DR     CORPUS CHRISTI   TX   78404-2832
1720   Affiliated   6893   Riverside Renal Center   Riverside Renal Center (P256)   13434 LEOPARD RD. SUITE A17     CORPUS CHRISTI   TX   78410-4466
1721   Affiliated   6894   South Texas Renal Center   South Texas Renal Center (P257)   4301 S PADRE ISLAND DR     CORPUS CHRISTI   TX   78411-4433
1722   Affiliated   6896   South Central Renal Center   Morgan Avenue Dialysis (P258)   2222 S MORGAN AVE   SUITE 114   CORPUS CHRISTI   TX   78405-1900
1723   Affiliated   6898   Northeast Texas   Dialylsis Care of Greenville (P260)   4805 WESLEY ST     GREENVILLE   TX   75401-5649

 

Page 78 of 136


1724   Affiliated   6899   Downtown Spokane   Downtown Spokane Renal Center (P261)   601 W 5TH ST   SUITE F   SPOKANE   WA   99205
1725   Affiliated   6900   North Spokane   North Spokane Renal Center (P262)   12610 E MARIBEAU PRKWY   STE 1   SPOKANE   WA   99216
1726   Affiliated   6901   Spokane Valley   Spokane Valley Renal Center (P263)   12610 EAST MIRABEAU PKY   SUITE 1   SPOKANE   WA   99208-1450
1727   Affiliated   6902   Kansas City   Kansas City Renal Center (P264)   4333 MADISON AVE     KANSAS CITY   MO   64111-3429
1728   Affiliated   6903   Butler Renal Center   Butler Renal Center (P266)   601 W NURSERY     BUTLER   MO   64730
1729   Affiliated   6904   Harrisonville   Harrisonville Renal Center (P267)   308 GALAXIE AVE     HARRISONVILLE   MO   64701-2084
1730   Affiliated   6905   Marshall Renal Center   Marshall Renal Center (P268)   359 W MORGAN     MARSHALL   MO   65340
1731   Affiliated   6907   Akron Renal Center   Akron Renal Center (P272)   525 EAST MARKET STREET     AKRON   OH   44304-1619
1732   Affiliated   6908   Kendallville Renal Center   Kendallville Renal Center (P274)   602 SAWYER RD     KENDALLVILLE   IN   46755- 2566
1733   Affiliated   6909   Greenwood Holly Renal Center   Greenwood Holly Renal Center (P276)   1533 HOLLY RD     CORPUS CHRISTI   TX   78417-2010
1734   Affiliated   6910   Plainfield Renal Center   Plainfield Renal Center (P278)   8110 NETWORK DR     PLAINFIELD   IN   46168-9024
1735   Affiliated   6911   Green Valley Renal Center   Green Valley Dialysis (P279)   1489 W WARM SPRINGS RD   STE 122   HENDERSON   NV   89014-7637
1736   Affiliated   6912   Las Vegas Renal Center   Las Vegas Renal Center (P280)   2333 RENAISSANCE DR     LAS VEGAS   NV   89119-6191
1737   Affiliated   6913   Lees Summit Renal Center   Lees Summit Renal Center (P281)   100 NE MISSOURI RD   STE 1   LEE’S SUMMIT   MO   64086-4702
1738   Affiliated   6914   Westport Renal Center   Westport Renal Center (P282)   3947 BROADWAY STREET     KANSAS CITY   MO   64111-2516
1739   Affiliated   6915   Greensboro Dialysis Center   Greensboro Dialysis Center (P284)   1220 SILOAM RD     GREENSBORO   GA   30642-0390
1740   Affiliated   5057   Forest Landing   DNVO-Forest Landing Dialysis (Harford Cty, Havre de Grace)-MD   2220 COMMERCE AVE   STE 1   FOREST HILL   MD   21050
1741   Affiliated   5033   University City   DNVO-University City Dialysis (Philadelphia)-PA   3020 MARKET ST   STE 13   PHILADELPHIA   PA   19104-2999
1742   Affiliated   2411   Parkland   DNVO-Parkland Dialysis-WA   311 140TH ST SO     TACOMA   WA   98444
1743   Affiliated   5094   Shelbyville Road   DNVO JV-Shelbyville Road Dialysis (DuPont, Louisville)-KY   4600 SHELBYVILLE RD   STE 31   LOUISVILLE   KY   40207
1744   Affiliated   5106   Fort Wayne West Dialysis   DNVO JV-Fort Wayne South-IN   302 E PETTIT AVE     FORT WAYNE   IN   468063007
1745   Affiliated   5671   Suburban Dialysis   ACQ-5671-NY   1542 MAPLE RD     WILLIAMSVILLE   NY   14221
1746   Affiliated   5672   Gates Circle Dialysis   ACQ-5672-NY   3 GATES CIRCLE   1ST FLR   BUFFALO   NY   14209
1747   Affiliated   5673   Orchard Park Dialysis   ACQ-5673-NY   3801 TAYLOR RD     ORCHARD PARK   NY   14127
1748   Affiliated   2420   TC Jester   DNVO-TC Jester-TX   1800 W 26TH ST   STE 11   HOUSTON   TX   77008-1419
1749   Affiliated   4436   Champions   DNVO-Champions Dialysis (Houston)-TX   4427 FM 1960 W   STE D   HOUSTON   TX   77068-3409
1750   Affiliated   5083   Magic City Dialysis MMC   DNVO-Magic City Dialysis (Birmingham)-AL   300 22ND ST SO     BIRMINGHAM   AL   35233-2209
1751   Affiliated   5084   Steel City Dialysis   DNVO-Steel City Dialysis (Birmingham)-AL   1809 AVE H (ENSLEY)     BIRMINGHAM   AL   35218
1752   Affiliated   5081   Jewel Dialysis   DNVO-Jewel Dialysis (Camellia, Birmingham)-AL   514 WEST TOWN PLAZA     BESSEMER   AL   35020
1753   Affiliated   660   Crystal River   Crystal River Dialysis   7435 W GULF TO LAKE HWY     CRYSTAL RIVER   FL   34429-7834
1754   Affiliated   1936   Southwest Kidney   Estrella Dialysis Center   8410 W THOMAS RD   STE 1 BLDG 1   PHOENIX   AZ   85037-3356
1755   Affiliated   1937   Gilbert Dialysis   Gilbert Dialysis Center   5222 E BASELINE RD   STE 14   GILBERT   AZ   85234-2963
1756   Affiliated   1938   Tempe Dialysis   Tempe Dialysis Center   2149 E WARNER RD   STE 11   TEMPE   AZ   85284-3496
1757   Affiliated   1939   Phoenix Dialysis   Phoenix Dialysis Center   337 E CORONADO RD   STE 11   PHOENIX   AZ   85004-1582
1758   Affiliated   1949   Arrowhead Lakes Dialysis   Arrowhead Lakes Dialysis   20325 N 51ST AVE   BLDG 11, STE 186   GLENDALE   AZ   85308-4625
1759   Affiliated   1952   Mountain Vista Dialysis   Mountain Vista Dialysis Center of Arizona   10238 E HAMPTON AVE   STE 18   MESA   AZ   85209-3317
1760   Affiliated   1977   South Meadows Dialysis Center   South Meadows Dialysis Center   10085 DOUBLE R BLVD   STE 16   RENO   NV   89521-4867
1761   Affiliated   1978   Reno Dialysis Center   Reno Dialysis Center   1500 E 2ND ST   STE 11   RENO   NV   89502-1189
1762   Affiliated   1979   Carson City Dialysis Center   Carson City Dialysis Center   3246 N. CARSON ST   STE 11   CARSON CITY   NV   89706-0248
1763   Affiliated   844   Sparks   Sparks Dialysis Center   4860 VISTA BLVD   STE 1   SPARKS   NV   89436-2817
1764   Affiliated   2015   Sierra Rose Dialysis   Sierra Rose Dialysis Center   685 SIERRA ROSE DR     RENO   NV   89511-2060
1765   Affiliated   2325   Northwest Tucson   Northwest Tucson Dialysis   2945 W INA RD   STE 15   TUCSON   AZ   85741-2366
1766   Affiliated   4355   Mesa   Central Mesa Dialysis Center   1134 E UNIVERSITY DR   STE 11   MESA   AZ   85203-8048
1767   Affiliated   4371   Raven   Raven Dialysis Center   3540 E BASELINE RD   STE 11   PHOENIX   AZ   85042-9628
1768   Affiliated   4374   Brookwood   Brookwood Dialysis Center   8910 N 43RD AVE   STE 17   GLENDALE   AZ   85302-5340
1769   Affiliated   4405   Ocotillo   Ocotillo Dialysis   975 W CHANDLER HEIGHTS RD   UNIT 11   CHANDLER   AZ   85248-5724
1770   Affiliated   4364   Maryvale   Maryvale Dialysis Center   4845 W MCDOWELL RD   STE 1A, 2A, 3A   PHOENIX   AZ   85035-4076
  Affiliated   1995   Winter Park Home PD Dialysis   Winter Park Home PD Dialysis   4100 METRIC DR   STE 2   WINTER PARK   FL   32792-6832
  Affiliated   4302   Lockport HHD PD At Home   Lockport Home Dialysis-PD   16626 W 159TH ST   STE 73   LOCKPORT   IL   60441-8019
  Affiliated   1972   HHD 6183 and PD 1972 in Shreveport   Shreveport Home Dialysis PD   1560 IRVING PL     SHREVEPORT   LA   71101-4604
  Affiliated   5618   Home Dialysis of Dayton – South   Home Dialysis of Dayton-South   4700 SPRINGBORO PIKE   STE 3   MORAINE   OH   45439-1964
  Affiliated   5619   Home Dialysis of Dayton   Home Dialysis of Dayton   627 S EDWIN C MOSES BLVD   STE 2B   DAYTON   OH   45417-3474
  Affiliated   144   Timpanogos Dialysis Center   Timpanogos Dialysis   1055 N 500 W   STE 222   PROVO   UT   84604-3329
  Affiliated   216   HOME DIALYSIS UNIT   Home Dialysis /CAPD Unit   825 S 8TH ST STE 1202     MINNEAPOLIS   MN   55404

 

Page 79 of 136


  Affiliated   284   MANZANITA HOME TRAINING CENTER   Manzanita Home Training Center (fka North CAPD)   4005 MANZANITA AVE   STE 18   CARMICHAEL   CA   95608-1779
  Affiliated   408   WICHITA DIALYSIS CENTER   Wichita Dialysis Center-PD Program   909 N TOPEKA ST     WICHITA   KS   67214-3620
  Affiliated   978   CENTRAL TULSA DIALYSIS CENTER   Central Tulsa PD   1124 S SAINT LOUIS AVE     TULSA   OK   74120-5413
  Affiliated   1748   ST PAUL CAPITAL PD   St. Paul Capital Dialysis at Home-PD (fka Capital PD Program)   555 PARK ST   STE 110   SAINT PAUL   MN   55103-2110
  Affiliated   1787   ASH TREE PD   Ash Tree PD   2666 N GROVE INDUSTRIAL DR     FRESNO   CA   93727-1552
  Affiliated   1821   EMERALD DIALYSIS   Emerald Dialysis PD (fka Hyde Park PD)   710 W 43RD ST     CHICAGO   IL   60609-3435
  Affiliated   1822   OLYMPIA FIELDS DIALYSIS   Olympia Fields PD   4557B LINCOLN HWY   STE B   MATTESON   IL   60443-2385
  Affiliated   1823   LAKE COUNTY DIALYSIS   Lake County PD   918 S MILWAUKEE AVE     LIBERTYVILLE   IL   60048-3229
  Affiliated   1825   COMPREHENSIVE RENAL CARE-GARY   CRC-Gary PD   4802 BROADWAY     GARY   IN   46408-4509
  Affiliated   1826   COMPREHENSIVE RENAL CARE-HAMMOND   CRC-Hammond PD   222 DOUGLAS ST     HAMMOND   IN   46320-1960
  Affiliated   1827   COMPREHENSIVE RENAL CARE-VALPARAISO   CRC-Valparaiso PD   606 E LINCOLNWAY     VALPARAISO   IN   46383-5728
  Affiliated   1828   COMPREHENSIVE RENAL CARE-MICHIGAN CITY   CRC-Michigan City PD   9836 WEST 400 NORTH     MICHIGAN CITY   IN   46360-2910
  Affiliated   1829   MERRILLVILLE PD   Merrillville Dialysis PD   9223 TAFT ST     MERRILLVILLE   IN   46410-6911
  Affiliated   1833   NAMPA DIALYSIS CENTER   Nampa Dialysis PD   846 PARKCENTRE WAY     NAMPA   ID   83651-1790
  Affiliated   1834   TABLE ROCK DIALYSIS CENTER   Table Rock Dialysis PD   5610 W GAGE ST     BOISE   ID   83706
  Affiliated   1835   TWIN FALLS DIALYSIS CENTER   Twin Falls Dialysis PD   1840 CANYON CREST DR     TWIN FALLS   ID   83301-3007
  Affiliated   1836   TREASURE VALLEY DIALYSIS CENTER   Treasure Valley Dialysis PD & Home   3525 E LOUISE DR   STE 155   MERIDIAN   ID   83642-6303
  Affiliated   1837   GATE CITY DIALYSIS CENTER   Gate City Dialysis PD   2001 BENCH RD     POCATELLO   ID   83201-2033
  Affiliated   1838   FOUR RIVERS DIALYSIS CENTER   Four Rivers Dialysis PD   515 EAST LN     ONTARIO   OR   97914-3953
  Affiliated   1869   LOWRY DIALYSIS CENTER   Lowry Dialysis PD   7465 E 1ST AVE   STE A   DENVER   CO   80230-6877
  Affiliated   1905   BURLEY DIALYSIS CENTER   Burley Dialysis PD   741 N OVERLAND AVE     BURLEY   ID   83318-3440
  Affiliated   1909   TURFWAY PD DIALYSIS   Turfway PD Training   11 SPIRAL DR   STE 15A   FLORENCE   KY   41042-1394
  Affiliated   1910   MARYVILLE DIALYSIS   Maryville Dialysis PD   2136B VADALABENE DR     MARYVILLE   IL   62062-5632
  Affiliated   1917   PDL ANNEX-PD   PDL Annex-PD (PDL=Physician Dialysis Lancaster)   2110 HARRISBURG PIKE   STE 310   LANCASTER   PA   17601-2644
  Affiliated   1924   KANKAKEE COUNTY DIALYSIS   Kankakee County Dialysis PD   581 WILLIAM R LATHAM SR DR   STE 104   BOURBONNAIS   IL   60914-2439
  Affiliated   1946   SNAKE RIVER DIALYSIS PD   DNVO-Snake River Dialysis PD (fka Blackfoot)-ID   1491 PARKWAY DR     BLACKFOOT   ID   83221-1667
  Affiliated   1953   NORTH HIGHLANDS DIALYSIS CENTER   North Highlands Dialysis Center PD   4986 WATT AVE   STE C   NORTH HIGHLANDS   CA   95660-5182
  Affiliated   1966   AMERY DIALYSIS   Amery Dialysis PD   970 ELDEN AVE     AMERY   WI   54001-1448
  Affiliated   1975   KIDNEY HOME CENTER   Kidney HOME (Home Operations & Medical Education) Center PD   2245 ROLLING RUN DR   STE 4   WINDSOR MILL   MD   21244-1858
  Affiliated   1988   MEMPHIS DOWNTOWN DIALYSIS   Memphis Downtown Dialysis PD   2076 UNION AVE   FL 2   MEMPHIS   TN   38104-4138
  Affiliated   1989   PGH HOME MODALITY COE   Pittsburgh Home Modality Center of Excellence PD   5171 LIBERTY AVE   STE A   PITTSBURGH   PA   15224-2254
  Affiliated   2223   LAKE VILLA DIALYSIS   Lake Villa Dialysis PD   37809 N IL RTE 59     LAKE VILLA   IL   60046-7332
  Affiliated   2232   RICHFIELD DIALYSIS   Richfield PD Program   6601 LYNDALE AVE S   STE 150   RICHFIELD   MN   55423-2490
  Affiliated   2297   TOKAY HOME DIALYSIS CENTER   Tokay Home Dialysis-PD   777 S HAM LN   STE L   LODI   CA   95242-3593
  Affiliated   2302   SPIVEY PERITONEAL AND HOME DIALYSIS CENTER   Spivey Peritoneal Dialysis and Home Dialysis Center   1423 STOCKBRIDGE RD   STE B   JONESBORO   GA   30236-3740
  Affiliated   2326   WARRENSVILLE HEIGHTS PD DIALYSIS   Warrensville Heights PD Dialysis   4200 WARRENSVILLE CENTER RD   STE 210   WARRENSVILLE HEIGHTS   OH   44122-7000
  Affiliated   2340   EASTGATE HOME   Eastgate Home Training   4435 AICHOLTZ RD   STE 800B   CINCINNATI   OH   45245-1692
  Affiliated   2366   WESLEY CHAPEL DIALYSIS   Wesley Chapel Dialysis (PD ONLY)   2255 GREEN HEDGES WAY     WESLEY CHAPEL   FL   33544-8183
  Affiliated   2400   FRESNO PD   Fresno At Home Center-PD Only   568 E HERNDON AVE   STE 301   FRESNO   CA   93720-2989
  Affiliated   2456   GRAND HOME DIALYSIS PD/HHD   Grand Home Dialysis (PD only)   14674 W MOUNTAIN VIEW BLVD   STE 204   SURPRISE   AZ   85374-2708
  Affiliated   2458   WASHINGTON COUNTY DIALYSIS   Washington County Dialysis PD Only (fka Hagerstown)   1136 OPAL CT     HAGERSTOWN   MD   21740-5940
  Affiliated   2477   SAN JOSE PD   San Jose At Home-PD Only (Freestanding)   4400 STEVENS CREEK BLVD   STE 50   SAN JOSE   CA   95129-1104
  Affiliated   2483   FREMONT HOME TRAINING JV   DNVO-Fremont At Home PD/HHD-CA   39355 CALIFORNIA AVE     FREMONT   CA   94538
  Affiliated   2490   HOME DIALYSIS OPTIONS OF BALDWIN COUNTY   Home Dialysis Options of Baldwin County-PD Only   27880 N MAIN ST   STE A   DAPHNE   AL   36526-7080
  Affiliated   3299   TRI COUNTIES HOME TRAINING   Tri Counties Home Dialysis   433 S BRIDGE ST     VISALIA   CA   93277-2801
  Affiliated   3640   WHITE OAK HOME TRAINING DIALYSIS   White Oak Home Training   5520 CHEVIOT RD   STE B   CINCINNATI   OH   45247-7069
  Affiliated   3683   BUTLER COUNTY HOME TRAINING DIALYSIS   Butler County Home Training   3497 S DIXIE HWY     FRANKLIN   OH   45005-5717
  Affiliated   3727   HANFORD AT HOME DIALYSIS   Hanford Home Dialysis PD   900 N DOUTY ST     HANFORD   CA   93230-3918
  Affiliated   3735   HIOAKS DIALYSIS PD   Hioaks Dialysis PD   681 HIOAKS RD   STE B   RICHMOND   VA   23225-4043
  Affiliated   3891   MEMPHIS EAST DIALYSIS PD   Memphis East Dialysis PD   50 HUMPHREYS CTR   STE 28B   MEMPHIS   TN   38120-2369
  Affiliated   3892   NASHVILLE HOME TRAINING DIALYSIS PD   Nashville Home Training Dialysis PD   1919 CHARLOTTE AVE   STE 200   NASHVILLE   TN   37203-2245
  Affiliated   3989   DEARBORN HOME DIALYSIS   Dearborn Home Dialysis-PD   22030 PARK ST     DEARBORN   MI   48124-2854
  Affiliated   4308   GALLERIA HOME TRAINING DIALYSIS   Galleria Home Training Dialysis PD (aka SW Tennessee)   9045 HIGHWAY 64   STE 102   LAKELAND   TN   38002-8394
  Affiliated   4310   GREATER TAMPA AT HOME   Greater Tampa At Home PD   4204 N MACDILL AVE   STE 1B NORTH BLDG   TAMPA   FL   33607-6364

 

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  Affiliated   4315   LORAIN COUNTY HOME DIALYSIS   DNVO-Lorain County Home Dialysis HHD/PD-OH   824 E BROAD ST     ELYRIA   OH   44035-6557
  Affiliated   4375   GARFIELD HOME PROGRAM   Garfield Home Program (PD Only)   228 N GARFIELD AVE   STE 301   MONTEREY PARK   CA   91754-1709
  Affiliated   4453   BINZ HOME TRAINING   Binz Home Training - PD only   1213 HERMANN DR   STE 180   HOUSTON   TX   77004-7018
  Affiliated   5021   FRANKLIN AT HOME PD   Franklin At Home PD   301 CALLOWHILL ST     PHILADELPHIA   PA   19123-4117
  Affiliated   5028   CALDWELL DIALYSIS CENTER PD   Caldwell Dialysis Center   821 S SMEED PKWY     CALDWELL   ID   83605-5130
  Affiliated   5170   FORT WAYNE HOME DIALYSIS   DNVO-Fort Wayne Home Dialysis (PD-HHD)-IN   3124 E STATE BLVD   STE 5B   FORT WAYNE   IN   46805-4763
  Affiliated   5556   VISALIA AT HOME   Visalia At Home PD   1120 N CHINOWTH ST     VISALIA   CA   93291-7896
  Affiliated   5569   BLUEMOUND PD   Bluemound PD   601 N 99TH ST STE 300     WAUWATOSA   WI   53226-4362
  Affiliated   5581   WOODLAWN HOME PROGRAM PD   Woodlawn Home Program PD Only   5841 S MARYLAND AVE   RM L-026   CHICAGO   IL   60637-1447
  Affiliated   5599   BEVERLY DIALYSIS PD   Beverly PD   8109 S WESTERN AVE     CHICAGO   IL   60620-5939
  Affiliated   5600   WOODLAWN PEDIATRIC HOME PROGRAM   Woodlawn Pediatrics Home Program PD Only   5841 S MARYLAND AVE L026     CHICAGO   IL   60615
  Affiliated   5616   SPRINGHILL HOME TRAINING DIALYSIS   Springhill Home Training (PD Only)   3401 SPRINGHILL DR   STE 330   NORTH LITTLE ROCK   AR   72117-2945
  Affiliated   5647   FIRST COLONIAL DAVITA PD   First Colonial DaVita PD   1157 FIRST COLONIAL RD   STE 200   VIRGINIA BEACH   VA   23454-2432
  Affiliated   5898   AMHERST AT HOME   Amherst At Home   3200 COOPER FOSTER PRK RD W     LORAIN   OH   44053-3654
  Affiliated   5900   CATHERDRAL CITY AT HOME   DNVO JV-Cathedral City At Home-CA   30-885 DATE PALM DR     CATHEDRAL CITY   CA   92234-2958
  Affiliated   5904   ROBBINSDALE AT HOME   Robbinsdale At Home   3461 WEST BROADWAY AVE     ROBBINSDALE   MN   55422-2955
  Affiliated   5905   NORTH PALM BEACH AT HOME   North Palm Beach At Home   2841 PGA BLVD     PALM BEACH GARDENS   FL   33410-2910
  Affiliated   5907   SOUTHTOWNS AT HOME   Southtowns At Home (Hamburg)   4910 CAMP RD   STE 100   HAMBURG   NY   14075-2617
  Affiliated   5909   FORT WAYNE HOME AT HOME   DNVO-Fort Wayne Home At Home   3124 E STATE BLVD   STE 5B   FORT WAYNE   IN   46805-4763
  Affiliated   5910   FORT WAYNE WEST AT HOME   DNVO JV-Fort Wayne West At Home   4916 ILLINOIS RD   STE 118   FORT WAYNE   IN   46804-5116
  Affiliated   5913   WINCHESTER AT HOME   Winchester At Home   2301 VALOR DR     WINCHESTER   VA   22601-6111
  Affiliated   5914   MARSHFIELD AT HOME   Marshfield At Home   123 NORTHRIDGE ST     MARSHFIELD   WI   54449-8341
  Affiliated   5915   MOSCOW AT HOME   Moscow At Home   212 RODEO DR   STE 110   MOSCOW   ID   83843-9791
  Affiliated   5919   AVON AT HOME   Avon At Home   9210 ROCKVILLE RD   STE D   INDIANAPOLIS   IN   46234-2670
  Affiliated   5923   NORTHSIDE AT HOME   Northside At Home   320 E NORTH AVE   4TH FLOOR SOUTH TOWER   PITTSBURGH   PA   15212-4756
  Affiliated   5926   PANAMA CITY AT HOME   Panama City At Home   615 HIGHWAY 231     PANAMA CITY   FL   32405-4704
  Affiliated   5927   MAGNOLIA OAKS AT HOME   Magnolia Oaks At Home (aka Hinesville, Satilla River)   2377 HIGHWAY 196 W   BLDG A MAGNOLIA OAKS   HINESVILLE   GA   31313-8036
  Affiliated   5928   WESTBANK AT HOME   Westbank At Home   3631 BEHRMAN PL     NEW ORLEANS   LA   70114-0906
  Affiliated   5931   ROCKSIDE AT HOME   Rockside At Home   4801 ACORN DR     INDEPENDENCE   OH   44131-2566
  Affiliated   5932   WADSWORTH AT HOME   Wadsworth At Home   195 WADSWORTH RD STE 302   FOUNDERS HALL 3RD FLOOR   WADSWORTH   OH   44281-9504
  Affiliated   5933   WOODLAWN AT HOME HHD   Woodlawn Home Program At Home   5841 S MARYLAND AVE   RM L-026   CHICAGO   IL   60637-1447
  Affiliated   5934   WESLEY CHAPEL AT HOME   Wesley Chapel At Home   2255 GREEN HEDGES WAY     WESLEY CHAPEL   FL   33544-8183
  Affiliated   5935   THOUSAND OAKS AT HOME   Thousand Oaks At Home   375 ROLLING OAKS DR   STE 100   THOUSAND OAKS   CA   91361-1024
  Affiliated   5936   SIMI VALLEY AT HOME   Simi Valley At Home   2950 SYCAMORE DR   STE 100   SIMI VALLEY   CA   93065-1210
  Affiliated   5937   MIDWEST FAIRBORN AT HOME   Midwest Fairborn At Home   1266 N BROAD ST     FAIRBORN   OH   45324
  Affiliated   5938   NORTH ST LOUIS COUNTY AT HOME   North St. Louis County At Home   13119 NEW HALLS FERRY RD     FLORISSANT   MO   63033-3228
  Affiliated   5939   BLUEMOUND AT HOME   Bluemound At Home   601 N 99TH ST   STE 110   WAUWATOSA   WI   53226
  Affiliated   5940   MESA COUNTY AT HOME   Mesa County At Home (Grand Junction)   561 25 RD   STE D   GRAND JUNCTION   CO   81505-1303
  Affiliated   5942   PLANO AT HOME   Plano At Home   481 SHILOH RD   STE 100   PLANO   TX   75074-7231
  Affiliated   5943   WEST BLOOMFIELD AT HOME   West Bloomfield At Home   6010 W MAPLE RD STE 215     WEST BLOOMFIELD   MI   48322-4406
  Affiliated   5945   BINZ HOME TRAINING AT HOME   Binz Home Training At Home   1213 HERMANN DR STE 180     HOUSTON   TX   77004-7070
  Affiliated   5947   HANNIBAL AT HOME   Hannibal At Home   3140 PALMYRA RD     HANNIBAL   MO   63401-2204
  Affiliated   5949   BEVERLY AT HOME   Beverly At Home   8109 SOUTH WESTERN AVE     CHICAGO   IL   60620-5939
  Affiliated   5950   NORTH JACKSON AT HOME   North Jackson At Home (fka Stonegate)   217 STERLING FARM DR     JACKSON   TN   38305-5727
  Affiliated   5951   PORTAGE AT HOME   Portage At Home   5823 US HIGHWAY 6     PORTAGE   IN   46368-4851
  Affiliated   5952   ROGUE VALLEY AT HOME   Rogue Valley At Home   760 GOLF VIEW DR UNIT 100     MEDFORD   OR   97504-9685
  Affiliated   5953   EVERETT AT HOME   Everett At Home   8130 EVERGREEN WAY STE C     EVERETT   WA   98203-6419
  Affiliated   5954   OLYMPIA AT HOME   Olympia At Home   335 COOPER POINT ROAD NW   SUITE 105   OLYMPIA   WA   98502-4436
  Affiliated   5955   LORAIN COUNTY HOME AT HOME   DNVO-Lorain County Home At Home   824 EAST BROAD ST     ELYRIA   OH   44035-6559
  Affiliated   5956   RENAISSANCE AT HOME   Renaissance At Home   1840 DARBY DR     FLORENCE   AL   35630-2623
  Affiliated   5957   POOLER AT HOME   Pooler At Home   54 TRADERS WAY   LIVE OAK PLAZA   POOLER   GA   31322-4158
  Affiliated   5958   GULF SHORES AT HOME   Gulf Shores At Home   3947 GULF SHORES PKWY   UNIT 150   GULF SHORES   AL   36542-2735
  Affiliated   5959   FRANKLIN AT HOME   Franklin At Home   301 CALLOWHILL ST     PHILADELPHIA   PA   19123-4117
  Affiliated   5961   RENO AT HOME   Reno At Home   1500 EAST 2ND STREET   STE 101, 106   RENO   NV   89502-1189

 

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  Affiliated   5963   JACKSONVILLE SOUTH AT HOME   Jacksonville South At Home   14965 OLD SAINT AUGUSTINE RD   UNIT 114   JACKSONVILLE   FL   32258-9481
  Affiliated   5964   LAKE ST LOUIS AT HOME   Lake St. Louis At Home   200 BREVCO PLZ   STE 202   LAKE ST LOUIS   MO   63367-2950
  Affiliated   5965   UNION CITY AT HOME (GA)   Union City At Home (GA)   6851 SHANNON PARKWAY   STE 200   UNION CITY   GA   30291-2049
  Affiliated   5966   WEBER VALLEY AT HOME   Weber Valley At Home   1920 W 250TH N     MARRIOTT-SLATERVILLE   UT   84404-9233
  Affiliated   5968   PARKER DIALYSIS CENTER   Parker At Home   10371 S PARK GLENN WAY   STE 180   PARKER   CO   80138-3871
  Affiliated   5971   KENNESTONE AT HOME   Kennestone At Home   200 COBB PKWY N   STE 318   MARIETTA   GA   30062-3558
  Affiliated   5973   NORTH COLORADO SPRINGS AT HOME   North Colorado Springs At Home   6071 E WOODMEN RD   STE 100   COLORADO SPRINGS   CO   80923-2610
  Affiliated   5974   PGH HOME MODALITY COD/HHD   Pittsburgh Home Modality Center of Excellence At Home   5171 LIBERTY AVE   STE A   PITTSBURGH   PA   15224-2254
  Affiliated   5977   FRESNO AT HOME CENTER   Fresno At Home Center-HHD Only   568 E HERNDON AVE   STE 301   FRESNO   CA   93720-2989
  Affiliated   5978   BLUFF CITY AT HOME   Bluff City At Home   2400 LUCY LEE PKWY   STE E   POPLAR BLUFF   MO   63901-2427
  Affiliated   5979   NORTH METRO AT HOME   North Metro At Home   12365 HURON ST   STE 500   WESTMINSTER   CO   80234-3498
  Affiliated   5980   FIVE STAR AT HOME   Five Star At Home (fka Las Vegas Multi-Care)   2400 TECH CENTER CT     LAS VEGAS   NV   89128-0804
  Affiliated   5981   KIDNEY HOME AT HOME   Kidney HOME (Home Operations & Medical Education) At Home   2245 ROLLING RUN DR   STE 3   WINDSOR MILL   MD   21244-1858
  Affiliated   5982   FARGO AT HOME   Fargo At Home   4474 23RD AVE S   STE M   FARGO   ND   58104-8795
  Affiliated   5983   GALLERIA HOME TRAINING AT HOME   Galleria Home Training At Home   9045 HIGHWAY 64   STE 102   LAKELAND   TN   38002-8394
  Affiliated   5986   BELDEN COMMUNITY AT HOME   Belden Community At Home   4685 FULTON DR NW     CANTON   OH   44718-2379
  Affiliated   5987   MAINPLACE AT HOME   Mainplace At Home   972 W TOWN AND COUNTRY RD     ORANGE   CA   92868-4714
  Affiliated   5988   PENNSAUKEN AT HOME   Pennsauken At Home   7024 KAIGHNS AVE     PENNSAUKEN   NJ   08109-4417
  Affiliated   5989   JEDBURG AT HOME   Jedburg At Home   2897 W 5TH NORTH ST     SUMMERVILLE   SC   29483-9674
  Affiliated   5993   CAPE CORAL SOUTH AT HOME   Cape Coral South At Home   3046 DEL PRADO BLVD S   STE 4A   CAPE CORAL   FL   33904-7232
  Affiliated   5994   GREATER TAMPA HOME AT HOME   Greater Tampa At Home   4204 N MACDILL AVE   STE 1B NORTH BLDG   TAMPA   FL   33607-6364
  Affiliated   5995   ATHENS EAST AT HOME   Athens East At Home   2026 S MILLEDGE AVE   STE A2   ATHENS   GA   30605-6480
  Affiliated   5996   UNIVERSITY UNIT RIVERSIDE AT HOME   University Unit Riverside At Home   1045 WESTGATE DR   STE 90   SAINT PAUL   MN   55114-1079
  Affiliated   5997   WOODRIDGE AT HOME   Woodridge Home At Home   7425 JANES AVE   STE 103   WOODRIDGE   IL   60517-2356
  Affiliated   5998   INDY SOUTH AT HOME   Indy South At Home   972 EMERSON PKWY   STE E   GREENWOOD   IN   46143-6202
  Affiliated   5999   LOCKPORT HOME AT HOME   Lockport Home Dialysis At Home   16626 W 159TH ST   STE 703   LOCKPORT   IL   60441-8019
  Affiliated   6000   CAMELBACK AT HOME HEMO   Camelback Dialysis At Home   7321 E OSBORN DR     SCOTTSDALE   AZ   85251-6418
  Affiliated   6002   WEST BOUNTIFUL DIALYSIS AT HOME   West Bountiful Dialysis At Home   724 W 500 S   STE 300   WEST BOUNTIFUL   UT   84087-1471
  Affiliated   6002   WEST BOUNTIFUL DIALYSIS AT HOME   West Bountiful Dialysis At Home   724 W 500 S   STE 300   WEST BOUNTIFUL   UT   84087-1471
  Affiliated   6004   CORNERSTONE DIALYSIS AT HOME   Cornerstone Dialysis At Home   23857 GREENFIELD RD     SOUTHFIELD   MI   48075-3122
  Affiliated   6006   DIALYSIS CARE OF MOORE COUNTY AT HOME   Dialysis Care of Moore County At Home (aka Pinehurst)   16 REGIONAL DR     PINEHURST   NC   28374-8850
  Affiliated   6007   HOME DIALYSIS AT HOME   Home Dialysis At Home (Minneapolis)   825 S 8TH ST   STE 1224   MINNEAPOLIS   MN   55404-1223
  Affiliated   6009   ST PAUL CAPITOL DIALYSIS AT HOME   St Paul Capital Dialysis At Home   555 PARK ST   STE 210   SAINT PAUL   MN   55103-2193
  Affiliated   6011   BALLENGER PT AT HOME   Ballenger Pt. At Home   2262 S BALLENGER HWY     FLINT   MI   48503-3447
  Affiliated   6012   LAKEWOOD AT HOME   Lakewood At Home   1750 PIERCE ST     LAKEWOOD   CO   80214-1434
  Affiliated   6013   MED-CENTER AT HOME   Med-Center at Home   7580 FANNIN ST   STE 230   HOUSTON   TX   77054-1939
  Affiliated   6014   UTAH VALLEY DIALYSIS AT HOME   Utah Valley Dialysis At Home   1055 N 500 W   STE 221   PROVO   UT   84604-3305
  Affiliated   6015   LOWRY AT HOME   Lowry At Home   7465 E 1ST AVE   STE A   DENVER   CO   80230-6877
  Affiliated   6016   MANZANITA AT HOME   Manzanita At Home   4005 MANZANITA AVE   STE 17   CARMICHAEL   CA   95608-1779
  Affiliated   6017   FIRST COLONIAL DAVITA AT HOME   First Colonial DaVita At Home   1157 FIRST COLONIAL RD   STE 200   VIRGINIA BEACH   VA   23454-2432
  Affiliated   6019   LAKEWOOD WASHINGTON AT HOME   Lakewood Washington At Home   5919 LAKEWOOD TOWNE CENTER BLVD SW   STE A   LAKEWOOD   WA   98499-6513
  Affiliated   6020   GRAPEVINE AT HOME   Grapevine At Home   1600 W NORTHWEST HWY   STE 100   GRAPEVINE   TX   76051-8131
  Affiliated   6021   GRAND RAPIDS AT HOME (CHERRY STREET)   Grand Rapids At Home (Cherry Street)   801 CHERRY ST SE     GRAND RAPIDS   MI   49506-1440
  Affiliated   6022   FEDERAL WAY AT HOME   Federal Way At Home   1015 S 348TH ST     FEDERAL WAY   WA   98003-7078
  Affiliated   6023   CENTURY CITY AT HOME   Century City At Home   10630 SANTA MONICA BLVD     LOS ANGELES   CA   90025
  Affiliated   6024   REDDING AT HOME   Redding At Home   1876 PARK MARINA DR     REDDING   CA   96001-0913
  Affiliated   6025   OLYMPIA FIELDS AT HOME   Olympia Fields At Home   4557B LINCOLN HWY   STE B   MATTESON   IL   60443-2318
  Affiliated   6026   MT VERNON AT HOME   Mount Vernon At Home   1800 JEFFERSON AVE     MOUNT VERNON   IL   62864-4300
  Affiliated   6028   YAKIMA AT HOME   Yakima At Home   1221 N 16TH AVE     YAKIMA   WA   98902-1347
  Affiliated   6029   MID-COLUMBIA AT HOME   Mid Columbia At Home   6825 BURDEN BLVD   STE A   PASCO   WA   99301-9584
  Affiliated   6030   GEORGETOWN ON THE POTOMAC AT HOME   Georgetown on the Potomac At Home   3323 K STREET NW   SUITE 110   WASHINGTON   DC   20007
  Affiliated   6031   SIOUX FALLS AT HOME   Sioux Falls At Home   800 E 21ST ST     SIOUX FALLS   SD   57105-1016
  Affiliated   6032   HILLSBORO AT HOME   Hillsboro At Home   2500 NW 229TH AVE   STE 300 BLDG E   HILLSBORO   OR   97124-7516
  Affiliated   6033   PIKES PEAK AT HOME   Pikes Peak At Home   2002 LELARAY ST   STE 130   COLORADO SPRINGS   CO   80909-2804

 

Page 82 of 136


  Affiliated   6034   WALNUT CREEK AT HOME   Walnut Creek At Home   400 N WIGET LN     WALNUT CREEK   CA   94598-2408
  Affiliated   6035   SAN ANTONIO AT HOME   San Antonio At Home   5284 MEDICAL DR   STE 100   SAN ANTONIO   TX   78229-4849
  Affiliated   6036   SANTA ROSA AT HOME   Santa Rosa At Home   5819 HIGHWAY 90     MILTON   FL   32583-1763
  Affiliated   6037   DUNMORE AT HOME   Dunmore At Home   1212 ONEILL HWY     DUNMORE   PA   18512-1717
  Affiliated   6038   PALMERTON AT HOME   Palmerton At Home   185 DELAWARE AVE   STE C   PALMERTON   PA   18071-1716
  Affiliated   6039   LONGVIEW AT HOME   Longview At Home   425 N FREDONIA ST     LONGVIEW   TX   75601-6464
  Affiliated   6040   JB ZACHARY AT HOME   JB Zachary At Home   333 CASSELL DR   STE 2300   BALTIMORE   MD   21224-6815
  Affiliated   6041   MEMPHIS EAST AT HOME   Memphis East At Home   50 HUMPHREYS CTR   STE 28B   MEMPHIS   TN   38120-2369
  Affiliated   6042   PLAINFIELD AT HOME   Plainfield At Home   1200 RANDOLPH RD   KENYAN HOUSE   PLAINFIELD   NJ   07060-3361
  Affiliated   6045   CHARLOTTE AT HOME   Charlotte (NC) At Home   2321 W MOREHEAD ST   STE 102   CHARLOTTE   NC   28208-5145
  Affiliated   6046   DALY CITY AT HOME   Daly City At Home   1498 SOUTHGATE AVE   STE 101   DALY CITY   CA   94015-4015
  Affiliated   6047   SALEM AT HOME   Salem At Home (OR)   3550 LIBERTY RD S   STE 100   SALEM   OR   97302-5700
  Affiliated   6048   OMAHA WEST AT HOME   Omaha West At Home   13014 W DODGE RD     OMAHA   NE   68154-2148
  Affiliated   6049   TUCSON EAST AT HOME   Tucson East At Home   6420 E BROADWAY BLVD   STE C300   TUCSON   AZ   85710-3512
  Affiliated   6050   WHITE OAK AT HOME   White Oak At Home   5520 CHEVIOT RD   STE B   CINCINNATI   OH   45247-7069
  Affiliated   6051   BELPRE AT HOME   Belpre At Home   2906 WASHINGTON BLVD     BELPRE   OH   45714-1848
  Affiliated   6052   BIRMINGHAM AT HOME   Birmingham At Home   2101 7TH AVE S     BIRMINGHAM   AL   35233-3105
  Affiliated   6053   STAMFORD AT HOME   Stamford At Home   30 COMMERCE RD     STAMFORD   CT   06902-4506
  Affiliated   6054   WHITEBRIDGE AT HOME   Whitebridge At Home   103 WHITE BRIDGE PIKE   STE 6   NASHVILLE   TN   37209-4539
  Affiliated   6055   ZANESVILLE AT HOME   Zanesville At Home   3120 NEWARK RD     ZANESVILLE   OH   43701-9659
  Affiliated   6056   TYSON’S CORNER AT HOME   Tyson’s Corner At Home   8391 OLD COURTHOUSE RD   STE 160   VIENNA   VA   22182-3819
  Affiliated   6057   BRADFORD AT HOME   Bradford At Home   665 E MAIN ST     BRADFORD   PA   16701-1869
  Affiliated   6059   NORTHLAND AT HOME   Northland At Home   2750 CLAY EDWARDS DR   STE 515   N KANSAS CITY   MO   64116-3258
  Affiliated   6060   LAKE WORTH AT HOME   Lake Worth At Home   2459 S CONGRESS AVE   STE 100   PALM SPRINGS   FL   33406-7616
  Affiliated   6061   MEADVILLE AT HOME   Meadville At Home   19050 PARK AVENUE PLZ     MEADVILLE   PA   16335-4012
  Affiliated   6063   WILLINGBORO AT HOME   Willingboro At Home   230 VAN SCIVER PKWY     WILLINGBORO   NJ   08046-1131
  Affiliated   6064   DERENNE AT HOME   DeRenne At Home   5303 MONTGOMERY ST     SAVANNAH   GA   31405-5138
  Affiliated   6065   BRUNSWICK AT HOME   Brunswick At Home   53 SCRANTON CONNECTOR     BRUNSWICK   GA   31525-1862
  Affiliated   6067   AIKEN AT HOME   Aiken At Home   775 MEDICAL PARK DR     AIKEN   SC   29801-6306
  Affiliated   6068   BRIDGEPORT AT HOME   Bridgeport At Home   900 MADISON AVE     BRIDGEPORT   CT   06606-5534
  Affiliated   6069   ST PETERSBURG AT HOME   St Petersburg At Home   2850 34TH ST S     ST PETERSBURG   FL   33711-3817
  Affiliated   6070   DENISON AT HOME   Denison At Home   1220 REBA MACENTIRE LN     DENISON   TX   75020-9057
  Affiliated   6072   ATLANTIC AT HOME   Atlantic At Home   6 INDUSTRIAL WAY W   STE B   EATONTOWN   NJ   07724-2258
  Affiliated   6073   NEWTOWN AT HOME   Newtown At Home (fka St. Mary)   60 BLACKSMITH RD     NEWTOWN   PA   18940-1847
  Affiliated   6075   FOX RIVER AT HOME   Fox River At Home   1910 RIVERSIDE DR     GREEN BAY   WI   54301-2319
  Affiliated   6076   TOKAY AT HOME   Tokay At Home   777 S HAM LN   STE L   LODI   CA   95242-3593
  Affiliated   6077   CAPITAL CITY AT HOME   Capital City At Home   307 N 46TH ST     LINCOLN   NE   68503-3714
  Affiliated   6081   GREATER MIAMI AT HOME   Greater Miami At Home   160 NW 176TH ST   STE 100   MIAMI   FL   33169-5023
  Affiliated   6083   EFFINGHAM AT HOME   Effingham At Home   904 MEDICAL PARK DR   STE 1   EFFINGHAM   IL   62401-2193
  Affiliated   6084   SPRINGFIELD CENTRAL AT HOME   Springfield Central At Home   932 N RUTLEDGE ST     SPRINGFIELD   IL   62702-3721
  Affiliated   6085   DECATUR EAST WOOD AT HOME   Decatur East Wood At Home   794 E WOOD ST     DECATUR   IL   62523-1155
  Affiliated   6086   ILLINI AT HOME   Illini At Home   507 E UNIVERSITY AVE     CHAMPAIGN   IL   61820-3828
  Affiliated   6087   JANESVILLE AT HOME   Janesville At Home   1305 WOODMAN RD     JANESVILLE   WI   53545-1068
  Affiliated   6088   NEW HAVEN AT HOME   New Haven At Home   100 CHURCH ST S   STE C   NEW HAVEN   CT   06519-1703
  Affiliated   6089   NASHUA AT HOME   Nashua At Home   38 TYLER ST   STE 100   NASHUA   NH   03060-2912
  Affiliated   6090   EAST EVANSVILLE AT HOME   East Evansville At Home   1312 PROFESSIONAL BLVD     EVANSVILLE   IN   47714-8007
  Affiliated   6095   BROOKRIVER AT HOME   Brookriver At Home   8101 BROOKRIVER DR     DALLAS   TX   75247-4003
  Affiliated   6098   METRO EAST AT HOME   Metro East At Home   5105 W MAIN ST     BELLEVILLE   IL   62226-4728
  Affiliated   6099   MARION AT HOME   Marion At Home   324 S 4TH ST     MARION   IL   62959-1241
  Affiliated   6100   ROXBURY AT HOME   Roxbury At Home   622 ROXBURY RD     ROCKFORD   IL   61107-5089
  Affiliated   6101   SYCAMORE AT HOME   Sycamore At Home   2200 GATEWAY DR     SYCAMORE   IL   60178-3113
  Affiliated   6103   WESTVIEW AT HOME   Westview At Home   3749 COMMERCIAL DR   STE B   INDIANAPOLIS   IN   46222-1676
  Affiliated   6105   OCALA AT HOME   Ocala At Home   2860 SE 1ST AVE     OCALA   FL   34471-0406
  Affiliated   6106   COMPLETE CARE AT HOME   Complete Care At Home   7850 W SAMPLE RD     MARGATE   FL   33065-4710

 

Page 83 of 136


  Affiliated   6107   INTERAMERICAN AT HOME   InterAmerican At Home   7815 CORAL WAY   STE 115   MIAMI   FL   33155-6541
  Affiliated   6109   PURCELLVILLE AT HOME   Purcellville At Home   280 N HATCHER AVE     PURCELLVILLE   VA   20132-3193
  Affiliated   6110   TABLE ROCK AT HOME   Table Rock At Home   5610 GAGE ST   STE B   BOISE   ID   83706
  Affiliated   6111   TWIN FALLS AT HOME   Twin Falls At Home   1840 CANYON CREST DR     TWIN FALLS   ID   83301-3007
  Affiliated   6113   FOUR RIVERS AT HOME   Four Rivers At Home   515 EAST LN     ONTARIO   OR   97914-3953
  Affiliated   6114   OLYMPIC VIEW AT HOME   Olympic View At Home   125 16TH AVE E   FL 5   SEATTLE   WA   98112-5211
  Affiliated   6115   SPIVEY AT HOME   Spivey At Home   1423 STOCKBRIDGE RD   STE B   JONESBORO   GA   30236-3740
  Affiliated   6116   EAST DES MOINES AT HOME   East Des Moines At Home   1301 PENNSYLVANIA AVE   STE 208   DES MOINES   IA   50316-2365
  Affiliated   6118   KETTERING AT HOME   Kettering At Home   5721 BIGGER RD     KETTERING   OH   45440-2752
  Affiliated   6119   CITRUS VALLEY AT HOME   Citrus Valley At Home   894 HARDT ST     SAN BERNARDINO   CA   92408-2854
  Affiliated   6124   MERIDIAN PARK AT HOME   Meridian Park At Home   19255 SW 65TH AVE   STE 100   TUALATIN   OR   97062-9712
  Affiliated   6125   MARYVILLE AT HOME   Maryville At Home   2136B VADALABENE DR     MARYVILLE   IL   62062-5632
  Affiliated   6128   PDI-WORCESTER AT HOME   PDI-Worcester At Home   19 GLENNIE ST   STE A   WORCESTER   MA   01605-3918
  Affiliated   6129   PDI-ROCKY HILL AT HOME   PDI-Rocky Hill At Home   30 WATERCHASE DR     ROCKY HILL   CT   06067-2110
  Affiliated   6133   WICHITA AT HOME   Wichita At Home   909 N TOPEKA ST     WICHITA   KS   67214-3620
  Affiliated   6134   ASHEVILLE KIDNEY AT HOME   Asheville Kidney At Home   1600 CENTERPARK DR     ASHEVILLE   NC   28805-6206
  Affiliated   6136   STRONGSVILLE AT HOME   Strongsville At Home   17792 PEARL RD     STRONGSVILLE   OH   44136-6909
  Affiliated   6137   BATON ROUGE AT HOME   DSI Divest-Baton Rouge At Home   3888 NORTH BLVD   STE 101   BATON ROUGE   LA   70806-3824
  Affiliated   6138   WEST BROADWAY DIALYSIS AT HOME   West Broadway At Home   720 W BROADWAY   STE 200   LOUISVILLE   KY   40202-3245
  Affiliated   6140   BRONX AT HOME   Bronx At Home   1615 EASTCHESTER RD     BRONX   NY   10461-2603
  Affiliated   6142   CLEVE HILL AT HOME   Cleve Hill At Home   1461 KENSINGTON AVE     BUFFALO   NY   14215-1436
  Affiliated   6144   WHITE PLAINS AT HOME   White Plains At Home   200 HAMILTON AVE   STE 13B   WHITE PLAINS   NY   10601-1859
  Affiliated   6146   LAKE VILLA AT HOME   Lake Villa At Home   37809 N IL ROUTE 59     LAKE VILLA   IL   60046-7332
  Affiliated   6148   TULSA AT HOME   Tulsa At Home   4436 S HARVARD AVE     TULSA   OK   74135-2605
  Affiliated   6151   LITHONIA AT HOME   Lithonia At Home   2485 PARK CENTRAL BLVD     DECATUR   GA   30035-3902
  Affiliated   6152   LANHAM AT HOME   Lanham At Home   8855 ANNAPOLIS RD   STE 200   LANHAM   MD   20706-2919
  Affiliated   6153   HAMMOND AT HOME   Hammond At Home   222 DOUGLAS ST     HAMMOND   IN   46320-1960
  Affiliated   6156   UNION CITY CENTER AT HOME (CA)   Union City Center At Home (CA)   32930 ALVARADO NILES RD   STE 300   UNION CITY   CA   94587-8101
  Affiliated   6157   CHICO AT HOME   Chico At Home   530 COHASSET RD     CHICO   CA   95926-2212
  Affiliated   6158   MONTCLAIR AT HOME   Montclair At Home   5050 PALO VERDE ST   STE 100   MONTCLAIR   CA   91763-2333
  Affiliated   6161   PDI - LANCASTER AT HOME   PDI-Lancaster At Home   1412 E KING ST     LANCASTER   PA   17602-3240
  Affiliated   6162   PDI JOHNSTOWN AT HOME   PDI-Johnstown At Home   344 BUDFIELD ST     JOHNSTOWN   PA   15904-3214
  Affiliated   6163   CAMP HILL AT HOME   Camp Hill At Home   425 N 21ST ST   PLAZA 21 BLDG 1ST FL   CAMP HILL   PA   17011-2202
  Affiliated   6164   PDI MONTGOMERY AT HOME   PDI-Montgomery At Home   1001 FOREST AVE     MONTGOMERY   AL   36106-1181
  Affiliated   6165   FAIRFAX AT HOME   Fairfax At Home   8501 ARLINGTON BLVD   STE 100   FAIRFAX   VA   22031-4625
  Affiliated   6170   WEST SACRAMENTO AT HOME   West Sacramento At Home   3450 INDUSTRIAL BLVD   STE 100   WEST SACRAMENTO   CA   95691-5003
  Affiliated   6171   EAST MACON AT HOME   East Macon At Home   165 EMERY HWY   STE 101   MACON   GA   31217-3666
  Affiliated   6178   GERMANTOWN AT HOME   Germantown At Home   20111 CENTURY BLVD   STE C   GERMANTOWN   MD   20874-9165
  Affiliated   6180   SEDC-WILMINGTON AT HOME   SEDC-Wilmington (NC) At Home   2215 YAUPON DR     WILMINGTON   NC   28401-7334
  Affiliated   6182   HERMISTON COMMUNITY AT HOME   Hermiston Community At Home   1155 W LINDA AVE     HERMISTON   OR   97838-9601
  Affiliated   6183   SHREVEPORT HHD LA   Shreveport Home Dialysis At Home   1560 IRVING PL     SHREVEPORT   LA   71101-4604
  Affiliated   6184   DOWNTOWN SAN ANTONIO AT HOME   Downtown San Antonio At Home   615 E QUINCY ST     SAN ANTONIO   TX   78212
  Affiliated   6186   COLUMBIA MO AT HOME   RTC-Columbia (MO) At Home   1701 E BROADWAY   STE G102   COLUMBIA   MO   65201-8029
  Affiliated   6188   REGENCY AT HOME   Regency At Home (fka Jacksonville)   9535 REGENCY SQUARE BLVD N     JACKSONVILLE   FL   32225-8128
  Affiliated   6193   WEST GEORGIA AT HOME   West Georgia At Home (fka Columbus (GA))   1216 STARK AVE     COLUMBUS   GA   31906-2500
  Affiliated   6194   BUFORD AT HOME   Buford At Home   1550 BUFORD HWY   STE 1E   BUFORD   GA   30518-3666
  Affiliated   6195   KALAMAZOO WEST AT HOME   Kalamazoo West At Home   1040 N 10TH ST     KALAMAZOO   MI   49009-6149
  Affiliated   6196   SOUTH VALLEY AT HOME   South Valley At Home   17815 VENTURA BLVD   STE 100   ENCINO   CA   91316-3600
  Affiliated   6204   QUEENS VILLAGE AT HOME   Queens Village At Home   22202 HEMPSTEAD AVE   STE 170   QUEENS VILLAGE   NY   11429-2123
  Affiliated   6207   LANSING AT HOME-MI   Lansing Home Hemodialysis At Home   1675 WATERTOWER PL   STE 700   EAST LANSING   MI   48823-6397
  Affiliated   6208   SOUTH COUNTY AT HOME   South County At Home (Deaconess)   4145 UNION RD     SAINT LOUIS   MO   63129-1064
  Affiliated   6211   TACOMA AT HOME   Tacoma At Home   3401 S 19TH ST     TACOMA   WA   98405-1909
  Affiliated   6213   CEDAR PARK AT HOME   Cedar Park At Home (fka North Austin)   1720 E WHITESTONE BLVD     CEDAR PARK   TX   78613-7640
  Affiliated   6214   SOUTH FORT WORTH DIALYSIS AT HOME   South Fort Worth At Home   6260 SOUTHWEST BLVD     BENBROOK   TX   76109-6906

 

Page 84 of 136


  Affiliated   6215   THE WOODLANDS AT HOME   DNVO-The Woodlands At Home   9301 PINECROFT DR     SHENANDOAH   TX   77380-3179
  Affiliated   6218   ARROWHEAD LAKES AT HOME   Arrowhead Lakes At Home   20325 N 51ST AVE   STE 184 BLDG 11   GLENDALE   AZ   85308-4625
  Affiliated   6220   COLUMBUS WEST HOME TRAINING   Columbus West Home Training At Home   1391 GEORGESVILLE RD     COLUMBUS   OH   43228-3611
  Affiliated   6221   RICHMOND KIDNEY CENTER AT HOME   Richmond Kidney Center At Home (Staten Island)   1366 VICTORY BLVD     STATEN ISLAND   NY   10301-3907
  Affiliated   6225   DIALYSIS CARE OF KANNAPOLIS AT HOME   Dialysis Care of Kannapolis At Home   1607 N MAIN ST     KANNAPOLIS   NC   28081-2317
  Affiliated   6226   BUTLER-FARM AT HOME   Butler Farm At Home   501 BUTLER FARM RD   STE A   HAMPTON   VA   23666-1777
  Affiliated   6228   NEW PORT RICHEY AT HOME   New Port Richey Kidney At Home   7421 RIDGE RD     PORT RICHEY   FL   34668-6933
  Affiliated   6229   GRAND HOME AT HOME   Grand Home At Home   14674 W MOUNTAIN VIEW BLVD   STE 204   SURPRISE   AZ   85374-2708
  Affiliated   6230   WILLIAMSBURG AT HOME   Williamsburg At Home (fka Yorktown)   500 SENTARA CIR   STE 103   WILLIAMSBURG   VA   23188-5727
  Affiliated   6231   BALDWIN COUNTY AT HOME   Home Dialysis Options of Baldwin County At Home   27880 N MAIN ST   STE A   DAPHNE   AL   36526-7080
  Affiliated   6232   CLINTON TOWNSHIP AT HOME   Clinton Township at Home   15918 19 MILE RD   STE 110   CLINTON TOWNSHIP   MI   48038-1101
  Affiliated   6233   GROSSE POINTE AT HOME   Grosse Pointe At Home   18000 E WARREN AVE   STE 100   DETROIT   MI   48224-1336
  Affiliated   6234   GREENSBURG AT HOME   Greensburg At Home   1531 N COMMERCE EAST DR   STE 6   GREENSBURG   IN   47240-3259
  Affiliated   6236   GULF BREEZE AT HOME   Gulf Breeze At Home   1519 MAIN ST     DUNEDIN   FL   34698-4650
  Affiliated   6237   JACKSONVILLE CENTRAL AT HOME   Jacksonville Central At Home   400 T P WHITE DR     JACKSONVILLE   AR   72076-3287
  Affiliated   6238   SAN JOSE AT HOME   San Jose At Home (Freestanding)   4400 STEVENS CREEK BLVD   STE 50   SAN JOSE   CA   95129-1104
  Affiliated   6243   ORLANDO AT HOME   Orlando At Home (0178)   14050 TOWN LOOP BLVD   STE 104B   ORLANDO   FL   32837-6190
  Affiliated   6244   KENNEDY HOME DIALYSIS-AT HOME   Kennedy Home Dialysis-At Home   5509 N CUMBERLAND AVE   STE 515   CHICAGO   IL   60656-4702
  Affiliated   6245   YPSILANTI AT HOME   Ypsilanti At Home   2762 WASHTENAW RD     YPSILANTI   MI   48197-1506
  Affiliated   6246   JACKSONVILLE AT HOME   SEDC (NC II) Jacksonville At Home   14 OFFICE PARK DR     JACKSONVILLE   NC   28546-7325
  Affiliated   6247   LEBANON AT HOME   Lebanon At Home   918 COLUMBUS AVE   STE 2 UNIT B   LEBANON   OH   45036-1402
  Affiliated   6248   SLIDELL KIDNEY CARE AT HOME   Slidell Kidney Care At Home   1150 ROBERT BLVD   STE 240   SLIDELL   LA   70458-2005
  Affiliated   6249   WATERBURY AT HOME   Waterbury At Home   150 MATTATUCK HEIGHTS RD     WATERBURY   CT   06705-3893
  Affiliated   6251   WHITE LANE AT HOME   White Lane At Home   7701 WHITE LN   STE D   BAKERSFIELD   CA   93309-0201
  Affiliated   6253   HANFORD AT HOME   Hanford At Home   900 N DOUTY ST     HANFORD   CA   93230-3918
  Affiliated   6254   ANAHEIM AT HOME   Anaheim At Home   1107 W LA PALMA AVE     ANAHEIM   CA   92801-2804
  Affiliated   6255   MERCED AT HOME   Merced At Home   3150 NORTH G ST   STE B   MERCED   CA   95340-1346
  Affiliated   6257   ST JOSEPH AT HOME   St. Joseph At Home   5514 CORPORATE DR   STE 100   SAINT JOSEPH   MO   64507-7752
  Affiliated   6258   CENTRAL LITTLE ROCK AT HOME   Central Little Rock At Home   5800 W 10TH ST   STE 510   LITTLE ROCK   AR   72204-1760
  Affiliated   6260   DURHAM WEST AT HOME   Durham West At Home   4307 WESTERN PARK PL   STE 101   DURHAM   NC   27705-1204
  Affiliated   6262   TOLEDO AT HOME   Toledo At Home   1614 S BYRNE RD     TOLEDO   OH   43614-3464
  Affiliated   6263   HIOAKS AT HOME   Hioaks At Home   681 HIOAKS RD   STE D   RICHMOND   VA   23225-4043
  Affiliated   6264   ELIZABETH AT HOME   Elizabeth At Home   201 MCKEESPORT RD     ELIZABETH   PA   15037-1623
  Affiliated   6265   ABINGTON AT HOME   Abington At Home   3940A COMMERCE AVE     WILLOW GROVE   PA   19090-1705
  Affiliated   6267   NORTH ORANGEBURG AT HOME   North Orangeburg At Home   124 FIRE TOWER RD     ORANGEBURG   SC   29118-1401
  Affiliated   6268   DEARBORN HOME DIALYSIS - AT HOME   Dearborn Home Dialysis-At Home   22030 PARK ST     DEARBORN   MI   48124-2854
  Affiliated   6269   OCEAN SPRINGS AT HOME   Ocean Springs At Home   13150 PONCE DEL LEON     OCEAN SPRINGS   MS   39564-2460
  Affiliated   6270   HAKC - HUNTINGTON AT HOME   HAKC-Huntington At Home   256 BROADWAY     HUNTINGTON STATION   NY   11746-1403
  Affiliated   6271   42ND ST AT HOME   Philadelphia 42nd Street At Home   4126 WALNUT ST     PHILADELPHIA   PA   19104-3511
  Affiliated   6275   CHARLOTTESVILLE NORTH AT HOME   Charlottesville North At Home   1800 TIMBERWOOD BLVD   STE C   CHARLOTTESVILLE   VA   22911-7544
  Affiliated   6276   HEARTLAND AT HOME   Heartland At Home   925 NE 8TH ST     OKLAHOMA CITY   OK   73104-5800
  Affiliated   6278   LAKELAND SOUTH AT HOME   Lakeland South At Home   5050 S FLORIDA AVE   STE 1   LAKELAND   FL   33813-2501
  Affiliated   6282   RAINBOW CITY AT HOME   Rainbow City At Home   2800 RAINBOW DR     RAINBOW CITY   AL   35906-5811
  Affiliated   6283   ATHENS AT HOME   Athens At Home   15953 ATHENS LIMESTONE DR   STE 15   ATHENS   AL   35613-2214
  Affiliated   6284   SYLACAUGA AT HOME   Sylacauga At Home   331 JAMES PAYTON BLVD     SYLACAUGA   AL   35150
  Affiliated   6287   PITTSBURGH AT HOME   Pittsburgh At Home   4312 PENN AVE     PITTSBURGH   PA   15224-1310
  Affiliated   6289   RADNOR AT HOME   Radnor At Home   250 KING OF PRUSSIA RD     RADNOR   PA   19087-5220
  Affiliated   6291   RADFORD AT HOME   Radford At Home   600 E MAIN ST   STE B   RADFORD   VA   24141-1826
  Affiliated   6292   HARRISONBURG AT HOME   Harrisonburg At Home   871 CANTRELL AVE   STE 100   HARRISONBURG   VA   22801-4323
  Affiliated   6293   KERRVILLE AT HOME   Kerrville At Home   515 GRANADA PL     KERRVILLE   TX   78028-5992
  Affiliated   6294   WEST TALLAHASSEE AT HOME   West Tallahassee At Home   2645 W TENNESSEE ST   STE 8   TALLAHASSEE   FL   32304-2521
  Affiliated   6295   ROME AT HOME   Rome At Home   15 JOHN MADDOX DR NW     ROME   GA   30165-1413
  Affiliated   6297   ST LOUIS WEST AT HOME   St. Louis West At Home   450 N LINDBERGH BLVD   STE 100C   CREVE COEUR   MO   63141-7858
  Affiliated   6298   COOKEVILLE AT HOME   Cookeville At Home   140 W 7TH ST     COOKEVILLE   TN   38501-1726

 

Page 85 of 136


  Affiliated   6300   DOTHAN AT HOME   Dothan At Home   216 GRACELAND DR     DOTHAN   AL   36305-7346
  Affiliated   6302   HENRICO COUNTY AT HOME   Henrico County At Home   5270 CHAMBERLAYNE RD     RICHMOND   VA   23227-2950
  Affiliated   6303   WEYMOUTH CLINIC AT HOME   Weymouth At Home   330 LIBBEY INDUSTRIAL PKWY   STE 900   WEYMOUTH   MA   02189-3122
  Affiliated   6304   ERIE AT HOME   Erie At Home   350 E BAYFRONT PKWY   STE A   ERIE   PA   16507-2410
  Affiliated   6305   WILSON AT HOME   Wilson At Home   1605 MEDICAL PARK DR W     WILSON   NC   27893-2799
  Affiliated   6306   NORTH FULTON AT HOME   North Fulton At Home   1250 NORTHMEADOW PKWY   STE 120   ROSWELL   GA   30076-4914
  Affiliated   6311   BRADENTON AT HOME   Bradenton At Home   3501 CORTEZ RD W   STE 104   BRADENTON   FL   34210-3104
  Affiliated   6312   COLUMBIA UNIVERSITY AT HOME   Columbia University At Home   60 HAVEN AVENUE     NEW YORK   NY   10032-2604
  Affiliated   6313   NEW BEDFORD AT HOME   New Bedford At Home   524 UNION ST     NEW BEDFORD   MA   02740-3546
  Affiliated   6314   MUSKEGON AT HOME   Muskegon At Home   1277 MERCY DR     MUSKEGON   MI   49444-4605
  Affiliated   6315   WELLINGTON CIRCLE AT HOME   Wellington Circle At Home   10 CABOT RD   STE 103B   MEDFORD   MA   02155-5173
  Affiliated   6316   FREDERICK AT HOME   Frederick At Home   140 THOMAS JOHNSON DR   STE 100   FREDERICK   MD   21702-4475
  Affiliated   6317   SELINSGROVE AT HOME   Selinsgrove At Home   1030 N SUSQUEHANNA TRL     SELINSGROVE   PA   17870-7767
  Affiliated   6318   LAKE CHARLES SOUTHWEST AT HOME   Lake Charles Southwest At Home   300 18th ST     LAKE CHARLES   LA   70601-7342
  Affiliated   6319   LENEXA AT HOME   Lenexa At Home   8630 HALSEY ST     LENEXA   KS   66215-2880
  Affiliated   6321   NASHVILLE HOME TRAINING AT HOME   Nashville Home Training At Home   1919 CHARLOTTE AVE   STE 200   NASHVILLE   TN   37203-2245
  Affiliated   6322   GOLDSBORO AT HOME   Goldsboro At Home   2609 HOSPITAL RD     GOLDSBORO   NC   27534-9424
  Affiliated   6323   MIAMI CAMPUS AT HOME   Miami Campus At Home   1500 NW 12TH AVE   STE 106   MIAMI   FL   33136-1028
  Affiliated   6324   DAYTONA BEACH AT HOME   Daytona Beach At Home   578 HEALTH BLVD     DAYTONA BEACH   FL   32114-1492
  Affiliated   6325   GRASS VALLEY AT HOME   Grass Valley At Home   360 CROWN POINT CIR   STE 210   GRASS VALLEY   CA   95945-2543
  Affiliated   6326   POMONA AT HOME   Pomona At Home   2111 NORTH GAREY AVENUE     POMONA   CA   91767
  Affiliated   6327   MID ATLANTA HOME AT HOME   MidAtlanta Home At Home   418 DECATUR ST SE   SUITE B   ATLANTA   GA   30312-1801
  Affiliated   6328   MARTINSVILLE AT HOME   Martinsville Dialysis   33 BRIDGE ST S     MARTINSVILLE   VA   24112-6214
  Affiliated   6329   HUBBARD ROAD AT HOME   Hubbard Road At Home   1963 HUBBARD RD     MADISON   OH   44057
  Affiliated   6350   PLAINFIELD RENAL CENTER AT HOME   Plainfield Renal At Home (P278)   8110 NETWORK DR     PLAINFIELD   IN   46168-9024
  Affiliated   6351   NORTH ANDOVER RENAL CENTER AT HOME   North Andover Renal At Home (P178)   201 SUTTON ST     NORTH ANDOVER   MA   1845
  Affiliated   6352   JACKSON NORTH DIALYSIS AT HOME   Jackson North At Home (P181)   571 BEASLEY RD   STE B   JACKSON   MS   39206-3042
  Affiliated   6353   SUMMIT RENAL AT HOME   Summit Renal At Home (P186)   73 MASSILLON RD     AKRON   OH   44312-1028
  Affiliated   6354   MARLTON DIALYSIS AT HOME   Marlton At Home (P200)   769 E RTE 70     MARLTON   NJ   08053-2341
  Affiliated   6355   CENTRAL FORT WAYNE DIALYSIS AT HOME   Central Fort Wayne At Home (P223)   1940 BLUFTON RD     FORT WAYNE   IN   46809-1307
  Affiliated   6356   LAS CRUCES RENAL CENTER AT HOME   Las Cruces Renal At Home (P237)   3961 E LOHMAN AVE   STE 29   LAS CRUCES   NM   88011-8272
  Affiliated   6357   NORTHEAST PORTLAND RENAL CENTER AT HOME   Northeast Portland Renal At Home (P240)   703 NE HANCOCK ST     PORTLAND   OR   97212-3955
  Affiliated   6358   KANSAS CITY RENAL CENTER AT HOME   Kansas City Renal At Home (P264)   4333 MADISON AVE     KANSAS CITY   MO   64111-3429
  Affiliated   6359   COASTAL DIALYSIS AT HOME   South Texas Renal At Home (P257)   4300 S PADRE ISLAND DR     CORPUS CHRISTI   TX   78411-4433
  Affiliated   6360   NORTH SPOKANE RENAL CENTER AT HOME   North Spokane Renal At Home (P262)   12610 E MARIBEAU PRKWY   STE 100   SPOKANE   WA   99216
  Affiliated   5659   TEMPE DIALYSIS PD   Tempe Dialysis Center PD   2149 EAST WARNER RD   STE 109   TEMPE   AZ   85284-3496
  Affiliated   5660   ARROWHEAD LAKES DIALYSIS PD   Arrowhead Lakes Dialysis PD   20325 N 51ST AVE   BLDG 11, STE 184   GLENDALE   AZ   85308-4625
  Affiliated   5916   SHAKER SQUARE AT HOME   Shaker Square At Home   12800 SHAKER BLVD   STE 1   CLEVELAND   OH   44120-2004
  Affiliated   6130   SIERRA ROSE AT HOME   Sierra Rose At Home   685 SIERRA ROSE DR     RENO   NV   89511-2060
  Affiliated   6217   TEMPE AT HOME   Tempe At Home   2149 E WARNER RD   STE 109   TEMPE   AZ   85284-3496
  Affiliated   6281   TUSCALOOSA AT HOME   Tuscaloosa At Home   805 OLD MILL ST     TUSCALOOSA   AL   35401-7132
TEMPORARY CLOSURES
(Included above are several centers that have temporarily suspended operations for a variety of reasons, but are scheduled to resume operations within the coming few months)
    614   Lynwood            
    643   Vidalia            
    3518   Huntingdon Valley Dialysis            
    626   Tuba City            
    903   Littleton            

 

Page 86 of 136


Exhibit D

Managed Centers List

 

Page 87 of 136


Exhibit D

Managed Centers List

 

Active
count

 

TYPE

 

CTR #

 

CENTER NAME

 

LEGAL NAME

 

ADDRESS

 

ADDRESS

 

CITY

 

STATE

 

ZIP

1771   Administrative Services   181   Childrens Hospital   MGD-Children’s National Medical Center   111 MICHIGAN AVE NW     WASHINGTON   DC   20010-2916
1772   Administrative Services   1624   Renal Care Seat Pleasant   MGD-Renal Care of Seat Pleasant   6274 CENTRAL AVE     SEAT PLEASANT   MD   20743
1773   Administrative Services   1715   Moses Taylor Hospital Renal Unit   Moses Taylor Hospital Renal Unit   700 QUINCY AVE     SCRANTON   PA   18510-1724
1774   Administrative Services   3330   Aurora Medical Group - Fond du Lac   Aurora Medical Group-Fond du Lac   210 WISCONSIN AMERICAN DR   ATTN DAVITA DIALYSIS (WEST END OF BLDG)   FOND DU LAC   WI   54937-2999
1775   Administrative Services   3331   Aurora Medical Group - Sheboygan   Aurora Medical Group-Sheboygan   2414 KOHLER MEMORIAL DR     SHEBOYGAN   WI   53081-3129
1776   Administrative Services   3338   Aurora Medical Group - Lake Geneva   Aurora Medical Group-Lake Geneva   146 E GENEVA SQ     LAKE GENEVA   WI   53147-9694
1777   Administrative Services   3555   Aurora Medical Group - Marinette Dialysis   Aurora Medical Group-Marinette Dialysis   4061 OLD PESHTIGO RD     MARINETTE   WI   54143
1778   Administrative Services   3607   Aurora Medical Group - Brown County Dialysis   Aurora Medical Group-Brown County Dialysis   1751 DECKNER AVE     GREEN BAY   WI   54302-2630
1779   Administrative Services   3641   Aurora Medical Group - Sturgeon Bay Dialysis   Aurora Medical Group-Sturgeon Bay Dialysis   108 S 10TH AVE     STURGEON BAY   WI   54235-1802
1780   Administrative Services   3653   Aurora Medical Group - Oshkosh West Dialysis   Aurora Medical Group-Oshkosh West Dialysis   855 N WESTHAVEN DR     OSHKOSH   WI   54904-7668
1781   Administrative Services   3665   Aurora Medical Group - Manitowoc Dialysis   Aurora Medical Group-Manitowoc Dialysis   601 REED AVE     MANITOWOC   WI   54220-2026
1782   Administrative Services   3672   Aurora Medical Group - Wautoma Dialysis   Aurora Medical Group-Wautoma Dialysis   900 EAST DIVISION ST     WAUTOMA   WI   54982-6944
1783   Administrative Services   1868   Maize Dialysis   Maize Dialysis Center   10001 GRADY AVE     MAIZE   KS   67101
1784   Administrative Services   1912   Kidney Dialysis Center   MGD-Kidney Dialysis Center, LLC (MMG Macon)   640 MARTIN LUTHER KING JR BLVD     MACON   GA   31201-3206
  Administrative Services   6079   MAGNOLIA WEST AT HOME   Magnolia West At Home   11161 MAGNOLIA AVE   STE B   RIVERSIDE   CA   92505-3605
  Administrative Services   1903   Riverside PD Central NAMG   Riverside PD Central   3660 PARK SIERRA DR   STE 18   RIVERSIDE   CA   92505-3071

 

Page 88 of 136


Exhibit E

Dialysis Center Committed Purchasers List

 

Page 89 of 136


Exhibit E

Dialysis Center Committed Purchasers List

 

Active
count

 

TYPE

 

CTR #

 

CENTER NAME

 

LEGAL NAME

 

ADDRESS

 

ADDRESS

 

CITY

 

STATE

 

ZIP

1   Affiliated   398   Los Angeles Dialysis Center   Los Angeles Dialysis Center (LADC)   3901 S WESTERN AVE     LOS ANGELES   CA   90062-1112
2   Affiliated   613   Garfield   Garfield Hemodialysis Center   118 HILLIARD AVE     MONTEREY PARK   CA   91754-1118
3   Affiliated   614   Lynwood   Kidney Dialysis Care Unit (Lynwood)   3600 E MARTIN LUTHER KING JR BLVD     LYNWOOD   CA   90262-2607
4   Affiliated   615   Lakewood Dialysis-CA   Lakewood Dialysis-CA   4611 SILVA ST     LAKEWOOD   CA   90712-2512
5   Affiliated   616   Valley Dialysis   Valley Dialysis   16149 HART ST     VAN NUYS   CA   91406-3906
6   Affiliated   617   Downey Dialysis   Downey Dialysis   8630 FLORENCE AVE   STE 1   DOWNEY   CA   90240-4017
7   Affiliated   618   Covina Dialysis   Covina Dialysis   1547 W GARVEY AVE N     WEST COVINA   CA   91790-2139
8   Affiliated   625   Four Corners Farmington   Four Corners Farmington   801 W BROADWAY     FARMINGTON   NM   87401-5650
9   Affiliated   626   Tuba City Dialysis   Tuba City Dialysis   500 EDGEWATER DR   PO BOX 291   TUBA CITY   AZ   86045-2905
10   Affiliated   627   Camelback Dialysis Center   Camelback Dialysis Center (fka Scottsdale Dialysis Center)   7321 E OSBORN DR     SCOTTSDALE   AZ   85251-6418
11   Affiliated   630   Westbank   Westbank Chronic Renal Center   3631 BEHRMAN PLACE     NEW ORLEANS   LA   70114
12   Affiliated   632   Fleur de Lis   Fleur de Lis Dialysis (fka Tri-Parish)   5555 BULLARD AVE     NEW ORLEANS   LA   70128-3450
13   Affiliated   637   Desert Mountain   Desert Mountain Dialysis   9220 E MOUNTAIN VIEW RD   STE 15   SCOTTSDALE   AZ   85258-5134
14   Affiliated   638   Chinle   Chinle Dialysis   US HWY 191   PO BOX 879   CHINLE   AZ   86503-0879
15   Affiliated   648   Central City   Central City Dialysis Center   1300 MURCHISON DR   STE 32   EL PASO   TX   79902-4840
16   Affiliated   651   Federal Way   Federal Way Community Dialysis Center   1015 S 348TH ST     FEDERAL WAY   WA   98003-7078
17   Affiliated   663   Beverly Hills   Beverly Hills Dialysis Center   50 N LA CIENEGA BLVD   3RD FLOOR, STE 3   BEVERLY HILLS   CA   90211-2205
18   Affiliated   667   Walnut Creek   Walnut Creek Dialysis Center   404 N WIGET LN     WALNUT CREEK   CA   94598-2408
19   Affiliated   672   Norwalk   Norwalk Dialysis Center   12375 E IMPERIAL HWY   STE D3   NORWALK   CA   90650-3129
20   Affiliated   673   El Monte   Greater El Monte Dialysis Center   1938 TYLER AVE   STE J-168   SOUTH EL MONTE   CA   91733-3623
21   Affiliated   676   Bayonet Point   Bayonet Point-Hudson Kidney   14144 NEPHRON LN     HUDSON   FL   34667-6504
22   Affiliated   677   New Port Richey   New Port Richey Kidney Center   7421 RIDGE RD     PORT RICHEY   FL   34668-6933
23   Affiliated   678   Hernando   Hernando Kidney Center, Inc   2985 LANDOVER BLVD     SPRING HILL   FL   34608-7258
24   Affiliated   681   Woodbridge   CDC Of Woodbridge   2751 KILLARNEY DR     WOODBRIDGE   VA   22192-4119
25   Affiliated   682   Manassas   CDC-Manassas Dialysis   10655 LOMOND DR   STE 11   MANASSAS   VA   20109-2877
26   Affiliated   683   Springfield   CDC-Springfield Dialysis   8350 TRAFORD LN   STE A   SPRINGFIELD   VA   22152-1671
27   Affiliated   684   Sterling   CDC-Sterling   46396 BENEDICT DR   STE 1   STERLING   VA   20164-6626
28   Affiliated   687   Alexandria   Springfield-Alexandria   5999 STEVENSON AVE   STE 1   ALEXANDRIA   VA   22304-3302
29   Affiliated   642   Statesboro   Nephrology Center of Statesboro fka Statesboro Dialysis   4B COLLEGE PLZ     STATESBORO   GA   30458-4928
30   Affiliated   643   Vidalia   Nephrology Center of Vidalia   1806 EDWINA DR     VIDALIA   GA   30474-8927
31   Affiliated   657   Papago Dialysis   Papago Dialysis Center (fka PD Central & Squaw Peak)   1401 N 24TH ST   STE 2   PHOENIX   AZ   85008-4638
32   Affiliated   658   Boca Raton   Boca Raton Artificial Kidney Center   998 NW 9TH CT     BOCA RATON   FL   33486-2214
33   Affiliated   644   Piedmont   Buckhead Dialysis   1575 NORTHSIDE DR NW   STE 365   ATLANTA   GA   30318-4210
34   Affiliated   311   Logan Square   Logan Square Dialysis Services   2659 N MILWAUKEE AVE   1ST FL   CHICAGO   IL   60647-1643
35   Affiliated   312   Lake County   Lake County Dialysis Services   918 S MILWAUKEE AVE     LIBERTYVILLE   IL   60048-3229
36   Affiliated   314   Lincoln Park   Lincoln Park Dialysis fka Lincoln Park Nephrology   3157 N LINCOLN AVE     CHICAGO   IL   60657-3111
37   Affiliated   318   Lincoln Pk-PD   Skyline Home Dialysis (fka Lincoln Park PD)   7009 W BELMONT AVE     CHICAGO   IL   60634-4533
38   Affiliated   670   West Palm Beach   Dialysis Associates of the Palm Beaches   2611 POINSETTIA AVE     WEST PALM BEACH   FL   33407-5919
39   Affiliated   693   Sunrise   Sunrise Dialysis Center   13039 HAWTHORNE BLVD     HAWTHORNE   CA   90250-4415
40   Affiliated   655   Kayenta   Kayenta Dialysis   PO BOX 217   US HWY 163 N   KAYENTA   AZ   86033-0217
41   Affiliated   321   Hyde Park   Emerald Dialysis (fka Hyde Park Kidney Center)   710 W 43RD ST     CHICAGO   IL   60609-3435
42   Affiliated   322   Olympia Fields   Olympia Fields Dialysis Center   4557B LINCOLN HWY   STE B   MATTESON   IL   60443-2318
43   Affiliated   351   CKD   Center for Kidney Disease at North Shore   1190 NW 95TH ST   STE 28   MIAMI   FL   33150-2065
44   Affiliated   352   Venture   Center for Kidney Disease at Venture   16855 NE 2ND AVE   STE 25   N MIAMI BEACH   FL   33162-1744
45   Affiliated   360   South Broward   South Broward Artifical Kidney   4401 HOLLYWOOD BLVD     HOLLYWOOD   FL   33021-6609
46   Affiliated   688   East End   East End Dialysis Center   2201 E MAIN ST   STE 1   RICHMOND   VA   23223-7071
47   Affiliated   354   Flamingo Park   Flamingo Park Kidney Cntr, Inc   901 E 10TH AVE   BAY 17   HIALEAH   FL   33010-3762
48   Affiliated   355   Interamerican   InterAmerican Dialysis Center   7815 CORAL WAY   STE 115   MIAMI   FL   33155-6541
49   Affiliated   356   Coral Gables Dialysis Center   Coral Gables Kidney Center (fka LeJeune)   3280 PONCE DE LEON BLVD     CORAL GABLES   FL   33134-7252

 

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50   Affiliated   370   Cielo Vista Dialysis   DaVita East Dialysis dba Cielo Vista Dialysis (fkaTotal Renal Care East Dialysis Center)   7200 GATEWAY BLVD E   STE B   EL PASO   TX   79915-1301
51   Affiliated   371   West Texas Dialysis   DaVita West Dialysis Center dba West Texas (fkaTotal Renal Care West Dialysis Center)   5595 ALAMEDA AVE B   STE B   EL PASO   TX   79905
52   Affiliated   656   Shiprock   Shiprock Dialysis   PO BOX 2156   US HWY 491 N   SHIPROCK   NM   87420-2156
53   Affiliated   202   Arden Hills   Arden Hills Dialysis Unit   3900 NORTHWOODS DR   STE 11   ARDEN HILLS   MN   55112-6911
54   Affiliated   203   Burnsville   Burnsville Dialysis Unit   501 E NICOLLET BLVD   STE 15   BURNSVILLE   MN   55337-6784
55   Affiliated   204   Coon Rapids   Coon Rapids Dialysis Unit   3960 COON RAPIDS BLVD NW   STE 39   COON RAPIDS   MN   55433-2598
56   Affiliated   205   Edina   Edina Dialysis Unit   6550 YORK AVE S   STE 1   EDINA   MN   55435-2332
57   Affiliated   206   Maplewood   Maplewood Dialysis Center   2785 WHITE BEAR AVE N   STE 21   MAPLEWOOD   MN   55109-1320
58   Affiliated   207   Minneapolis   Minneapolis Dialysis Unit   825 S EIGHTH ST   STE SL42   MINNEAPOLIS   MN   55404-1208
59   Affiliated   208   Minnetonka   Minnetonka Dialysis Unit   17809 HUTCHINS DR     MINNETONKA   MN   55345-4100
60   Affiliated   209   St. Paul Dialysis   St. Paul Dialysis Unit   555 PARK ST   STE 18   SAINT PAUL   MN   55103-2192
61   Affiliated   210   Special Needs   University Dialysis Unit Riverside (Minneapolis-Special Needs Dialysis)   1045 WESTGATE DR   STE 9   SAINT PAUL   MN   55114-1079
62   Affiliated   211   West St. Paul   West St. Paul Dialysis   1555 LIVINGSTON AVE     WEST ST PAUL   MN   55118-3411
63   Affiliated   213   Cass Lake   Cass Lake Dialysis Unit   602 GRANT UTLEY ST   PO BOX 757   CASS LAKE   MN   56633-0757
64   Affiliated   215   Faribault   Faribault Dialysis Unit   201 LYNDALE AVE S   STE F   FARIBAULT   MN   55021-5758
65   Affiliated   217   Marshall   Marshall Dialysis Unit   300 S BRUCE ST   AVERA MARSHALL REGIONAL MEDICAL CENTER   MARSHALL   MN   56258-1934
66   Affiliated   218   Montevideo   Montevideo Dialysis Center   824 N 11TH ST   MONTEVIDEO HOSPITAL   MONTEVIDEO   MN   56265-1629
67   Affiliated   220   Pine City   TRC-Pine City (fka-Pine City Dialysis Unit)   129 6TH AVE SE   LAKESIDE MEDICAL CENTER   PINE CITY   MN   55063-1913
68   Affiliated   222   Red Wing   Red Wing Dialysis Unit   3028 N SERVICE DR     RED WING   MN   55066-1921
69   Affiliated   223   Redwood Falls   Redwood Falls Dialysis Center   100 FALLWOOD RD     REDWOOD FALLS   MN   56283-1828
70   Affiliated   240   Mitchell   Mitchell Dialysis   525 N FOSTER   QUEEN OF PEACE HOSPITAL   MITCHELL   SD   57301-2966
71   Affiliated   242   Rosebud   Rosebud Dialysis   1 SOLDIER CREEK RD     ROSEBUD   SD   57570-0610
72   Affiliated   243   Sioux Falls   Sioux Falls Dialysis Community Unit   1325 S CLIFF AVE   STE 46   SIOUX FALLS   SD   57105-1016
73   Affiliated   250   St. Croix Falls   St. Croix Falls Dialysis   744 E LOUISIANA ST     SAINT CROIX FALLS   WI   54024-9501
74   Affiliated   260   Hayward   Hayward Dialysis Center   21615 HESPERIAN BLVD   STE F   HAYWARD   CA   94541-7026
75   Affiliated   262   Pleasanton   Pleasanton Dialysis Center (HEMO) (fka Dublin)   5720 STONERIDGE MALL RD   STE 16   PLEASANTON   CA   94588-2882
76   Affiliated   263   Union City   Union City Dialysis Center (aka TRC-Union City)   32930 ALVARADO NILES RD   STE 3   UNION CITY   CA   94587-8101
77   Affiliated   264   East Bay - PD   East Bay Peritoneal Dialysis Center   13939 E 14TH ST   STE 11   SAN LEANDRO   CA   94578-2613
78   Affiliated   383   Greer   Greer Kidney Center   211 VILLAGE DR     GREER   SC   29651-1238
79   Affiliated   382   Upstate   Upstate Dialysis Center   308 MILLS AVE     GREENVILLE   SC   29605-4022
80   Affiliated   390   Kenner   Kenner Regional Dialysis Center   200 W ESPLANADE AVE   STE 1   KENNER   LA   70065-2473
81   Affiliated   689   Downtown Dialysis   Downtown Dialysis Center   821 N EUTAW ST   STE 41   BALTIMORE   MD   21201-6304
82   Affiliated   331   Eaton Canyon   Eaton Canyon Dialysis   2551 E WASHINGTON BLVD     PASADENA   CA   91107-1446
83   Affiliated   190   Georgetown   Georgetown on the Potomac   3223 K ST NW   STE 11   WASHINGTON   DC   20007-4412
84   Affiliated   395   St. Mary   Newtown Dialysis Center (fka St. Mary Dialysis)   60 BLACKSMITH RD     NEWTOWN   PA   18940-1847
85   Affiliated   393   Bertha Sirk   Bertha Sirk Dialysis Center   5820 YORK RD   STE 1   BALTIMORE   MD   21212-3620
86   Affiliated   394   Greenspring   Greenspring Dialysis Center   4701 MOUNT HOPE DR   STE C   BALTIMORE   MD   21215-3246
87   Affiliated   378   Houston Kidney - NW   Northwest Kidney Center (Houston)   11029 NORTHWEST FWY     HOUSTON   TX   77092-7311
88   Affiliated   379   NorthStar Dialysis   NorthStar Dialysis Center (fka North Houston Kidney Center)   380 W LITTLE YORK RD     HOUSTON   TX   77076-1303
89   Affiliated   363   Port Charlotte   Port Charlotte Artificial Kidney Center   4300 KINGS HWY STE 406     PORT CHARLOTTE   FL   33980
90   Affiliated   364   Gulf Coast PD   Gulf Coast Dialysis   3300 TAMIAMI TRL   STE 11A   PORT CHARLOTTE   FL   33952-8054
91   Affiliated   649   Loma Vista   Loma Vista Dialysis Center Partnership   1382 LOMALAND DR   STE A   EL PASO   TX   79935-5204
92   Affiliated   332   Paramount   Paramount Dialysis Center   8319 ALONDRA BLVD     PARAMOUNT   CA   90723-4403
93   Affiliated   334   East LA   Doctors Dialysis of East LA (aka East Los Angeles Dialysis)   950 S EASTERN AVE     LOS ANGELES   CA   90022-4801
94   Affiliated   335   Montebello   Doctors Dialysis of Montebello   1721 W WHITTIER BLVD     MONTEBELLO   CA   90640-4004
95   Affiliated   361   Pine Island   Pine Island Kidney Center   1871 N PINE ISLAND RD     PLANTATION   FL   33322-5208
96   Affiliated   365   Complete   Complete Dialysis Care   7850 W SAMPLE RD     MARGATE   FL   33065-4710
97   Affiliated   122   Lone Star Dialysis   Lone Star Dialysis (fka Hobby Dialysis)   8560 MONROE RD     HOUSTON   TX   77061-4815
98   Affiliated   255   Forest Lake   Forest Lake Dialysis   1068 S LAKE ST   STE 11   FOREST LAKE   MN   55025-2633
99   Affiliated   690   USC Phase II   TRC/USC Dialysis Center   2310 ALCAZAR ST     LOS ANGELES   CA   90033-5327
100   Affiliated   396   TRC/Union Plaza Ctr   Union Plaza Dialysis Center   810 1ST ST NE   STE 1   WASHINGTON   DC   20002-4227
101   Affiliated   130   Mid-Columbia Kidney   Mid Columbia Kidney Center   6825 BURDEN BLVD   STE A   PASCO   WA   99301-9584
102   Affiliated   131   Mt. Adams Kidney Ctr   Mt. Adams Kidney Center   3220 PICARD PL     SUNNYSIDE   WA   98944-8400
103   Affiliated   650   Lakewood   Lakewood Community Dialysis Center   5919 LAKEWOOD TOWNE CENTER BLVD SW   STE A   LAKEWOOD   WA   98499-6513

 

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104   Affiliated   228   St. Paul Ramsey   St. Paul Capitol Dialysis   555 PARK ST   STE 23   SAINT PAUL   MN   55103-2193
105   Affiliated   229   River City Dialysis   River City Dialysis (fka Lakeview Dialysis)   1970 NORTHWESTERN AVE S     STILLWATER   MN   55082-6567
106   Affiliated   231   Woodbury   Woodbury Dialysis   1850 WEIR DR   STE 3   WOODBURY   MN   55125-2260
107   Affiliated   281   Alhambra   Alhambra Dialysis Center   1315 ALHAMBRA BLVD   STE 1   SACRAMENTO   CA   95816-5245
108   Affiliated   282   Antelope   Antelope Dialysis Center   6406 TUPELO DR   STE A   CITRUS HEIGHTS   CA   95621-1780
109   Affiliated   283   Chico   Chico Dialysis Center (aka Chico Clinic)   530 COHASSET RD     CHICO   CA   95926-2212
110   Affiliated   285   North Clinic   Manzanita Dialysis Center (aka North Clinic)   4005 MANZANITA AVE   STE 17   CARMICHAEL   CA   95608-1779
111   Affiliated   286   Placerville   Cameron Park Dialysis (fka Placerville)   3311 COACH LN   STE C   CAMERON PARK   CA   95682
112   Affiliated   288   South Sacramento   South Sacramento Dialysis Center   7000 FRANKLIN BLVD   STE 88   SACRAMENTO   CA   95823-1838
113   Affiliated   289   Redding   Redding Dialysis Center   1876 PARK MARINA DR     REDDING   CA   96001-0913
114   Affiliated   291   Yuba City   Yuba City Dialysis Center   1525 PLUMAS CT   STE A   YUBA CITY   CA   95991-2971
115   Affiliated   292   University Clinic   University Dialysis Center   777 CAMPUS COMMONS RD   STE 1   SACRAMENTO   CA   95825-8344
116   Affiliated   372   Mesa Vista   Mesa Vista Dialysis Center (El Paso)   2400 N OREGON ST   STE C   EL PASO   TX   79902-3135
117   Affiliated   694   Hollywood   Hollywood Dialysis Center   5108 W SUNSET BLVD     LOS ANGELES   CA   90027-5708
118   Affiliated   697   UCLA Harbor   TRC/Harbor-UCLA MFI Total Renal Dialysis Center   21602 S VERMONT AVE     TORRANCE   CA   90502-1940
119   Affiliated   325   Brighton   Brighton Dialysis (fka Michigan Kidney Center of Brighton)   7960 GRAND RIVER RD   STE 21   BRIGHTON   MI   48114-7336
120   Affiliated   326   Macomb   Macomb Kidney Center (fka Macomb Dialysis)   28295 SCHOENHERR RD   STE A   WARREN   MI   48088-4300
121   Affiliated   327   North Oakland   North Oakland Dialysis   450 N TELEGRAPH RD   STE 6   PONTIAC   MI   48341-1037
122   Affiliated   328   Novi   Novi Dialysis   47250 W 10 MILE RD     NOVI   MI   48374-2932
123   Affiliated   329   Southfield   Cornerstone Dialysis (fka Southfield)   23857 GREENFIELD RD     SOUTHFIELD   MI   48075-3122
124   Affiliated   319   Children’s Mem’l Hosp.   TRC Children’s Dialysis Center aka Children’s Chicago/Children’s Memorial Hospital   2611 N HALSTED ST     CHICAGO   IL   60614-2301
125   Affiliated   151   New Center   New Center Dialysis   3011 W GRAND BLVD   STE 65   DETROIT   MI   48202-3012
126   Affiliated   2003   Whittier   Whittier Dialysis Center (fka Whittier Hills)   10055 WHITTWOOD DR     WHITTIER   CA   90603-2313
127   Affiliated   357   Miami Lakes   Miami Lakes Artificial Kidney Center (ALTHIN)   14600 NW 60TH AVE     MIAMI LAKES   FL   33014-2811
128   Affiliated   571   Anson County   Dialysis Care of Anson County   923 E CASWELL ST     WADESBORO   NC   28170-2305
129   Affiliated   573   Edgecomb County   Dialysis Care of Edgecomb County   3206 WESTERN BLVD     TARBORO   NC   27886-1828
130   Affiliated   574   Franklin County   Dialysis Care of Franklin County   1706 NC HWY 39 N     LOUISBURG   NC   27549-8329
131   Affiliated   575   Hoke County   Dialysis Care of Hoke County   403 S MAIN ST     RAEFORD   NC   28376-3222
132   Affiliated   576   Martin County   Dialysis Care of Martin County   100 MEDICAL DR     WILLIAMSTON   NC   27892-2156
133   Affiliated   578   Montgomery County   Dialysis Care of Montgomery County (aka Montgomery)   323 W MAIN ST     BISCOE   NC   27209-9528
134   Affiliated   579   Moore County   Dialysis Care of Moore County (aka Pinehurst)   16 REGIONAL DR     PINEHURST   NC   28374-8850
135   Affiliated   580   Richmond County   Dialysis Care of Richmond County   771 CHERAW RD     HAMLET   NC   28345-7158
136   Affiliated   581   Rockingham County   Dialysis Care of Rockingham County   251 W KINGS HWY     EDEN   NC   27288-5009
137   Affiliated   582   Rowan County   Dialysis Care of Rowan County   111 DORSETT DR     SALISBURY   NC   28144-2278
138   Affiliated   583   Rutherford County   Dialysis Care of Rutherford County   226 COMMERCIAL ST     FOREST CITY   NC   28043-2851
139   Affiliated   399   Monterey Park   Monterey Park Dialysis Center   2560 CORPORATE PL   STE 1-11 BLDG D   MONTEREY PARK   CA   91754-7612
140   Affiliated   183   Mason Dixon   Mason-Dixon Baltimore County   9635-A LIBERTY RD   STE 1   RANDALLSTOWN   MD   21133-2436
141   Affiliated   184   Carrol County   Carroll County Dialysis Facility   412 MALCOLM DR   STE 31   WESTMINSTER   MD   21157-6167
142   Affiliated   167   South Brooklyn   South Brooklyn Nephrology Center   3915 AVENUE V   STE 14   BROOKLYN   NY   11234-5150
143   Affiliated   843   Phenix City   Phenix City Dialysis Center   1900 OPELIKA RD     PHENIX CITY   AL   36867-3640
144   Affiliated   876   Brea   Brea Dialysis Center   595 TAMARACK AVE   STE A   BREA   CA   92821-3125
145   Affiliated   878   Hemet   Hemet Dialysis Center   3050 W FLORIDA AVE     HEMET   CA   92545-3619
146   Affiliated   883   Temecula   Temecula Dialysis Center   40945 COUNTY CENTER DR   STE G   TEMECULA   CA   92591-6006
147   Affiliated   880   Riverside   Riverside Dialysis Center   4361 LATHAM ST   STE 1   RIVERSIDE   CA   92501-1767
148   Affiliated   870   Napa   Napa Dialysis Center   3900 BEL AIRE PLZ   STE C   NAPA   CA   94558-2823
149   Affiliated   875   Santa Ana   Santa Ana Dialysis Center   1820 E DEERE AVE     SANTA ANA   CA   92705-5721
150   Affiliated   879   Valley View Dialysis Center   Valley View Dialysis Center (aka Morneo Valley)   26900 CACTUS AVE     MORENO VALLEY   CA   92555-3912
151   Affiliated   884   Orange   Mainplace Dialysis Center (fka Orange Dialysis Center)   972 W TOWN AND COUNTRY RD     ORANGE   CA   92868-4714
152   Affiliated   882   San Bernadino   Mountain Vista Dialysis Center (fka San Bernadino Dailysis Center (Mountain Vista))   4041 NORTH UNIVERSITY PKWY     SAN BERNARDINO   CA   92407-1823
153   Affiliated   871   Lakeport   Lakeport Dialysis Center   804 11TH ST   STE 2   LAKEPORT   CA   95453-4102
154   Affiliated   873   Vacaville   Vacaville Dialysis Center   941 MERCHANT ST     VACAVILLE   CA   95688-5315
155   Affiliated   877   Corona   Corona Dialysis Center   1820 FULLERTON AVE   STE 18   CORONA   CA   92881-3147
156   Affiliated   872   Fairfield   Fairfield Dialysis Center   4660 CENTRAL WAY     FAIRFIELD   CA   94534-1803
157   Affiliated   902   Westminster   Westminster Dialysis Center (Federal Heights)   9053 HARLAN ST   STE 9   WESTMINSTER   CO   80031-2908

 

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158   Affiliated   901   Aurora   Aurora Dialysis Center   1411 S POTOMAC ST   AMC II STE 1   AURORA   CO   80012-4536
159   Affiliated   900   Denver   Denver Dialysis Center   2900 DOWNING ST   STE C   DENVER   CO   80205-4699
160   Affiliated   903   Littleton   Littleton Dialysis Center   209 W COUNTY LINE RD     LITTLETON   CO   80129-1901
161   Affiliated   904   South Denver   South Denver Dialysis Center   850 E HARVARD AVE   STE 6   DENVER   CO   80210-5030
162   Affiliated   946   Lee Street Dialysis   Lee Street Dialysis (fka Grant Park Dialysis Center)   5155 LEE ST NE     WASHINGTON   DC   20019-4051
163   Affiliated   868   Leesburg   Leesburg Dialysis Center   801 E DIXIE AVE   STE 18A   LEESBURG   FL   34748-7699
164   Affiliated   866   Panama City   Panama City Dialysis Center   615 HIGHWAY 231     PANAMA CITY   FL   32405-4704
165   Affiliated   867   Marianna   Marianna Dialysis Center   2930 OPTIMIST DR     MARIANNA   FL   32448-7703
166   Affiliated   864   Venice   Venice Dialysis Center   816 PINEBROOK RD     VENICE   FL   34285-7103
167   Affiliated   827   Buena Vista   Buena Vista Dialysis Center   349 GENEVA RD     BUENA VISTA   GA   31803-1701
168   Affiliated   828   Decatur   Decatur Dialysis Center   1987 CANDLER RD     DECATUR   GA   30032-4212
169   Affiliated   825   Moultrie   Moultrie Dialysis Center   2419 S MAIN ST     MOULTRIE   GA   31768-6531
170   Affiliated   820   SW Atlanta   Southwest Atlanta Dialysis Center   3620 MARTIN LUTHER KING DR SW     ATLANTA   GA   30331-3711
171   Affiliated   818   Griffin   Griffin Dialysis Center   731 S 8TH ST     GRIFFIN   GA   30224-4818
172   Affiliated   826   Columbus   Columbus Dialysis Center   6228 BRADLEY PARK DR   STE B   COLUMBUS   GA   31904-3604
173   Affiliated   829   East Macon   East Macon Dialysis Center   165 EMERY HWY   STE 11   MACON   GA   31217-3666
174   Affiliated   817   Jonesboro   Jonesboro Dialysis Center   129 KING ST     JONESBORO   GA   30236-3656
175   Affiliated   824   Milledgeville   Milledgeville Dialysis Center   400 S WAYNE ST     MILLEDGEVILLE   GA   31061-3446
176   Affiliated   823   Fort Valley   Fort Valley Dialysis Center   557 BLUEBIRD BLVD     FORT VALLEY   GA   31030-5083
177   Affiliated   821   Midtown   Linden Dialysis (fka Midtown-Atlanta)   121 LINDEN AVE NE     ATLANTA   GA   30308-2432
178   Affiliated   953   E. St. Louis   Sauget Dialysis (fka East St. Louis Dialysis Center)   2061 GOOSE LAKE RD     SAUGET   IL   62206-2822
179   Affiliated   952   Granite City   Granite City Dialysis Center   9 AMERICAN VLG     GRANITE CITY   IL   62040-3706
180   Affiliated   937   Batesville   Batesville Dialysis Center Aka Renal Treatment Centers-Batesville   232 STATE ROAD 129 S     BATESVILLE   IN   47006-7694
181   Affiliated   938   Lawrenceburg   Lawrenceburg Dialysis Center   721 RUDOLPH WAY     GREENDALE   IN   47025-8378
182   Affiliated   939   Madison   Madison Dialysis Center   220 CLIFTY DR   UNIT K   MADISON   IN   47250-1669
183   Affiliated   836   Newton   Renal Treatment Center-Newton aka-Newton Dialysis Center   1223 WASHINGTON RD     NEWTON   KS   67114-4855
184   Affiliated   837   Derby   Renal Treatment Center-Derby aka Derby Dialysis Center   250 W RED POWELL DR     DERBY   KS   67037-2626
185   Affiliated   834   Winfield   Renal Treatment Center-Winfield aka, Winfield Dialysis Center   1315 E 4TH AVE     WINFIELD   KS   67156-2457
186   Affiliated   830   Wichita   Wichita Dialysis Center   909 N TOPEKA ST     WICHITA   KS   67214-3620
187   Affiliated   833   Garden City   Renal Treatment Center-Garden City Aka-Garden City Dialysis Center   401 N MAIN ST     GARDEN CITY   KS   67846-5429
188   Affiliated   831   E. Wichita   East Wichita Dialysis Center   320 N HILLSIDE ST     WICHITA   KS   67214-4918
189   Affiliated   832   Independance   Independence Dialysis Center   801 W MYRTLE ST     INDEPENDENCE   KS   67301-3239
190   Affiliated   835   Parson, KS   Parsons Dialysis Center   1902 S US HWY 59   BLDG B   PARSONS   KS   67357-4948
191   Affiliated   814   Wheaton   Wheaton Dialysis Center   11941 GEORGIA AVE     WHEATON   MD   20902
192   Affiliated   812   Rockville   Rockville Dialysis Center   14915 BROSCHART RD   STE 1   ROCKVILLE   MD   20850-3367
193   Affiliated   815   Owing Mills   Owings Mills Dialysis Center (fka-Renal Treatment Center-Owings Mills)   10 CROSSROADS DR   STE 11   OWINGS MILLS   MD   21117-5463
194   Affiliated   811   Berlin   Berlin Dialysis Center   314 FRANKLIN AVE   STE 36   BERLIN   MD   21811-1238
195   Affiliated   810   Easton   Easton Dialysis Center   402 MARVEL CT     EASTON   MD   21601-4052
196   Affiliated   813   Chestertown   Chestertown Dialysis Center (fka Renal Treatment Centers-Chestertown)   100 BROWN ST     CHESTERTOWN   MD   21620
197   Affiliated   951   Hope Again   Hope Again Dialysis Center- fka Kennett Dialysis Center   1207 STATE ROUTE VV     KENNETT   MO   63857-3823
198   Affiliated   950   Poplar Bluff   Bluff City Dialysis Center   2400 LUCY LEE PKWY   STE E   POPLAR BLUFF   MO   63901-2429
199   Affiliated   949   Crystal City   Crystal City Dialysis Center   960 SO TRUMAN BLVD     CRYSTAL CITY   MO   63019-1329
200   Affiliated   947   St. Louis   St. Louis Dialysis Center (fka Renal Treatment Center-St. Louis)   2610 CLARK AVE     SAINT LOUIS   MO   63103-2502
201   Affiliated   944   Burlington   Burlington Dialysis   873 HEATHER RD     BURLINGTON   NC   27215-6288
202   Affiliated   838   Scottsbluff   Scottsbluff Dialysis Center   3812 AVENUE B     SCOTTSBLUFF   NE   69361-4780
203   Affiliated   802   Bridgewater   Bridgewater Dialysis Center (fka Renal Treatment Center-Bridgewater)   2121 US HWY 22     BOUND BROOK   NJ   08805-1546
204   Affiliated   845   West Las Vegas   Las Vegas Dialysis Center   150 S VALLEY VIEW BLVD     LAS VEGAS   NV   89107
205   Affiliated   846   North Las Vegas   North Las Vegas Dialysis Center   2300 MCDANIEL ST     NORTH LAS VEGAS   NV   89030-6318
206   Affiliated   940   Cincinnati   Eastgate Dialysis (fka Cincinnati)   4435 AICHOLTZ RD     CINCINNATI   OH   45245-1690
207   Affiliated   885   Tulsa   Tulsa Dialysis   4436 S HARVARD AVE     TULSA   OK   74135-2605
208   Affiliated   897   NW Bethany   Northwest Bethany Dialysis Center   7800 NW 23RD ST   STE A   BETHANY   OK   73008-4948
209   Affiliated   890   Duncan   Duncan Dialysis Center   2645 W ELK AVE     DUNCAN   OK   73533-1572
210   Affiliated   893   Shawnee   Shawnee Dialysis Center   4409 N KICKAPOO AVE   STE 113   SHAWNEE   OK   74804-1224
211   Affiliated   895   Stillwater   Stillwater Dialysis Center   406 E HALL OF FAME AVE   STE 3   STILLWATER   OK   74075-5447

 

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212   Affiliated   955   Midwest City   Midwest City Dialysis Center   7221 E RENO AVE     MIDWEST CITY   OK   73110-4474
213   Affiliated   886   Broken Arrow   Broken Arrow Dialysis Center   1700 N 9TH ST     BROKEN ARROW   OK   74012
214   Affiliated   888   Tahlequah   Tahlequah Dialysis Center   1373 E BOONE ST     TAHLEQUAH   OK   74464-3330
215   Affiliated   899   Edmund   Edmond Dialysis   50 S BAUMANN AVE     EDMOND   OK   73034-5676
216   Affiliated   889   Altus   Altus Dialysis Center   205 S PARK LN   STE 13   ALTUS   OK   73521-5756
217   Affiliated   896   Elk City   Elk City Dialysis Center   1601 W 2ND ST     ELK CITY   OK   73644-4427
218   Affiliated   887   Claremore   Claremore Dialysis Center   202 E BLUE STARR DR     CLAREMORE   OK   74017-4223
219   Affiliated   891   Norman   Norman Dialysis Center   1818 W LINDSEY ST   STE 14 BLDG B   NORMAN   OK   73069-4159
220   Affiliated   862   Pocono   Pocono Dialysis Center   100 PLAZA CT   STE B   EAST STROUDSBURG   PA   18301-8258
221   Affiliated   861   Palmerton   Palmerton Dialysis Center   185 DELAWARE AVE   STE C   PALMERTON   PA   18071-1716
222   Affiliated   860   Jennersville   Jennersville Dialysis Center   1011 W BALTIMORE PIKE     WEST GROVE   PA   19390-9446
223   Affiliated   858   Lewistown   Lewistown Dialysis Center   611 ELECTRIC AVE     LEWISTOWN   PA   17044-1128
224   Affiliated   854   Lemoyne   Camp Hill Dialysis Center (fka Lemoyne Dialysis Center (York Hospital Acutes))   425 N 21ST ST   LOWER LEVEL   CAMP HILL   PA   17011-2223
225   Affiliated   856   Upland   Upland Dialysis Center   1 MEDICAL CENTER BLVD   STE 12   CHESTER   PA   19013-3902
226   Affiliated   848   South Philadelphia   So. Philadelphia Dialysis Center   109 DICKINSON ST     PHILADELPHIA   PA   19147-6107
227   Affiliated   857   Exton   Exton Dialysis Center   710 SPRINGDALE DR     EXTON   PA   19341-2828
228   Affiliated   847   Northeast Philadelphia   NE Philadelphia Dialysis Center   518 KNORR ST     PHILADELPHIA   PA   19111-4604
229   Affiliated   934   Longview   Longview Dialysis Center   425 N FREDONIA ST     LONGVIEW   TX   75601-6464
230   Affiliated   935   Marshall-RTC   Marshall Dialysis Center   1301 S WASHINGTON AVE     MARSHALL   TX   75670-6215
231   Affiliated   933   Conroe   Conroe Dialysis Center   500 MEDICAL CENTER BLVD   STE 175   CONROE   TX   77304-2899
232   Affiliated   928   San Marcos   Hill Country Dialysis Center Of San Marcos   1820 PETER GARZA DR     SAN MARCOS   TX   78666-7407
233   Affiliated   923   Sherman   Sherman Dialysis Center   205 W LAMBERTH RD     SHERMAN   TX   75092-2659
234   Affiliated   932   Tomball   Tomball Dialysis Center   27720A TOMBALL PKWY     TOMBALL   TX   77375-
235   Affiliated   919   Cleveland   Cleveland Dialysis Center   600 E HOUSTON   STE 63   CLEVELAND   TX   77327-4689
236   Affiliated   921   Livingston   Livingston Dialysis Center   209 W PARK     LIVINGSTON   TX   77351-7020
237   Affiliated   920   Kingwood   Kingwood Dialysis Center   2300 GREEN OAK DR   STE 5   KINGWOOD   TX   77339-2053
238   Affiliated   930   North Houston   North Houston Dialysis Center   129 LITTLE YORK RD     HOUSTON   TX   77076-1020
239   Affiliated   926   Omni   Omni Dialysis Center (fka Hamilton Dialysis Center)   9350 KIRBY DR   STE 11   HOUSTON   TX   77054-2528
240   Affiliated   925   Victoria   Victoria Dialysis Center   1405 VICTORIA STATION DR     VICTORIA   TX   77901-3092
241   Affiliated   922   Lufkin   Lufkin Dialysis Center   700 S JOHN REDDITT DR     LUFKIN   TX   75904-3145
242   Affiliated   927   Gonzales   Gonzales Dialysis Center   1406 N SARAH DEWITT DR     GONZALES   TX   78629-2702
243   Affiliated   924   Denison   Denison Dialysis Center   1220 REBA MCENTIRE LANE     DENISON   TX   75020-9057
244   Affiliated   918   South San Antonio   South San Antonio Dialysis Center   1313 SE MILITARY DR   STE 111   SAN ANTONIO   TX   78214-2850
245   Affiliated   913   Austin   Waterloo Dialysis Center (fka Austin Dialysis Center)   5310 BURNET RD   UNIT 122   AUSTIN   TX   78756-2003
246   Affiliated   916   S. Austin   El Milagro Dialysis Unit (fka South Austin Dialysis Center)   2800 S INTERSTATE HWY 35   STE 12   AUSTIN   TX   78704-5700
247   Affiliated   929   SW San Antonio   Southwest San Antonio Dialysis Center   7515 BARLITE BLVD     SAN ANTONIO   TX   78224-1311
248   Affiliated   936   Bedford   HEB Dialysis Center (Bedford)   1401 BROWN TRL   STE A   BEDFORD   TX   76022-6416
249   Affiliated   917   TRC Med Cntr   Med-Center Dialysis, fka Plaza Dialysis Center & Houston Kidney Center #376   5610 ALMEDA RD     HOUSTON   TX   77004-7515
250   Affiliated   908   Chesapeake   Chesapeake Dialysis Center   1400 CROSSWAYS BLVD   CROSSWAYS II STE 16   CHESAPEAKE   VA   23320-2839
251   Affiliated   912   Hopewell   Hopewell Dialysis Center   301 W BROADWAY AVE     HOPEWELL   VA   23860-2645
252   Affiliated   911   Newport News   Newport News Dialysis Center   711 79TH ST     NEWPORT NEWS   VA   23605-2767
253   Affiliated   907   Norfolk   Norfolk Dialysis Center   962 NORFOLK SQ     NORFOLK   VA   23502-3235
254   Affiliated   909   Virginia Beach   Virginia Beach Dialysis Center   740 INDEPENDENCE CIR     VIRGINIA BEACH   VA   23455-6438
255   Affiliated   171   Palmer   Palmer Dialysis Center   30 COMMUNITY DR     EASTON   PA   18045-2658
256   Affiliated   589   Burgaw   SEDC (NC II) Burgaw Dialysis Center   704 S DICKERSON ST   PO BOX 1391   BURGAW   NC   28425-4904
257   Affiliated   590   Elizabethtown   SEDC (NC II) Elizabethtown Dialysis Center   101 DIALYSIS DR     ELIZABETHTOWN   NC   28337-9048
258   Affiliated   591   Jacksonville   SEDC (NC II) Jacksonville Dialysis Center   14 OFFICE PARK DR     JACKSONVILLE   NC   28546-7325
259   Affiliated   592   Kenansville   SEDC (NC II) Kenansville Dialysis Center   305 BEASLEY ST     KENANSVILLE   NC   28349-8798
260   Affiliated   593   Shallotte   SEDC (NC II) Shallotte Dialysis Center   4770 SHALLOTTE AVE     SHALLOTTE   NC   28470-6596
261   Affiliated   594   Whiteville   SEDC (NC II) Whiteville Dialysis Center   608 PECAN LN     WHITEVILLE   NC   28472-2949
262   Affiliated   595   Wilmington   SEDC (NC II) Wilmington Dialysis Center   2215 YAUPON DR     WILMINGTON   NC   28401-7334
263   Affiliated   175   Deerfield   Deerfield Beach Artificial Kidney Center   1983 W HILLSBORO BLVD     DEERFIELD BEACH   FL   33442-1418
264   Affiliated   176   Pampano Beach   Pompano Beach Artificial Kidney Center   600 SW 3RD ST   STE 11   POMPANO BEACH   FL   33060-6936
265   Affiliated   177   Tamarack   Tamarac Artificial Kidney Center   7140 W MCNAB RD     TAMARAC   FL   33321-5306

 

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266   Affiliated   168   Atlantic AKC   Atlantic Artificial Kidney Center   6 INDUSTRIAL WAY W   STE B   EATONTOWN   NJ   07724-2258
267   Affiliated   587   Rowan/Kannapolis   Dialysis Care of Kannapolis   1607 N MAIN ST     KANNAPOLIS   NC   28081-2317
268   Affiliated   654   Cortez   Cortez Dialysis   610 E MAIN ST   STE C   CORTEZ   CO   81321-3308
269   Affiliated   142   West Bountiful 4/6/98   West Bountiful Dialysis   724 W 500 S   STE 3   WEST BOUNTIFUL   UT   84087-1471
270   Affiliated   187   Meherrin   Meherrin Dialysis Center   201A WEAVER AVE     EMPORIA   VA   23847-1248
271   Affiliated   436   Montclair   Montclair Dialysis Center   5050 PALO VERDE ST   STE 1   MONTCLAIR   CA   91763-2329
272   Affiliated   259   Pipestone   Pipestone Dialysis   916 4TH AVE SW     PIPESTONE   MN   56164-1054
273   Affiliated   236   Washington   Washington Dialysis Center   154 WASHINGTON PLZ     WASHINGTON   GA   30673-2074
274   Affiliated   235   Elberton   Elberton Dialysis Center   894 ELBERT ST     ELBERTON   GA   30635-2628
275   Affiliated   174   Gulf Breeze   Gulf Breeze Dialysis Center   1519 MAIN ST     DUNEDIN   FL   34698-4650
276   Affiliated   526   Asheville   Asheville Kidney Center   1600 CENTRE PARK DR     ASHEVILLE   NC   28805-6206
277   Affiliated   528   Sylva   Sylva Dialysis Center   655 ASHEVILLE HWY     SYLVA   NC   28779-2747
278   Affiliated   527   Hendersonville   Hendersonville Dialysis Center   500 BEVERLY HANKS CTR   HWY 25 N   HENDERSONVILLE   NC   28792
279   Affiliated   389   Memorial   Memorial Dialysis   4427 S ROBERTSON ST     NEW ORLEANS   LA   70115-6308
280   Affiliated   127   Warner Robbins   Dialysis Center of Middle Georgia-Warner Robins   509 N HOUSTON RD     WARNER ROBINS   GA   31093-8844
281   Affiliated   126   Macon - Middle Georgia   Dialysis Center of Middle Georgia-Macon   747 2ND ST     MACON   GA   31201-6835
282   Affiliated   344   Oakland PD   Oakland Peritoneal Dialysis Center (Piedmont PD)   5352 CLAREMONT AVE     OAKLAND   CA   94618
283   Affiliated   384   Fairfax   Fairfax Dialysis Center   8501 ARLINGTON BLVD   STE 1   FAIRFAX   VA   22031-4625
284   Affiliated   374   Houston SW   Houston Kidney Center Southwest   11111 BROOKLET DR   STE 1 BLDG 1   HOUSTON   TX   77099-3555
285   Affiliated   545   Pikes Peak   Pikes Peak Dialysis Center   2002 LELARAY ST   STE 13   COLORADO SPRINGS   CO   80909-2804
286   Affiliated   546   Printers Place   Printers Place Dialysis   2802 INTERNATIONAL CIR     COLORADO SPRINGS   CO   80910-3127
287   Affiliated   541   Lakewood Colorado   Lakewood Dialysis Center   1750 PIERCE ST     LAKEWOOD   CO   80214-1434
288   Affiliated   543   Boulder   Boulder Dialysis Center   2880 FOLSOM ST   STE 11   BOULDER   CO   80304-3769
289   Affiliated   542   Thornton   Thornton Dialysis Center   8800 FOX DR     THORNTON   CO   80260-6880
290   Affiliated   544   Arvada   Arvada Dialysis Center   9950 W 80TH AVE   STE 25   ARVADA   CO   80005-3914
291   Affiliated   173   Ft. Lauderdale   CDC South-Ft Lauderdale Renal Associates   6264 N FEDERAL HWY     FORT LAUDERDALE   FL   33308-1904
292   Affiliated   380   Houston Cypress Station   Houston Kidney Center Cypress Station   221 FM 1960 RD W   STE H   HOUSTON   TX   77090-3537
293   Affiliated   169   Erie County   Cleve Hill Dialysis Center (Fka Cleve Hill Limited Partnership-Erie Dialysis &ECMC Dialysis Center At Cleve Hill )   1461 KENSINGTON AVE     BUFFALO   NY   14215-1436
294   Affiliated   430   UCLA Pediatrics   Century City Dialysis (fka UCLA, DaVita Westwood UCLA)   10630 SANTA MONICA BLVD     LOS ANGELES   CA   90025-4837
295   Affiliated   501   Bronx   Bronx Dialysis Center   1615 EASTCHESTER RD     BRONX   NY   10461-2603
296   Affiliated   502   Catskill   Catskill Dialysis Center   139 FORESTBURGH RD     MONTICELLO   NY   12701-2364
297   Affiliated   505   Riverdale   Riverdale Dialysis Center   170 W 233RD ST     BRONX   NY   10463-5639
298   Affiliated   506   South Bronx   South Bronx Dialysis Center   1940 WEBSTER AVE     BRONX   NY   10457-4261
299   Affiliated   507   Stanten Island   Richmond Kidney Center (Staten Island)   1366 VICTORY BLVD     STATEN ISLAND   NY   10301-3907
300   Affiliated   238   McDonough   McDonough Dialysis Center   114 DUNN ST     MCDONOUGH   GA   30253-2347
301   Affiliated   192   Milford   Delaware Valley Dialysis Center (fka Milford)   102 DAVITA DR     MILFORD   PA   18337-9390
302   Affiliated   191   Honesdale   Honesdale Dialysis Center-NE Regional   RR 6 BOX 6636   STOURBRIDGE MALL   HONESDALE   PA   18431-9649
303   Affiliated   247   Memorial   Memorial Dialysis Center   11621 KATY FWY     HOUSTON   TX   77079-1801
304   Affiliated   246   Katy Dialysis Center   Grand Parkway Dialysis Center   403 W GRAND PKWY S   STE T   KATY   TX   77494-8358
305   Affiliated   245   Cyfair Dialysis Center   Cyfair Dialysis Center   9110 JONES RD   STE 11   HOUSTON   TX   77065-4489
306   Affiliated   165   Port Chester   Port Chester Dialysis and Renal Center   38 BULKLEY AVE     PORT CHESTER   NY   10573-3902
307   Affiliated   193   Franklin Dialysis   Franklin Dialysis Center   150 SOUTH INDEPENDENCE WEST   11 PUBLIC LEDGER BLDG   PHILADELPHIA   PA   19106-3413
308   Affiliated   156   Grand Blanc   Grand Blanc Dialysis Center   3625 GENESYS PKWY     GRAND BLANC   MI   48439-8070
309   Affiliated   397   Oxford Court   Oxford Court Dialysis   930 TOWN CENTER DR   STE G1   LANGHORNE   PA   19047-4260
310   Affiliated   348   Antioch   Antioch Dialysis   3100 DELTA FAIR BLVD     ANTIOCH   CA   94509-4001
311   Affiliated   401   North Palm Beach   North Palm Beach Dialysis Center   2841 PGA BLVD     PALM BEACH GARDENS   FL   33410-2910
312   Affiliated   277   Lodi   Lodi Dialysis Center   1610 W KETTLEMAN LN   STE D   LODI   CA   95242-4210
313   Affiliated   438   United   United Dialysis Center   3111 LONG BEACH BLVD     LONG BEACH   CA   90807-5015
314   Affiliated   437   Premier   Premier Dialysis Center   7612 ATLANTIC AVE     CUDAHY   CA   90201-5020
315   Affiliated   349   Salinas   Salinas Dialysis Center   955 BLANCO CIR   STE C   SALINAS   CA   93901-4452
316   Affiliated   428   Lowry I   Lowry Dialysis Center   7465 E 1ST AVE   STE A   DENVER   CO   80230-6877
317   Affiliated   154   Ypsilanti   Ypsilanti Dialysis   2766 WASHTENAW RD     YPSILANTI   MI   48197-1506
318   Affiliated   237   Eastpoint   East Point Dialysis   2669 CHURCH ST     EAST POINT   GA   30344-3115
319   Affiliated   520   Celia Dill   Celia Dill Dialysis Center   667 STONELEIGH AVE   STE 123 BARNS OFFICE CENTER   CARMEL   NY   10512-2454

 

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320   Affiliated   248   Elmbrook   Brookriver Dialysis   8101 BROOKRIVER DR     DALLAS   TX   75247-4003
321   Affiliated   402   Ocala East   OCALA Regional Kidney Center-East   2870 SE 1ST AVE     OCALA   FL   34471-0406
322   Affiliated   403   Ocala West   OCALA Regional Kidney Center-West   9401 SW HWY 200   BLDG 6   OCALA   FL   34481-9612
323   Affiliated   404   Ocala South   OCALA Regional Kidney Center-South   13940 N US HWY 441   BLDG 4   LADY LAKE   FL   32159-8908
324   Affiliated   417   Delta Sierra Dialysis   Delta-Sierra Dialysis Center   555 W BENJAMIN HOLT DR   STE 2   STOCKTON   CA   95207-3839
325   Affiliated   552   Olympic View   Olympic View Dialysis Center   125 16TH AVE E CSB   5TH FL   SEATTLE   WA   98112
326   Affiliated   148   Pratt   Pratt Dialysis Center   203 WATSON ST   STE 11   PRATT   KS   67124-3092
327   Affiliated   196   Buffalo   Renal Care of Buffalo   550 ORCHARD PARK RD     WEST SENECA   NY   14224-2646
328   Affiliated   555   Woodland   Woodland Dialysis Center   912 WOODLAND DR   STE B   ELIZABETHTOWN   KY   42701-2795
329   Affiliated   556   Taylor   Taylor County Dialysis Center   101 KINGSWOOD DR     CAMPBELLSVILLE   KY   42718-9634
330   Affiliated   491   Gary   Comprehensive Renal Care (CRC)-Gary   4802 BROADWAY     GARY   IN   46408-4509
331   Affiliated   492   Hammond   Comprehensive Renal Care (CRC)-Hammond   222 DOUGLAS ST     HAMMOND   IN   46320-1960
332   Affiliated   493   Valparaiso   Comprehensive Renal Care (CRC)-Valparaiso   606 E LINCOLNWAY     VALPARAISO   IN   46383-5728
333   Affiliated   494   Michigan City   Comprehensive Renal Care (CRC)-Michigan City   9836 WEST 400 NORTH     MICHIGAN CITY   IN   46360-2910
334   Affiliated   495   Munster   Comprehensive Renal Care (CRC)-Munster   9100 CALUMET AVE     MUNSTER   IN   46321-1737
335   Affiliated   497   South County-Deaconess   South County Dialysis (Deaconess)   4145 UNION RD     SAINT LOUIS   MO   63129-1064
336   Affiliated   266   South Hayward   South Hayward Dialysis Center   254 JACKSON ST     HAYWARD   CA   94544-1907
337   Affiliated   164   Dyker Heights   Dyker Heights Dialysis Center   1435 86TH ST     BROOKLYN   NY   11228-3435
338   Affiliated   152   Clarkston   Clarkston Dialysis Center   6770 DIXIE HWY   STE 25   CLARKSTON   MI   48346-2089
339   Affiliated   534   Hudson Valley   Hudson Valley Dialysis Center   155 WHITE PLAINS RD     TARRYTOWN   NY   10591-5523
340   Affiliated   971   Central Tulsa   Central Tulsa Dialysis Center   1124 S SAINT LOUIS AVE     TULSA   OK   74120-5413
341   Affiliated   972   Okmulgee   Okmulgee Dialysis Center   201 SO DELAWARE AVE     OKMULGEE   OK   74447-5528
342   Affiliated   974   Muskogee   Muskogee Community Dialysis   2316 W SHAWNEE ST     MUSKOGEE   OK   74401-2228
343   Affiliated   975   Miami-Oklahoma   Tri-State Dialysis Center (fka Miami Dialysis Center (OK))   2510 N MAIN ST     MIAMI   OK   74354-1602
344   Affiliated   977   Stilwell   Stilwell Dialysis Center   80851 HWY 59     STILWELL   OK   74960
345   Affiliated   496   East Chicago   Comprehensive Renal Care (CRC)-East Chicago   4320 FIR ST   UNIT 44   EAST CHICAGO   IN   46312-3078
346   Affiliated   549   Bright Dialysis   Bright Dialysis (fka Fort Pierce Artificial Kidney Center, TRC of Fort Pierce-AKC)   1801 S 23RD ST   STE 1   FORT PIERCE   FL   34950-4830
347   Affiliated   153   Detroit   Detroit Dialysis Center (Eastern Market, Brewery Park Development)   2674 E JEFFERSON AVE     DETROIT   MI   48207-4129
348   Affiliated   166   White Plains   White Plains Dialysis Center   200 HAMILTON AVE   STE 13B   WHITE PLAINS   NY   10601-1859
349   Affiliated   337   Crescent Heights   Crescent Heights Dialysis Center   8151 BEVERLY BLVD     LOS ANGELES   CA   90048-4514
350   Affiliated   547   Pahrump Dialysis   Pahrump Dialysis Center   330 S LOLA LN   STE 1   PAHRUMP   NV   89048-0884
351   Affiliated   598   Cherokee Dialysis Center   Cherokee Dialysis Center   53 ECHOTA CHURCH RD     CHEROKEE   NC   28719-9702
352   Affiliated   444   Utah Valley   Utah Valley Dialysis Center   1055 N 500 W   STE 221   PROVO   UT   84604-3305
353   Affiliated   439   Washington Plaza   Washington Plaza Dialysis Center   516 E WASHINGTON BLVD   # 522   LOS ANGELES   CA   90015-3723
354   Affiliated   539   Commerce City   Commerce City Dialysis Center   6320 HOLLY ST     COMMERCE CITY   CO   80022-3325
355   Affiliated   251   Bloomington Dialysis   Bloomington Dialysis Unit of TRC (fka Richfield)   8591 LYNDALE AVE S     BLOOMINGTON   MN   55420-2237
356   Affiliated   133   Kent Community Dialysis   Kent Dialysis Center   21501 84TH AVE S     KENT   WA   98032-1960
357   Affiliated   278   Florin Dialyis   Florin Dialysis Center   7000 STOCKTON BLVD     SACRAMENTO   CA   95823-2312
358   Affiliated   540   South Las Vegas Dialysis   South Las Vegas Dialysis Center (Palms)   2250 S RANCHO DR   STE 115   LAS VEGAS   NV   89102-4456
359   Affiliated   538   Longmont Dialysis   Longmont Dialysis Center   1715 IRON HORSE DR   STE 17   LONGMONT   CO   80501-9617
360   Affiliated   500   Great Bridge   Great Bridge Dialysis (fka Chesapeake II)   745 BATTLEFIELD BLVD N   STE 1   CHESAPEAKE   VA   23320-0305
361   Affiliated   569   Weaverville Dialysis   Weaverville Dialysis Facility   329 MERRIMON AVE     WEAVERVILLE   NC   28787-9253
362   Affiliated   427   Lakewood Crossing   Lakewood Crossing Dialysis   1057 S WADSWORTH BLVD   STE 1   LAKEWOOD   CO   80226-4361
363   Affiliated   155   Jackson   Jackson Dialysis Center   234 W LOUIS GLICK HWY     JACKSON   MI   49201-1326
364   Affiliated   429   Englewood   Englewood Dialysis Center   3247 S LINCOLN ST     ENGLEWOOD   CO   80113-2505
365   Affiliated   387   Harford Road Dialysis   Harford Road Dialysis Center   5800 HARFORD RD     BALTIMORE   MD   21214-1847
366   Affiliated   179   Arcadia   Arcadia Dialysis Center   1341 E OAK ST     ARCADIA   FL   34266-8902
367   Affiliated   388   Richmond Community   Richmond Community Hospital Dialysis (fkaTRC @ Richmond Community/Richmond II)   1510 N 28TH ST   STE 11   RICHMOND   VA   23223-5311
368   Affiliated   119   Henderson   Henderson Dialysis Center   1002 US HWY 79 N     HENDERSON   TX   75652-6008
369   Affiliated   253   Augusta   Nephrology Center of South Augusta   1631 GORDON HWY STE 1B     AUGUSTA   GA   30906
370   Affiliated   510   Boston Post Road   Boston Post Road Dialysis Center fka Co Op City Dialysis   4026 BOSTON RD     BRONX   NY   10475-1122
371   Affiliated   512   Peekskill   Peekskill Cortlandt Dialysis Center   2050 E MAIN ST   STE 15   CORTLANDT MANOR   NY   10567-2502
372   Affiliated   513   Queens   Queens Dialysis Center   11801 GUY R BREWER BLVD     JAMAICA   NY   11434-2101
373   Affiliated   517   Soundview   Soundview Dialysis Center   1622 BRUCKNER BLVD   STE 24   BRONX   NY   10473-4553

 

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374   Affiliated   516   Port Washington   Port Washington Dialysis Center   50 SEAVIEW BLVD     PORT WASHINGTON   NY   11050-4615
375   Affiliated   515   Lynbrook   Lynbrook Dialysis Center   147 SCRANTON AVE     LYNBROOK   NY   11563-2808
376   Affiliated   518   Yonkers Dialysis Center   Yonkers Dialysis   575 YONKERS AVE     YONKERS   NY   10704-2601
377   Affiliated   537   IHS - Queens Village   Queens Village Dialysis Center   22202 HEMPSTEAD AVE   STE 17   QUEENS VILLAGE   NY   11429-2123
378   Affiliated   536   Coney Island - IHS   Sheepshead Bay Renal Care Center (fka Coney Island)   26 BRIGHTON 11TH ST     BROOKLYN   NY   11235-5304
379   Affiliated   521   Garden City I.H.S   Garden City Dialysis Center   1100 STEWART AVE   STE 2   GARDEN CITY   NY   11530-4839
380   Affiliated   267   Kenneth Hahn- I.R.A   Kenneth Hahn Plaza Dialysis Center (Willowbrook)   11854 S WILMINGTON AVE     LOS ANGELES   CA   90059-3016
381   Affiliated   279   North Highland   North Highlands Dialysis Center   4986 WATT AVE   STE F   NORTH HIGHLANDS   CA   95660-5182
382   Affiliated   294   TRC Orangevale   Orangevale Dialysis Center   9267 GREENBACK LN   STE A2   ORANGEVALE   CA   95662-4864
383   Affiliated   554   Forest Park Dialysis Center   Forest Park Dialysis Center   380 FOREST PKWY   STE C   FOREST PARK   GA   30297-2107
384   Affiliated   446   Grant Park Nursing Home Dialysis   Grant Park Dialysis (fka Grants Park Nursing Home)   5000 NANNIE HELEN BURROUGHS AVE NE     WASHINGTON   DC   20019-5506
385   Affiliated   455   Fourth Street Dialysis   Fourth Street Dialysis   3101 N 4TH ST   STE B   LONGVIEW   TX   75605-5146
386   Affiliated   274   Bay Breeze   Bay Breeze Dialysis   11465 ULMERTON RD     LARGO   FL   33778-1602
387   Affiliated   416   Hopi   Hopi Dialysis Center- fka First Mesa   PO BOX 964   HWY 264   POLACCA   AZ   86042
388   Affiliated   178   Orlando Dialysis   Orlando Dialysis   14050 TOWN LOOP BLVD   STE 14A   ORLANDO   FL   32837-6190
389   Affiliated   170   Celebration Dialysis   Celebration Dialysis   1154 CELEBRATION BLVD     CELEBRATION   FL   34747-4605
390   Affiliated   1500   Mt. Dora Dialysis   Mt. Dora Dialysis   2735 W OLD US HIGHWAY 441     MOUNT DORA   FL   32757-3526
391   Affiliated   1501   Lake Dialysis   Lake Dialysis   221 N 1ST ST     LEESBURG   FL   34748-5150
392   Affiliated   146   Puyallup Community Dialysis   Puyallup Dialysis Center   716 SOUTH HILL PARK DR   STE C   PUYALLUP   WA   98373-1445
393   Affiliated   562   Towson Dialysis   Dulaney Towson Dialysis Center   113 WEST RD   STE 21   TOWSON   MD   21204-2318
394   Affiliated   188   Purcellville   Purcellville Dialysis Center   280 N HATCHER AVE     PURCELLVILLE   VA   20132-3193
395   Affiliated   476   Iris City   Iris City Dialysis (aka Griffin)   521 N EXPRESSWAY   STE 159   GRIFFIN   GA   30223-2073
396   Affiliated   1521   Slidell Kidney Care   Slidell Kidney Care   1150 ROBERT BLVD   STE 24   SLIDELL   LA   70458-2005
397   Affiliated   385   Rivertowne Dialysis   Rivertowne Dialysis (fka Oxon Hill Dialysis)   6192 OXON HILL RD   1ST FL   OXON HILL   MD   20745-3114
398   Affiliated   477   Pearland Dialysis   Pearland Dialysis   6516 BROADWAY ST   STE 122   PEARLAND   TX   77581-7879
399   Affiliated   419   East Aurora Dialysis   East Aurora Dialysis (aka Aurora II)   482 S CHAMBERS RD     AURORA   CO   80017-2092
400   Affiliated   1507   Merrillville Dialysis   CRC-Merrillville Dialysis Center   9223 TAFT ST     MERRILLVILLE   IN   46410-6911
401   Affiliated   563   Bricktown Dialysis   Bricktown Dialysis Center   525 JACK MARTIN BLVD   FL 2   BRICK   NJ   08724-7735
402   Affiliated   423   Sapulpa   Sapulpa Dialysis (fka Jenks-Sapulpa)   9647 RIDGEVIEW ST     TULSA   OK   74131-6205
403   Affiliated   1526   Ellijay Dialysis   Ellijay Dialysis   449 INDUSTRIAL BLVD   STE 24   ELLIJAY   GA   30540-6724
404   Affiliated   1527   Gainesville Dialysis   Gainesville Dialysis   2545 FLINTRIDGE RD   STE 13   GAINESVILLE   GA   30501-7428
405   Affiliated   1528   Newnan Dialysis   Newnan Dialysis   1565 E HWY 34   STE 13   NEWNAN   GA   30265
406   Affiliated   405   Ocala Regional Kidney Center - North   OCALA North Dialysis Center   2620 W HWY 316     CITRA   FL   32113-3555
407   Affiliated   1516   Pin Oak Dialysis   Pin Oak Dialysis Center (aka Katy II)   1302 PIN OAK RD     KATY   TX   77494-6848
408   Affiliated   1523   Imperial Care Dialysis   Imperial Care Dialysis Center   4345 E IMPERIAL HWY     LYNWOOD   CA   90262-2318
409   Affiliated   1533   St. Louis Park Dialysis   St. Louis Park Dialysis Center   3505 LOUISIANA AVE S     ST LOUIS PARK   MN   55426-4121
410   Affiliated   1517   Minneapolis NE Dialysis   Minneapolis NE Dialysis   1049 10TH AVE SE     MINNEAPOLIS   MN   55414-1312
411   Affiliated   298   Flushing Dialysis   Flushing Dialysis Center   3469 PIERSON PL   STE A   FLUSHING   MI   48433-2413
412   Affiliated   1535   Dialysis Systems of Covington   Dialysis Systems of Covington   210 GREENBRIAR BLVD     COVINGTON   LA   70433-7235
413   Affiliated   1536   Dialysis Systems of Hammond   Dialysis Systems of Hammond   15799 PROFESSIONAL PLZ     HAMMOND   LA   70403-1452
414   Affiliated   433   Soledad Dialysis   Soledad Dialysis Center   901 LOS COCHES DR     SOLEDAD   CA   93960-2995
415   Affiliated   443   Lake Elsinore Dialysis   Lake Elsinore Dialysis   32291 MISSION TRL   BLDG S   LAKE ELSINORE   CA   92530
416   Affiliated   1511   Clinton Dialysis Center   Clinton Dialysis Center   150 S 31ST ST     CLINTON   OK   73601-9118
417   Affiliated   456   Bakers Ferry   Bakers Ferry Dialysis   3645 BAKERS FERRY RD SW     ATLANTA   GA   30331-3712
418   Affiliated   1509   Hermiston   Hermiston Community Dialysis Center   1155 W LINDA AVE     HERMISTON   OR   97838-9601
419   Affiliated   1539   Yakima   Yakima Dialysis Center   1221 N 16TH AVE     YAKIMA   WA   98902-1347
420   Affiliated   409   Madison   Madison Dialysis Center   302 HIGHWAY ST     MADISON   NC   27025-1672
421   Affiliated   1508   Swannanoa Dialysis   Swannanoa Dialysis Center (fka Black Mountain, NC)   2305 US HIGHWAY 70     SWANNANOA   NC   28778-8207
422   Affiliated   2009   NE Wichita Dialysis   NE Wichita Dialysis Center   2630 N WEBB RD   STE 1 BLDG 1   WICHITA   KS   67226-8174
423   Affiliated   2005   Chadbourn Dialysis   Chadbourn Dialysis Center (fkaColumbus County)   210 STRAWBERRY BLVD     CHADBOURN   NC   28431-1418
424   Affiliated   1506   Western Home Dialysis   Mile High Home Dialysis PD (fka Western Home)   1750 PIERCE ST   STE A   LAKEWOOD   CO   80214-1434
425   Affiliated   2019   Tustin Dialysis   Tustin Dialysis (aka Santa Ana)   2090 N TUSTIN AVE   STE 1   SANTA ANA   CA   92705-7869
426   Affiliated   182   Appomatox   Appomattox Dialysis (Petersburg)   15 W OLD ST     PETERSBURG   VA   23803-3221
427   Affiliated   2002   Maryville Dialysis   Maryville Dialysis   2130 VADALABENE DR     MARYVILLE   IL   62062-5632

 

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428   Affiliated   2001   Mission Hills   Mission Hills Dialysis (aka Cristo Rey)   2700 N STANTON ST     EL PASO   TX   79902-2500
429   Affiliated   125   Moncrief   Moncrief Dialysis Partners   800 W 34TH ST   STE 11   AUSTIN   TX   78705-1144
430   Affiliated   295   Southfield West Dialysis   Southfield West Dialysis   21900 MELROSE AVE   STE 4   SOUTHFIELD   MI   48075-7967
431   Affiliated   525   Neptune Dialysis   Neptune Dialysis Center   2180 BRADLEY AVE     NEPTUNE   NJ   07753-4427
432   Affiliated   2014   Portsmouth Dialysis   Portsmouth Dialysis Center   2000 HIGH ST     PORTSMOUTH   VA   23704-3012
433   Affiliated   2016   Tokay Dialysis   Tokay Dialysis Center (fka East Lodi, CA)   312 S FAIRMONT AVE   STE A   LODI   CA   95240-3840
434   Affiliated   1504   Mt. Pocono Dialysis   Mt. Pocono Dialysis   100 COMMUNITY DR   STE 16   TOBYHANNA   PA   18466-8986
435   Affiliated   1544   Greater Portsmouth   Greater Portsmouth (aka Bon View Dialysis & Mid Town Hampton Road Dialysis)   3516 QUEEN ST     PORTSMOUTH   VA   23707-3238
436   Affiliated   1545   Peninsula Dialysis   Peninsula Dialysis Center (aka Immaculate Dialysis)   716 DENBIGH BLVD   STE D1 AND D2   NEWPORT NEWS   VA   23608-4414
437   Affiliated   1540   Saginaw Dialysis   Saginaw Dialysis   1527 E GENESEE AVE     SAGINAW   MI   48607-1755
438   Affiliated   1560   Churchview Dialysis   Churchview Dialysis   5970 CHURCHVIEW DR     ROCKFORD   IL   61107-2574
439   Affiliated   1562   Freeport Dialysis   Freeport Dialysis   1028 S KUNKLE BLVD     FREEPORT   IL   61032-6914
440   Affiliated   1563   Rockford Dialysis   Rockford Dialysis   3339 N ROCKTON AVE     ROCKFORD   IL   61103-2839
441   Affiliated   1564   Whiteside Dialysis   Whiteside Dialysis   2600 N LOCUST   STE D   STERLING   IL   61081-4602
442   Affiliated   2021   Pikesville Dialysis   Pikesville Dialysis   1500 REISTERSTOWN RD   STE 22   PIKESVILLE   MD   21208-3836
443   Affiliated   2000   Waynesville Dialysis   Waynesville Dialysis Center (fka Haywood, NC)   11 PARK TERRACE DR     CLYDE   NC   28721-7445
444   Affiliated   296   Davison Dialysis   Davison Dialysis   1011 S STATE RD     DAVISON   MI   48423-1903
445   Affiliated   1557   Flint Dialysis   Flint Dialysis Center   2 HURLEY PLZ   STE 115   FLINT   MI   48503-5904
446   Affiliated   1558   Hallwood Dialysis   Hallwood Dialysis Center   4929 CLIO RD   STE B   FLINT   MI   48504-1886
447   Affiliated   1559   Park Plaza Dialysis   Park Plaza Dialysis   G1075 N BALLENGER HWY     FLINT   MI   48504-4431
448   Affiliated   1518   Rosemead Springs Dialysis   Rosemead Springs Dialysis Center   3212 ROSEMEAD BLVD     EL MONTE   CA   91731-2807
449   Affiliated   2022   Scottsdale Dialysis   Scottsdale Dialysis Center   4725 N SCOTTSDALE RD   STE 1   SCOTTSDALE   AZ   85251-7621
450   Affiliated   1570   Washington Parish Dialysis   Washington Parish Dialysis   724 WASHINGTON ST     FRANKLINTON   LA   70438-1790
451   Affiliated   2027   Brookhollow Dialysis   Brookhollow Dialysis   4918 W 34TH ST     HOUSTON   TX   77092-6606
452   Affiliated   2017   Creekside   Creekside Dialysis Center (fka So. Vacaville, CA)   141 PARKER ST     VACAVILLE   CA   95688-3921
453   Affiliated   529   Middletown   Middletown Dialysis Center (fka-Red Bank)   500 STATE ROUTE 35   UNION SQUARE PLAZA   RED BANK   NJ   07701-5038
454   Affiliated   1541   Southwest Ohio Dialysis   Southwest Ohio Dialysis (Xenia-SWORC)   215 S ALLISON AVE     XENIA   OH   45385-3694
455   Affiliated   369   Oak Park   Oak Park Dialysis Center   13481 W 10 MILE RD     OAK PARK   MI   48237-4633
456   Affiliated   2042   Eden Prairie   Eden Prairie Dialysis   14852 SCENIC HEIGHTS RD   STE 255 BLDG B   EDEN PRAIRIE   MN   55344-2320
457   Affiliated   1530   Owensboro Dialysis   Owensboro Dialysis Center   1930 E PARRISH AVE     OWENSBORO   KY   42303-1443
458   Affiliated   1531   Tell City Dialysis   CRC-Tell City Dialysis Center   1602 MAIN ST     TELL CITY   IN   47586-1310
459   Affiliated   1576   Crestwood Dialysis   Crestwood Dialysis (fka Health Research Group-St. Louis (HRG))   9901 WATSON RD   STE 125   SAINT LOUIS   MO   63126-1855
460   Affiliated   2004   Copperfield Dialysis   Copperfield Dialysis (fka Cabarrus County-NC, and Concord)   1030 VINEHAVEN DR     CONCORD   NC   28025-2438
461   Affiliated   1572   Grand Island Dialysis   Grand Island Dialysis   603 S WEBB RD     GRAND ISLAND   NE   68803-5141
462   Affiliated   1573   Harlan Dialysis   Harlan Dialysis   1213 GARFIELD AVE     HARLAN   IA   51537-2057
463   Affiliated   1574   Shenandoah Dialysis   Shenandoah Dialysis   300 PERSHING AVE     SHENANDOAH   IA   51601-2355
464   Affiliated   2053   Germantown Dialysis   Germantown Dialysis   20111 CENTURY BLVD   STE C   GERMANTOWN   MD   20874-9165
465   Affiliated   2051   Lamplighter Dialysis   Lamplighter Dialysis   12654 LAMPLIGHTER SQUARE     ST LOUIS   MO   63128
466   Affiliated   1578   Kidney Care of Largo   Kidney Care of Largo   1300 MERCANTILE LN   STE 194   UPPER MARLBORO   MD   20774
467   Affiliated   1579   Kidney Care of Laurel   Kidney Care of Laurel   14631 LAUREL BOWIE ROAD   UNITS 1-15   LAUREL   MD   20707
468   Affiliated   2024   Durant Dialysis   Durant Dialysis Center   411 WESTSIDE DR     DURANT   OK   74701-2932
469   Affiliated   2038   Palm Brook Dialysis   Palm Brook Dialysis Center   14664 N DEL WEBB BLVD     SUN CITY   AZ   85351-2137
470   Affiliated   2043   Cambridge Dialysis   Cambridge Dialysis Center   300 BYRN ST     CAMBRIDGE   MD   21613-1908
471   Affiliated   2059   Reston Dialysis Center   Reston Dialysis Center   1875 CAMPUS COMMONS DR   STE 11   RESTON   VA   20191-1564
472   Affiliated   2040   Franconia Dialysis   Franconia Dialysis Centre   5695 KING CENTRE DRIVE     ALEXANDRIA   VA   22315-5744
473   Affiliated   2041   Eagan Dialysis   Eagan Dialysis Unit   2750 BLUE WATER RD   SUITE 3   EAGAN   MN   55121-1400
474   Affiliated   1594   Central Des Moines Dialysis   Central Des Moines Dialysis   1215 PLEASANT ST   STE 16   DES MOINES   IA   50309-1409
475   Affiliated   1595   West Des Moines Dialysis   West Des Moines Dialysis   6800 LAKE DR   STE 185   WEST DES MOINES   IA   50266-2544
476   Affiliated   1596   Creston Dialysis   Creston Dialysis   1700 W TOWNLINE ST     CRESTON   IA   50801-1054
477   Affiliated   1597   Atlantic Dialysis   Atlantic Dialysis   1500 E 10TH ST     ATLANTIC   IA   50022-1935
478   Affiliated   1598   Newton Dialysis   Newton Dialysis   204 N 4TH AVE E   STE 134   NEWTON   IA   50208-3135
479   Affiliated   2046   Dialysis of Des Moines   Riverpoint Dialysis Unit   501 SW 7TH ST   STE B   DES MOINES   IA   50309-4538
480   Affiliated   2060   Bellevue Dialysis   Bellevue Dialysis Center   3535 FACTORIA BLVD SE   STE 15   BELLEVUE   WA   98006-1293
481   Affiliated   414   Somerset Dialysis   Somerset Dialysis Center   240 CHURCHILL AVE     SOMERSET   NJ   08873-3451

 

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482   Affiliated   2031   East Ft. Lauderdale Dialysis   East Ft. Lauderdale Dialysis Center (fka No. Broward)   1301 S ANDREWS AVE   STE 11   FT LAUDERDALE   FL   33316-1823
483   Affiliated   1593   Spring Branch Dialysis   Spring Branch Dialysis   1425 BLALOCK   STE 1   HOUSTON   TX   77055-4446
484   Affiliated   1599   Battle Creek Dialysis   Battle Creek Dialysis   220 E GOODALE AVE     BATTLE CREEK   MI   49037-2728
485   Affiliated   2025   Hampton Avenue Dialysis   Hampton Avenue Dialysis-MO (Forest Park)   1425 HAMPTON AVE     SAINT LOUIS   MO   63139-3115
486   Affiliated   1605   Bogalusa Kidney Care   Bogalusa Kidney Care   2108 SOUTH AVE F     BOGALUSA   LA   70427
487   Affiliated   2055   Bardstown Dialysis   Bardstown Dialysis Center   210 W JOHN FITCH AVE     BARDSTOWN   KY   40004-1115
488   Affiliated   2050   Southern Pines   Southern Pines Dialysis Center   209 WINDSTAR PL     SOUTHERN PINES   NC   28387-7086
489   Affiliated   2030   Montclare Dialysis   Montclare Dialysis Center (aka Belmont Ave)   7009 W BELMONT AVE     CHICAGO   IL   60634-4533
490   Affiliated   2048   Southern Hills   Southern Hills Dialysis Center   9280 W SUNSET RD   STE 11   LAS VEGAS   NV   89148-4861
491   Affiliated   2068   Kilgore Dialysis   Kilgore Dialysis Center   209 HWY 42 NORTH     KILGORE   TX   75662-5019
492   Affiliated   2067   Brighton Dialysis   Brighton Dialysis   4700 E BROMLEY LN   STE 13   BRIGHTON   CO   80601-7821
493   Affiliated   2023   Union Gap   Union Gap Dialysis (aka Yakima)   1236 AHTANUM RIDGE DR   AHTANUM RIDGE BUSINESS PARK   UNION GAP   WA   98903-1813
494   Affiliated   2039   Dallas North Dialysis   Dallas North Dialysis Center (aka Greenville)   11886 GREENVILLE AVE   STE 1B   DALLAS   TX   75243-9743
495   Affiliated   2061   Grovepark Dialysis   Grovepark Dialysis Center (fka Jackson Dialysis)   794 MCDONOUGH RD     JACKSON   GA   30233-1572
496   Affiliated   1583   Eastern Kentucky Dialysis   Eastern Kentucky Dialysis   167 WEDDINGTON BRANCH RD     PIKEVILLE   KY   41501-3204
497   Affiliated   1584   Paintsville Dialysis   Paintsville Dialysis   4750 S KY ROUTE 321     HAGERHILL   KY   41222
498   Affiliated   1582   West Virginia Dialysis   West Virginia Dialysis   300 PROSPERITY LANE   STE 15   LOGAN   WV   25601-3494
499   Affiliated   2049   Reidsville Dialysis   Reidsville Dialysis   1307 FREEWAY DR     REIDSVILLE   NC   27320-7104
500   Affiliated   2034   Elk Grove Dialysis   Elk Grove Dialysis   9281 OFFICE PARK CIR   STE 15   ELK GROVE   CA   95758-8069
501   Affiliated   2035   Weston Dialysis   Weston Dialysis Center (fka Cleveland Clinic)   2685 EXECUTIVE PARK DR   STE 1   WESTON   FL   33331-3651
502   Affiliated   1600   McCook Dialysis   McCook Dialysis Center   801 W C ST     MCCOOK   NE   69001-3591
503   Affiliated   1601   Hastings Dialysis   Hastings Dialysis Center   1900 N SAINT JOSEPH AVE     HASTINGS   NE   68901-2652
504   Affiliated   1602   Capital City Dialysis   Capital City Dialysis   307 N 46TH ST     LINCOLN   NE   68503-3714
505   Affiliated   1616   Renal Care of Bowie   Renal Care of Bowie   4861 TELSA DRIVE   STES G-H   BOWIE   MD   20715-4318
506   Affiliated   1617   Renal Care of Takoma Park   Takoma Park Dialysis (fka Renal Care of Takoma Park)   1502 UNIVERSITY BLVD E     HYATTSVILLE   MD   20783
507   Affiliated   1618   Renal Care of Lanham   Renal Care of Lanham   8855 ANNAPOLIS RD   STE 2   LANHAM   MD   20706-2942
508   Affiliated   1619   Parma Dialysis   Parma Dialysis Center   6735 AMES RD     CLEVELAND   OH   44129-5601
509   Affiliated   1620   Middleburg Heights Dialysis   Middleburg Hts. Dialysis   7360 ENGLE RD     MIDDLEBURG HTS   OH   44130
510   Affiliated   1621   Rocky River Dialysis   Rocky River Dialysis   20220 CENTER RIDGE RD   STE 5   ROCKY RIVER   OH   44116-3567
511   Affiliated   1606   Diamond Valley Dialysis   Diamond Valley Dialysis   1030 E FLORIDA AVE     HEMET   CA   92543-4511
512   Affiliated   1607   Murrieta Dialysis   Murrieta Dialysis   25100 HANCOCK AVE   STE 11   MURRIETA   CA   92562-5973
513   Affiliated   2057   South Chico Dialysis   South Chico Dialysis Center   2345 FOREST AVE     CHICO   CA   95928-7641
514   Affiliated   2099   Dixon Kidney Center   Dixon Kidney Center   1131 N GALENA AVE     DIXON   IL   61021-1015
515   Affiliated   1640   Grand Rapids   PDI-Grand Rapids   801 CHERRY ST SE     GRAND RAPIDS   MI   49506-1440
516   Affiliated   1641   Grand Rapids East   PDI-Grand Rapids East   1230 EKHART ST NE     GRAND RAPIDS   MI   49503-1372
517   Affiliated   1642   Grand Haven   PDI-Grand Haven   16964 ROBBINS RD     GRAND HAVEN   MI   49417-2796
518   Affiliated   1644   Highland Park   PDI-Highland Park   64 VICTOR ST     HIGHLAND PARK   MI   48203-3128
519   Affiliated   1645   Cadieux   PDI-Cadieux   6150 CADIEUX ROAD     DETROIT   MI   48224-2006
520   Affiliated   1646   Montgomery   PDI-Montgomery   1001 FOREST AVE     MONTGOMERY   AL   36106-1181
521   Affiliated   1647   East Montgomery   PDI-East Montgomery   6890 WINTON BLOUNT BLVD     MONTGOMERY   AL   36117-3516
522   Affiliated   1648   Prattville   PDI-Prattville   1815 GLYNWOOD DR     PRATTVILLE   AL   36066-5584
523   Affiliated   1649   Elmore   PDI-Elmore   125 HOSPITAL DR     WETUMPKA   AL   36092-1626
524   Affiliated   1650   Fitchburg   PDI-Fitchburg   551 ELECTRIC AVE     FITCHBURG   MA   01420-5371
525   Affiliated   1652   Rocky Hill   PDI-Rocky Hill   30 WATERCHASE DR     ROCKY HILL   CT   06067-2110
526   Affiliated   1653   Middlesex   PDI-Middlesex Dialysis Center   100 MAIN ST   STE A   MIDDLETOWN   CT   06457-3477
527   Affiliated   1655   Johnstown   PDI-Johnstown   344 BUDFIELD ST     JOHNSTOWN   PA   15904-3214
528   Affiliated   1656   Ebensburg   PDI-Ebensburg   236 JAMESWAY RD     EBENSBURG   PA   15931-4207
529   Affiliated   1657   Walnut Tower   PDI-Walnut Tower   834 WALNUT ST     PHILADELPHIA   PA   19107-5109
530   Affiliated   1659   Lancaster   PDI-Lancaster   1412 E KING ST     LANCASTER   PA   17602-3240
531   Affiliated   1660   Ephrata   PDI-Ephrata   67 W CHURCH ST     STEVENS   PA   17578-9203
532   Affiliated   2083   Pinecrest Dialysis   Pinecrest Dialysis (aka North Marshall-TX)   913 E PINECREST DR     MARSHALL   TX   75670-7309
533   Affiliated   551   Westwood Dialysis   Westwood Dialysis Center (aka West Seattle)   2615 SW TRENTON ST     SEATTLE   WA   98126-3745
534   Affiliated   2107   Louisville Dialysis   Louisville Dialysis   8037 DIXIE HWY     LOUISVILLE   KY   40258-1344
535   Affiliated   2018   Fair Oaks Dialysis   Fair Oaks Dialysis Center (fka Chantilly & Centreville)   3955 PENDER DR   ONE PENDER BUSINESS PARK   FAIRFAX   VA   22030-6091

 

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536   Affiliated   421   Oak Cliff   Oak Cliff Dialysis   2000 S LLEWELLYN AVE     DALLAS   TX   75224-1804
537   Affiliated   2126   Gilmer Dialysis   Gilmer Dialysis Center   519 N WOOD ST     GILMER   TX   75644-1746
538   Affiliated   1608   Chicago Heights Dialysis   Chicago Heights Dialysis   177 W JOE ORR RD   STE B   CHICAGO HEIGHTS   IL   60411-1733
539   Affiliated   1623   East Georgia Dialysis   East Georgia Dialysis   450 GEORGIA AVE   STE A   STATESBORO   GA   30458-5590
540   Affiliated   1639   Northlake Dialysis   Northlake Dialysis   1350 MONTREAL RD   STE 2   TUCKER   GA   30084-8144
541   Affiliated   1680   Down River Dialysis   Downriver Kidney Center   5600 ALLEN RD     ALLEN PARK   MI   48101-2604
542   Affiliated   2063   Belcaro   Belcaro Dialysis Center   755 S COLORADO BLVD     DENVER   CO   80246-8005
543   Affiliated   2076   Sherwood Dialysis Center   Sherwood Dialysis Center   21035 SW PACIFIC HWY     SHERWOOD   OR   97140-8062
544   Affiliated   2054   Lonetree Dialysis   Lonetree Dialysis Center (aka Skyridge)   9777 MOUNT PYRAMID CT   STE 14   ENGLEWOOD   CO   80112-6017
545   Affiliated   2078   River Park Dialysis   River Park Dialysis (aka Conroe)   2010 S LOOP 336 W   STE 2   CONROE   TX   77304-3313
546   Affiliated   2058   Northshore Dialysis   Northshore Kidney Center (fka Slidell II)   106 MEDICAL CENTER DR     SLIDELL   LA   70461-5575
547   Affiliated   2036   Marysville Dialysis   Marysville Dialysis Center   1015 8TH ST     MARYSVILLE   CA   95901-5271
548   Affiliated   2070   West Georgia Dialysis   West Georgia Dialysis   1216 STARK AVE     COLUMBUS   GA   31906-2500
549   Affiliated   2102   East Dearborn Dialysis   Westland Dialysis (aka Canton)   36588 FORD RD     WESTLAND   MI   48185-3769
550   Affiliated   2045   Downtown Houston Dialysis   Downtown Houston Dialysis Center   2207 CRAWFORD ST     HOUSTON   TX   77002-8915
551   Affiliated   2066   Concord Dialysis   Concord Dialysis Center   2300 STANWELL DR   STE C   CONCORD   CA   94520-4841
552   Affiliated   2087   Pendleton Dialysis   Pendleton Dialysis (aka Clemson, Tri-County)   7703 HIGHWAY 76     PENDLETON   SC   29670-1818
553   Affiliated   2106   New Albany Dialysis   New Albany Dialysis   2669 CHARLESTON RD     NEW ALBANY   IN   47150-2573
554   Affiliated   1585   Whitesburg Dialysis   Whitesburg Dialysis   222 HOSPITAL RD   STE D   WHITESBURG   KY   41858-7627
555   Affiliated   2047   Jacinto Dialysis   Jacinto Dialysis Center (aka East Houston)   11515 MARKET STREET RD     HOUSTON   TX   77029-2305
556   Affiliated   2088   Transmountain Dialysis   Transmountain Dialysis (aka Northeast El Paso, Rushfair)   5255 WOODROW BEAN   STE B18   EL PASO   TX   79924-3832
557   Affiliated   2029   Southcrest Dialysis   Southcrest Dialysis (aka South Creek)   9001 S 101ST EAST AVE   STE 11   TULSA   OK   74133-5799
558   Affiliated   2071   Lake Hearn   Lake Hearn Dialysis (aka Dunwoody, Roswell, Northside)   1150 LAKE HEARN DR NE   STE 1   ATLANTA   GA   30342-1566
559   Affiliated   2118   Mt. Greenwood   Mt. Greenwood Dialysis   3401 W 111TH ST     CHICAGO   IL   60655-3329
560   Affiliated   2086   Citrus Valley Dialysis Center   Citrus Valley Dialysis (aka San Bernadino II)   894 HARDT STREET     SAN BERNARDINO   CA   92408-2854
561   Affiliated   2095   McDowell County Dialysis   McDowell County Dialysis Center   100 SPAULDING RD   STE 2   MARION   NC   28752-5116
562   Affiliated   2115   Leigh Dialysis Center   Leigh Dialysis Center (aka Leigh-Kempville-VA)   420 N CENTER DR   STE 128   NORFOLK   VA   23502-4019
563   Affiliated   2120   Dialysis of Lithonia   Dialysis of Lithonia   2485 PARK CENTRAL BLVD     DECATUR   GA   30035-3902
564   Affiliated   2114   Embassy Lake Artificial Kidney Center   Embassy Lake Artificial Kidney Center (fka Davie & South Broward AKC)   11011 SHERIDAN ST   STE 38   HOLLYWOOD   FL   33026-1505
565   Affiliated   2056   Sun City Dialysis   Sun City Dialysis (akaTexas Tech II)   600 NEWMAN ST     EL PASO   TX   79902-5543
566   Affiliated   1651   PDI Worcester   PDI-Worcester Dialysis   19 GLENNIE ST   STE A   WORCESTER   MA   01605-3918
567   Affiliated   2130   Davenport Dialysis Center   Davenport Dialysis Center (aka Haines City II)   45597 HIGHWAY 27   RIDGEVIEW PLAZA   DAVENPORT   FL   33897-4519
568   Affiliated   2081   Cinema Dialysis   Cinema Dialysis (aka OKC South)   3909 S WESTERN AVE     OKLAHOMA CITY   OK   73109-3405
569   Affiliated   2037   Greenwood Dialysis Center   Greenwood Dialysis Center (North Tulsa)   1345 N LANSING AVE     TULSA   OK   74106-5911
570   Affiliated   1712   TRC Alamosa Diakysis   Alamosa Dialysis   612 DEL SOL DR     ALAMOSA   CO   81101-8548
571   Affiliated   1682   South Austin   South Austin Dialysis   6114 S 1ST ST     AUSTIN   TX   78745-4008
572   Affiliated   2109   Durango Dialysis Center   Durango Dialysis Center   72 SUTTLE STREET   STE D   DURANGO   CO   81303-6829
573   Affiliated   1700   Bolivar Dialysis   Bolivar Dialysis   515 PECAN DR     BOLIVAR   TN   38008-1611
574   Affiliated   1701   Brownsville Dialysis   Brownsville Dialysis   380 N DUPREE AVE     BROWNSVILLE   TN   38012-2332
575   Affiliated   1702   Camden Dialysis   Camden Dialysis   168 W MAIN ST   STE A   CAMDEN   TN   38320-1767
576   Affiliated   1703   Collierville Dialysis   Collierville Dialysis   791 W POPLAR AVE     COLLIERVILLE   TN   38017-2543
577   Affiliated   1705   Galleria Dialysis   Galleria Dialysis   9160 HIGHWAY 64     LAKELAND   TN   38002-4766
578   Affiliated   1706   Humboldt Dialysis   Humboldt Dialysis   2214 OSBORNE ST     HUMBOLDT   TN   38343-3044
579   Affiliated   1707   Stonegate Dialysis   North Jackson Dialysis (fka Stonegate)   217 STERLING FARM DR     JACKSON   TN   38305-5727
580   Affiliated   1708   Lexington Dialysis   Lexington Dialysis   317 W CHURCH ST     LEXINGTON   TN   38351-2096
581   Affiliated   1709   Pickwick Dialysis   Pickwick Dialysis   121 PICKWICK ST     SAVANNAH   TN   38372-1953
582   Affiliated   1710   Selmber Dialysis   Selmer Dialysis   251 OAKGROVE RD     SELMER   TN   38375-1881
583   Affiliated   1713   Childs Dialysis   Childs Dialysis   101 MAIN ST     CHILDS   PA   18407-2614
584   Affiliated   1714   Dunmore Dialysis   Dunmore Dialysis   1212 O’NEIL HWY     DUNMORE   PA   18512-1717
585   Affiliated   1716   Old Forge Dialysis   Old Forge Dialysis   325 S MAIN ST     OLD FORGE   PA   18518-1677
586   Affiliated   1717   Scranton Dialysis   Scranton Dialysis   475 MORGAN HWY     SCRANTON   PA   18508-2605
587   Affiliated   1718   Tunkhannock Dialysis   Tunkhannock Dialysis   5950 SR 6     TUNKHANNOCK   PA   18657-7905
588   Affiliated   1725   East Evansville Dialysis   East Evansville Dialysis   1312 PROFESSIONAL BLVD     EVANSVILLE   IN   47714-8007
589   Affiliated   1726   North Evansville Dialysis   North Evansville Dialysis   1151 W BUENA VISTA RD     EVANSVILLE   IN   47710-3334

 

Page 100 of 136


590

  Affiliated   1728   Jasper Dialysis   Jasper Dialysis   721 W 13TH ST   STE 15   JASPER   IN   47546-1856

591

  Affiliated   1729   Daviess County Dialysis   Daviess County Dialysis   310 NE 14TH ST     WASHINGTON   IN   47501-2137

592

  Affiliated   1730   Gardenside Dialysis   Gardenside Dialysis   70 N GARDENMILE RD     HENDERSON   KY   42420-5529

593

  Affiliated   1732   PD Evansville Dialysis   East Evansville Dialysis PD   1312 PROFESSIONAL BLVD     EVANSVILLE   IN   47714-8007

594

  Affiliated   2098   Meridian Dialysis Center   Meridian Dialysis Center (aka Bayshore)   201 W FAIRMONT PKWY   STE A   LA PORTE   TX   77571-6303

595

  Affiliated   2100   Sycamore Dialysis   Sycamore Dialysis (aka DeKalb)   2200 GATEWAY DR     SYCAMORE   IL   60178-3113

596

  Affiliated   2104   Ballenger Pointe Dialysis   Ballenger Pointe Dialysis (aka West Flint)   2262 S BALLENGER HWY     FLINT   MI   48503-3447

597

  Affiliated   2139   Leitchfield Dialysis   Leitchfield Dialysis   912 WALLACE AVE   STE 16   LEITCHFIELD   KY   42754-2405

598

  Affiliated   2097   Roxbury Dialysis Center   Roxbury Dialysis   622 ROXBURY RD     ROCKFORD   IL   61107-5089

599

  Affiliated   2148   LaGrange Dialysis   La Grange Dialysis   240 PARKER DR     LA GRANGE   KY   40031-1200

600

  Affiliated   2132   Des Moines East   East Des Moines Dialysis (aka Des Moines II)   1301 PENNSYLVANIA AVE   STE 28   DES MOINES   IA   50316-2365

601

  Affiliated   2119   Lake Villa Dialysis   Lake Villa Dialysis   37809 N IL ROUTE 59     LAKE VILLA   IL   60046-7332

602

  Affiliated   159   Seneca Dialysis   Seneca County Dialysis   65 SAINT FRANCIS AVE     TIFFIN   OH   44883-3413

603

  Affiliated   407   Perry   Perry Dialysis Center   1027 KEITH DR     PERRY   GA   31069-2948

604

  Affiliated   661   Wilshire   Wilshire Dialysis   1212 WILSHIRE BLVD     LOS ANGELES   CA   90017-1902

605

  Affiliated   692   University Park   University Park Dialysis Center   3986 S FIGUEROA ST     LOS ANGELES   CA   90037-1222

606

  Affiliated   1720   Metro East Dialysis   Metro East Dialysis   5105 W MAIN ST     BELLEVILLE   IL   62226-4728

607

  Affiliated   2196   Ocala Regional Kidney Centers   Ocala Regional Kidney Centers Home Dialysis Division PD   2860 SE 1ST AVE     OCALA   FL   34471-0406

608

  Affiliated   2133   Little Village Dialysis   Little Village Dialysis (Chicago)   2335 W CERMAK RD     CHICAGO   IL   60608-3811

609

  Affiliated   2112   Crossroads   Crossroads Dialysis (aka Fullerton Dialysis)   3214 YORBA LINDA BLVD     FULLERTON   CA   92831-1707

610

  Affiliated   1727   Vincennes Dialysis   Vincennes Dialysis   700 WILLOW ST     VINCENNES   IN   47591-1028

611

  Affiliated   1723   Spring Dialysis   Spring Dialysis   607 TIMBERDALE LN   STE 1   HOUSTON   TX   77090-3043

612

  Affiliated   2190   River Center   Rivercenter Dialysis (aka Central San Antonio)   1123 N MAIN AVE   STE 15   SAN ANTONIO   TX   78212-4738

613

  Affiliated   2193   Southcross Dialysis Center   Southcross Dialysis (aka SouthEast San Antonio)   4602 E SOUTHCROSS BLVD     SAN ANTONIO   TX   78222-4911

614

  Affiliated   2125   Bonham Dialysis   Bonham Dialysis   201 W 5TH ST     BONHAM   TX   75418-4302

615

  Affiliated   2192   Northwest Medical Center Dialysis   NW Medical Center Dialysis (aka NorthWest San Antonio)   5284 MEDICAL DR   STE 1   SAN ANTONIO   TX   78229-4849

616

  Affiliated   2124   Ontario Dialysis   Ontario Dialysis (aka Dr. Handoko)   1950 S GROVE AVE   STE 11-15   ONTARIO   CA   91761-5693

617

  Affiliated   1750   Chipley Community Dialysis   Chipley Dialysis   877 3RD ST   STE 2   CHIPLEY   FL   32428-1855

618

  Affiliated   1751   North Ikaloosa   North Okaloosa Dialysis   320 REDSTONE AVE W     CRESTVIEW   FL   32536-6433

619

  Affiliated   1752   West Florida Dialysis   West Florida Dialysis   8333 N DAVIS HWY   1ST FLOOR ATTN DIALYSIS ROOM   PENSACOLA   FL   32514-6049

620

  Affiliated   1753   Santa Rosa Dialysis   Santa Rosa Dialysis   5819 HIGHWAY 90     MILTON   FL   32583-1763

621

  Affiliated   1755   Atmore Dialysis   Atmore Dialysis Center   807 E CRAIG ST     ATMORE   AL   36502-3017

622

  Affiliated   1756   South Baldwin Dialysis   South Baldwin Dialysis Center   150 W PEACHTREE AVE     FOLEY   AL   36535-2244

623

  Affiliated   1731   Olney Dialysis   Olney Dialysis Center (aka Good Samaritan Hospital)   117 N BOONE ST     OLNEY   IL   62450-2109

624

  Affiliated   2156   Lancaster Dialysis   Lancaster Dialysis   2424 W PLEASANT RUN RD     LANCASTER   TX   75146-4005

625

  Affiliated   2136   Columbia Dialysis   RTC-Columbia Dialysis (MO)   1701 E BROADWAY   STE G12   COLUMBIA   MO   65201-8029

626

  Affiliated   2194   Las Palmas Dialysis Center   Las Palmas Dialysis Center (aka West San Antonio)   803 CASTROVILLE RD   STE 415   SAN ANTONIO   TX   78237-3148

627

  Affiliated   2116   South Shore Dialysis Center   South Shore Dialysis (aka Horizon)   212 GULF FWY S   STE G3   LEAGUE CITY   TX   77573-3957

628

  Affiliated   2191   Marymount Dilaysis Center   Marymont Dialysis (aka NorthEast San Antonio)   2391 NE LOOP 410   STE 211   SAN ANTONIO   TX   78217-5675

629

  Affiliated   1744   Fox River Dialysis   Fox River Dialysis   1910 RIVERSIDE DR     GREEN BAY   WI   54301-2319

630

  Affiliated   1745   Titletown Dialysis   Titletown Dialysis   120 SIEGLER ST     GREEN BAY   WI   54303-2636

631

  Affiliated   1746   Northwoods Dialysis   Green Bay Northwood Dialysis   W 7305 ELM AVENUE     SHAWANO   WI   54166-1024

632

  Affiliated   1758   North Charleston Dialysis   North Charleston Dialysis   5900 RIVERS AVE   STE E   NORTH CHARLESTON   SC   29406

633

  Affiliated   1759   Charleston County Dialysis   Faber Place Dialysis   3801 FABER PLACE DR     NORTH CHARLESTON   SC   29405-8533

634

  Affiliated   1760   Goose Creek Dialysis   Goose Creek Dialysis   109 GREENLAND DR     GOOSE CREEK   SC   29445-5354

635

  Affiliated   2501   Bridgeport Dialysis   Bridgeport Dialysis   900 MADISON AVE   STE 221   BRIDGEPORT   CT   06606-5534

636

  Affiliated   2503   Greater Waterbury Dialysis   Greater Waterbury Dialysis   209 HIGHLAND AVE     WATERBURY   CT   06708-3026

637

  Affiliated   2506   Shelton Dialysis   Shelton Dialysis   750 BRIDGEPORT AVE     SHELTON   CT   06484-4734

638

  Affiliated   2508   Yuma Dialysis   Yuma Dialysis   2130 W 24TH ST     YUMA   AZ   85364-6122

639

  Affiliated   2509   Pittsburgh Dialysis   Pittsburgh Dialysis   4312 PENN AVE     PITTSBURGH   PA   15224-1310

640

  Affiliated   2510   Elizabeth Dialysis   Elizabeth Dialysis   201 MCKEESPORT RD     ELIZABETH   PA   15037-1623

641

  Affiliated   2511   Brandon East Dialysis   Brandon East Dialysis   114 E BRANDON BLVD     BRANDON   FL   33511-5219

642

  Affiliated   2513   North Rolling Road Dialysis   North Rolling Road Dialysis   1108 N ROLLING RD     BALTIMORE   MD   21228-3826

643

  Affiliated   2521   Memphis South Dialysis   Memphis South Dialysis   1205 MARLIN RD     MEMPHIS   TN   38116-5812

 

Page 101 of 136


644

  Affiliated   2524   Hartford Dialysis   Hartford Dialysis   675 TOWER AVE   RENAL UNIT 2ND FL   HARTFORD   CT   6112

645

  Affiliated   2538   New Orleans Uptown Dialysis   New Orleans Uptown Dialysis   1401 FOUCHER ST   4TH FLOOR DIALYSIS   NEW ORLEANS   LA   70115-3515

646

  Affiliated   2540   Omaha West Dialysis   Omaha West Dialysis   13014 W DODGE RD     OMAHA   NE   68154-2148

647

  Affiliated   2541   White Memorial Dialysis   East Los Angeles Plaza Dialysis (fka White Memorial)   1700 E CESAR E CHAVEZ AVE   STE L 1   LOS ANGELES   CA   90033-2424

648

  Affiliated   2542   Imperial Dialysis   Imperial Dialysis   2738 W IMPERIAL HWY     INGLEWOOD   CA   90303-3111

649

  Affiliated   2546   North Hollywood Dialysis   North Hollywood Dialysis   12126 VICTORY BLVD     NORTH HOLLYWOOD   CA   91606-3205

650

  Affiliated   2555   Mountain View Dialysis   Mountain View Dialysis   2881 BUSINESS PARK CT   STE 13   LAS VEGAS   NV   89128-9019

651

  Affiliated   2560   San Juan Capistrano South Dialysis   San Juan Capistrano South Dialysis   31736 RANCHO VIEJO RD   STE B   SAN JUAN CAPISTRANO   CA   92675-2783

652

  Affiliated   2564   Mission Viejo Dialysis   Mission Viejo Dialysis   27640 MARGUERITE PKWY     MISSION VIEJO   CA   92692-3604

653

  Affiliated   2568   HI-Desert Dialysis   HI-Desert Dialysis   58457 29 PALMS HWY   STE 12   YUCCA VALLEY   CA   92284-5879

654

  Affiliated   2571   Banning Dialysis   Banning Dialysis   6090 W RAMSEY ST     BANNING   CA   92220-3052

655

  Affiliated   2601   Rainbow City Dialysis   Rainbow City Dialysis   2800 RAINBOW DR     RAINBOW CITY   AL   35906-5811

656

  Affiliated   2604   Gadsden Dialysis   Gadsden Dialysis   409 S 1ST ST     GADSDEN   AL   35901-5358

657

  Affiliated   2605   Chateau Dialysis   Chateau Dialysis   720 VILLAGE RD     KENNER   LA   70065-2751

658

  Affiliated   2606   Donaldsonville Dialysis   Donaldsonville Dialysis   101 PLIMSOL DR     DONALDSONVILLE   LA   70346-4357

659

  Affiliated   2609   Dothan Dialysis   Dothan Dialysis   216 GRACELAND DR     DOTHAN   AL   36305-7346

660

  Affiliated   2614   Birmingham East Dialysis   Birmingham East Dialysis   1105 E PARK DR     BIRMINGHAM   AL   35235-2560

661

  Affiliated   2615   Tuscaloosa Dialysis   Tuscaloosa Dialysis   805 OLD MILL ST     TUSCALOOSA   AL   35401-7132

662

  Affiliated   2616   Demopolis Dialysis   Demopolis Dialysis   511 S CEDAR AVE     DEMOPOLIS   AL   36732-2235

663

  Affiliated   2623   Singing River Dialysis   Singing River Dialysis   4907 TELEPHONE RD     PASCAGOULA   MS   39567-1823

664

  Affiliated   2624   Ocean Springs Dialysis   Ocean Springs Dialysis   13150 PONCE DE LEON DR     OCEAN SPRINGS   MS   39564-2460

665

  Affiliated   2625   Lucedale Dialysis   Lucedale Dialysis   652 MANILA ST     LUCEDALE   MS   39452-5962

666

  Affiliated   2707   Holmdel Dialysis   Holmdel Dialysis   668 N BEERS ST     HOLMDEL   NJ   07733-1526

667

  Affiliated   2855   Alameda County Dialysis   Alameda County Dialysis   10700 MACARTHUR BLVD   STE 14   OAKLAND   CA   94605-5260

668

  Affiliated   2908   Elizabeth City Dialysis   Elizabeth City Dialysis   1840 W CITY DR     ELIZABETH CITY   NC   27909-9632

669

  Affiliated   2914   Cookeville Dialysis   Cookeville Dialysis   140 W 7TH ST     COOKEVILLE   TN   38501-1726

670

  Affiliated   3001   Inglewood Dialysis   Inglewood Dialysis   125 E ARBOR VITAE ST     INGLEWOOD   CA   90301-3839

671

  Affiliated   3002   Rome Dialysis   Rome Dialysis   15 JOHN MADDOX DR NW     ROME   GA   30165-1413

672

  Affiliated   3004   Pomona Dialysis   Pomona Dialysis   2111 N GAREY AVE     POMONA   CA   91767-2328

673

  Affiliated   3005   Oak Street Dialysis   Oak Street Dialysis (fka Valdosta)   2704 N OAK ST   BLDG H   VALDOSTA   GA   31602-1723

674

  Affiliated   3006   Channelview Dialysis   Channelview Dialysis   777 SHELDON RD   STE C   CHANNELVIEW   TX   77530-3509

675

  Affiliated   3007   Sagemont Dialysis   Sagemont Dialysis   10851 SCARSDALE BLVD   STE 2   HOUSTON   TX   77089-5738

676

  Affiliated   3008   San Jacinto Dialysis   San Jacinto Dialysis   11430 EAST FWY   STE 33   HOUSTON   TX   77029-1959

677

  Affiliated   3009   Victor Valley Dialysis   Victor Valley Dialysis   16049 KAMANA RD     APPLE VALLEY   CA   92307-1331

678

  Affiliated   3010   Delran Dialysis   Delran Dialysis   8008 ROUTE 130     DELRAN   NJ   08075-1869

679

  Affiliated   3011   Central Houston Dialysis   Central Houston Dialysis   610 S WAYSIDE DR   UNIT B   HOUSTON   TX   77011-4605

680

  Affiliated   3012   Southern Lane Dialysis   Southern Lane Dialysis   1840 SOUTHERN LN     DECATUR   GA   30033-4033

681

  Affiliated   3013   Northumberland Dialysis   Northumberland Dialysis   103 W STATE ROUTE 61     MOUNT CARMEL   PA   17851-2539

682

  Affiliated   3014   Pryor Dialysis   Pryor Dialysis   309 E GRAHAM AVE     PRYOR   OK   74361-2434

683

  Affiliated   3015   Oklahoma City South Dialysis   Oklahoma City South Dialysis   5730 S MAY AVE     OKLAHOMA CITY   OK   73119-5604

684

  Affiliated   3016   Abington Dialysis   Abington Dialysis   3940A COMMERCE AVE     WILLOW GROVE   PA   19090-1705

685

  Affiliated   3017   Memphis Central Dialysis   Memphis Central Dialysis   889 LINDEN AVE     MEMPHIS   TN   38126-2412

686

  Affiliated   3018   Memphis East Dialysis   Memphis East Dialysis   50 HUMPHREYS CTR   STE 42   MEMPHIS   TN   38120-2372

687

  Affiliated   3019   Clarksville Dialysis   Clarksville Dialysis   231 HILLCREST DR     CLARKSVILLE   TN   37043-5093

688

  Affiliated   3020   Miami Campus Dialysis   Miami Campus Dialysis   1500 NW 12TH AVE   STE 16   MIAMI   FL   33136-1028

689

  Affiliated   3021   Orlando Dialysis   Orlando Dialysis   116 STURTEVANT ST     ORLANDO   FL   32806-2021

690

  Affiliated   3024   Durham Dialysis   Durham Dialysis   601 FAYETTEVILLE ST     DURHAM   NC   27701-3910

691

  Affiliated   3025   Candler County Dialysis   Candler County Dialysis   325 CEDAR ST     METTER   GA   30439-4043

692

  Affiliated   3027   Kerrville Dialysis   Kerrville Dialysis   515 GRANADA PL     KERRVILLE   TX   78028-5992

693

  Affiliated   3028   Floresville Dialysis   Floresville Dialysis   543 10TH ST     FLORESVILLE   TX   78114-3107

694

  Affiliated   3029   Pearsall Dialysis   Pearsall Dialysis   1305 N OAK ST     PEARSALL   TX   78061-3414

695

  Affiliated   3030   Nogales Dialysis   Nogales Dialysis   1231 W TARGET RANGE RD     NOGALES   AZ   85621-2417

696

  Affiliated   3032   Wilson Dialysis   Wilson Dialysis   1605 MEDICAL PARK DR W     WILSON   NC   27893-2799

697

  Affiliated   3033   Goldsboro Dialysis   Goldsboro Dialysis   2609 HOSPITAL RD     GOLDSBORO   NC   27534-9424

 

Page 102 of 136


698

  Affiliated   3034   Roxboro Dialysis   Roxboro Dialysis   718 RIDGE RD     ROXBORO   NC   27573-4508

699

  Affiliated   3035   Boston Dialysis   Boston Dialysis   660 HARRISON AVE     BOSTON   MA   02118-2304

700

  Affiliated   3037   Jesup Dialysis   Jesup Dialysis   301 PEACHTREE ST     JESUP   GA   31545-0245

701

  Affiliated   3038   Sheffield Dialysis   Sheffield Dialysis   1120 S JACKSON HWY   ST 17   SHEFFIELD   AL   35660-5777

702

  Affiliated   3039   Berkeley Dialysis   Berkeley Dialysis   2920 TELEGRAPH AVE     BERKELEY   CA   94705-2031

703

  Affiliated   3040   Douglas Dialysis   Douglas Dialysis   190 WESTSIDE DR   STE A   DOUGLAS   GA   31533-3534

704

  Affiliated   3041   Hopkinsville Dialysis   Hopkinsville Dialysis   1914 S VIRGINIA ST     HOPKINSVILLE   KY   42240-3610

705

  Affiliated   3042   Roxborough Dialysis   Roxborough Dialysis   5003 UMBRIA ST     PHILADELPHIA   PA   19128-4301

706

  Affiliated   3043   New Haven Dialysis   New Haven Dialysis   100 CHURCH ST S   STE C   NEW HAVEN   CT   06519-1703

707

  Affiliated   3044   Ocoee Dialysis   Ocoee Dialysis   11140 W COLONIAL DR   STE 5   OCOEE   FL   34761-3300

708

  Affiliated   3045   Waverly Dialysis   Waverly Dialysis   407 E BALTIMORE PIKE     MORTON   PA   19070-1042

709

  Affiliated   3046   Sells Dialysis   Sells Dialysis   PO BOX 3030   HWY 86 MILEPOST 113   SELLS   AZ   85634-3030

710

  Affiliated   3047   Sierra Vista Dialysis   Sierra Vista Dialysis   629 N HIGHWAY 90   STE 6   SIERRA VISTA   AZ   85635-2257

711

  Affiliated   3048   Callaghan Road Dialysis   San Antonio West Dialysis (fka Callaghan Road)   4530 CALLAGHAN RD     SAN ANTONIO   TX   78228

712

  Affiliated   3049   Houston Dialysis   Houston Dialysis   7543 SOUTH FWY     HOUSTON   TX   77021-5928

713

  Affiliated   3050   South Yuma Dialysis   South Yuma Dialysis   7179 E 31ST PLACE     YUMA   AZ   85365-8392

714

  Affiliated   3052   Cherry Hill Dialysis   Cherry Hill Dialysis   1030 KINGS HWY N   STE 1   CHERRY HILL   NJ   08034-1907

715

  Affiliated   3055   Escondido Dialysis   Escondido Dialysis   203 E 2ND AVE     ESCONDIDO   CA   92025-4212

716

  Affiliated   3056   Brookline Dialysis   Brookline Dialysis   322 WASHINGTON ST     BROOKLINE   MA   02445-6850

717

  Affiliated   3057   Reliant Dialysis   Reliant Dialysis   1335 LA CONCHA LN     HOUSTON   TX   77054-1809

718

  Affiliated   3058   Fullerton Dialysis   Fullerton Dialysis   238 ORANGEFAIR MALL     FULLERTON   CA   92832-3037

719

  Affiliated   3059   Huntington Beach Dialysis   Huntington Beach Dialysis   16892 BOLSA CHICA ST   STE 1   HUNTINGTON BEACH   CA   92649-3571

720

  Affiliated   3060   Eastlake Dialysis   Eastlake Dialysis (fka South Dekalb)   1757 CANDLER RD     DECATUR   GA   30032-3276

721

  Affiliated   3061   Mt. Olive Dialysis   Mt. Olive Dialysis   105 MICHAEL MARTIN RD     MOUNT OLIVE   NC   28365-1112

722

  Affiliated   3062   Southwest San Antonio Dialysis   Southwest San Antonio Dialysis   1620 SOMERSET RD     SAN ANTONIO   TX   78211-3021

723

  Affiliated   3064   North Loop East Dialysis   North Loop East Dialysis   7139 NORTH LOOP E     HOUSTON   TX   77028-5903

724

  Affiliated   3065   Katy Cinco Ranch Dialysis   Katy Cinco Ranch Dialysis   1265 ROCK CANYON DR     KATY   TX   77450-3831

725

  Affiliated   3067   Palm Springs Dialysis   Palm Springs Dialysis   1061 N INDIAN CANYON DR     PALM SPRINGS   CA   92262-4854

726

  Affiliated   3069   Muskegon Dialysis   Muskegon Dialysis   1277 MERCY DR     MUSKEGON   MI   49444-4605

727

  Affiliated   3070   Loomis Road Dialysis   Loomis Road Dialysis   4120 W LOOMIS RD     GREENFIELD   WI   53221-2052

728

  Affiliated   3071   Ludington Dialysis   Ludington Dialysis   5 N ATKINSON DR   STE 11   LUDINGTON   MI   49431-2918

729

  Affiliated   3073   Walterboro Dialysis   Walterboro Dialysis   302 RUBY ST     WALTERBORO   SC   29488-2758

730

  Affiliated   3074   K Street   K Street Dialysis (fka GWU N Street Dialysis)   2131 K ST NW     WASHINGTON   DC   20037-1898

731

  Affiliated   3075   GWU Southeast Dialysis   GWU Southeast Dialysis   3857A PENNSYLVANIA AVE SE     WASHINGTON   DC   20020-1309

732

  Affiliated   3076   Lakeside Dialysis   Lakeside Dialysis   10401 HOSPITAL DR   STE G2   CLINTON   MD   20735-3113

733

  Affiliated   3077   Summit Dialysis   Summit Dialysis   1139 SPRUCE DR     MOUNTAINSIDE   NJ   07092-2221

734

  Affiliated   3078   Aiken Dialysis   Aiken Dialysis   775 MEDICAL PARK DR     AIKEN   SC   29801-6306

735

  Affiliated   3092   Ozark Dialysis   Ozark Dialysis   214 HOSPITAL AVE     OZARK   AL   36360-2038

736

  Affiliated   3094   Wylds Road Dialysis   Wylds Road Dialysis (fka Augusta South)   1815 WYLDS RD     AUGUSTA   GA   30909-4430

737

  Affiliated   3104   Douglasville Dialysis   Douglasville Dialysis   3899 LONGVIEW DR     DOUGLASVILLE   GA   30135-1373

738

  Affiliated   3106   Brunswick Dialysis   Brunswick Dialysis   53 SCRANTON CONNECTOR     BRUNSWICK   GA   31525-1862

739

  Affiliated   3109   Benicia Dialysis   Benicia Dialysis   560 1ST ST   STE 13 BLDG D   BENICIA   CA   94510-3295

740

  Affiliated   3111   Atlanta Dialysis   Atlanta Dialysis   567 NORTH AVE NE   STE 2   ATLANTA   GA   30308-2719

741

  Affiliated   3115   Rolla Dialysis   Rolla Dialysis   1503 E 10TH ST     ROLLA   MO   65401-3696

742

  Affiliated   3119   East Atlanta Dialysis   East Atlanta Dialysis   1308 MORELAND AVE SE     ATLANTA   GA   30316-3224

743

  Affiliated   3120   Brunswick South Dialysis   Brunswick South Dialysis   2930 SPRINGDALE RD     BRUNSWICK   GA   31520

744

  Affiliated   3121   Thomaston Dialysis   Thomaston Dialysis   1065 US HIGHWAY 19 NORTH     THOMASTON   GA   30286-2233

745

  Affiliated   3128   Piedmont Dialysis   Piedmont Dialysis   105 COLLIER RD NW   STE B   ATLANTA   GA   30309-1730

746

  Affiliated   3130   Athens West Dialysis   Athens West Dialysis   2047 PRINCE AVE   STE A   ATHENS   GA   30606-6033

747

  Affiliated   3131   Florence Dialysis   Florence Dialysis   422 E DR HICKS BLVD   STE B   FLORENCE   AL   35630-5763

748

  Affiliated   3138   Atwater Dialysis   Atwater Dialysis   1201 COMMERCE AVE     ATWATER   CA   95301

749

  Affiliated   3143   North Merced Dialysis   Merced Dialysis   3150 G ST   STE A   MERCED   CA   95340-1346

750

  Affiliated   3169   Wisconsin Avenue Dialysis   Wisconsin Avenue Dialysis   3801 W WISCONSIN AVE     MILWAUKEE   WI   53208-3155

751

  Affiliated   3171   River Center Dialysis   River Center Dialysis   117 N JEFFERSON ST     MILWAUKEE   WI   53202-6160

 

Page 103 of 136


752

  Affiliated   3175   South Fulton Dialysis   South Fulton Dialysis   2685 METROPOLITAN PKWY SW   STE F   ATLANTA   GA   30315-7926

753

  Affiliated   3201   Heartland Dialysis   Heartland Dialysis   925 NE 8TH ST     OKLAHOMA CITY   OK   73104-5800

754

  Affiliated   3202   Hospital Hill Dialysis   Hospital Hill Dialysis   2250 HOLMES ST     KANSAS CITY   MO   64108-2639

755

  Affiliated   3203   Tucson South Dialysis   Tucson South Dialysis   3662 S 16TH AVE     TUCSON   AZ   85713-6001

756

  Affiliated   3204   Greene County Dialysis   Greene County Dialysis (AL)   544 US HIGHWAY 43     EUTAW   AL   35462-4017

757

  Affiliated   3205   Fayette Dialysis   Fayette Dialysis   2450 TEMPLE AVE N     FAYETTE   AL   35555-1160

758

  Affiliated   3206   Tuscaloosa University Dialysis   Tuscaloosa University Dialysis   220 15TH STREET     TUSCALOOSA   AL   35401

759

  Affiliated   3207   Goldsboro South Dialysis   Goldsboro South Dialysis   1704 WAYNE MEMORIAL DR     GOLDSBORO   NC   27534-2240

760

  Affiliated   3208   Orlando North Dialysis   Orlando North Dialysis   5135 ADANSON ST   STE 7   ORLANDO   FL   32804-1338

761

  Affiliated   3209   UT Southwestern-Dallas Dialysis   UT Southwestern-Dallas Dialysis   204 E AIRPORT FREEWAY     IRVING   TX   75062

762

  Affiliated   3210   San Diego South Dialysis   San Diego South Dialysis   995 GATEWAY CENTER WAY   STE 11   SAN DIEGO   CA   92102-4550

763

  Affiliated   3211   Santa Monica Dialysis   Santa Monica Dialysis   1260 15TH ST   STE 12   SANTA MONICA   CA   90404-1136

764

  Affiliated   3212   Airport Dialysis   Airport Dialysis   4632 W CENTURY BLVD     INGLEWOOD   CA   90304-1456

765

  Affiliated   3220   Plantation Dialysis   Plantation Dialysis   7061 CYPRESS RD   STE 13   PLANTATION   FL   33317-2243

766

  Affiliated   3224   Laurens County Dialysis   Laurens County Dialysis   2400 BELLEVUE RD   STE 8   DUBLIN   GA   31021-2856

767

  Affiliated   3225   Ford Factory Square Dialysis   Ford Factory Square Dialysis   567 NORTH AVE NE   STE 1   ATLANTA   GA   30308-2719

768

  Affiliated   3226   North Fulton Dialysis   North Fulton Dialysis   1250 NORTHMEADOW PKWY   STE 12   ROSWELL   GA   30076-4914

769

  Affiliated   3228   Freehold Dialysis   Freehold Dialysis   300 CRAIG RD     MANALAPAN   NJ   07726-8742

770

  Affiliated   3229   Neptune Dialysis   Neptune Route 66 Dialysis   3297 STATE ROUTE 66     NEPTUNE   NJ   07753-2762

771

  Affiliated   3231   East Orange Dialysis   East Orange Dialysis   90 WASHINGTON ST   BSMT   EAST ORANGE   NJ   07017-1050

772

  Affiliated   3234   UT Southwestern-Oakcliff Dialysis   UT Southwestern-Oakcliff Dialysis   610 WYNNEWOOD DR     DALLAS   TX   75224

773

  Affiliated   3236   Atlanta West Dialysis   Atlanta West Dialysis   2538 MARTIN LUTHER KING JR DR SW     ATLANTA   GA   30311-1779

774

  Affiliated   3237   Columbia University Dialysis Center   Columbia University Dialysis Center   60 HAVEN AVE     NEW YORK   NY   10032-2604

775

  Affiliated   3238   Northeast Cambridge Dialysis   Northeast Cambridge Dialysis   799 CONCORD AVE     CAMBRIDGE   MA   02138-1048

776

  Affiliated   3239   New Bedford Dialysis   New Bedford Dialysis   524 UNION ST     NEW BEDFORD   MA   02740-3546

777

  Affiliated   3242   Weymouth Dialysis   Weymouth Dialysis   330 LIBBEY INDUSTRIAL PARK   STE 9   WEYMOUTH   MA   02189-3122

778

  Affiliated   3243   Woburn Dialysis   Woburn Dialysis   23 WARREN AVE     WOBURN   MA   01801-7906

779

  Affiliated   3248   Bryan Dialysis   College Station Dialysis (fka Bryan Dialysis)   701 UNIVERSITY DR E   STE 41   COLLEGE STATION   TX   77840-1866

780

  Affiliated   3249   Brenham Dialysis   Brenham Dialysis   2815 HIGHWAY 36 SO     BRENHAM   TX   77833

781

  Affiliated   3250   Huntsville Dialysis   Huntsville Dialysis   521 IH 45S   STE 2   HUNTSVILLE   TX   77340-5651

782

  Affiliated   3252   Utica Avenue Dialysis Center   Utica Avenue Dialysis Center   1305 UTICA AVE     BROOKLYN   NY   11203-5911

783

  Affiliated   3254   New London Dialysis   New London Dialysis   5 SHAWS COVE   STE 1   NEW LONDON   CT   06320-4974

784

  Affiliated   3258   Baxley Dialysis   Baxley Dialysis   539 FAIR ST     BAXLEY   GA   31513-0112

785

  Affiliated   3261   Pascua Yaqui Tribe Dialysis   Pascua Yaqui Tribe Dialysis   7490 S CAMINO DE OESTE     TUCSON   AZ   85746-9308

786

  Affiliated   3262   JHHS North Bond Street Dialysis   JHHS North Bond Street Dialysis   409 N CAROLINE ST     BALTIMORE   MD   21231-1003

787

  Affiliated   3263   Syosset Kidney Center   Syosset Kidney Center   1 LOCUST LN     SYOSSET   NY   11791-4834

788

  Affiliated   3264   Freeport Kidney Center   Freeport Kidney Center   267 W MERRICK RD     FREEPORT   NY   11520-3346

789

  Affiliated   3265   Huntington Station Dialysis Center   HAKC-Huntington   256 BROADWAY     HUNTINGTON STATION   NY   11746-1403

790

  Affiliated   3266   Medford Kidney Center   Medford Kidney Center   1725 N OCEAN AVE     MEDFORD   NY   11763-2649

791

  Affiliated   3267   Blue Ash Dialysis   Blue Ash Dialysis   10600 MCKINLEY RD     CINCINNATI   OH   45242-3716

792

  Affiliated   3269   Mt. Auburn Dialysis   Mt. Auburn Dialysis   2109 READING RD     CINCINNATI   OH   45202-1417

793

  Affiliated   3272   Charlottesville Dialysis   Charlottesville Dialysis   1460 PANTOPS MOUNTAIN PLACE     CHARLOTTESVILLE   VA   22911

794

  Affiliated   3273   Alexandria Dialysis   Alexandria Dialysis   5150 DUKE ST     ALEXANDRIA   VA   22304-2906

795

  Affiliated   3275   Sebastian Dialysis   Sebastian Dialysis   1424 US HWY 1   STE C   SEBASTIAN   FL   32958-1619

796

  Affiliated   3276   Crestview Hills Dialysis   Crestview Hills Dialysis   400 CENTERVIEW BLVD     CRESTVIEW HILLS   KY   41017-3478

797

  Affiliated   3278   Washington Square Dialysis   Washington Square Dialysis   1112 WASHINGTON SQ     WASHINGTON   MO   63090-5336

798

  Affiliated   3279   Florissant Dialysis   Florissant Dialysis   11687 W FLORISSANT AVE     FLORISSANT   MO   63033-6711

799

  Affiliated   3282   Ithaca Dialysis Center   Ithaca Dialysis Center   201 DATES DR   STE 26   ITHACA   NY   14850-1345

800

  Affiliated   3289   Fairfield Dialysis   Fairfield Dialysis   1210 HICKS BLVD     FAIRFIELD   OH   45014-1921

801

  Affiliated   3290   Fairfield Home Training Dialysis   Fairfield Home Training Dialysis   1210 HICKS BLVD     FAIRFIELD   OH   45014-1921

802

  Affiliated   3291   South Hill Dialysis   South Hill Dialysis   525 ALEXANDRIA PIKE   STE 12   SOUTHGATE   KY   41071-3243

803

  Affiliated   3292   Silver Spring Dialysis   Silver Spring Dialysis   8412 GEORGIA AVE     SILVER SPRING   MD   20910-4406

804

  Affiliated   3295   Philadelphia PMC Dialysis   Philadelphia PMC Dialysis   51 N 39TH ST     PHILADELPHIA   PA   19104-2640

805

  Affiliated   3298   Tulare Dialysis   Tulare Dialysis   545 E TULARE AVE     TULARE   CA   93274-4220

 

Page 104 of 136


806

  Affiliated   3300   Visalia Dialysis   Visalia Dialysis   5429 W CYPRESS AVE     VISALIA   CA   93277-8341

807

  Affiliated   3310   Falls Road Dialysis   Falls Road Dialysis   10753 FALLS RD   STE 115   LUTHERVILLE   MD   21093-4572

808

  Affiliated   3312   Malden Dialysis   Wellington Circle Dialysis Center (fka Malden)   10 CABOT RD   STE 13B   MEDFORD   MA   02155-5173

809

  Affiliated   3313   Salem Northeast Dialysis   Salem Northeast Dialysis (MA)   10 COLONIAL RD   STE 25   SALEM   MA   01970-2947

810

  Affiliated   3314   Lexington   Lexington Prison Unit (OK)   15151 STATE HWY 39 E   PO BOX 26   LEXINGTON   OK   73051-0260

811

  Affiliated   3315   Macon County Dialysis   Macon County Dialysis   1090 W MCKINLEY AVE     DECATUR   IL   62526-3208

812

  Affiliated   3316   Effingham Dialysis   Effingham Dialysis   904 MEDICAL PARK DR   STE 1   EFFINGHAM   IL   62401-2193

813

  Affiliated   3317   Jacksonville Dialysis   Jacksonville Dialysis   1515 W WALNUT ST     JACKSONVILLE   IL   62650-1150

814

  Affiliated   3318   Litchfield Dialysis   Litchfield Dialysis   915 ST FRANCES WAY     LITCHFIELD   IL   62056-1775

815

  Affiliated   3319   Mattoon Dialysis   Mattoon Dialysis   6051 DEVELOPMENT DR     CHARLESTON   IL   61920-9467

816

  Affiliated   3320   Springfield Central Dialysis   Springfield Central Dialysis   932 N RUTLEDGE ST     SPRINGFIELD   IL   62702-3721

817

  Affiliated   3321   Taylorville Dialysis   Taylorville Dialysis   901 W SPRESSER ST     TAYLORVILLE   IL   62568-1831

818

  Affiliated   3322   Lincoln Dialysis   Lincoln Dialysis   2100 WEST FIFTH     LINCOLN   IL   62656-9115

819

  Affiliated   3323   J. B. Zachary Dialysis Center   J. B. Zachary Dialysis Center   333 CASSELL DR   STE 23   BALTIMORE   MD   21224-6815

820

  Affiliated   3324   Whitesquare Dialysis   Whitesquare Dialysis   1 NASHUA CT STE E     BALTIMORE   MD   21221

821

  Affiliated   3325   25th Street Dialysis   25th Street Dialysis   920 E 25TH ST     BALTIMORE   MD   21218-5503

822

  Affiliated   3326   Perth Amboy Dialysis   Perth Amboy Dialysis   530 NEW BRUNSWICK AVE     PERTH AMBOY   NJ   08861-3654

823

  Affiliated   3327   Old Bridge Dialysis   Old Bridge Dialysis   3 HOSPITAL PLZ   STE 11   OLD BRIDGE   NJ   08857-3084

824

  Affiliated   3328   Pear Tree Dialysis   Pear Tree Dialysis (fka Ukiah)   126 N ORCHARD AVE     UKIAH   CA   95482-4502

825

  Affiliated   3334   Hubbard Road Dialysis   Hubbard Road Dialysis   1963 HUBBARD RD     MADISON   OH   44057-2105

826

  Affiliated   3335   St. Charles Dialysis   St. Charles Dialysis   2125 BLUESTONE DR     SAINT CHARLES   MO   63303-6704

827

  Affiliated   3336   Bel Air Dialysis   Bel Air Dialysis   2225 OLD EMMORTON RD   STE 15   BEL AIR   MD   21015-6122

828

  Affiliated   3339   Cedarburg Dialysis   Cedarburg Dialysis   N 54 W 6135 MILL ST     CEDARBURG   WI   53012-2021

829

  Affiliated   3340   Western Hills Dialysis   Western Hills Dialysis   3267 WESTBOURNE DR     CINCINNATI   OH   45248-5130

830

  Affiliated   3341   Winton Road Dialysis   Winton Road Dialysis   6550 WINTON RD     CINCINNATI   OH   45224-1327

831

  Affiliated   3342   Stamford Dialysis   Stamford Dialysis   30 COMMERCE RD     STAMFORD   CT   06902-4550

832

  Affiliated   3343   Boaz Dialysis   Boaz Dialysis   16 CENTRAL HENDERSON RD     BOAZ   AL   35957-5922

833

  Affiliated   3344   Guernsey County Dialysis   Guernsey County Dialysis   1300 CLARK ST     CAMBRIDGE   OH   43725-8875

834

  Affiliated   3345   Marietta Dialysis   Marietta Dialysis   1019 PIKE ST     MARIETTA   OH   45750-3500

835

  Affiliated   3346   Zanesville Dialysis   Zanesville Dialysis   3120 NEWARK RD     ZANESVILLE   OH   43701-9659

836

  Affiliated   3351   Orlando East Dialysis   Orlando East Dialysis   1160 S SEMORAN BLVD   STE C   ORLANDO   FL   32807-1461

837

  Affiliated   3352   Norwich Dialysis   Norwich Dialysis   113 SALEM TPKE     NORWICH   CT   06360-6484

838

  Affiliated   3354   Columbus Dialysis   Columbus Dialysis   3830 OLENTANGY RIVER RD     COLUMBUS   OH   43214-5404

839

  Affiliated   3362   Pasadena Dialysis   Pasadena Dialysis   8894 FORT SMALLWOOD RD   STE 12   PASADENA   MD   21122-7608

840

  Affiliated   3369   Baltimore Geriatric & Rehab Dialysis Center   Baltimore Geriatric & Rehab Dialysis Center   4940 EASTERN AVE   FLOOR 5   BALTIMORE   MD   21224-2735

841

  Affiliated   3373   Frederick Dialysis   Frederick Dialysis   140 THOMAS JOHNSON DR   STE 1   FREDERICK   MD   21702-4475

842

  Affiliated   3376   Fayetteville Dialysis   Fayetteville Dialysis   1279 HIGHWAY 54 W   STE 11   FAYETTEVILLE   GA   30214-4551

843

  Affiliated   3377   Birmingham Central Dialysis   Birmingham Central Dialysis   728 RICHARD ARRINGTON JR BLVD S     BIRMINGHAM   AL   35233-2106

844

  Affiliated   3379   Birmingham North Dialysis   Birmingham North Dialysis   1917 32ND AVE N     BIRMINGHAM   AL   35207-3333

845

  Affiliated   3380   Bessemer Dialysis   Bessemer Dialysis   901 W LAKE MALL     BESSEMER   AL   35020

846

  Affiliated   3382   Ensley Dialysis   Ensley Dialysis   2630 AVENUE E     BIRMINGHAM   AL   35218-2163

847

  Affiliated   3383   Sylacauga Dialysis   Sylacauga Dialysis   331 JAMES PAYTON BLVD     SYLACAUGA   AL   35150

848

  Affiliated   3385   Branford Dialysis   Branford Dialysis   249 W MAIN ST     BRANFORD   CT   06405-4048

849

  Affiliated   3386   Shrewsbury Dialysis   Shrewsbury Dialysis   7435 WATSON RD   STE 119   SAINT LOUIS   MO   63119-4472

850

  Affiliated   3389   Milford Dialysis   Milford Dialysis   470 BRIDGEPORT AVE     MILFORD   CT   06460-4167

851

  Affiliated   3414   Cedartown Dialysis   Cedartown Dialysis   325 WEST AVE     CEDARTOWN   GA   30125-3439

852

  Affiliated   3416   Brookfield Dialysis   Brookfield Dialysis   19395 W CAPITOL DR   BLDG C   BROOKFIELD   WI   53045-2736

853

  Affiliated   3417   Henrico County Dialysis   Henrico County Dialysis   5270 CHAMBERLAYNE RD     RICHMOND   VA   23227-2950

854

  Affiliated   3418   St. Louis West Dialysis   St. Louis West Dialysis   400 N LINDBERGH BLVD     SAINT LOUIS   MO   63141-7814

855

  Affiliated   3420   Springfield Montvale Dialysis   Springfield Montvale Dialysis   2930 MONTVALE DR   STE A   SPRINGFIELD   IL   62704-5376

856

  Affiliated   3422   South Norwalk Dialysis   South Norwalk Dialysis   31 STEVENS ST     NORWALK   CT   06850-3805

857

  Affiliated   3425   Decatur East Wood Dialysis   Decatur East Wood Dialysis   794 E WOOD ST     DECATUR   IL   62523-1155

858

  Affiliated   3426   Schaeffer Drive Dialysis   Schaeffer Drive Dialysis   18100 SCHAEFER HWY     DETROIT   MI   48235-2600

859

  Affiliated   3427   Redford Dialysis   Redford Dialysis   22711 GRAND RIVER AVE     DETROIT   MI   48219-3113

 

Page 105 of 136


860

  Affiliated   3428   Kresge Dialysis   Kresge Dialysis   4145 CASS AVE     DETROIT   MI   48201-1707

861

  Affiliated   3429   Motor City Dialysis   Motor City Dialysis   4727 SAINT ANTOINE ST   STE 11   DETROIT   MI   48201-1461

862

  Affiliated   3431   Whitebridge Dialysis   Whitebridge Dialysis   103 WHITE BRIDGE PIKE   STE 6   NASHVILLE   TN   37209-4539

863

  Affiliated   3432   Columbia Dialysis   Columbia Dialysis (TN)   1705 GROVE ST     COLUMBIA   TN   38401-3517

864

  Affiliated   3433   Murfreesboro Dialysis   Murfreesboro Dialysis   1346 DOW ST     MURFREESBORO   TN   37130-2470

865

  Affiliated   3434   Lawrenceburg Dialysis   Lawrenceburg Dialysis (TN)   2022 N LOCUST AVE     LAWRENCEBURG   TN   38464-2336

866

  Affiliated   3436   Sumner Dialysis   Sumner Dialysis   300 STEAM PLANT RD   STE 27   GALLATIN   TN   37066-3019

867

  Affiliated   3437   Cumberland Dialysis   Cumberland Dialysis   312 HOSPITAL DR   STE 5   MADISON   TN   37115-5037

868

  Affiliated   3438   Williamson County Dialysis   Williamson County Dialysis   3983 CAROTHERS PKWY   STE E-4   FRANKLIN   TN   37067-5936

869

  Affiliated   3441   Cumming Dialysis   Cumming Dialysis   911 MARKET PLACE BLVD   STE 3   CUMMING   GA   30041-7938

870

  Affiliated   3443   Silverton Dialysis   Silverton Dialysis   6929 SILVERTON AVE     CINCINNATI   OH   45236-3701

871

  Affiliated   3445   Atlanta South Dialysis   Atlanta South Dialysis   3158 EAST MAIN ST   STE A   EAST POINT   GA   30344-4800

872

  Affiliated   3447   St. Petersburg Dialysis   St. Petersburg Dialysis   1117 ARLINGTON AVE N     ST PETERSBURG   FL   33705-1521

873

  Affiliated   3449   Alton Dialysis   Alton Dialysis   3511 COLLEGE AVE     ALTON   IL   62002-5009

874

  Affiliated   3451   Edison Dialysis   Edison Dialysis   29 MERIDIAN RD     EDISON   NJ   08820-2823

875

  Affiliated   3452   Dundalk Dialysis   Dundalk Dialysis   14 COMMERCE ST     DUNDALK   MD   21222-4307

876

  Affiliated   3454   Columbus East Dialysis   Columbus East Dialysis   299 OUTERBELT ST     COLUMBUS   OH   43213-1529

877

  Affiliated   3455   Dallas East Dialysis   Dallas East Dialysis   3312 N BUCKNER BLVD   STE 213   DALLAS   TX   75228-5642

878

  Affiliated   3456   San Ysidro Dialysis   San Ysidro Dialysis   1445 30TH ST   STE A   SAN DIEGO   CA   92154-3496

879

  Affiliated   3457   Olathe Dialysis   Olathe Dialysis   732 W FRONTIER LN     OLATHE   KS   66061-7202

880

  Affiliated   3459   Orange City Dialysis   Orange City Dialysis   242 TREEMONT DR   BLDG II   ORANGE CITY   FL   32763-7945

881

  Affiliated   3460   Miami East Dialysis   Miami East Dialysis   1250 NW 7TH ST   STE 16   MIAMI   FL   33125-3744

882

  Affiliated   3462   Temple Terrace Dialysis   Temple Terrace Dialysis   11306 N 53RD ST     TEMPLE TERRACE   FL   33617-2214

883

  Affiliated   3463   Midlothian Dialysis   Midlothian Dialysis   14281 MIDLOTHIAN TPKE   BLDG B   MIDLOTHIAN   VA   23113-6560

884

  Affiliated   3464   Christian County Dialysis   Christian County Dialysis   200 BURLEY AVE     HOPKINSVILLE   KY   42240-8725

885

  Affiliated   3465   St. Louis West PD Dialysis   St. Louis West PD Dialysis   450 N LINDBERGH BLVD   STE 1C   CREVE COEUR   MO   63141-7858

886

  Affiliated   3467   Atlanta Midtown Dialysis   Atlanta Midtown Dialysis PD   418 DECATUR ST SE   STE A   ATLANTA   GA   30312-1801

887

  Affiliated   3468   Silverton Home Training Dialysis   Silverton Home Training Dialysis   6929 SILVERTON AVE     CINCINNATI   OH   45236-3701

888

  Affiliated   3472   Philadelphia 42nd Street Dialysis   Philadelphia 42nd Street Dialysis   4126 WALNUT ST     PHILADELPHIA   PA   19104-3511

889

  Affiliated   3473   Radnor Dialysis   Radnor Dialysis   250 KING OF PRUSSIA RD     RADNOR   PA   19087-5220

890

  Affiliated   3475   St. Louis Dialysis   St. Louis Dialysis   324 DE BALIVIERE AVE     SAINT LOUIS   MO   63112-1804

891

  Affiliated   3477   Elkins Park Dialysis   Wyncote Dialysis (fka Elkins Park)   1000 EASTON RD   STE 25   WYNCOTE   PA   19095-2934

892

  Affiliated   3478   Mainland Dialysis   Mainland Dialysis   2600 GULF FWY     LA MARQUE   TX   77568-4922

893

  Affiliated   3479   Island Dialysis   Island Dialysis   5920 BROADWAY ST     GALVESTON   TX   77551-4305

894

  Affiliated   3481   Orlando Home Training Dialysis   Orlando Home Training Dialysis   116 STURTEVANT ST   STE 2   ORLANDO   FL   32806-2021

895

  Affiliated   3482   Mechanicsville Dialysis   Mechanicsville Dialysis   8191 ATLEE RD     MECHANICSVILLE   VA   23116-1807

896

  Affiliated   3484   San Diego East Dialysis   San Diego East Dialysis   292 EUCLID AVE   STE 1   SAN DIEGO   CA   92114-3629

897

  Affiliated   3485   Russellville Dialysis   Russellville Dialysis   14897 HIGHWAY 43     RUSSELLVILLE   AL   35653-1954

898

  Affiliated   3486   Encinitas Dialysis   Encinitas Dialysis   332 SANTA FE DR   STE 1   ENCINITAS   CA   92024-5143

899

  Affiliated   3491   Rushville Dialysis   Rushville Dialysis   112 SULLIVAN DRIVE     RUSHVILLE   IL   62681-1293

900

  Affiliated   3493   Plainfield Dialysis   Plainfield Dialysis   1200 RANDOLPH RD   MUHLENBURG CAMPUS   PLAINFIELD   NJ   07060-3361

901

  Affiliated   3494   Parkersburg Dialysis   Parkersburg Dialysis   1824 MURDOCH AVE   STE 44   PARKERSBURG   WV   26101-3230

902

  Affiliated   3497   Tucson South Central Dialysis   Tucson South Central Dialysis   2024 E IRVINGTON RD   STE 7   TUCSON   AZ   85714-1825

903

  Affiliated   3499   Hazelwood Dialysis   Hazelwood Dialysis   637 DUNN RD     HAZELWOOD   MO   63042-1755

904

  Affiliated   3503   Durham West Dialysis   Durham West Dialysis   4307 WESTERN PARK PL     DURHAM   NC   27705-1204

905

  Affiliated   3504   Liberty Dialysis   Liberty Dialysis   2525 GLEN HENDREN DR     LIBERTY   MO   64068-9625

906

  Affiliated   3506   Chino Dialysis   Chino Dialysis   4445 RIVERSIDE DR     CHINO   CA   91710-3961

907

  Affiliated   3507   Greenview Dialysis   Greenview Dialysis   18544 W 8 MILE RD     SOUTHFIELD   MI   48075-4194

908

  Affiliated   3508   Perry Dialysis   Perry Dialysis   118 W MAIN ST     PERRY   FL   32347-2656

909

  Affiliated   3511   Ashtabula Dialysis   Ashtabula Dialysis   1614 W 19TH ST     ASHTABULA   OH   44004-3036

910

  Affiliated   3513   Northland Dialysis   Northland Dialysis   2750 CLAY EDWARDS DR   STE 1   N KANSAS CITY   MO   64116-3257

911

  Affiliated   3516   Lake St. Louis Dialysis   Lake St. Louis Dialysis   200 BREVCO PLZ   STE 21   LAKE SAINT LOUIS   MO   63367-2950

912

  Affiliated   3517   Wyandotte West Dialysis   Wyandotte West Dialysis   8919 PARALLEL PKWY   STE 121   KANSAS CITY   KS   66112-1655

913

  Affiliated   3518   Huntingdon Valley Dialysis   Temp CLSD-Huntingdon Valley Dialysis   769 HUNTINGDON PIKE   STE 18   HUNTINGDON VALLEY   PA   19006-8362

 

Page 106 of 136


914

  Affiliated   3519   Glendale Dialysis   Glendale Dialysis   1000 E PALMER AVE     GLENDALE   CA   91205-3532

915

  Affiliated   3520   Toledo Dialysis   Toledo Dialysis   1614 S BYRNE RD     TOLEDO   OH   43614-3464

916

  Affiliated   3523   Cameron Dialysis   Cameron Dialysis   1003 W 4TH ST     CAMERON   MO   64429-1466

917

  Affiliated   3524   Omaha Central Dialysis   Omaha Central Dialysis   144 S 40TH ST     OMAHA   NE   68131-3004

918

  Affiliated   3525   Chillicothe Dialysis   Chillicothe Dialysis   588 E BUSINESS 36     CHILLICOTHE   MO   64601-3721

919

  Affiliated   4210   Council Bluffs Dialysis   Council Bluffs Dialysis Center   300 W BROADWAY   STE 15   COUNCIL BLUFFS   IA   51503-9077

920

  Affiliated   3528   DeRidder Dialysis   DeRidder Dialysis   239 E 1ST ST     DERIDDER   LA   70634-4105

921

  Affiliated   3530   Dodge County Dialysis   Dodge County Dialysis   1949 E 23RD AVE S     FREMONT   NE   68025-2452

922

  Affiliated   3533   Omaha North Dialysis   Omaha North Dialysis   6572 AMES AVE     OMAHA   NE   68104-1931

923

  Affiliated   3534   Omaha South Dialysis   Omaha South Dialysis   3427 L ST   STE 16   OMAHA   NE   68107-2577

924

  Affiliated   3535   Lake Charles Southwest Dialysis   Lake Charles Southwest Dialysis   300 W 18th ST     LAKE CHARLES   LA   70601-7342

925

  Affiliated   3536   St. Joseph Dialysis   St. Joseph Dialysis   5514 CORPORATE DR   STE 1   SAINT JOSEPH   MO   64507-7752

926

  Affiliated   3537   Sulphur Dialysis   Sulphur Dialysis   944 BEGLIS PKWY     SULPHUR   LA   70663-5102

927

  Affiliated   3539   Tipton County Dialysis   Tipton County Dialysis   107 TENNESSEE AVE     COVINGTON   TN   38019-3902

928

  Affiliated   3540   Dyersburg Dialysis   Dyersburg Dialysis   1575 PARR AVE     DYERSBURG   TN   38024-3151

929

  Affiliated   3544   Effingham North Dialysis   Effingham North Dialysis   301 N PINE ST     SPRINGFIELD   GA   31329-3076

930

  Affiliated   3545   Westminster South Dialysis   Westminster South Dialysis   14014 MAGNOLIA ST.     WESTMINSTER   CA   92683-4736

931

  Affiliated   3546   Williams Street Dialysis   Williams Street Dialysis   2812 WILLIAMS ST     SAVANNAH   GA   31404-4134

932

  Affiliated   3547   DeRenne Dialysis   DeRenne Dialysis   5303 MONTGOMERY ST     SAVANNAH   GA   31405-5138

933

  Affiliated   3548   Abercorn Dialysis   Abercorn Dialysis   11706 MERCY BLVD   STE 9   SAVANNAH   GA   31419-1751

934

  Affiliated   3551   Fort Myers North Dialysis   Fort Myers North Dialysis   16101 N CLEVELAND AVE     N FT MYERS   FL   33903-2148

935

  Affiliated   3552   Butler County Dialysis   Butler County Dialysis   3497 S DIXIE HWY     FRANKLIN   OH   45005-5717

936

  Affiliated   3556   Willingboro   Willingboro Dialysis   230 VAN SCIVER PKWY     WILLINGBORO   NJ   08046-1131

937

  Affiliated   3557   McKeesport West Dialysis   McKeesport West Dialysis   101 9TH ST     MCKEESPORT   PA   15132-3953

938

  Affiliated   3559   College Dialysis   College Dialysis   6535 UNIVERSITY AVE     SAN DIEGO   CA   92115-5810

939

  Affiliated   3560   Montezuma Dialysis   Montezuma Dialysis   114 DEVAUGHN AVE     MONTEZUMA   GA   31063-1708

940

  Affiliated   3561   Romulus Dialysis   Romulus Dialysis   31470 ECORSE RD     ROMULUS   MI   48174-1963

941

  Affiliated   3564   Wrightsville Dialysis   Wrightsville Dialysis   2240 W ELM ST     WRIGHTSVILLE   GA   31096-2016

942

  Affiliated   3565   Tower Dialysis   Tower Dialysis   8635 W 3RD ST   STE 56W   LOS ANGELES   CA   90048-6110

943

  Affiliated   3566   Columbus Downtown Dialysis   Columbus Downtown Dialysis   415 E MOUND ST     COLUMBUS   OH   43215-5512

944

  Affiliated   3568   Charlotte East Dialysis   Charlotte East Dialysis   3204 N SHARON AMITY RD     CHARLOTTE   NC   28205-6541

945

  Affiliated   3569   Carmel Mountain Dialysis   Carmel Mountain Dialysis   9850 CARMEL MOUNTAIN RD     SAN DIEGO   CA   92129-2892

946

  Affiliated   3571   Lenexa Dialysis   Lenexa Dialysis   8630 HALSEY ST     LENEXA   KS   66215-2880

947

  Affiliated   3577   Nashua Dialysis   Nashua Dialysis   38 TYLER ST   STE 1   NASHUA   NH   03060-2912

948

  Affiliated   3580   Illini Renal Dialysis   Illini Renal Dialysis   507 E UNIVERSITY AVE     CHAMPAIGN   IL   61820-3828

949

  Affiliated   3586   Loring Heights Dialysis   Loring Heights Dialysis   1575 NORTHSIDE DR NW   STE 45   ATLANTA   GA   30318-4211

950

  Affiliated   3588   Forest Hills Dialysis   Forest Hills Dialysis   2693 FOREST HILLS RD SW     WILSON   NC   27893-8611

951

  Affiliated   3589   St. Peters Dialysis   St. Peters Dialysis   300 FIRST EXECUTIVE AVE   STE A   SAINT PETERS   MO   63376-1655

952

  Affiliated   3591   Platte Woods Dialysis   Platte Woods Dialysis   7667 NW PRAIRIE VIEW RD     KANSAS CITY   MO   64151-1544

953

  Affiliated   3593   Fresno North Dialysis   Fresno Palm Bluffs Dialysis (fka Fresno North)   770 W PINEDALE AVE     FRESNO   CA   93711-5744

954

  Affiliated   3594   Middlesex County Dialysis   Burlington Regional Dialysis (fka Middlesex County)   31 MALL RD   STE 1B   BURLINGTON   MA   01803-4138

955

  Affiliated   3596   Clearfield Dialysis   Clearfield Dialysis   1033 TURNPIKE AVE   STE 1   CLEARFIELD   PA   16830-3061

956

  Affiliated   3597   Papillion Dialysis   Papillion Dialysis   1502 S WASHINGTON ST   STE 1   PAPILLION   NE   68046-3136

957

  Affiliated   3598   Birmingham Home Training Dialysis   Birmingham Home Training Dialysis   2101 7TH AVE S     BIRMINGHAM   AL   35233-3105

958

  Affiliated   3603   Bayou Dialysis   Magnolia Dialysis   210 E SPILLMAN ST     GONZALES   LA   70737-4604

959

  Affiliated   3609   Radford Dialysis   Radford Dialysis   600 E MAIN ST   STE F   RADFORD   VA   24141-1826

960

  Affiliated   3610   Eufaula Dialysis   Eufaula Dialysis   220 S ORANGE AVE     EUFAULA   AL   36027-1612

961

  Affiliated   3612   Coshocton Dialysis   Coshocton Dialysis   1404 CHESTNUT ST EAST     COSHOCTON   OH   43812-1401

962

  Affiliated   3614   Costa Mesa Dialysis   Costa Mesa Dialysis   1590 SCENIC AVE     COSTA MESA   CA   92626-1400

963

  Affiliated   3615   Little Rock Dialysis   Central Little Rock Dialysis   5800 W 10TH ST   STE 51   LITTLE ROCK   AR   72204-1760

964

  Affiliated   3619   Northport Dialysis   Northport Dialysis   2401 HOSPITAL DR     NORTHPORT   AL   35476-3392

965

  Affiliated   3632   Pageland Dialysis   Pageland Dialysis   505A S PEARL ST     PAGELAND   SC   29728-2222

966

  Affiliated   3633   Bakersfield South Dialysis   White Lane Dialysis (fka Bakersfield South)   7701 WHITE LN   STE D   BAKERSFIELD   CA   93309-0201

967

  Affiliated   3634   Newaygo County Dialysis   Newaygo County Dialysis   1317 W MAIN ST     FREMONT   MI   49412-1478

 

Page 107 of 136


968

  Affiliated   3636   Cedar Lane Dialysis   Cedar Lane Dialysis   6334 CEDAR LN   STE 11   COLUMBIA   MD   21044-3898

969

  Affiliated   3639   Torrington Dialysis   Torrington Dialysis   780 LITCHFIELD ST   STE 1   TORRINGTON   CT   06790-6268

970

  Affiliated   3642   Janesville Dialysis   Janesville Dialysis   1305 WOODMAN RD     JANESVILLE   WI   53545-1068

971

  Affiliated   3643   Bloomfield Dialysis   Bloomfield Dialysis   29 GRIFFIN RD S     BLOOMFIELD   CT   06002-1351

972

  Affiliated   3645   Anthem Village Dialysis   Anthem Village Dialysis   2530 ANTHEM VILLAGE DR     HENDERSON   NV   89052-5548

973

  Affiliated   3646   Glen Burnie Dialysis   Glen Burnie Dialysis   120 LANGLEY RD N     GLEN BURNIE   MD   21060-6578

974

  Affiliated   3655   Melbourne Dialysis   Melbourne Dialysis   2235 S BABCOCK ST     MELBOURNE   FL   32901-5305

975

  Affiliated   3656   St. Petersburg South Dialysis   St. Petersburg South Dialysis   2850 34TH ST S     ST PETERSBURG   FL   33711-3817

976

  Affiliated   3663   Belpre Dialysis   Belpre Dialysis   2906 WASHINGTON BLVD     BELPRE   OH   45714-1848

977

  Affiliated   3666   Stockton Home Training Dialysis   Stockton Home Training Dialysis   545 E CLEVELAND ST   STE A   STOCKTON   CA   95204-5535

978

  Affiliated   3670   Rock Prairie Road Dialysis   Rock Prairie Road Dialysis   1605 ROCK PRAIRIE RD   STE 11   COLLEGE STATION   TX   77845-8358

979

  Affiliated   3675   Market Street   Market Street Dialysis   3701 MARKET ST   STE 1   PHILADELPHIA   PA   19104-5503

980

  Affiliated   3677   Northwood   Northwood Dialysis (aka Toledo East)   611 LEMOYNE RD     NORTHWOOD   OH   43619-1811

981

  Affiliated   3701   Tyson's Corner Dialysis   Tyson's Corner Dialysis   8391 OLD COURTHOUSE RD   STE 16   VIENNA   VA   22182-3819

982

  Affiliated   3704   Southern Maryland Dialysis   Southern Maryland Dialysis   9211 STUART LN   4TH FL   CLINTON   MD   20735-2712

983

  Affiliated   3707   Brentwood Dialysis   Brentwood Dialysis   1231 BRENTWOOD RD NE     WASHINGTON   DC   20018-1019

984

  Affiliated   3708   Amelia Dialysis   Amelia Dialysis   15151 PATRICK HENRY HWY     AMELIA COURT HOUSE   VA   23002-4700

985

  Affiliated   3714   Eighth Street Dialysis   Eighth Street Dialysis   300 8TH ST NE     WASHINGTON   DC   20002-6108

986

  Affiliated   3715   Chester Dialysis   Chester Dialysis   10360 IRONBRIDGE RD     CHESTER   VA   23831-1425

987

  Affiliated   3716   Howard County Dialysis   Howard County Dialysis   5999 HARPERS FARM RD   STE 11E   COLUMBIA   MD   21044-3023

988

  Affiliated   3717   Catonsville Dialysis   Catonsville Dialysis   1581 SULPHUR SPRING RD   STE 112   BALTIMORE   MD   21227

989

  Affiliated   3718   Mercy Dialysis   Mercy Dialysis   315 N CALVERT ST   STE 3   BALTIMORE   MD   21202-3611

990

  Affiliated   3719   Harbor Park Dialysis   Harbor Park Dialysis   111 CHERRY HILL RD     BALTIMORE   MD   21225-1392

991

  Affiliated   3732   Dabney Dialysis   Three Chopt Dialysis (fka Dabney)   8813 THREE CHOPT RD     RICHMOND   VA   23229

992

  Affiliated   3733   Hioaks Dialysis   Hioaks Dialysis   671 HIOAKS RD   STE A   RICHMOND   VA   23225-4072

993

  Affiliated   3757   Arlington Dialysis   Arlington Dialysis   4805 1st ST N     ARLINGTON   VA   22203

994

  Affiliated   3759   Landover Dialysis   Landover Dialysis   1200 MERCANTILE LN   STE 15   UPPER MARLBORO   MD   20774-5389

995

  Affiliated   3761   Staunton Dialysis   Staunton Dialysis   29 IDLEWOOD BLVD     STAUNTON   VA   24401-9355

996

  Affiliated   3762   Covington Dialysis   Covington Dialysis   2504 VALLEY RIDGE RD     COVINGTON   VA   24426-6339

997

  Affiliated   3763   Culpeper Dialysis   Culpeper Dialysis   430 SOUTHRIDGE PARKWAY     CULPEPER   VA   22701-3791

998

  Affiliated   3764   Greenbrier Dialysis   Greenbrier Dialysis   129 SENECA TRL     LEWISBURG   WV   24901-1564

999

  Affiliated   3765   Harrisonburg Dialysis   Harrisonburg Dialysis   871 CANTRELL AVE   STE 1   HARRISONBURG   VA   22801-4323

1000

  Affiliated   3766   Lexington Dialysis   Lexington Dialysis   756 N LEE HWY     LEXINGTON   VA   24450-3724

1001

  Affiliated   3802   Manteca Dialysis   Manteca Dialysis   1156 S MAIN ST     MANTECA   CA   95337-9505

1002

  Affiliated   3804   Roseburg/Mercy Dialysis   Roseburg/Mercy Dialysis   2599 NW EDENBOWER BLVD     ROSEBURG   OR   97471-6220

1003

  Affiliated   3805   Daly City Dialysis   Daly City Dialysis   1498 SOUTHGATE AVE   STE 11   DALY CITY   CA   94015-4015

1004

  Affiliated   3806   Vallejo Dialysis   Vallejo Dialysis   121 HOSPITAL DR     VALLEJO   CA   94589-2562

1005

  Affiliated   3812   Salem Dialysis   Salem Dialysis (OR)   3550 LIBERTY RD S   STE 1   SALEM   OR   97302-5700

1006

  Affiliated   3817   Fresno Dialysis   Fresno Dialysis   1111 E WARNER AVE     FRESNO   CA   93710-4030

1007

  Affiliated   3818   Oakland Dialysis   Oakland Dialysis   5354 CLAREMONT AVE     OAKLAND   CA   94618-1035

1008

  Affiliated   3820   Bakersfield Dialysis   Bakersfield Brimhall Dialysis (fka California Ave.)   8501 BRIMHALL RD   BLDG 5   BAKERSFIELD   CA   93311-2252

1009

  Affiliated   3821   Northeast Bakersfield Dialysis   Northeast Dialysis (fka NE Bakersfield)   3761 MALL VIEW RD     BAKERSFIELD   CA   93306-3048

1010

  Affiliated   3830   San Francisco Dialysis   San Francisco Dialysis   1499 WEBSTER ST     SAN FRANCISCO   CA   94115-3705

1011

  Affiliated   3831   Hanford Dialysis   Hanford Dialysis   402 W 8TH ST     HANFORD   CA   93230-4536

1012

  Affiliated   3840   San Pablo Dialysis   San Pablo Dialysis   14020 SAN PABLO AVE     SAN PABLO   CA   94806-3604

1013

  Affiliated   3847   Chinatown Dialysis   Chinatown Dialysis   636 CLAY ST     SAN FRANCISCO   CA   94111-2502

1014

  Affiliated   3849   El Cerrito Dialysis   El Cerrito Dialysis   10690 SAN PABLO AVE     EL CERRITO   CA   94530-2620

1015

  Affiliated   3857   Tracy Dialysis   Tracy Dialysis   425 W BEVERLY PL   STE A   TRACY   CA   95376-3086

1016

  Affiliated   3858   Salem North Dialysis   Salem North Dialysis (OR)   1220 LIBERTY ST NE     SALEM   OR   97301-7330

1017

  Affiliated   3860   Auburn Dialysis   Auburn Dialysis   3126 PROFESSIONAL DR   STE 1   AUBURN   CA   95603-2411

1018

  Affiliated   3861   Grass Valley Dialysis   Grass Valley Dialysis   360 CROWN POINT CIRCLE   STE 21   GRASS VALLEY   CA   95945-2543

1019

  Affiliated   3901   Santee Dialysis   Santee Dialysis   228 BRADFORD BLVD     SANTEE   SC   29142-8677

1020

  Affiliated   3903   Upland Dialysis   Upland Dialysis   600 N 13TH AVE     UPLAND   CA   91786-4957

1021

  Affiliated   3906   Vance County Dialysis   Vance County Dialysis   854 S BECKFORD DR     HENDERSON   NC   27536-3487

 

Page 108 of 136


1022

  Affiliated   3907   Edenton Dialysis   Edenton Dialysis   703 LUKE ST     EDENTON   NC   27932-9694

1023

  Affiliated   3909   Ahoskie Dialysis   Ahoskie Dialysis   129 HERTFORD COUNTY HIGH RD     AHOSKIE   NC   27910-8131

1024

  Affiliated   3914   Allendale County Dialysis   Allendale County Dialysis   202 HAMPTON AVE N     FAIRFAX   SC   29827-4510

1025

  Affiliated   3916   North Orangeburg Dialysis   North Orangeburg Dialysis   124 FIRE TOWER RD     ORANGEBURG   SC   29118-1443

1026

  Affiliated   3917   South Orangeburg Dialysis   South Orangeburg Dialysis   1080 SUMMERS AVE     ORANGEBURG   SC   29115-4920

1027

  Affiliated   3931   Greenwood Dialysis   Greenwood Dialysis   109 OVERLAND DR     GREENWOOD   SC   29646-4053

1028

  Affiliated   3933   Union County Dialysis   Union County Dialysis   701 E ROOSEVELT BLVD   STE 4   MONROE   NC   28112-4107

1029

  Affiliated   3934   South Charlotte Dialysis   South Charlotte Dialysis   6450 BANNINGTON RD     CHARLOTTE   NC   28226-1327

1030

  Affiliated   3935   Lancaster SC Dialysis   Lancaster SC Dialysis   980 N WOODLAND DR   STE 1   LANCASTER   SC   29720-1964

1031

  Affiliated   3952   Central Bamberg Dialysis   Central Bamberg Dialysis   67 SUNSET DR     BAMBERG   SC   29003-1181

1032

  Affiliated   4001   West Tallahassee Dialysis   West Tallahassee Dialysis   2645 W TENNESSEE ST     TALLAHASSEE   FL   32304-2547

1033

  Affiliated   4002   Daytona South Dialysis   Daytona South Dialysis   1801 S NOVA RD   STE 36   SOUTH DAYTONA   FL   32119-1775

1034

  Affiliated   4003   Daytona Beach Dialysis   Daytona Beach Dialysis   578 HEALTH BLVD     DAYTONA BEACH   FL   32114-1492

1035

  Affiliated   4004   West Tampa Dialysis   West Tampa Dialysis   4515 GEORGE RD   STE 3   TAMPA   FL   33634-7300

1036

  Affiliated   4005   Fontana Dialysis   Fontana Dialysis   17590 FOOTHILL BLVD     FONTANA   CA   92335-8416

1037

  Affiliated   4007   Fort Myers Dialysis   Fort Myers Dialysis   4220 EXECUTIVE CIRCLE   STE 38   FORT MYERS   FL   33916-7993

1038

  Affiliated   4009   Lehigh Acres Dialysis   Lehigh Acres Dialysis   2719 4TH ST W     LEHIGH ACRES   FL   33971-1942

1039

  Affiliated   4010   Los Banos Dialysis   Los Banos Dialysis   222 I ST     LOS BANOS   CA   93635-4132

1040

  Affiliated   4013   Kissimmee Dialysis   Kissimmee Dialysis   802 N JOHN YOUNG PKWY     KISSIMMEE   FL   34741-4912

1041

  Affiliated   4014   New Smyrna Beach Dialysis   New Smyrna Beach Dialysis   110 S ORANGE ST     NEW SMYRNA BEACH   FL   32168-7153

1042

  Affiliated   4017   Lake Wales Dialysis   Lake Wales Dialysis   1125 BRYN MAWR AVE     LAKE WALES   FL   33853-4333

1043

  Affiliated   4018   Dearborn Dialysis   Dearborn Dialysis   1185 MONROE ST     DEARBORN   MI   48124-2814

1044

  Affiliated   4020   Greater Miami Dialysis   Greater Miami Dialysis   160 NW 176TH ST   STE 1   MIAMI   FL   33169-5023

1045

  Affiliated   4021   Burbank Dialysis   Burbank Dialysis   1211 N SAN FERNANDO BLVD     BURBANK   CA   91504-4234

1046

  Affiliated   4024   Lakeland Dialysis   Lakeland Dialysis   515 E BELLA VISTA ST     LAKELAND   FL   33805-3005

1047

  Affiliated   4025   Burlington North Dialysis   Burlington North Dialysis   1164 E ROUTE 130     BURLINGTON   NJ   08016-2954

1048

  Affiliated   4026   Delano Dialysis   Delano Dialysis   905 MAIN ST     DELANO   CA   93215-1729

1049

  Affiliated   4027   Erie Dialysis   Erie Dialysis   350 E BAYFRONT PKWY   STE A   ERIE   PA   16507-2410

1050

  Affiliated   4028   Homestead Dialysis   Homestead Dialysis   207 W 7TH AVE     W HOMESTEAD   PA   15120-1002

1051

  Affiliated   4029   Plant City Dialysis   Plant City Dialysis   1211 W REYNOLDS ST     PLANT CITY   FL   33563-4321

1052

  Affiliated   4030   Winter Haven Dialysis   Winter Haven Dialysis   1625 UNITY WAY NW     WINTER HAVEN   FL   33881

1053

  Affiliated   4032   Charlotte Dialysis   Charlotte Dialysis   2321 W MOREHEAD ST   STE 12   CHARLOTTE   NC   28208-5145

1054

  Affiliated   4034   McKeesport Dialysis   McKeesport Dialysis   2001 LINCOLN WAY   OAK PARK MALL   MCKEESPORT   PA   15131-2419

1055

  Affiliated   4035   Broward Dialysis   Broward Dialysis   1500 N FEDERAL HWY   STE 1   FT LAUDERDALE   FL   33304-5600

1056

  Affiliated   4036   Athens Dialysis   Athens Dialysis   15953 ATHENS LIMESTONE DR     ATHENS   AL   35613-2214

1057

  Affiliated   4038   Bradenton Dialysis   Bradenton Dialysis   3501 CORTEZ RD W   STE 14   BRADENTON   FL   34210-3104

1058

  Affiliated   4039   Deland Dialysis   Deland Dialysis   350 E NEW YORK AVE     DELAND   FL   32724-5510

1059

  Affiliated   4040   Boynton/North Delray Dialysis   Boynton/North Delray Dialysis   2655 W ATLANTIC AVE     DELRAY BEACH   FL   33445-4400

1060

  Affiliated   4041   Lake Worth Dialysis   Lake Worth Dialysis   2459 S CONGRESS AVE   STE 1   PALM SPRINGS   FL   33406-7616

1061

  Affiliated   4042   Palm Coast Dialysis   Palm Coast Dialysis   13 KINGSWOOD DR   STE A   PALM COAST   FL   32137-4614

1062

  Affiliated   4043   Fort Myers South Dialysis   Fort Myers South Dialysis   8570 GRANITE CT     FORT MYERS   FL   33908-4102

1063

  Affiliated   4044   Woodburn Dialysis   Woodburn Dialysis   1840 NEWBERG HWY   STE 14   WOODBURN   OR   97071-3187

1064

  Affiliated   4045   Four Freedoms   Four Freedoms Dialysis (fka Range Street)   289 SW RANGE AVE   STE A   MADISON   FL   32340-2351

1065

  Affiliated   4046   West Philadelphia Dialysis   West Philadelphia Dialysis   7609 LINDBERGH BLVD     PHILADELPHIA   PA   19153-2301

1066

  Affiliated   4048   Tucson West Dialysis   Tucson West Dialysis   1780 W ANKLAM RD     TUCSON   AZ   85745-2632

1067

  Affiliated   4049   Tucson East Dialysis   Tucson East Dialysis   6420 E BROADWAY BLVD   STE C3   TUCSON   AZ   85710-3512

1068

  Affiliated   4053   Tallahassee South Dialysis   Tallahassee South Dialysis   2410 S ADAMS ST     TALLAHASSEE   FL   32301-6325

1069

  Affiliated   4054   Selma Dialysis   Selma Dialysis   2711 CINEMA WAY   STE 111   SELMA   CA   93662-2662

1070

  Affiliated   4055   Hinesville Dialysis   Hinesville Dialysis   522 ELMA G MILES PKWY     HINESVILLE   GA   31313-4021

1071

  Affiliated   4056   Los Angeles Downtown Dialysis   Los Angeles Downtown Dialysis   2021 S FLOWER ST     LOS ANGELES   CA   90007-1342

1072

  Affiliated   4057   Anaheim Dialysis   Anaheim Dialysis   1107 W LA PALMA AVE     ANAHEIM   CA   92801-2804

1073

  Affiliated   4058   Martinsville Dialysis   Martinsville Dialysis   33 BRIDGE ST S     MARTINSVILLE   VA   24112-6214

1074

  Affiliated   4060   Jefferson Dialysis   Jefferson Dialysis   14 CLAIRTON BLVD     PITTSBURGH   PA   15236-3911

1075

  Affiliated   4061   Saddleback Dialysis   Saddleback Dialysis   23141 PLAZA POINTE DR     LAGUNA HILLS   CA   92653-1425

 

Page 109 of 136


1076

  Affiliated   4064   Sun City Center Dialysis   Sun City Center Dialysis   783 CORTARO DR     RUSKIN   FL   33573-6812

1077

  Affiliated   4065   Paris Dialysis   Paris Dialysis   32 STEUBENVILLE PK     PARIS   PA   15021

1078

  Affiliated   4066   Central Tampa Dialysis   Central Tampa Dialysis   4204 N MACDILL AVE   SOUTH BLDG   TAMPA   FL   33607-6342

1079

  Affiliated   4068   Zephyrhills Dialysis   Zephyrhills Dialysis   6610 STADIUM DR     ZEPHYRHILLS   FL   33542-7510

1080

  Affiliated   4069   Bartow Dialysis   Bartow Dialysis   1190 E CHURCH ST     BARTOW   FL   33830-4117

1081

  Affiliated   4070   Ormond Beach Dialysis   Ormond Beach Dialysis   495 S NOVA RD   STE 19   ORMOND BEACH   FL   32174-8444

1082

  Affiliated   4071   Lakeland South Dialysis   Lakeland South Dialysis   5050 S FLORIDA AVE     LAKELAND   FL   33813-2501

1083

  Affiliated   4072   St. Mary’s Dialysis   St. Mary’s Dialysis   2714 OSBORNE RD     ST MARY’S   GA   31558-4049

1084

  Affiliated   4073   Miami North Dialysis   Miami North Dialysis   860 NE 125TH ST     NORTH MIAMI   FL   33161-5743

1085

  Affiliated   4074   Naples Dialysis   Naples Dialysis   661 9TH ST N     NAPLES   FL   34102-8132

1086

  Affiliated   4075   Bonita Springs Dialysis   Bonita Springs Dialysis   9134 BONITA BEACH RD SE     BONITA SPRINGS   FL   34135-4281

1087

  Affiliated   4076   Orlando Southwest Dialysis   Orlando Southwest Dialysis   6925 LAKE ELLENOR DR   STE 65   ORLANDO   FL   32809-4670

1088

  Affiliated   4088   Quincy Dialysis   Quincy Dialysis   878 STRONG RD     QUINCY   FL   32351-5243

1089

  Affiliated   4089   Tallahassee Dialysis   Tallahassee Dialysis   1607 PHYSICIANS DR     TALLAHASSEE   FL   32308-4620

1090

  Affiliated   4095   South Beach Dialysis   South Beach Dialysis   4701 N MERIDIAN AVE     MIAMI BEACH   FL   33140-2910

1091

  Affiliated   4124   Americus Dialysis   Americus Dialysis   227 N LEE ST     AMERICUS   GA   31709-3525

1092

  Affiliated   4204   Corry Dialysis   Corry Dialysis   300 YORK ST     CORRY   PA   16407-1420

1093

  Affiliated   4208   Elizabethtown Dialysis   Elizabethtown Dialysis   844 N HANOVER ST     ELIZABETHTOWN   PA   17022-1303

1094

  Affiliated   4209   Lumberton Dialysis   Lumberton Dialysis   668 MAIN ST     LUMBERTON   NJ   08048-5016

1095

  Affiliated   4211   Cobbs Creek Dialysis   Cobbs Creek Dialysis   1700 S 60TH ST     PHILADELPHIA   PA   19142-1404

1096

  Affiliated   4214   Westland Dialysis   Garden West Dialysis (fka Westland)   5715 N VENOY RD     WESTLAND   MI   48185-2830

1097

  Affiliated   4215   Meadville Dialysis   Meadville Dialysis   19050 PARK AVENUE PLZ     MEADVILLE   PA   16335-4012

1098

  Affiliated   4217   Bradford Dialysis   Bradford Dialysis   665 E MAIN ST     BRADFORD   PA   16701-1869

1099

  Affiliated   4219   Southgate Dialysis   Southgate Dialysis   14752 NORTHLINE RD     SOUTHGATE   MI   48195-2467

1100

  Affiliated   4223   Waynesburg Dialysis   Waynesburg Dialysis   248 ELM DR     WAYNESBURG   PA   15370-8269

1101

  Affiliated   4224   Selinsgrove Dialysis   Selinsgrove Dialysis   1030 N SUSQUEHANNA TRAIL     SELINSGROVE   PA   17870-7767

1102

  Affiliated   2153   Arlington Dialysis   Arlington Dialysis   1250 E PIONEER PKWY   STE 7   ARLINGTON   TX   76010-6423

1103

  Affiliated   2154   Grapevine Dialysis   Grapevine Dialysis   1600 W NORTHWEST HWY   STE 1   GRAPEVINE   TX   76051-8131

1104

  Affiliated   1740   Willow Dialysis   Willow Dialysis   1675 ALEX DR     WILMINGTON   OH   45177-2446

1105

  Affiliated   1767   New Braunfels Dialysis   New Braunfels Dialysis   900 LOOP 337     NEW BRAUNFELS   TX   78130-3555

1106

  Affiliated   2080   Chickasha Dialysis   Chickasha Dialysis   228 S 29TH ST     CHICKASHA   OK   73018-2502

1107

  Affiliated   2184   Sugarloaf   Sugarloaf Dialysis (fka Lawrenceville)   1705 BELLE MEADE CT   STE 11   LAWRENCEVILLE   GA   30043-5895

1108

  Affiliated   2166   Buford Dialysis   Buford Dialysis   1550 BUFORD HWY   STE 1E   BUFORD   GA   30518-3666

1109

  Affiliated   1749   St. Louis Park PD   St. Louis Park Dialysis Center PD   3505 LOUISIANA AVE S     ST LOUIS PARK   MN   55426-4121

1110

  Affiliated   1769   Front Royal Dialysis   Front Royal Dialysis   1077D N SHENANDOAH AVE     FRONT ROYAL   VA   22630-3546

1111

  Affiliated   1770   Winchester Dialysis   Winchester Dialysis   2301 VALOR DR     WINCHESTER   VA   22601-6111

1112

  Affiliated   2200   New Hope Dialysis   New Hope Dialysis (aka Minneapolis, Golden Valley)   5640 INTERNATIONAL PKWY     NEW HOPE   MN   55428-3047

1113

  Affiliated   2175   Richfield Dialysis   Richfield Dialysis   6601 LYNDALE AVE S   STE 15   RICHFIELD   MN   55423-2490

1114

  Affiliated   2162   Fairborne Dialysis   Fairborn Dialysis   3070 PRESIDENTIAL DR   STE A   FAIRBORN   OH   45324-6273

1115

  Affiliated   1694   Benton Dialysis   Benton Dialysis   1151 ROUTE 14 W     BENTON   IL   62812-1500

1116

  Affiliated   1695   Centralia Dialysis   Centralia Dialysis   1231 STATE ROUTE 161     CENTRALIA   IL   62801-6739

1117

  Affiliated   1696   Marion Dialysis   Marion Dialysis   324 S 4TH ST     MARION   IL   62959-1241

1118

  Affiliated   1697   Mount Vernon Dialysis   Mount Vernon Dialysis   1800 JEFFERSON AVE     MOUNT VERNON   IL   62864-4300

1119

  Affiliated   2121   Bayou City Dialysis   Bayou City Dialysis (fka Hanson)   10655 EASTEX FWY     HOUSTON   TX   77093-4323

1120

  Affiliated   2117   Metarie Dialysis Center   Metairie Dialysis   7100 AIRLINE DR     METAIRIE   LA   70003-5950

1121

  Affiliated   1784   Stony Creek Dialysis   Stony Creek Dialysis   9115 S CICERO AVE     OAK LAWN   IL   60453-1895

1122

  Affiliated   1785   Beverly Dialysis   Beverly Dialysis   8109 SOUTH WESTERN AVE     CHICAGO   IL   60620-5939

1123

  Affiliated   2089   Summit Dialysis   Summit Dialysis Center   3150 POLK ST     HOUSTON   TX   77003-4631

1124

  Affiliated   2212   Upper Valley Dialysis   Upper Valley Dialysis (fka West El Paso)   7933 N MESA ST   STE H   EL PASO   TX   79932-1699

1125

  Affiliated   2134   Dallas County   Perry Dialysis (fka Dallas County)   610 10TH ST   STE L1   PERRY   IA   50220-2221

1126

  Affiliated   1813   Nampa Dialysis Center   Nampa Dialysis   846 PARKCENTRE WAY     NAMPA   ID   83651-1790

1127

  Affiliated   1814   Table Rock Dialysis   Table Rock Dialysis   5610 W GAGE ST   STE B   BOISE   ID   83706

1128

  Affiliated   1815   Twin Falls Dialysis   Twin Falls Dialysis   1840 CANYON CREST DR     TWIN FALLS   ID   83301-3007

1129

  Affiliated   1816   Burley Dialysis Center   Burley Dialysis   741 N OVERLAND AVE     BURLEY   ID   83318-3440

 

Page 110 of 136


1130

  Affiliated   1817   Gate City Dialysis Center   Gate City Dialysis   2001 BENCH RD     POCATELLO   ID   83201-2033

1131

  Affiliated   1818   Four Rivers Dialysis   Four Rivers Dialysis   515 EAST LN     ONTARIO   OR   97914-3953

1132

  Affiliated   2231   River Parishes   River Parishes Dialysis (aka La Place)   2880 W AIRLINE HWY     LA PLACE   LA   70068-2922

1133

  Affiliated   2177   South Lincoln   South Lincoln Dialysis   3401 PLANTATION DR   STE 14   LINCOLN   NE   68516-4712

1134

  Affiliated   2105   Rochester Hills   Rochester Hills Dialysis (aka Sterling Heights)   1886 W AUBURN RD   STE 1   ROCHESTER HILLS   MI   48309-3865

1135

  Affiliated   2101   Willowbrook Dialysis   Willowbrook Dialysis   12120 JONES RD   STE G   HOUSTON   TX   77070-5280

1136

  Affiliated   2195   Springhurst Dialysis   Springhurst Dialysis (aka Louisville)   10201 CHAMPION FARMS DR     LOUISVILLE   KY   40241-6150

1137

  Affiliated   2012   Magnolia West   Magnolia West Dialysis (aka Riverside II)   11161 MAGNOLIA AVE     RIVERSIDE   CA   92505-3605

1138

  Affiliated   2206   Garrisonville Dialysis   Garrisonville Dialysis   70 DOC STONE RD   STE 11   STAFFORD   VA   22556-4628

1139

  Affiliated   2152   Strongsville Dialysis   Strongsville Dialysis   17792 PEARL RD     STRONGSVILLE   OH   44136-6909

1140

  Affiliated   984   Summerlin Dialysis   Summerlin Dialysis Center, LV   653 N TOWN CENTER DR   STE 7 BLDG 2   LAS VEGAS   NV   89144-0503

1141

  Affiliated   2127   Red Bluff Dialysis   Red Bluff Dialysis Center   2455 SISTER MARY COLUMBA DR     RED BLUFF   CA   96080-4364

1142

  Affiliated   1638   Cobb Dialysis   Cobb Dialysis   3865 MEDICAL PARK DR     AUSTELL   GA   30106-1109

1143

  Affiliated   1693   Paulding Dialysis   Paulding Dialysis   4019 JOHNS RD     DALLAS   GA   30132-3420

1144

  Affiliated   1839   Sweetwater Dialysis   Sweetwater Dialysis   7117 S SWEETWATER RD     LITHIA SPRINGS   GA   30122-2446

1145

  Affiliated   3671   Charlottesville North   Charlottesville North Dialysis   1800 TIMBERWOOD BLVD   STE C   CHARLOTTESVILLE   VA   22911-7544

1146

  Affiliated   2186   Southern Crescent   Southern Crescent Dialysis Center (fka Riverdale)   275 UPPER RIVERDALE RD SW   STE B   RIVERDALE   GA   30274-2556

1147

  Affiliated   2169   Meridian Park   Meridian Park Dialysis Center (fka Lake Oswego)   19255 SW 65TH AVE   STE 1   TUALATIN   OR   97062-9712

1148

  Affiliated   1812   Treasure Valley Dialysis   Treasure Valley Dialysis   3525 E LOUISE ST   STE 155   MERIDIAN   ID   83642-6303

1149

  Affiliated   3637   White Oak   White Oak Dialysis (Chronic)   5520 CHEVIOT RD   STE B   CINCINNATI   OH   45247-7069

1150

  Affiliated   1786   Ash Tree   Ash Tree Dialysis   2666 N GROVE INDUSTRIAL DR     FRESNO   CA   93727-1552

1151

  Affiliated   2242   Madera Dialysis   Almond Wood Dialysis (fka Madera)   501 E ALMOND AVE     MADERA   CA   93637-5661

1152

  Affiliated   2209   Carrollton   Carrollton Dialysis   1544 VALWOOD PKWY   STE 114   CARROLLTON   TX   75006-8425

1153

  Affiliated   2202   Edna Dialysis   Edna Dialysis   1008 N WELLS ST     EDNA   TX   77957-2153

1154

  Affiliated   2208   Bear Creek Dialysis   Bear Creek Dialysis (fka Clay Road)   4978 HIGHWAY 6 N   STE I   HOUSTON   TX   77084-5282

1155

  Affiliated   1820   Windham Dialysis   Windham Dialysis   375 TUCKIE RD   STE C   NORTH WINDHAM   CT   06256-1345

1156

  Affiliated   1819   Vernon Dialysis   Vernon Dialysis   460 HARTFORD TPKE STE C     VERNON ROCKVILLE   CT   6066

1157

  Affiliated   2092   Fountain Dialysis   Fountain Dialysis (aka Security)   6910 BANDLEY DR     FOUNTAIN   CO   80817-2617

1158

  Affiliated   1846   Grand Junction   Grand Junction Dialysis Center   710 WELLINGTON AVE   STE 2   GRAND JUNCTION   CO   81501-6100

1159

  Affiliated   2183   Fort Mill   Fort Mill Dialysis   1975 CAROLINA PLACE DR     FORT MILL   SC   29708-6922

1160

  Affiliated   2215   Mrytle Beach   JV-Myrtle Beach Dialysis   3919 MAYFAIR ST     MYRTLE BEACH   SC   29577-5773

1161

  Affiliated   2032   Oakwood   Oakwood Dialysis Center   148 HECTOR AVE     GRETNA   LA   70056-2531

1162

  Affiliated   2168   SP Hillsboro   Hillsboro Dialysis   2500 NW 229TH AVE   STE 3 BLDG E   HILLSBORO   OR   97124-7516

1163

  Affiliated   2269   Kettering   Kettering Dialysis   5721 BIGGER RD     KETTERING   OH   45440-2752

1164

  Affiliated   2246   Mansfield   Mansfield Dialysis Center (aka Dallas)   987 N WALNUT CREEK DR   STE 11   MANSFIELD   TX   76063-8016

1165

  Affiliated   2290   Cottage Grove   Cottage Grove Dialysis   8800 E POINT DOUGLAS RD S   STE 1   COTTAGE GROVE   MN   55016-4160

1166

  Affiliated   2257   Scott County Dialysis   Scott County Dialysis   7456 S PARK DR     SAVAGE   MN   55378

1167

  Affiliated   1773   Virginia Beach   Camelot Dialysis Center   1800 CAMELOT DR   STE 1   VIRGINIA BEACH   VA   23454-2440

1168

  Affiliated   1627   Amelia Island   Amelia Island Dialysis   1525 LIME ST   STE 12   FERNANDINA BEACH   FL   32034-3015

1169

  Affiliated   2179   Laurel Manor at the Villages   Laurel Manor Dialysis Center at the Villages   1950 LAUREL MANOR DR   STE 19   LADY LAKE   FL   32162-5603

1170

  Affiliated   2160   East Deerborn   East Dearborn Dialysis   13200 W WARREN AVE     DEARBORN   MI   48126-2410

1171

  Affiliated   1661   North Houston   PDI-North Houston   7115 NORTH LOOP E     HOUSTON   TX   77028-5948

1172

  Affiliated   1663   South Houston   PDI-South Houston   5989 SOUTH LOOP E     HOUSTON   TX   77033-1017

1173

  Affiliated   1856   Ralph McGill Dialysis Center   Ralph McGill Dialysis   418 DECATUR ST SE     ATLANTA   GA   30312-1801

1174

  Affiliated   2144   Chelsea   Chelsea Dialysis   1620 COMMERCE PARK DR   STE 2   CHELSEA   MI   48118-2136

1175

  Affiliated   2214   Smokey Mountain   Smoky Mountain Dialysis   1611 ANDREWS RD     MURPHY   NC   28906-5100

1176

  Affiliated   3680   Miami Gardens   Miami Gardens Dialysis   3363 NW 167TH ST     MIAMI GARDENS   FL   33056-4254

1177

  Affiliated   2222   Deerbrook   Deerbrook Dialysis   9660 FM 1960 BYPASS RD W     HUMBLE   TX   77338-4039

1178

  Affiliated   2227   Downtown Dallas   DaVita Downtown Dallas Dialysis Center (fka Grove)   3515 SWISS AVE   STE A   DALLAS   TX   75204-6223

1179

  Affiliated   2197   Henderson   Siena Henderson Dialysis Center   2865 SIENNA HEIGHTS DR   STE 141   HENDERSON   NV   89052-4168

1180

  Affiliated   2292   Wyandotte   Wyandotte Central Dialysis   3737 STATE AVE     KANSAS CITY   KS   66102-3830

1181

  Affiliated   2235   Westview   Westview Dialysis   3749 COMMERCIAL DR   LAFAYETTE PLACE SHOPPING CENTER   INDIANAPOLIS   IN   46222-1676

1182

  Affiliated   2286   Garland   Garland Dialysis   776 E CENTERVILLE RD     GARLAND   TX   75041-4640

1183

  Affiliated   2333   Aberdeen   Aberdeen Dialysis   780 W BEL AIR AVE     ABERDEEN   MD   21001-2236

 

Page 111 of 136


1184

  Affiliated   2259   Mountain Park   Mountain Park Dialysis   5235 MEMORIAL DR     STONE MOUNTAIN   GA   30083-3112

1185

  Affiliated   2229   Downtown San Antonio   Downtown San Antonio Dialysis (Brooklyn St)   615 E QUINCY ST     SAN ANTONIO   TX   78215-1600

1186

  Affiliated   2237   Medlock Bridge   Medlock Bridge Dialysis (aka Duluth)   10680 MEDLOCK BRIDGE RD   STE 13   DULUTH   GA   30097-8420

1187

  Affiliated   2234   Greene County Dialysis   Greene County Dialysis Center (NC)   1025 KINGOLD BLVD     SNOW HILL   NC   28580-1616

1188

  Affiliated   2243   West Broadway Dialysis   West Broadway Dialysis   720 W BROADWAY     LOUISVILLE   KY   40202-2240

1189

  Affiliated   2072   St. Pauls Dialysis   St. Pauls Dialysis (aka Robeson County)   564 W MCLEAN ST     SAINT PAULS   NC   28384-1421

1190

  Affiliated   2123   Carquinez Dialyis   Carquinez Dialysis (fka SW Vallejo)   125 CORPORATE PL   STE C   VALLEJO   CA   94590-6968

1191

  Affiliated   2159   DaVita East   DaVita East Dialysis Clinic (fka La Bamba)   11989 PELLICANO DR     EL PASO   TX   79936-6287

1192

  Affiliated   2187   Natomas   Natomas Dialysis   30 GOLDEN LAND CT   BLDG G   SACRAMENTO   CA   95834-2420

1193

  Affiliated   2228   Tennesse Valley   Tennessee Valley Dialysis Center (aka Johnson City)   107 WOODLAWN DR   STE 2   JOHNSON CITY   TN   37604-6287

1194

  Affiliated   2174   Turfway Dialysis   Turfway Dialysis (fka Florence)   11 SPIRAL DR   STE 15   FLORENCE   KY   41042-1394

1195

  Affiliated   2291   Leavenworth   Leavenworth Dialysis   501 OAK ST     LEAVENWORTH   KS   66048-2646

1196

  Affiliated   2270   Franklin Dialysis   Franklin Dialysis (IN)   1140 W JEFFERSON ST   STE A   FRANKLIN   IN   46131-2101

1197

  Affiliated   2011   Norco   Norco Dialysis (fka Corona II)   1901 TOWN AND COUNTRY DR   STE 1   NORCO   CA   92860-3611

1198

  Affiliated   2240   Andover   Andover Dialysis   488 S MAIN ST     ANDOVER   OH   44003-9602

1199

  Affiliated   1863   Little Rock   Jacksonville Central Dialysis Center   400 T P WHITE DR     JACKSONVILLE   AR   72076-3287

1200

  Affiliated   1864   North Little Rock Dialysis   North Little Rock Center   4505 E MCCAIN BLVD     NORTH LITTLE ROCK   AR   72117-2902

1201

  Affiliated   2233   Anadarko   Anadarko Dialysis   412 SE 11TH STREET     ANADARKO   OK   73005-4442

1202

  Affiliated   2331   Desert Springs   Desert Springs Dialysis   2110 E FLAMINGO RD   STE 18   LAS VEGAS   NV   89119-5191

1203

  Affiliated   2213   Livingston   Vancouver Dialysis Center   9120 NE VANCOUVER MALL DR   STE 16   VANCOUVER   WA   98662-9401

1204

  Affiliated   2300   Vancouver   Livingston TN Dialysis   308 OAK ST     LIVINGSTON   TN   38570-1729

1205

  Affiliated   2225   Fenton Dialysis   Fenton Dialysis   17420 SILVER PKWY     FENTON   MI   48430-4429

1206

  Affiliated   2332   Cold Spring   Cold Springs Dialysis   430 CROSS ROADS BLVD     COLD SPRING   KY   41076-2341

1207

  Affiliated   2094   Yucaipa   Yucaipa Dialysis   33487 YUCAIPA BLVD     YUCAIPA   CA   92399-2064

1208

  Affiliated   1900   Florida Renal Center   Florida Renal Center   3500 NW 7TH ST     MIAMI   FL   33125-4016

1209

  Affiliated   2140   Harbor UCLA   Long Beach Harbor Dialysis (aka UCLA)   1075 E PACIFIC COAST HWY     LONG BEACH   CA   90806-5089

1210

  Affiliated   2210   Seaton Drive   Seton Drive Dialysis (fka Greensprings II)   4800 SETON DR     BALTIMORE   MD   21215-3210

1211

  Affiliated   1865   South Valley   South Valley Dialysis   17815 VENTURA BLVD   STE 1   ENCINO   CA   91316-3600

1212

  Affiliated   2305   West Pensacola   West Pensacola Dialysis   598 N FAIRFIELD DR   STE 1   PENSACOLA   FL   32506-4320

1213

  Affiliated   2073   Mar Vista   Mar Vista Dialysis Center (UCLA-Santa Monica)   2020 SANTA MONICA BLVD   STE 1   SANTA MONICA   CA   90404-2139

1214

  Affiliated   2082   Riddle Dialysis   Riddle Dialysis   100 GRANITE DR   STE 16   MEDIA   PA   19063-5134

1215

  Affiliated   2346   Uptown   Minneapolis Uptown Dialysis   3601 LYNDALE AVE S     MINNEAPOLIS   MN   55409-1103

1216

  Affiliated   1907   Lake Griffith East Dialysis   Lake Griffin East Dialysis   401 E NORTH BLVD     LEESBURG   FL   34748-5256

1217

  Affiliated   2170   West Linn   West Linn Dialysis   19056 WILLAMETTE DR     WEST LINN   OR   97068-1715

1218

  Affiliated   2330   Cape Coral South Dialysis   Cape Coral South Dialysis   3046 DEL PRADO BLVD S   STE 4A   CAPE CORAL   FL   33904-7232

1219

  Affiliated   2241   Ceres   Ceres Dialysis Center   1768 MITCHELL RD   STE 38   CERES   CA   95307-2156

1220

  Affiliated   1862   Shaker Square   Shaker Square Dialysis   12800 SHAKER BLVD   STE 1   CLEVELAND   OH   44120-2004

1221

  Affiliated   1906   St. Cloud Dialysis   St. Cloud Dialysis   4750 OLD CANOE CREEK RD     SAINT CLOUD   FL   34769-1430

1222

  Affiliated   1915   Turlock Dialysis Center   Turlock Dialysis Center   50 W SYRACUSE AVE     TURLOCK   CA   95380-3143

1223

  Affiliated   2268   Haymarket   Haymarket Dialysis (fka Gainesville)   14664 GAP WAY     GAINESVILLE   VA   20155-1683

1224

  Affiliated   2272   Hackettstown   Hackettstown Dialysis   657 WILLOW GROVE ST   WEST WING MEDICAL PLAZA STE 22   HACKETTSTOWN   NJ   07840-1713

1225

  Affiliated   2274   Regency   Regency Dialysis Center (fka Jacksonville)   9535 REGENCY SQUARE BLVD N     JACKSONVILLE   FL   32225-8128

1226

  Affiliated   2149   Williamsburg   Williamsburg Dialysis (fka Yorktown)   500 SENTARA CIR   STE 13   WILLIAMSBURG   VA   23188-5727

1227

  Affiliated   2141   Commerce Township   Commerce Township Dialysis   120 W COMMERCE RD     COMMERCE TOWNSHIP   MI   48382-3915

1228

  Affiliated   2147   Kankakee   Kankakee County Dialysis   581 WILLIAM R LATHAM SR DR   STE 14   BOURBONNAIS   IL   60914-2439

1229

  Affiliated   2283   Sandusky   Sandusky Dialysis Center   795 BARDSHAR RD     SANDUSKY   OH   44870-1505

1230

  Affiliated   2252   Ionia   Ionia Dialysis   2622 HEARTLAND BLVD     IONIA   MI   48846-8757

1231

  Affiliated   2289   Indian River   Indian River Dialysis Center   2150 45TH ST   UNIT 12   VERO BEACH   FL   32967-6281

1232

  Affiliated   2360   North Henry   North Henry Dialysis (fka Stockbridge)   5627 N HENRY BLVD   STE I1   STOCKBRIDGE   GA   30281-3244

1233

  Affiliated   2077   Tacoma Dialysis   Tacoma Dialysis Center   3401 S 19TH ST     TACOMA   WA   98405-1909

1234

  Affiliated   1908   Hileah Kidney Center I   Hialeah Artificial Kidney Center   2750 W 68TH ST   STE 27   HIALEAH   FL   33016-5450

1235

  Affiliated   2315   St. Francis   Charter Colony Dialysis Center (fka St. Francis Dialysis)   2312 COLONY CROSSING PL     MIDLOTHIAN   VA   23112-4280

1236

  Affiliated   2138   Bellflower   Bellflower Dialysis Center (aka Widerhorn)   15736 WOODRUFF AVE     BELLFLOWER   CA   90706-4018

1237

  Affiliated   2301   Smyrna   Smyrna Dialysis   537 STONECREST PKWY     SMYRNA   TN   37167-6884

 

Page 112 of 136


1238

  Affiliated   2122   Clearlake   Clearlake Dialysis   14400 OLYMPIC DR     CLEARLAKE   CA   95422-8809

1239

  Affiliated   1853   Dialysis Center of Erie   Dialysis Center of Erie   1641 SASSAFRAS ST     ERIE   PA   16502-1858

1240

  Affiliated   1854   Warren Dialysis   Warren Dialysis   2 W CRESCENT PARK     WARREN   PA   16365-2111

1241

  Affiliated   2322   Maysville   Maysville Dialysis   489 TUCKER DR     MAYSVILLE   KY   41056-9111

1242

  Affiliated   2429   Fridley   East River Road Dialysis (fka Fridley Dialysis Unit)   5301 E RIVER RD   STE 117   FRIDLEY   MN   55421-3778

1243

  Affiliated   2189   West Sacramento   West Sacramento Dialysis   3450 INDUSTRIAL BLVD   STE 1   WEST SACRAMENTO   CA   95691-5003

1244

  Affiliated   2293   Anderson   Anderson Dialysis Center   7502 STATE RD   STE 116   CINCINNATI   OH   45255

1245

  Affiliated   2383   North County   North St. Louis County Dialysis   13119 NEW HALLS FERRY RD     FLORISSANT   MO   63033-3228

1246

  Affiliated   2439   Fargo   Fargo Dialysis Center   4474 23RD AVE S   STE M   FARGO   ND   58104-8795

1247

  Affiliated   2008   Eastchester   Eastchester Road Dialysis Center (Bronx II)   1515 JARRETT PL     BRONX   NY   10461-2606

1248

  Affiliated   2224   Fallon   Fallon Dialysis   1103 NEW RIVER PKWY     FALLON   NV   89406-6899

1249

  Affiliated   2279   Clarksville North   Clarksville North Dialysis   3071 CLAY LEWIS RD     CLARKSVILLE   TN   37040-5141

1250

  Affiliated   2308   Eaton   Eaton Dialysis   105 E WASHINGTON JACKSON RD     EATON   OH   45320-9789

1251

  Affiliated   2447   Wallace   Wallace Dialysis   5650 S NC 41 HWY     WALLACE   NC   28466-6094

1252

  Affiliated   2288   Central Kalazmazoo   Kalamazoo Central Dialysis   535 S BURDICK ST   STE 11   KALAMAZOO   MI   49007-5261

1253

  Affiliated   2287   West Kalamazoo   Kalamazoo West Dialysis   1040 N 10TH ST     KALAMAZOO   MI   49009-6149

1254

  Affiliated   1921   Bakersfield   Bakersfield Dialysis Center   5143 OFFICE PARK DR     BAKERSFIELD   CA   93309-0660

1255

  Affiliated   1930   Antelope Valley Dialysis   Antelope Valley Dialysis   1759 W AVENUE J   STE 12   LANCASTER   CA   93534-2703

1256

  Affiliated   1931   Indian Wells Valley Dialysis   Indian Wells Valley Dialysis   212 S RICHMOND RD     RIDGECREST   CA   93555-4434

1257

  Affiliated   1932   Palmdale Regional Dialysis   Palmdale Regional   1643 E PALMDALE BLVD     PALMDALE   CA   93550-4847

1258

  Affiliated   2185   South Star / Adamsville   Southstar Adamsville Dialysis (fka Cascade)   3651 BAKERS FERRY RD SW     ATLANTA   GA   30331-3712

1259

  Affiliated   2314   Union City   Union City Dialysis   6851 SHANNON PKWY   STE 2   UNION CITY   GA   30291-2049

1260

  Affiliated   2345   Waterbury   Waterbury Dialysis Center   150 MATTATUCK HEIGHTS RD     WATERBURY   CT   06705-3893

1261

  Affiliated   2421   Butler Farm   Butler Farm Dialysis (Hope II)   501 BUTLER FARM RD     HAMPTON   VA   23666-1777

1262

  Affiliated   2337   Blue Mtn Kidney Center   Blue Mountain Kidney Center (aka Wild Horse, Pendleton)   72556 COYOTE RD     PENDLETON   OR   97801-1002

1263

  Affiliated   2249   Talladega   Talladega Dialysis   726 BATTLE ST E   STE A   TALLADEGA   AL   35160-2583

1264

  Affiliated   2281   Athens East   Athens East Dialysis   2026 S MILLEDGE AVE   STE A2   ATHENS   GA   30605-6480

1265

  Affiliated   2412   Mayland   Mayland Dialysis Center (aka Spruce Pine)   575 ALTAPASS HWY     SPRUCE PINE   NC   28777-3012

1266

  Affiliated   2236   Salem   Salem Dialysis Center (IN)   1201 N JIM DAY RD   STE 13   SALEM   IN   47167-7219

1267

  Affiliated   2239   Lake Cliff   Lake Cliff Dialysis Center   805 N BECKLEY AVE     DALLAS   TX   75203-1612

1268

  Affiliated   2363   DVA Mid Cities Dialysis   Mid Cities Dialysis Center   117 E HARWOOD RD     HURST   TX   76054-3043

1269

  Affiliated   2362   Boerne   Boerne Dialysis Center   1369 S MAIN ST   STE 11   BOERNE   TX   78006-2860

1270

  Affiliated   2318   Columbus West   Columbus West Dialysis   1395 GEORGESVILLE RD     COLUMBUS   OH   43228-3611

1271

  Affiliated   2306   Point Place   Point Place Dialysis   4747 SUDER AVE   STE 17   TOLEDO   OH   43611-2869

1272

  Affiliated   2350   Delhi Dialysis   Delhi Dialysis   5040 DELHI AVE     CINCINNATI   OH   45238-5388

1273

  Affiliated   2253   Pataskala   Pataskala Dialysis Center   642 E BROAD ST     PATASKALA   OH   43062-7627

1274

  Affiliated   2384   Eastland   Eastland Dialysis (fka Independence)   19101 E VALLEY VIEW PKWY   STE E   INDEPENDENCE   MO   64055-6907

1275

  Affiliated   2254   Wauseon   Wauseon Dialysis Center   721 S SHOOP AVE     WAUSEON   OH   43567-1729

1276

  Affiliated   2327   Lebanon Dialysis   Lebanon Dialysis Center (Chronic Only)   918B COLUMBUS AVE     LEBANON   OH   45036-

1277

  Affiliated   2460   Horton   Horton Dialysis   1901 EUCLID AVE     HORTON   KS   66439-1238

1278

  Affiliated   2280   Lone Peak Dialysis   Lone Peak Dialysis   1175 E 50 S   STE 111   AMERICAN FORK   UT   84003-2845

1279

  Affiliated   2347   Mena   Mena Dialysis Center   1200 CRESTWOOD CIR     MENA   AR   71953-5516

1280

  Affiliated   1941   FAYETTEVILLE DIALYSIS   Fayetteville Dialysis   509 E MILLSAP RD   STE 111   FAYETTEVILLE   AR   72703-4862

1281

  Affiliated   1942   BENTONVILLE DIALYSIS   Bentonville Dialysis   1104 SE 30TH ST     BENTONVILLE   AR   72712-4290

1282

  Affiliated   1943   SILOAM SPRINGS DIALYSIS   Siloam Springs Dialysis   500 S MOUNT OLIVE ST   STE 17   SILOAM SPRINGS   AR   72761-3602

1283

  Affiliated   1944   SPRINGDALE DIALYSIS   Springdale Dialysis   708 QUANDT AVE     SPRINGDALE   AR   72764-5309

1284

  Affiliated   2273   Grosse Pointe   Grosse Pointe Dialysis   18000 E WARREN AVE   STE 1   DETROIT   MI   48224-1336

1285

  Affiliated   2448   Indy South Dialysis   Indy South Dialysis   972 EMERSON PKWY   STE E   GREENWOOD   IN   46143-6202

1286

  Affiliated   2358   Greensburg Dialysis   Greensburg Dialysis   1531 N COMMERCE EAST DR   STE 6   GREENSBURG   IN   47240-3259

1287

  Affiliated   2319   Grove City   Grove City Dialysis   4155 KELNOR DR     GROVE CITY   OH   43123-2960

1288

  Affiliated   2338   West Beach   West Beach Dialysis Center   16201 PANAMA CITY BEACH HWY   STE 12   PANAMA CITY BEACH   FL   32413-5301

1289

  Affiliated   2371   Birmingham   Center Point Dialysis (aka Birmingham Center)   2337 1ST ST NE     CENTER POINT   AL   35215-3619

1290

  Affiliated   2445   Eureka   Eureka Dialysis Center   419 MERAMEC BLVD     EUREKA   MO   63025-3906

1291

  Affiliated   2313   Tifton   Tifton Dialysis   624 LOVE AVE     TIFTON   GA   31794-4406

 

Page 113 of 136


1292

  Affiliated   2146   Woodlands   The Woodlands Dialysis   9301 PINECROFT DR   STE 13   SHENANDOAH   TX   77380-3178

1293

  Affiliated   2266   Exerter   Exeter Dialysis   1116 W VISALIA RD   STE 16   EXETER   CA   93221-1482

1294

  Affiliated   2396   Wayne County   Wayne County Dialysis (fka Fairfield)   303 NW 11TH ST   STE 1   FAIRFIELD   IL   62837-1203

1295

  Affiliated   2415   Cordele Dialysis   Cordele Dialysis   1013 E 16TH AVE     CORDELE   GA   31015-1539

1296

  Affiliated   2304   Winter Park   Winter Park Dialysis (aka Orlando)   3727 N GOLDENROD RD   STE 11   WINTER PARK   FL   32792-8611

1297

  Affiliated   2449   Carmel   Carmel Dialysis   180 E CARMEL DR     CARMEL   IN   46032-2633

1298

  Affiliated   2298   Corydon   Corydon Dialysis   1937 OLD HWY 135 NW     CORYDON   IN   47112-2013

1299

  Affiliated   2382   Memphis Southeast   Memphis Southeast Dialysis (aka Midtown)   1805 MORIAH WOODS BLVD   STE 11   MEMPHIS   TN   38117-7119

1300

  Affiliated   2399   Rim Country   Rim Country Dialysis   809 W LONGHORN RD     PAYSON   AZ   85541-4280

1301

  Affiliated   2201   Cedar Park   Cedar Park Dialysis (fka North Austin)   1720 E WHITESTONE BLVD     CEDAR PARK   TX   78613-7640

1302

  Affiliated   2368   Ellensburg   Ellensburg Dialysis   2101 W DOLARWAY RD   STE 1   ELLENSBURG   WA   98926-9310

1303

  Affiliated   2260   Santa Fe Springs   Santa Fe Springs Dialysis   11147 WASHINGTON BLVD     WHITTIER   CA   90606-3007

1304

  Affiliated   1950   Snapfinger Dialysis   Snapfinger Dialysis   5255 SNAPFINGER PARK DR   STE 115   DECATUR   GA   30035-4066

1305

  Affiliated   1951   East Dekalb Dialysis   East DeKalb Dialysis   2801 CANDLER RD   STE 23   DECATUR   GA   30034-1429

1306

  Affiliated   2258   Meadows East   Meadows East Dialysis   2529 SIX MILE LN     LOUISVILLE   KY   40220-2934

1307

  Affiliated   2226   First Colony   First Colony Dialysis (aka Sugarland, Great Woods)   1447 HIGHWAY 6   STE 14   SUGAR LAND   TX   77478-5094

1308

  Affiliated   1612   Coastal Kidney Center   Coastal Kidney Center   510 N MACARTHUR AVE     PANAMA CITY   FL   32401-3636

1309

  Affiliated   2211   Clinton Township   Clinton Township Dailysis   15918 19 MILE RD   STE 11   CLINTON TOWNSHIP   MI   48038-1101

1310

  Affiliated   2207   West Brook   Westbrook Dialysis (fka Palm Brook II)   13907 W CAMINO DEL SOL   STE 13   SUN CITY WEST   AZ   85375-4405

1311

  Affiliated   1954   Johnson County   Johnson County Dialysis   10453 W 84TH TER     LENEXA   KS   66214-1641

1312

  Affiliated   1956   Wyandotte County   Wyandotte County Dialysis   5001 STATE AVE     KANSAS CITY   KS   66102-3459

1313

  Affiliated   2479   Maple Grove   Maple Grove Dialysis Unit   15655 GROVE CIR N     MAPLE GROVE   MN   55369-4489

1314

  Affiliated   4336   East End   East End-Pittsburgh Dialysis (fka Wilkinsburg)   7714 PENN AVE PARK PLAZA     PITTSBURGH   PA   15221

1315

  Affiliated   2493   Westminster II - North Metro   North Metro Dialysis Center (aka Denver, Westminster II)   12365 HURON ST   STE 5   WESTMINSTER   CO   80234-3498

1316

  Affiliated   1960   Vidalia   Vidalia First Street Dialysis   906 E 1ST ST     VIDALIA   GA   30474-4207

1317

  Affiliated   2357   Highland Park   Highland Park Dialysis   1559 W 7TH ST     SAINT PAUL   MN   55102-4238

1318

  Affiliated   2367   Centennial Parkway   Centennial Dialysis Center   8775 DEER SPRINGS WAY     LAS VEGAS   NV   89149-0416

1319

  Affiliated   2250   Lord Baltimore   Northwest Dialysis Center (aka Lord Baltimore, N. Rolling Road II, Owings Mills II)   2245 ROLLING RUN DR   STE 1   WINDSOR MILL   MD   21244-1858

1320

  Affiliated   3944   North Charlotte   North Charlotte Dialysis   6620 OLD STATESVILLE RD     CHARLOTTE   NC   28269

1321

  Affiliated   2410   Sun Ray Dialysis   Sun Ray Dialysis Unit (fka East St. Paul)   1758 OLD HUDSON RD   STE 1   SAINT PAUL   MN   55106-6161

1322

  Affiliated   2425   Vandalia   Vandalia Dialysis   301 MATTES AVE     VANDALIA   IL   62471-2061

1323

  Affiliated   2428   Westwood Hills   Westwood Hills Dialysis (fka Minneapolis, Excelsior)   7525 WAYZATA BLVD     SAINT LOUIS PARK   MN   55426-1621

1324

  Affiliated   4305   Amery   Amery Dialysis   970 ELDEN AVE     AMERY   WI   54001-1448

1325

  Affiliated   2434   Wadsworth   Wadsworth Dialysis   195 WADSWORTH RD   STE 32   WADSWORTH   OH   44281-9504

1326

  Affiliated   2419   Dublin   Dublin Dialysis   6770 PERIMETER DR     DUBLIN   OH   43016-8063

1327

  Affiliated   4314   Weber Valley   Weber Valley Dialysis (fka Ogden)   1920 W 250TH N     MARRIOTT-SLATERVILLE   UT   84404-9233

1328

  Affiliated   2343   West Elk Grove   West Elk Grove Dialysis   2208 KAUSEN DR   STE 1   ELK GROVE   CA   95758-7174

1329

  Affiliated   2355   Bedford Park   Bedford Park Dialysis Center   3119 WEBSTER AVE   1ST FLR   BRONX   NY   10467-4905

1330

  Affiliated   1747   Cuero Lakeview Dialysis   Cuero Lakeview Dialysis   1105 E BROADWAY ST     CUERO   TX   77954

1331

  Affiliated   1961   Madisonville Dialysis   Madisonville Dialysis Center   255 E NORTH ST     MADISONVILLE   KY   42431

1332

  Affiliated   2467   Crescent City   Crescent City Dialysis Center   3909 BIENVILLE ST   STE B   NEW ORLEANS   LA   70119-5152

1333

  Affiliated   4318   Callowhill   Callowhill Dialysis Center   313 CALLOWHILL ST     PHILADELPHIA   PA   19123-4103

1334

  Affiliated   2406   Oak Creek   Oak Creek Dialysis (fka South Milwaukee)   8201 S HOWELL AVE   STE 6   OAK CREEK   WI   53154-8336

1335

  Affiliated   4395   Leesburg Virginia   Leesburg Virginia Dialysis   224D CORNWALL ST NW   STE 1   LEESBURG   VA   20176-2700

1336

  Affiliated   2386   Joy of Dixon   Joy of Dixon Dialysis Center   1640 N LINCOLN ST     DIXON   CA   95620-9255

1337

  Affiliated   2137   Long Beach JV -Bixby Knolls   Bixby Knolls Dialysis (fka Long Beach)   3744 LONG BEACH BLVD     LONG BEACH   CA   90807-3310

1338

  Affiliated   1790   Alliance Community Dialysis   Alliance Community Dialysis   270 E STATE ST   STE 11   ALLIANCE   OH   44601-4309

1339

  Affiliated   1791   Belden Community Dialysis   Belden Community Dialysis   4685 FULTON DR NW     CANTON   OH   44718-2379

1340

  Affiliated   1792   Mercy Canton Dialysis   Mercy Canton Dialysis   1320 MERCY DR NW     CANTON   OH   44708-2614

1341

  Affiliated   2294   Marrero   Marrero Dialysis   1908 JUTLAND DR     HARVEY   LA   70058-2359

1342

  Affiliated   2351   Miramar   Miramar Kidney Center   2501 DYKES RD   STE 2   MIRAMAR   FL   33027-4217

1343

  Affiliated   2418   Chesterton   Chesterton Dialysis   711 PLAZA DR   STE 6   CHESTERTON   IN   46304-5506

1344

  Affiliated   4368   St. John   St. John Dialysis   10033 WICKER AVE   STE 6   SAINT JOHN   IN   46373-8777

1345

  Affiliated   2256   Princeton   Princeton Dialysis   2227 SHERMAN DR     PRINCETON   IN   47670-1062

 

Page 114 of 136


1346   Affiliated   4332   Black Rock   Black Rock Dialysis (aka Faifield)   427 STILLSON RD     FAIRFIELD   CT   06824-3153
1347   Affiliated   2422   Williamstown   Williamstown Dialysis (fka Dry Ridge)   103 BARNES RD   STE A   WILLIAMSTOWN   KY   41097-9468
1348   Affiliated   4376   Renaissance   Renaissance Dialysis   1840 DARBY DR     FLORENCE   AL   35630-2623
1349   Affiliated   4360   Portage   Portage Dialysis   5823 US HIGHWAY 6     PORTAGE   IN   46368-4851
1350   Affiliated   2393   Opelika   Opelika Dialysis Center   2340 PEPPERELL PKWY     OPELIKA   AL   36801-6240
1351   Affiliated   2435   Urbana   Urbana Dialysis Center   1880 E US HIGHWAY 36     URBANA   OH   43078-9600
1352   Affiliated   1913   Port Lavaca Dialysis   Port Lavaca Dialysis   1300 N VIRGINIA ST   STE 12   PORT LAVACA   TX   77979-2512
1353   Affiliated   2276   Cornerhouse Dialysis   Cornerhouse Dialysis Center (aka Santa Clara)   2005 NAGLEE AVE     SAN JOSE   CA   95128-4801
1354   Affiliated   2167   Snellville   Snellville Dialysis   2135 MAIN ST E   STE 13   SNELLVILLE   GA   30078-6424
1355   Affiliated   4334   Bloomfield   Bloomfield-Pittsburgh Dialysis   5171 LIBERTY AVE   STE C   PITTSBURGH   PA   15224-2254
1356   Affiliated   2489   Pennsauken   Pennsauken Dialysis   7024 KAIGHNS AVE     PENNSAUKEN   NJ   08109-4417
1357   Affiliated   2433   Logan   Logan Dialysis   12880 GREY ST     LOGAN   OH   43138-9638
1358   Affiliated   2454   Forest Fair   Forest Fair Dialysis (fka Forest Park)   1145 KEMPER MEADOW DR     CINCINNATI   OH   45240-4118
1359   Affiliated   4307   Knoxville   Knoxville Central Dialysis   9141 CROSS PARK DR   STE 12   KNOXVILLE   TN   37923-4557
1360   Affiliated   4338   Kennestone   Kennestone Dialysis (aka Cobb II)   200 COBB PKWY N   STE 318 BLDG 3   MARIETTA   GA   30062-3558
1361   Affiliated   4343   Wiregrass Kidney Center   Wiregrass Kidney Center (fka Ross Circle)   1450 ROSS CLARK CIR     DOTHAN   AL   36301-4765
1362   Affiliated   2432   Memphis Downtown   Memphis Downtown Dialysis   2076 UNION AVE     MEMPHIS   TN   38104-4138
1363   Affiliated   3953   Marshville   Marshville Dialysis Center   7260 E MARSHVILLE BLVD     MARSHVILLE   NC   28103-1191
1364   Affiliated   4356   Shamrock   Shamrock Dialysis   1016 CLAXTON DAIRY RD   STE 1A   DUBLIN   GA   31021-7971
1365   Affiliated   4367   North Colorado Springs   North Colorado Springs Dialysis   6071 E WOODMEN RD   STE 1   COLORADO SPRINGS   CO   80923-2610
1366   Affiliated   2466   Oakes   Oakes Dialysis   413 S 7TH ST     OAKES   ND   58474-1920
1367   Affiliated   1976   Pinnacle Dialysis of Boca Raton   Pinnacle Dialysis of Boca Raton   2900 N MILITARY TRL   STE 195   BOCA RATON   FL   33431-6308
1368   Affiliated   1980   Cedar Valley Dialysis   Cedar Valley Dialysis   1661 W RIDGEWAY AVE     WATERLOO   IA   50701-4541
1369   Affiliated   1981   West Union Dialysis   West Union Dialysis   405 HIGHWAY 150 N     WEST UNION   IA   52175-1003
1370   Affiliated   2161   Rockside   Rockside Dialysis (aka Independence, Parma II)   4801 ACORN DR     INDEPENDENCE   OH   44131-2566
1371   Affiliated   2263   Sunset   Sunset Dialysis Center (fka Sunrise II)   3071 GOLD CANAL DR     RANCHO CORDOVA   CA   95670-6129
1372   Affiliated   2442   Yosemite Street   Yosemite Street Dialysis   1650 W YOSEMITE AVE     MANTECA   CA   95337-5193
1373   Affiliated   2335   Jedburg   Jedburg Dialysis   2897 W 5TH NORTH ST     SUMMERVILLE   SC   29483-9674
1374   Affiliated   2441   Parker Dialysis   Parker Dialysis   10371 S PARK GLENN WAY   STE 18   PARKER   CO   80138-3885
1375   Affiliated   2296   Northgate   Northgate Dialysis Center (aka San Rafael-Terra)   650 LAS GALLINAS AVE     SAN RAFAEL   CA   94903-3620
1376   Affiliated   2271   The Nevada Center   The Nevada Dialysis Center (fka Warm Springs, Green Valley)   1510 W WARM SPRINGS RD   STE 1   HENDERSON   NV   89014-3586
1377   Affiliated   2091   Aventura   Aventura Kidney Center   22 SW 11TH ST   FLOOR 2   HALLANDALE BEACH   FL   33009-7038
1378   Affiliated   2408   US Grant Dialysis   US Grant Dialysis (fka Georgetown, Brown County)   458 HOME ST     GEORGETOWN   OH   45121-1408
1379   Affiliated   4400   Arbor Place   Arbor Place Dialysis   9559 HIGHWAY 5   STE 1   DOUGLASVILLE   GA   30135-1573
1380   Affiliated   4389   South Jacksonville   Jacksonville South Dialysis Center   14965 OLD SAINT AUGUSTINE RD   UNIT 114   JACKSONVILLE   FL   32258-9481
1381   Affiliated   2385   Somerville   Somerville Dialysis   12475 US HIGHWAY 64     SOMERVILLE   TN   38068-6029
1382   Affiliated   4321   District Heights   District Heights Dialysis (aka Pennsylvania Ave)   5701 SILVER HILL RD     DISTRICT HEIGHTS   MD   20747-1102
1383   Affiliated   2414   Edwardsville   Edwardsville Dialysis   235 S BUCHANAN ST     EDWARDSVILLE   IL   62025-2108
1384   Affiliated   2361   Broad St   South Broad Street Dialysis (aka S. Philadelphia II)   1172 S BROAD ST     PHILADELPHIA   PA   19146-3142
1385   Affiliated   2342   Las Vegas Pedidatrics   Las Vegas Pediatrics Dialysis (fka UMC Peds, DaVita Peds)   7271 W SAHARA AVE   STE 12   LAS VEGAS   NV   89117-2862
1386   Affiliated   1990   Apopka Dialysis   Apopka Dialysis   640 EXECUTIVE PARK CT     APOPKA   FL   32703-6075
1387   Affiliated   1991   Cassellberry Dialysis   Casselberry Dialysis   4970 S US HWY 17/92     CASSELBERRY   FL   32707-3888
1388   Affiliated   1992   Central Orlando Dialysis   Central Orlando Dialysis   2548 N ORANGE BLOSSOM TRL   STE 4   ORLANDO   FL   32804-4863
1389   Affiliated   1993   Sanford Dialysis   Sanford Dialysis   1701 W 1ST ST     SANFORD   FL   32771-1605
1390   Affiliated   1994   Winter Park Hemo Dialysis   Winter Park Hemo Dialysis   4100 METRIC DR   STE 3   WINTER PARK   FL   32792-6832
1391   Affiliated   2173   Graham   Graham Dialysis Center   10219 196TH ST CT E   STE C   GRAHAM   WA   98338-7792
1392   Affiliated   2316   Batavia   Batavia Dialysis   4000 GOLDEN AGE DR     BATAVIA   OH   45103-1913
1393   Affiliated   1967   Klamath Falls   Klamath Falls Dialysis   2230 N ELDORADO AVE     KLAMATH FALLS   OR   97601-6418
1394   Affiliated   2336   Longs   Longs Dialysis (fka Conway)   90 CLOVERLEAF DR   STE 36   LONGS   SC   29568-9262
1395   Affiliated   2452   Pooler   Pooler Dialysis   54 TRADERS WAY     POOLER   GA   31322-
1396   Affiliated   4380   Ohio Pike Dialysis   Ohio Pike Dialysis (aka Amelia)   1761 STATE ROUTE 125     AMELIA   OH   45102-2039
1397   Affiliated   2285   Canyon Springs   Canyon Springs Dialysis (aka Moreno Valley)   22555 ALESSANDRO BLVD     MORENO VALLEY   CA   92553-8533
1398   Affiliated   4306   Williamson   South Williamson Dialysis   204 APPALACHIAN PLAZA     SOUTH WILLIAMSON   KY   41503-9404
1399   Affiliated   4402   Gulf Shores   Gulf Shores Dialysis Center   3947 GULF SHORES PKWY   UNIT 15   GULF SHORES   AL   36542-2737

 

Page 115 of 136


1400

  Affiliated   2496   Las Vegas Multi-Care Five Star   Five Star Dialysis Center (fka Las Vegas Multi-Care)   2400 TECH CENTER CT     LAS VEGAS   NV   89128-0804

1401

  Affiliated   4358   North Vernon   North Vernon Dialysis   2340 N STATE HWY 7     NORTH VERNON   IN   47265-7183

1402

  Affiliated   4316   Olympia   Olympia Dialysis Center   335 COOPER POINT RD NW   STE 15   OLYMPIA   WA   98502-4436

1403

  Affiliated   4335   Monroeville   Monroeville Dialysis   2690 MONROEVILLE BLVD     MONROEVILLE   PA   15146-2302

1404

  Affiliated   2317   East Galbraith   East Galbraith Dialysis   3877 E GALBRAITH RD   BLDG C   CINCINNATI   OH   45236-1500

1405

  Affiliated   2261   San Marcos   San Marcos Dialysis Center   2135 MONTIEL RD   BLDG B   SAN MARCOS   CA   92069-3511

1406

  Affiliated   4408   Winter Garden   Winter Garden Dialysis   1222 WINTER GARDEN VINELAND RD   BLDG 3 STE 1   WINTER GARDEN   FL   34787

1407

  Affiliated   1926   Bremer County Dialysis   Relo-Bremer County Dialysis (5022-Cedar Valley Waverly Dialysis)   220 10th ST SW     WAVERLY   IA   50677-2930

1408

  Affiliated   1927   Black Hawk Dialysis   Black Hawk Dialysis (Waterloo)   3421 W 9TH ST     WATERLOO   IA   50702-5401

1409

  Affiliated   2218   Downey Landing   Downey Landing Dialysis Center (aka Downey-Kaiser)   11611 BELLFLOWER BLVD     DOWNEY   CA   90241-5408

1410

  Affiliated   2427   Tucson Central   Tucson Central Dialysis   2901 E GRANT RD     TUCSON   AZ   85716-2717

1411

  Affiliated   4377   Hamburg   Hamburg Dialysis (fka Lexington)   1745 ALYSHEBA WAY     LEXINGTON   KY   40509-9013

1412

  Affiliated   2150   Midtown Norfolk   Midtowne Norfolk Dialysis (aka Ghent II)   2201 COLONIAL AVE     NORFOLK   VA   23517-1928

1413

  Affiliated   2394   Yonkers II   Yonkers East Dialysis Center   5 ODELL PLZ   STE 131   YONKERS   NY   10701-1406

1414

  Affiliated   2364   Caldwell   Caldwell Dialysis Center   821 S SMEED PKWY     CALDWELL   ID   83605-5130

1415

  Affiliated   2278   Hesperia   Hesperia Dialysis Center   14135 MAIN ST   UNIT 51   HESPERIA   CA   92345-8097

1416

  Affiliated   2339   Sealy   Sealy Dialysis   2242 CHAMPIONSHIP DR     SEALY   TX   77474-8026

1417

  Affiliated   2438   Hearne   Hearne Dialysis Center   106 CEDAR ST     HEARNE   TX   77859-2523

1418

  Affiliated   1998   Stockton Kidney Center   Stockton Kidney Center   1523 E MARCH LN   STE 2   STOCKTON   CA   95210-5607

1419

  Affiliated   5525   University of South Florida   USF Dialysis   10770 N 46TH ST STE A100     TAMPA   FL   33617-3465

1420

  Affiliated   4424   Westborough   Westborough Dialysis Center (fka South San Francisco, Daly City)   925 EL CAMINO REAL     SOUTH SAN FRANCISCO   CA   94080-3203

1421

  Affiliated   4359   Rush County   Rush County Dialysis   1400 N CHERRY ST     RUSHVILLE   IN   46173-1097

1422

  Affiliated   4339   Defuniak Springs   Defuniak Springs Dialysis   1045 US HWY 331 S   DEFUNIAK SHOPPING PLAZA   DEFUNIAK SPRINGS   FL   32435-3375

1423

  Affiliated   2181   Foster city   Foster City Dialysis (fka Belmont)   1261 E HILLSDALE BLVD   STE 2   FOSTER CITY   CA   94404-1236

1424

  Affiliated   4427   Red Bank   Redbank Village Dialysis (Cincinnati)   3960 RED BANK RD   STE 16   CINCINNATI   OH   45227-3421

1425

  Affiliated   4448   Southport   Southport Dialysis Center   1513 N HOWE ST   STE 15   SOUTHPORT   NC   28461-2770

1426

  Affiliated   4446   Orlando Park   Orlando Park Dialysis   5397 W COLONIAL DR   STE 12   ORLANDO   FL   32808-7647

1427

  Affiliated   4431   Harrisburg   Harrisburg Dialysis Center (aka Concord)   3310 PERRY ST     CONCORD   NC   28027-3901

1428

  Affiliated   2352   Waycross   Satilla River Dialysis   308 CARSWELL AVE     WAYCROSS   GA   31501-4762

1429

  Affiliated   4455   Timberlake   Timberlake Dialysis (Kansas City)   12110 HOLMES RD     KANSAS CITY   MO   64145-1707

1430

  Affiliated   4447   Dexter   Dexter Dialysis   2010 N OUTER RD     DEXTER   MO   63841

1431

  Affiliated   4426   Norwood   Norwood Dialysis (Cincinnati)   2300 WALL ST     CINCINNATI   OH   45212-2781

1432

  Affiliated   4420   Peachtree City   Peachtree City Dialysis   2830 W HWY 54   BLDG 1 STE J AND K   PEACHTREE CITY   GA   30269-1026

1433

  Affiliated   5516   Rogue Valley   Rogue Valley Dialysis   760 GOLF VIEW DR   UNIT 1   MEDFORD   OR   97504-9685

1434

  Affiliated   5517   Redwood Dialysis   Redwood Dialysis   201 SW L ST     GRANTS PASS   OR   97526-2913

1435

  Affiliated   4410   Tucker   Tucker Dialysis   4434 HUGH HOWELL RD     TUCKER   GA   30084-4905

1436

  Affiliated   4386   Shepherdsville   Shepherdsville Dialysis Center   150 BROOKS WAY   STE 15   BROOKS   KY   40109-6105

1437

  Affiliated   4399   Muscle Shoals   Muscle Shoals Dialysis   712 STATE ST     MUSCLE SHOALS   AL   35661-2940

1438

  Affiliated   2463   Tel Huron   Tel-Huron Dialysis (fka Waterford)   225 SUMMIT DR     WATERFORD   MI   48328-3364

1439

  Affiliated   2481   Cherry Valley   Cherry Valley Dialysis (aka Newark)   1627 W MAIN ST     NEWARK   OH   43055-1345

1440

  Affiliated   2437   Taylor   Taylor Dialysis   3100 W 2ND ST     TAYLOR   TX   76574

1441

  Affiliated   4430   Forrest City   Forrest City Dialysis   1501 N WASHINGTON ST     FORREST CITY   AR   72335-2152

1442

  Affiliated   4309   Kaufman   Kaufman Dialysis   2851 MILLENNIUM DR     KAUFMAN   TX   75142-8865

1443

  Affiliated   4348   Artesia   Artesia Dialysis   702 N 13TH ST     ARTESIA   NM   88210-1166

1444

  Affiliated   2381   North Hills   North Hills Dialysis   7927 BOULEVARD 26     NORTH RICHLAND HILLS   TX   76180-7103

1445

  Affiliated   4428   Millington   Millington Dialysis   8510 WILKINSVILLE RD   STE 121   MILLINGTON   TN   38053-1537

1446

  Affiliated   5519   Adams County   Adams County Dialysis   436 N 10TH ST     QUINCY   IL   62301-4152

1447

  Affiliated   5518   Hannibal   Hannibal Dialysis   3140 PALMYRA ROAD     HANNIBAL   MO   63401-2204

1448

  Affiliated   5520   Pittsfield   Pittsfield Dialysis   640 W WASHINGTON ST     PITTSFIELD   IL   62363-1350

1449

  Affiliated   4463   Villa of Waterbury   Villa of Waterbury (fka Kissker Microcenter)   929 WATERBURY FALLS DR     O’FALLON   MO   63368-2202

1450

  Affiliated   2465   Washington DC Nursing Facility   Washington DC Nursing Facility   2425 25TH ST SE     WASHINGTON   DC   20020-3408

1451

  Affiliated   4325   Moscow   Moscow Dialysis Center   212 RODEO DR   STE 11   MOSCOW   ID   83843-9798

1452

  Affiliated   2402   Chinook Kidney Center   Chinook Kidney Center (aka Richland)   1315 AARON DR   BLDG C1   RICHLAND   WA   99352-4678

1453

  Affiliated   4416   River’s Edge   Rivers Edge Dialysis (aka Athens)   1006 E STATE ST   STE B   ATHENS   OH   45701-2121

 

Page 116 of 136


1454

  Affiliated   5530   North Glendale Dialysis   North Glendale Dialysis   1505 WILSON TER STE 190     GLENDALE   CA   91206-4015

1455

  Affiliated   4373   Everett   Everett Dialysis Center (fka Snohomish 2)   8130 EVERGREEN WAY     EVERETT   WA   98203-6419

1456

  Affiliated   2069   Harbourview   Harbour View Dialysis (aka Churchland, Suffolk)   1039 CHAMPIONS WAY   BLDG 4   SUFFOLK   VA   23435-3761

1457

  Affiliated   4357   Capelville   Capelville Dialysis Center   7008 E SHELBY DR     MEMPHIS   TN   38125-3416

1458

  Affiliated   4485   San Leandro   San Leandro Dialysis (Bayfair Mall)   15555 E 14TH   STE 52   SAN LEANDRO   CA   94578-1900

1459

  Affiliated   4317   Mill Creek   Mill Creek Dialysis Center (Snohomish/Everett)   18001 BOTHELL EVERETT HWY   STE 112   BOTHELL   WA   98012-1661

1460

  Affiliated   2470   Seaview   Seaview Dialysis Center   101 18TH ST SE     LONG BEACH   WA   98631

1461

  Affiliated   2461   East Tampa   East Tampa Dialysis (Ybor City)   1701 E 9TH AVE     YBOR CITY   FL   33605-3801

1462

  Affiliated   5522   Detroit Road Dialysis   Detroit Road Dialysis   7901 DETROIT AVE     CLEVELAND   OH   44102-2828

1463

  Affiliated   5523   St V Quadrangle Dialysis   St V Quadrangle Dialysis   2302 COMMUNITY COLLEGE AVE     CLEVELAND   OH   44115-3117

1464

  Affiliated   5524   Westshore Dialysis   Westshore Dialysis   29000 CENTER RIDGE RD     WESTLAKE   OH   44145-5293

1465

  Affiliated   2468   Magnolia Dialysis Center Texas   Magnolia Dialysis Center   17649 FM 1488 RD     MAGNOLIA   TX   77354-5235

1466

  Affiliated   4471   Highland County   Highland County Dialysis (Hillsboro)   120 ROBERTS LN   STE 4   HILLSBORO   OH   45133-7608

1467

  Affiliated   4313   Rockwall   Rockwall Dialysis   2455 RIDGE RD   STE 11   ROCKWALL   TX   75087-5530

1468

  Affiliated   4354   Great Northern   Villa of Great Northern (fka North Olmsted)   22710 FAIRVIEW CENTER DR   STE 1   FAIRVIEW PARK   OH   44126-3607

1469

  Affiliated   2440   Ridgeland   Ridgeland Dialysis   112 WEATHERSBY ST     RIDGELAND   SC   29936-9514

1470

  Affiliated   2334   Livermore   Livermore Dialysis   3201 DOOLAN RD   STE 175   LIVERMORE   CA   94551-9605

1471

  Affiliated   2265   Westlake Daly city   Westlake Daly City Dialysis (fka Colma)   2201 JUNIPERO SERRA BLVD   STE 175   DALY CITY   CA   94014-1908

1472

  Affiliated   4488   12th Street Covington   12th Street Covington Dialysis   1500 JAMES SIMPSON JR WAY   STE 11   COVINGTON   KY   41011

1473

  Affiliated   4384   Bourbon County   Bourbon County Dialysis (fka Paris)   213 LETTON DR   PARIS TOWNE SQUARE   PARIS   KY   40361-2251

1474

  Affiliated   2499   Calverton   Calverton Dialysis   4780 CORRIDOR PL   STE C   BELTSVILLE   MD   20705-1165

1475

  Affiliated   2199   Aborn   Aborn Dialysis (fka East San Jose)   3162 S WHITE RD   STE 1   SAN JOSE   CA   95148-4019

1476

  Affiliated   4438   Clermont   Clermont County Dialysis (Milford,Goshen)   5901 MONTCLAIR BLVD   STE 1   MILFORD   OH   45150-2547

1477

  Affiliated   4365   Rita Ranch   Rita Ranch Dialysis (aka Tucson East II)   7355 S HOUGHTON RD   STE 11   TUCSON   AZ   85747-9379

1478

  Affiliated   4333   Wake Forest   Wake Forest Dialysis Center   11001 INGLESIDE PL     RALEIGH   NC   27614-8577

1479

  Affiliated   4472   Colonial Springs   Colonial Springs Dialysis (fka Powder Springs)   2840 EAST WEST CONNECTOR   STE 35   AUSTELL   GA   30106-6813

1480

  Affiliated   2474   Central Dallas   DaVita Central Dallas Dialysis   9500 N CENTRAL EXPY     DALLAS   TX   75231-5002

1481

  Affiliated   2188   Sanger   Sanger Sequoia Dialysis   2517 JENSEN AVE   BLDG B   SANGER   CA   93657-2251

1482

  Affiliated   4421   Conyers   Conyers Dialysis   1501 MILSTEAD RD NE     CONYERS   GA   30012-3838

1483

  Affiliated   4337   Duncanville   Duncanville Dialysis (Cedar Hill)   270 E HIGHWAY 67   STE 1   DUNCANVILLE   TX   75137-4428

1484

  Affiliated   4417   Gateway   Gateway Dialysis (Ft.Myers)   5705 LEE BLVD     LEHIGH ACRES   FL   33971-6342

1485

  Affiliated   4487   Derry   Derry Dialysis   1 ACTION BLVD   STE 2   LONDONDERRY   NH   03053-3428

1486

  Affiliated   4461   Villa of Wentzville Microcenter   Villa of Wentzville (Microcenter)   1126 W PEARCE BLVD   STE 116 & 118   WENTZVILLE   MO   63385-1053

1487

  Affiliated   1925   Buchanan County Dialysis   Buchanan County Dialysis (Independence)   1600 1ST ST E     INDEPENDENCE   IA   50644-3155

1488

  Affiliated   2450   Hoosier Hills   Hoosier Hills Dialysis   143 S KINGSTON DR     BLOOMINGTON   IN   47408-6342

1489

  Affiliated   4492   Palm Breeze   Palm Breeze Dialysis (fka North Port)   14942 TAMIAMI TRL   STE E   NORTH PORT   FL   34287-2705

1490

  Affiliated   4362   Big Oaks   Big Oaks Dialysis   5623 W TOUHY AVE     NILES   IL   60714-4019

1491

  Affiliated   4407   Pinellas West Shore   Pinellas West Shore Dialysis   3451 66TH ST N   STE A   ST PETERSBURG   FL   33710-1568

1492

  Affiliated   2267   Plano   Plano Dialysis   481 SHILOH RD   STE 1   PLANO   TX   75074-7231

1493

  Affiliated   4350   Fairview   Villa of Fairview Park (fka Fairview Park Dialysis)   19050 LORAIN RD     FAIRVIEW PARK   OH   44126-1915

1494

  Affiliated   2380   Ave Marisa   Ave Maria Dialysis (fka Immokalee)   5340 USEPPA DR     AVE MARIA   FL   34142-5051

1495

  Affiliated   5037   Warminster   Franklin Commons Dialysis (fka Warminster)   720 JOHNSVILLE BLVD   STE 8   WARMINSTER   PA   18974-3546

1496

  Affiliated   2446   Ripley   Ripley Dialysis Center   854 HWY 51 S     RIPLEY   TN   38063-5536

1497

  Affiliated   5538   St Charles / Riverbend   River Bend Dialysis (St. Charles Parish)   1057 PAUL MAILLARD RD   ST B135   LULING   LA   70070-4349

1498

  Affiliated   5570   Midwest Springfield   Midwest Springfield Dialysis   2200 N LIMESTONE ST STE 104     SPRINGFIELD   OH   45503-2692

1499

  Affiliated   5571   Midwest Fairborn   Midwest Fairborn Dialysis   1266 N BROAD ST     FAIRBORN   OH   45324-5549

1500

  Affiliated   5572   Midwest Urbana   Midwest Urbana Dialysis   1430 E US HIGHWAY 36     URBANA   OH   43078-9112

1501

  Affiliated   5531   Camarillo   Camarillo Dialysis   2438 N PONDEROSA DR STE C101     CAMARILLO   CA   93010-2465

1502

  Affiliated   5532   Thousand Oaks   Thousand Oaks Dialysis   375 ROLLING OAKS DR STE 100     THOUSAND OAKS   CA   91361-1024

1503

  Affiliated   5533   Simi Valley   Simi Valley Dialysis   2950 SYCAMORE DR STE 100     SIMI VALLEY   CA   93065-1210

1504

  Affiliated   5534   Santa Paula   Santa Paula Dialysis   253 MARCH ST     SANTA PAULA   CA   93060-2511

1505

  Affiliated   5548   Ventura   Ventura Dialysis   2705 LOMA VISTA RD STE 101     VENTURA   CA   93003-1596

1506

  Affiliated   4468   Villa of St. John   Villa of St John (Crossing Microcenter-MO)   9030 SAINT CHARLES ROCK RD     SAINT LOUIS   MO   63114-4246

1507

  Affiliated   4372   Whidbey Island   Whidbey Island Dialysis Center   32650 STATE RD 20   BLDG E STE 18   OAK HARBOR   WA   98277-2641

 

Page 117 of 136


1508

  Affiliated   4437   Baytown   Baytown Dialysis   4665 GARTH RD   STE 9   BAYTOWN   TX   77521-2261

1509

  Affiliated   2475   Highland Ranch   Highland Ranch Dialysis Center   7223 CHURCH ST STE A14     HIGHLAND   CA   92346-6837

1510

  Affiliated   4474   Tiptonville   Tiptonville Dialysis   795 HAMRA ST     TIPTONVILLE   TN   38079-1663

1511

  Affiliated   1902   Carabello   Carabello Dialysis Center   757 E WASHINGTON BLVD     LOS ANGELES   CA   90021-3016

1512

  Affiliated   5573   Palmetto   Palmetto Dialysis   317 PROFESSIONAL PARK RD     CLINTON   SC   29325-7625

1513

  Affiliated   5574   Greer South   Greer South Dialysis   3254 BRUSHY CREEK RD     GREER   SC   29650-1000

1514

  Affiliated   5575   Greenville West End   Greenville West End Dialysis   605 S ACADEMY ST     GREENVILLE   SC   29601-2407

1515

  Affiliated   5576   Fountain Inn   Fountain Inn Dialysis   298 CHAPMAN RD     FOUNTAIN INN   SC   29644-6129

1516

  Affiliated   5558   Sellersville   Sellersville Dialysis   1112 OLD BETHLEHEM PIKE     SELLERSVILLE   PA   18960-1423

1517

  Affiliated   5564   Humbolt Ridge   Humboldt Ridge Dialysis   2211 N HUMBOLDT BLVD     MILWAUKEE   WI   53212-3507

1518

  Affiliated   5565   West Appleton   West Appleton Dialysis   10130 W APPLETON AVE   STE 5   MILWAUKEE   WI   53225-2579

1519

  Affiliated   5566   Bay Shore   Bay Shore Dialysis   5650 N GREEN BAY AVE   STE 15   GLENDALE   WI   53209-4449

1520

  Affiliated   5567   South Ridge   South Ridge Dialysis   4848 S 76TH ST   STE 1   GREENFIELD   WI   53220-4361

1521

  Affiliated   5568   Bluemound   Bluemound Dialysis   601 N 99TH ST   STE 1   MILWAUKEE   WI   53226-4362

1522

  Affiliated   4385   Versailles   Versailles Dialysis   480 LEXINGTON RD     VERSAILLES   KY   40383-1918

1523

  Affiliated   5035   Magnolia Oaks   Magnolia Oaks Dialysis (aka Hinesville)   2377 HWY 196 W     HINESVILLE   GA   31313-8036

1524

  Affiliated   4489   Mesa County   Mesa County Dialysis (Grand Junction)   561 25 RD   STE D   GRAND JUNCTION   CO   81505-1303

1525

  Affiliated   297   West Bloomfield   West Bloomfield Dialysis   6010 W MAPLE RD   STE 215   WEST BLOOMFIELD   MI   48322-4406

1526

  Affiliated   5550   Crystal Springs Dialysis   Crystal Springs Dialysis   720 COG CIRCLE     CRYSTAL LAKE   IL   60014-7301

1527

  Affiliated   5551   Cobblestone Dialysis   Cobblestone Dialysis   934 CENTER ST   STE A   ELGIN   IL   60120-2125

1528

  Affiliated   5586   Oak Springs Dialysis   Oak Springs Dialysis   764 LOCUST AVE     WASHINGTON   PA   15301-2756

1529

  Affiliated   5010   Maple Valley Plaza   Maple Valley Plaza Dialysis (Farmington)   649 MAPLE VALLEY DR     FARMINGTON   MO   63640-1993

1530

  Affiliated   4433   Floyd Curl   Floyd Curl Dialysis (San Antonio)   9238 FLOYD CURL DR   STE 12   SAN ANTONIO   TX   78240-1691

1531

  Affiliated   2387   Mission Valley   Mission Valley Dialysis (aka McAllen)   1203 ST CLAIRE BLVD 9B     MISSION   TX   78572-6601

1532

  Affiliated   2180   Silver Lake   Silver Lake Dialysis   2723 W TEMPLE ST     LOS ANGELES   CA   90026-4723

1533

  Affiliated   5578   Lake Park Dialysis   Lake Park Dialysis   1531 E HYDE PARK BLVD     CHICAGO   IL   60615-3039

1534

  Affiliated   5579   Stoney Island Dialysis   Stony Island Dialysis   8725 S STONY ISLAND AVE     CHICAGO   IL   60617-2709

1535

  Affiliated   5580   Woodlawn Dialysis   Woodlawn Dialysis   1164 E 55TH ST     CHICAGO   IL   60615-5115

1536

  Affiliated   4440   Jefferson Ave   Jefferson Avenue Dialysis (aka Village Parkway, Hampton)   11234 JEFFERSON AVE     NEWPORT NEWS   VA   23601-2207

1537

  Affiliated   4381   Robinson   Robinson Dialysis   1215 N ALLEN ST   STE B   ROBINSON   IL   62454-1100

1538

  Affiliated   4320   Gateway Plaza   Gateway Plaza Dialysis (aka Willowbrook)   1580 W ROSECRANS AVE     COMPTON   CA   90222-3700

1539

  Affiliated   4329   Pasadena Foothills   Pasadena Foothills Dialysis (fka Arcadia)   3722 E COLORADO BLVD     PASADENA   CA   91107-3803

1540

  Affiliated   914   Live Oak Dialysis   Live Oak Dialysis (fka San Antonio)   6700 RANDOLPH BLVD   STE 11   LIVE OAK   TX   78233-4222

1541

  Affiliated   5031   Frackville   Frackville Dialysis (aka JV_Pottsville)   801 SCHUYLKILL MALL     FRACKVILLE   PA   17931-2524

1542

  Affiliated   5038   Castor   Cottman Kidney Center (Castor, NE Philadelphia)   7198 CASTOR AVE     PHILADELPHIA   PA   19149-1105

1543

  Affiliated   4351   Villa of North Ridgevelle   Villa of North Ridgeville   35143 CENTER RIDGE RD     NORTH RIDGEVILLE   OH   44039-3089

1544

  Affiliated   5503   Thorn Run Dialysis   Thorn Run Dialysis   1136 THORN RUN RD   STE J1   MOON TOWNSHIP   PA   15108

1545

  Affiliated   5504   Allegheny Valley   Allegheny Valley Dialysis   1620 PACIFIC AVE   HEIGHTS PLAZA SHOPPING CENTER   NATRONA HEIGHTS   PA   15065-2101

1546

  Affiliated   5506   Northside   Northside Dialysis (fka Allegheny General)   320 E NORTH AVE   4TH FL, SOUTH TOWER   PITTSBURGH   PA   15212-4756

1547

  Affiliated   5507   Somerset   Somerset County Dialysis   229 S KIMBERLY AVE   STE 1   SOMERSET   PA   15501-2022

1548

  Affiliated   4493   Carthage   Carthage Dialysis   165 SAVANNAH GARDENS DR     CARTHAGE   NC   28327

1549

  Affiliated   2464   Riverwood Dialysis   Riverwood Dialysis (fka Nine Mile, Tree City & Southfield)   24467 W 10 MILE RD     SOUTHFIELD   MI   48033-2931

1550

  Affiliated   4415   Burton   Burton Dialysis (fka Flint Northeast)   4015 DAVISON RD     BURTON   MI   48509-1401

1551

  Affiliated   4490   Black Canyon   Black Canyon Dialysis (Montrose)   3421 S RIO GRANDE AVE   UNIT D   MONTROSE   CO   81401-4840

1552

  Affiliated   4394   Memphis Midtown   Memphis Midtown Dialysis   3430 SUMMER AVE     MEMPHIS   TN   38122-3610

1553

  Affiliated   5539   Stonecrest Dialysis   Stonecrest Dialysis   1302 E STATE ST     ROCKFORD   IL   61104-2228

1554

  Affiliated   4412   West Plano   West Plano Dialysis   5036 TENNYSON PKWY     PLANO   TX   75024-3002

1555

  Affiliated   2217   Redwood City   Redwood City Dialysis (fka Palo Alto)   1000 MARSHALL ST     REDWOOD CITY   CA   94063-2027

1556

  Affiliated   1592   State Fair   State Fair Dialysis   19800 WOODWARD AVE     DETROIT   MI   48203-5102

1557

  Affiliated   5589   ADC of Ft Lauderdale   Advanced Dialysis Center of Fort Lauderdale   911 E OAKLAND PARK BLVD     OAKLAND PARK   FL   33334-2725

1558

  Affiliated   5008   Dover   Dover Community Dialysis (New Philadelphia)   899 E IRON AVE     DOVER   OH   44622-2097

1559

  Affiliated   5045   McMinnville   McMinnville Dialysis   200 NE NORTON LN     MCMINNVILLE   OR   97128-8470

1560

  Affiliated   5007   Sparta   Sparta Dialysis   150 SAM WALTON DR   STE 8   SPARTA   TN   38583-8818

1561

  Affiliated   4409   Kendall   Kendall Kidney Center (fka Dadeland)   8364 MILLS DR   STE 174   MIAMI   FL   33183-4806

 

Page 118 of 136


1562

  Affiliated   4397   Abbeville   Abbeville Dialysis   904 W GREENWOOD ST     ABBEVILLE   SC   29620

1563

  Affiliated   2453   Delta View   Delta View Dialysis   1150 E LELAND RD     PITTSBURG   CA   94565-5319

1564

  Affiliated   5013   Wolf River   Wolf River Dialysis (Germantown)   7990 TRINITY PL   STE 11   CORDOVA   TN   38018-7731

1565

  Affiliated   5601   San Luis Obispo Dialysis   San Luis Obispo Dialysis   1043 MARSH ST     SAN LUIS OBISPO   CA   93401-3629

1566

  Affiliated   5602   Templeton Dialysis   Templeton Dialysis   1310 LAS TABLAS RD   STE 11   TEMPLETON   CA   93465-9746

1567

  Affiliated   5603   Pismo Beach Dialysis   Pismo Beach Dialysis   320 JAMES WAY   STE 11   PISMO BEACH   CA   93449-2813

1568

  Affiliated   5583   Lincoln Way Dialysis   Lincoln Way Dialysis   1303 LINCOLN WAY STE A     WHITE OAK   PA   15131-1603

1569

  Affiliated   5023   Grundy Center   Grundy Center Dialysis   101 E J AVENUE     GRUNDY CENTER   IA   50638-2031

1570

  Affiliated   3862   Pickens County   Pickens County Dialysis   289 WILLIAM E HILL DR.   STE A   CARROLLTON   AL   35447

1571

  Affiliated   5032   Willow Grove   Willow Grove Dialysis (Abington-Maplewood)   1849 DAVISVILLE RD     WILLOW GROVE   PA   19090-4111

1572

  Affiliated   2255   Amherst   Amherst Dialysis (Lorain County)   3200 COOPER FOSTER PRK RD W     LORAIN   OH   44053-3654

1573

  Affiliated   2220   South Fort Worth   South Fort Worth Dialysis   6260 SOUTHWEST BLVD     BENBROOK   TX   76109-6906

1574

  Affiliated   5521   Jerseyville Dialysis   Jerseyville Dialysis   917 S STATE ST     JERSEYVILLE   IL   62052-2344

1575

  Affiliated   5605   Independence County Dialysis   Independence County Dialysis   1700 HARRISON ST   STE F   BATESVILLE   AR   72501-7315

1576

  Affiliated   5606   Jackson County Dialysis   Jackson County Dialysis   1912 MCLAIN ST   PRATT SQUARE   NEWPORT   AR   72112-3659

1577

  Affiliated   5607   Searcy Dialysis   Searcy Dialysis   3208 LANGLEY DR     SEARCY   AR   72143-6020

1578

  Affiliated   5608   Springhill Dialysis   Springhill Dialysis   3401 SPRINGHILL DR   STE 19   NORTH LITTLE ROCK   AR   72117-2925

1579

  Affiliated   5609   Pulaski County Dialysis   Pulaski County Dialysis   202 JOHN HARDEN DR     JACKSONVILLE   AR   72076-3775

1580

  Affiliated   5610   Little Rock Midtown Dialysis   Little Rock Midtown Dialysis   2 LILE CT   STE 12A   LITTLE ROCK   AR   72205-6241

1581

  Affiliated   5611   Saline County Dialysis   Saline County Dialysis   1200 N MAIN ST   STE 2   BENTON   AR   72015-3341

1582

  Affiliated   5612   Conway Dialysis   Conway Dialysis   2445 CHRISTINA LANE     CONWAY   AR   72034

1583

  Affiliated   5614   Valley Baptist Harlingen Dialysis   Valley Baptist-Harlingen Dialysis   2220 HAINE DR STE 40     HARLINGEN   TX   78550-8584

1584

  Affiliated   5615   Valley Baptist Raymondville Dialysis   Valley Baptist-Raymondville Dialysis   894 FM 3168     RAYMONDVILLE   TX   78580-4519

1585

  Affiliated   2455   Hawaiian Gardens   Hawaiian Gardens Dialysis   12191 226TH ST     HAWAIIAN GARDENS   CA   90716-1510

1586

  Affiliated   2310   Huntington park   Huntington Park Dialysis   5942 RUGBY AVE     HUNTINGTON PARK   CA   90255-2803

1587

  Affiliated   2462   Poinciana   Poinciana Dialysis   1002 CYPRESS PKWY     KISSIMMEE   FL   34758-3328

1588

  Affiliated   5005   Southtowns   Southtowns Dialysis (Hamburg)   4910 CAMP RD   STE 1   HAMBURG   NY   14075-2617

1589

  Affiliated   5635   Parma Heights Dialysis   Parma Heights Dialysis   9050 N CHURCH DR     PARMA HEIGHTS   OH   44130-4701

1590

  Affiliated   5636   Hillard Dialysis   Hilliard Dialysis   19133 HILLIARD BLVD     ROCKY RIVER   OH   44116-2907

1591

  Affiliated   5546   Pacific Dialysis   Pacific Dialysis   2351 CLAY ST   FL 4   SAN FRANCISCO   CA   94115-1931

1592

  Affiliated   5547   Davies Dialysis   Davies Dialysis   45 CASTRO ST   SOUTH TOWER 2ND FL   SAN FRANCISCO   CA   94114-1032

1593

  Affiliated   4486   Newburgh   Newburgh Dialysis   4311 HIGHWAY 261   STE A   NEWBURGH   IN   47630-2653

1594

  Affiliated   5052   Enterprise   Enterprise Dialysis (fka Geneva)   6002 BOLL WEEVIL CIRCLE     ENTERPRISE   AL   36330-9420

1595

  Affiliated   4387   State Line   State Line Dialysis   2049 E SHELBY DR     MEMPHIS   TN   38116-7639

1596

  Affiliated   5108   Cape Coral North   Cape Coral North Dialysis   1315 SE 8TH TERRACE     CAPE CORAL   FL   33990-3213

1597

  Affiliated   5044   Willard Ave   Willard Avenue Dialysis (Newington)   445E WILLARD AVE     NEWINGTON   CT   06111-2318

1598

  Affiliated   4363   West Lawn   West Lawn Dialysis (aka Midway)   7000 S PULASKI RD     CHICAGO   IL   60629-5842

1599

  Affiliated   4353   Villa of Lakewood   Villa of Lakewood (Northcoast)   14050 MADISON AVE     LAKEWOOD   OH   44107-4530

1600

  Affiliated   5054   North Carrolton   North Carrollton Dialysis (Parkview)   195 PARKWOOD CIRCLE     CARROLLTON   GA   30117-8756

1601

  Affiliated   5620   Sikeston Jaycee Regional Dialysis   Sikeston Jaycee Regional Dialysis   135 PLAZA DR STE 101     SIKESTON   MO   63801-5148

1602

  Affiliated   2244   Radcliff   Radcliff Dialysis   180 E LINCOLN TRAIL BLVD     RADCLIFF   KY   40160-1254

1603

  Affiliated   4452   McAfee   McAfee Dialysis (Candler Road Decatur)   1987 CANDLER RD   STE C   DECATUR   GA   30032-4212

1604

  Affiliated   5036   Avon   Avon Dialysis (Indy West)   9210 ROCKVILLE RD   STE D   INDIANAPOLIS   IN   46234-2669

1605

  Affiliated   2485   Anaheim West   Anaheim West Dialysis   1821 W LINCOLN AVE     ANAHEIM   CA   92801-6731

1606

  Affiliated   5043   Port Saint Joe   Port Saint Joe Dialysis   3871 HIGHWAY 98 E   STE 11   PORT ST. JOE   FL   32456-5318

1607

  Affiliated   5056   Hayward Mission Hills   Hayward Mission Hills Dialysis   1661 INDUSTRIAL PKWY W     HAYWARD   CA   94544-7046

1608

  Affiliated   2472   Cypress Woods Northwest   Cypress Woods Northwest Dialysis (aka NW Houston)   20320 NORTHWEST FWY   STE 1   HOUSTON   TX   77065-

1609

  Affiliated   5641   Willow Creek Dialysis   Willow Creek Dialysis   1139 WARWICK WAY     RACINE   WI   53406-5661

1610

  Affiliated   5642   Harbor View Dialysis   Harbor View Dialysis   818 6TH ST     RACINE   WI   53403-1176

1611

  Affiliated   4451   Red River   Red River Dialysis (fka Shreveport South)   9205 LINWOOD AVE     SHREVEPORT   LA   71106-7006

1612

  Affiliated   2392   South Dade Kidney Center   South Dade Kidney Center (Coral Reef)   11040 SW 184TH ST     CUTLER BAY   FL   33157-6602

1613

  Affiliated   5604   Niagara Falls Memorial Dialysis   Niagara Falls Memorial Dialysis (was NF Kidney Care Center)   621 10TH ST     NIAGARA FALLS   NY   14301-1813

1614

  Affiliated   5617   Silverado Dialysis   Silverado Dialysis   1100 TRANCAS ST   STE 266 AND 267   NAPA   CA   94558-2921

1615

  Affiliated   5621   Prairie River Dialysis   Prairie River Dialysis   601 S CENTER AVE     MERRILL   WI   54452-3404

 

Page 119 of 136


1616

  Affiliated   5622   Stevens Point Dialysis   Stevens Point Dialysis   900 ILLINOIS AVE   5th FLR   STEVENS POINT   WI   54481-2885

1617

  Affiliated   5623   Grand Seasons Dialysis   Grand Seasons Dialysis   190 GRAND SEASONS DR     WAUPACA   WI   54981-8219

1618

  Affiliated   5624   Wausau Dialysis   Wausau Dialysis   2600 STEWART AVE   STE 144   WAUSAU   WI   54401-1403

1619

  Affiliated   5625   Pine Crest Dialysis   Pine Crest Dialysis   232 S COURTNEY ST   STE 2   RHINELANDER   WI   54501-3319

1620

  Affiliated   5626   Meadow Lane Dialysis   Meadow Lane Dialysis   1120 PINE ST     STANLEY   WI   54768-1297

1621

  Affiliated   5627   Wisconsin Rapids Dialysis   Wisconsin Rapids Dialysis   1041B HILL ST     WISCONSIN RAPIDS   WI   54494-5221

1622

  Affiliated   5628   Marshfield Dialysis   Marshfield Dialysis   123 NORTHRIDGE ST     MARSHFIELD   WI   54449-8341

1623

  Affiliated   5629   Northern Star Dialysis   Northern Star Dialysis   311 ELM ST     WOODRUFF   WI   54568-9190

1624

  Affiliated   5632   Ames Mary Greeley Dialysis   Ames Mary Greeley Dialysis   2322 E 13TH ST     AMES   IA   50010-5669

1625

  Affiliated   5633   Marshalltown Mary Greeley Dialysis   Marshalltown Mary Greeley Dialysis   3120 S 2ND ST     MARSHALLTOWN   IA   50158-4614

1626

  Affiliated   5634   Iowa Falls Mary Greeley Dialysis   Iowa Falls Mary Greeley Dialysis   701 WASHINGTON AVE     IOWA FALLS   IA   50126-2100

1627

  Affiliated   5649   Dialysis Center of Hutchinson   Dialysis Center of Hutchinson   1901 N WALDRON ST     HUTCHINSON   KS   67502-1129

1628

  Affiliated   5650   Amarillo Dialysis   Amarillo Dialysis   8604 S COULTER ST     AMARILLO   TX   79119-7379

1629

  Affiliated   4495   Sagemeadow   Sagemeadow Dialysis (Houston)   10923 SCARSDALE BLVD     HOUSTON   TX   77089-6024

1630

  Affiliated   5009   McKinney   McKinney Dialysis   4717 MEDICAL CENTER DR     MCKINNEY   TX   75069-1870

1631

  Affiliated   4499   Scottsburg   Scottsburg Dialysis   1619 W MCCLAIN AVE     SCOTTSBURG   IN   47170-1161

1632

  Affiliated   2108   Snake River   Snake River Dialysis Center (fka Blackfoot)   1491 PARKWAY DR     BLACKFOOT   ID   83221-1667

1633

  Affiliated   5034   Southpoint   Southpoint Dialysis (aka Durham South)   415 W NC HWY 54     DURHAM   NC   27713-7516

1634

  Affiliated   5643   Burlingame Dialysis   Burlingame Dialysis   1720 EL CAMINO REAL   STE 12   BURLINGAME   CA   94010-3225

1635

  Affiliated   5644   Mills Dialysis   Mills Dialysis   100 S SAN MATEO DR     SAN MATEO   CA   94401-3805

1636

  Affiliated   5646   Stuebenville   Steubenville Dialysis   4000 JOHNSON RD     STEUBENVILLE   OH   43952-2300

1637

  Affiliated   5656   Premiere Kidney Center of Newark   Premiere Kidney Center of Newark   65 SOUTH TERRACE AVE     NEWARK   OH   43055-1355

1638

  Affiliated   5029   Calvine   Calvine Dialysis (Sacramento)   8243 E STOCKTON BLVD   STE 1   SACRAMENTO   CA   95828-8200

1639

  Affiliated   4445   Durham Corners dialysis   Durham Corners Dialysis (South Plainfield)   241 DURHAM AVE     SOUTH PLAINFIELD   NJ   07080-2504

1640

  Affiliated   4475   Mt Morris   Mt Morris Dialysis (aka North Flint)   6141 N. SAGINAW RD     MOUNT MORRIS   MI   48458-2403

1641

  Affiliated   2176   Grandview   Grandview Dialysis   13812 S US HIGHWAY 71     GRANDVIEW   MO   64030-3685

1642

  Affiliated   4450   Lemoore   Lemoore Dialysis   1345 W BUSH ST     LEMOORE   CA   93245-3303

1643

  Affiliated   5663   Middlebrook Dialysis   Middlebrook Dialysis   12401 MIDDLEBROOK RD   STE 16   GERMANTOWN   MD   20874-1523

1644

  Affiliated   5664   Catoctin Dialysis   Catoctin Dialysis   405 W 7TH ST     FREDERICK   MD   21701-4505

1645

  Affiliated   5648   Central New York Dialysis Center   Central New York Dialysis Center   910 ERIE BLVD E     SYRACUSE   NY   13210-1060

1646

  Affiliated   5014   South Jackson   South Jackson Dialysis   46 HARTS BRIDGE RD     JACKSON   TN   38301-7512

1647

  Affiliated   2344   Los Alamitos   Los Alamitos Dialysis   4141 KATELLA AVE     LOS ALAMITOS   CA   90720-3406

1648

  Affiliated   5048   Robbinsdale   Robbinsdale Dialysis   3461 W BROADWAY AVE     ROBBINSDALE   MN   55422-2955

1649

  Affiliated   5557   Oxnard   Oxnard Dialysis   1900 OUTLET CENTER DR     OXNARD   CA   93036-0677

1650

  Affiliated   4429   Marked Tree   DNVO-Marked Tree-AR   216 HESTER PARKER DR     MARKED TREE   AR   72365-2023

1651

  Affiliated   5669   Louisa Dialysis   Louisa Dialysis   2145 HWY 2565     LOUISA   KY   41230

1652

  Affiliated   5670   Point Pleasant Dialysis   Point Pleasant Dialysis   3683 OHIO RIVER DR     POINT PLEASANT   WV   25550

1653

  Affiliated   6802   Marion   Renal Care of Marion (P150)   2921 HWY 77   SUITE #8   MARION   AR   72364-2368

1654

  Affiliated   6803   Osceola   Osceola Dialysis (P151)   1420 W KEISER AVE     OSCEOLA   AR   72370-2800

1655

  Affiliated   6805   Cottonwood   Cottonwood Dialysis (P153)   203 S CANDY LANE     COTTONWOOD   AZ   86326-8115

1656

  Affiliated   6808   Prescott   Prescott Dialysis (P157)   980 WILLOW CREEK RD.   SUITE 11   PRESCOTT   AZ   86301-1619

1657

  Affiliated   6811   Naples   Collier County Dialysis (P160)   6625 HILLWAY CIRCLE     NAPLES   FL   34112

1658

  Affiliated   6813   Catersville   Cartersville Renal Center (P162)   203 S TENNESSEE ST     CARTERSVILLE   GA   30120

1659

  Affiliated   6816   Arlington Heights Renal Center   Arlington Heights Renal Center (P165)   17 W GOLF RD     ARLINGTON HEIGHTS   IL   60006

1660

  Affiliated   6817   Hazel Crest Renal Center   Hazel Crest Renal Center (P166)   3470 W 183RD ST     HAZEL CREST   IL   60429

1661

  Affiliated   6818   Loop Renal Center   Loop Renal Center (P167)   1101 S CANAL ST   11TH FLR   CHICAGO   IL   60607

1662

  Affiliated   6819   Markham Renal Center   Markham Renal Center (P168)   3053 W 159TH ST     MARKHAM   IL   60426

1663

  Affiliated   6821   South Holland Renal Center   South Holland Renal Center (P170)   16136 S PARK AVE.     SOUTH HOLLAND   IL   60473

1664

  Affiliated   6822   Waukegan Renal Center   Waukegan Renal Center (P171)   1616 GRAND AVE.   STE. C   WAUKEGAN   IL   60085

1665

  Affiliated   6936   Waukegan Home Renal Center   Waukegan Home Training (P172)   1616 GRAND AVE   STE F   WAUKEGAN   IL   60085

1666

  Affiliated   6825   Baton Rouge   East Baton Rouge Dialysis (P174)   1333 ONEAL LANE     BATON ROUGE   LA   70816

1667

  Affiliated   6826   Houma Renal Center   Houma Dialysis (P175)   108 PICONE RD     HOUMA   LA   70363

1668

  Affiliated   6827   Amesbury   Amesbury Renal Center (P177)   24 MORRILL PLACE     AMESBURY   MA   1913

1669

  Affiliated   6828   North Andover   North Andover Renal Center (P178)   201 SUTTON ST     NORTH ANDOVER   MA   1845

 

Page 120 of 136


1670

  Affiliated   6829   Canton   Canton Renal Center (P179)   620 E PEACE ST     CANTON   MS   39046-4729

1671

  Affiliated   6830   Hazelhurst   Hazlehurst Dialysis (P180)   201 N HALEY ST     HAZLEHURST   MS   39083

1672

  Affiliated   6831   Jackson North   Jackson North Dialysis (P181)   571 BEASLEY RD   SUITE B   JACKSON   MS   39206-3042

1673

  Affiliated   6832   Jackson South   Jackson South Dialysis (P182)   2460 TERRY RD   SUITE 27-J   JACKSON   MS   39204-5767

1674

  Affiliated   6833   Jackson Southwest   Jackson Southwest Dialysis (P183)   1828 RAYMOND RD     JACKSON   MS   39204-4126

1675

  Affiliated   6834   Lexington   Renal Care of Lexington (P184)   22579 DEPOT STREET     LEXINGTON   MS   39095

1676

  Affiliated   6835   Munroe Falls   Munroe Falls Dialysis (P185)   265 N MAIN ST     MUNROE FALLS   OH   44262

1677

  Affiliated   6836   Summit   Summit Renal Center (P186)   73 MASSILLON ROAD     AKRON   OH   44312

1678

  Affiliated   6837   White Ponds   White Ponds Dialysis (P187)   534 WHITE POND DRIVE   SUITE A   AKRON   OH   44320

1679

  Affiliated   6838   Philadelphia   Memphis Street Renal Center (P189)   3310 24 MEMPHIS ST     PHILADELPHIA   PA   19134-4510

1680

  Affiliated   6839   Memphis Central Renal Center   Renal Care of Central Memphis (P190)   1331 UNION AVE.   SUITE 11   MEMPHIS   TN   38104-7559

1681

  Affiliated   6840   Memphis Graceland Renal Center   Memphis Graceland Renal Center (P191)   4180 AUBURN RD     MEMPHIS   TN   38116-6202

1682

  Affiliated   6841   Memphis Midtown Renal Center   Renal Care of Midtown Memphis (P192)   1166 MONROE AVE.     MEMPHIS   TN   38104-6614

1683

  Affiliated   6842   Memphis North Renal Center   Renal Care of Memphis North (P193)   4913 RALEIGH COMMON DR.   SUITE 1   MEMPHIS   TN   38128-2485

1684

  Affiliated   6844   Whitehaven Renal Center   Whitehaven Renal Center (P195)   3420 ELVIS PRESLEY BLVD.     MEMPHIS   TN   38116-3260

1685

  Affiliated   6846   Edinburg   Edinburg Renal Center (P197)   4302 S SUGAR RD   STE 15   EDINBURG   TX   78539-9140

1686

  Affiliated   6847   Mcallen   Dialysis Care of McAllen (P198)   411 LINDBERG AVE     MCALLEN   TX   78501-2921

1687

  Affiliated   6848   Weslaco   Weslaco Renal Center (P199)   910 SOUTH UTAH     WESLACO   TX   78596-4270

1688

  Affiliated   6849   Marlton Dialysis Center   Marlton Dialysis (P200)   769 E ROUTE 70     MARLTON   NJ   08053-2341

1689

  Affiliated   6850   Lawrenceville Renal Center   Lawrenceville Renal Center (P201)   1840 PRINCETON AVE     LAWRENCEVILLE   NJ   8648

1690

  Affiliated   6851   Austell Renal Center   Austell Renal Center (P202)   3642 MARATHON CIRCLE     AUSTELL   GA   30106- 6821

1691

  Affiliated   6852   Bartlett Renal Center   Bartlett Renal Center (P203_P290_P8203)   2920 COVINGTON PIKE     MEMPHIS   TN   38128-6007

1692

  Affiliated   6854   Beaverton Dialysis Center   Beaverton Dialysis Center (P206)   15050 SW KOLL PARKWAY   SUITE J   BEAVERTON   OR   97006-6002

1693

  Affiliated   6858   Walker County Dialysis   Walker County Dialysis (P212)   589 HIGHWAY 78W     JASPER   AL   35501

1694

  Affiliated   6861   Lakewood   Manatee County Dialysis (P215)   8470 COOPER CREEK BVLD     UNIVERSITY PARK   FL   34201

1695

  Affiliated   6862   Canton   Northwest Georgia Dialysis (P216)   260 HOSPITAL RD     CANTON   GA   30114

1696

  Affiliated   6863   Buffulo Grove Renal Center   Buffalo Grove Dialysis (P218)   1291 W DUNDEE RD     BUFFALO GROVE   IL   60089

1697

  Affiliated   6864   Evanston Renal Center   Evanston Renal Center (P219)   1715 CENTRAL ST     EVANSTON   IL   60201

1698

  Affiliated   6865   Schaumburg Renal Center   Schaumburg Renal Center (P220)   1156 S. ROSELLE ROAD     SCHAUMBURG   IL   60193

1699

  Affiliated   6937   Schaumburg Home Renal Center   Schaumburg Home Training (P270)   17 W GOLF RD     ARLINGTON HEIGHTS   IL   60005

1700

  Affiliated   6866   Blue River Valley   Blue River Valley Renal Center (P222)   2309 S MILLER STREET   SUITE 1   SHELBYVILLE   IN   46176-9350

1701

  Affiliated   6867   Central Fort Wayne   Central Fort Wayne Dialysis (P223)   1940 BLUFTON RD     FORT WAYNE   IN   46809-1307

1702

  Affiliated   6869   Huntington   Renal Care of Huntington (P225)   3040 WEST PARK DRIVE     HUNTINGTON   IN   46750-8956

1703

  Affiliated   6870   Lake Avenue Dialysis Renal Center   Lake Avenue Dialysis (P226)   3525 LAKE AVE   STE 4   FORT WAYNE   IN   46805-5545

1704

  Affiliated   6871   Marion County   Marion County Dialysis (P229)   3834 S EMERSON AVE   BLDG B   INDIANAPOLIS   IN   46203-5902

1705

  Affiliated   6873   Quad Counties Dialysis   Quad Counties Dialysis (P232)   528 NORTH GRANDSTAFF     AUBURN   IN   46706-1660

1706

  Affiliated   6875   South Anthony   South Anthony Dialysis (P234)   7017 SOUTH ANTHONY BLVD.     FORT WAYNE   IN   46816-2016

1707

  Affiliated   6876   Brandon   Brandon Renal Center (P235)   101 CHRISTIAN DR     BRANDON   MS   39042-2678

1708

  Affiliated   6877   Carthage   Renal Care of Carthage (P236)   312 ELLIS STREET     CARTHAGE   MS   39051

1709

  Affiliated   6878   Las Cruces Renal Center   Las Cruces Renal Center (P237)   3961 E LOHMAN AVE   STE 29   LAS CRUCES   NM   88011-8272

1710

  Affiliated   6879   Northeast Portland   Northeast Portland Renal Center (P240)   703 NE HANCOCK ST     PORTLAND   OR   97212-3955

1711

  Affiliated   6880   Oregon Kidney Center   Dialysis Care of Portland (P241)   5318 NE IRVING     PORTLAND   OR   97213

1712

  Affiliated   6881   Sunnyside   Sunnyside Renal Center (P242)   6902 SE LAKE ROAD   SUITE 1   MILWAUKIE   OR   97267-2148

1713

  Affiliated   6882   Willamette Valley   Williamette Valley Renal Center (P243)   1510 DIVISION STREET   SUITE 9   OREGON CITY   OR   97045-1572

1714

  Affiliated   6883   Northern Philadelphia   Northern Philadelphia Dialysis (P244)   5933 N BROAD ST     PHILADELPHIA   PA   19141

1715

  Affiliated   6884   North Providence Renal Center   North Providence Renal Center (P246)   1635 MINERAL SPRING AVE     NORTH PROVIDENCE   RI   02904-4025

1716

  Affiliated   6889   Alice Renal Center   Alice Renal Center (P252)   2345 ALICE REGIONAL BLVD.     ALICE   TX   78332-7291

1717

  Affiliated   6890   Beeville Renal Center   Beeville Renal Center (P253)   1905 NW FRONTAGE     BEEVILLE   TX   78102-2954

1718

  Affiliated   6891   Brownsville   Brownsville Renal Center (P254)   2945 CENTRAL BLVD     BROWNSVILLE   TX   78520-8958

1719

  Affiliated   6892   Corpus Christi Renal Center   Corpus Christi Dialysis (P255)   2733 SWANTNER DR     CORPUS CHRISTI   TX   78404-2832

1720

  Affiliated   6893   Riverside Renal Center   Riverside Renal Center (P256)   13434 LEOPARD RD. SUITE A17     CORPUS CHRISTI   TX   78410-4466

1721

  Affiliated   6894   South Texas Renal Center   South Texas Renal Center (P257)   4301 S PADRE ISLAND DR     CORPUS CHRISTI   TX   78411-4433

1722

  Affiliated   6896   South Central Renal Center   Morgan Avenue Dialysis (P258)   2222 S MORGAN AVE   SUITE 114   CORPUS CHRISTI   TX   78405-1900

1723

  Affiliated   6898   Northeast Texas   Dialylsis Care of Greenville (P260)   4805 WESLEY ST     GREENVILLE   TX   75401-5649

 

Page 121 of 136


1724

  Affiliated   6899   Downtown Spokane   Downtown Spokane Renal Center (P261)   601 W 5TH ST   SUITE F   SPOKANE   WA   99205

1725

  Affiliated   6900   North Spokane   North Spokane Renal Center (P262)   12610 E MARIBEAU PRKWY   STE 1   SPOKANE   WA   99216

1726

  Affiliated   6901   Spokane Valley   Spokane Valley Renal Center (P263)   12610 EAST MIRABEAU PKY   SUITE 1   SPOKANE   WA   99208-1450

1727

  Affiliated   6902   Kansas City   Kansas City Renal Center (P264)   4333 MADISON AVE     KANSAS CITY   MO   64111-3429

1728

  Affiliated   6903   Butler Renal Center   Butler Renal Center (P266)   601 W NURSERY     BUTLER   MO   64730

1729

  Affiliated   6904   Harrisonville   Harrisonville Renal Center (P267)   308 GALAXIE AVE     HARRISONVILLE   MO   64701-2084

1730

  Affiliated   6905   Marshall Renal Center   Marshall Renal Center (P268)   359 W MORGAN     MARSHALL   MO   65340

1731

  Affiliated   6907   Akron Renal Center   Akron Renal Center (P272)   525 EAST MARKET STREET     AKRON   OH   44304-1619

1732

  Affiliated   6908   Kendallville Renal Center   Kendallville Renal Center (P274)   602 SAWYER RD     KENDALLVILLE   IN   46755- 2566

1733

  Affiliated   6909   Greenwood Holly Renal Center   Greenwood Holly Renal Center (P276)   1533 HOLLY RD     CORPUS CHRISTI   TX   78417-2010

1734

  Affiliated   6910   Plainfield Renal Center   Plainfield Renal Center (P278)   8110 NETWORK DR     PLAINFIELD   IN   46168-9024

1735

  Affiliated   6911   Green Valley Renal Center   Green Valley Dialysis (P279)   1489 W WARM SPRINGS RD   STE 122   HENDERSON   NV   89014-7637

1736

  Affiliated   6912   Las Vegas Renal Center   Las Vegas Renal Center (P280)   2333 RENAISSANCE DR     LAS VEGAS   NV   89119-6191

1737

  Affiliated   6913   Lees Summit Renal Center   Lees Summit Renal Center (P281)   100 NE MISSOURI RD   STE 1   LEE’S SUMMIT   MO   64086-4702

1738

  Affiliated   6914   Westport Renal Center   Westport Renal Center (P282)   3947 BROADWAY STREET     KANSAS CITY   MO   64111-2516

1739

  Affiliated   6915   Greensboro Dialysis Center   Greensboro Dialysis Center (P284)   1220 SILOAM RD     GREENSBORO   GA   30642-0390

1740

  Affiliated   5057   Forest Landing   DNVO-Forest Landing Dialysis (Harford Cty, Havre de Grace)-MD   2220 COMMERCE AVE   STE 1   FOREST HILL   MD   21050

1741

  Affiliated   5033   University City   DNVO-University City Dialysis (Philadelphia)-PA   3020 MARKET ST   STE 13   PHILADELPHIA   PA   19104-2999

1742

  Affiliated   2411   Parkland   DNVO-Parkland Dialysis-WA   311 140TH ST SO     TACOMA   WA   98444

1743

  Affiliated   5094   Shelbyville Road   DNVO JV-Shelbyville Road Dialysis (DuPont, Louisville)-KY   4600 SHELBYVILLE RD   STE 31   LOUISVILLE   KY   40207

1744

  Affiliated   5106   Fort Wayne West Dialysis   DNVO JV-Fort Wayne South-IN   302 E PETTIT AVE     FORT WAYNE   IN   468063007

1745

  Affiliated   5671   Suburban Dialysis   ACQ-5671-NY   1542 MAPLE RD     WILLIAMSVILLE   NY   14221

1746

  Affiliated   5672   Gates Circle Dialysis   ACQ-5672-NY   3 GATES CIRCLE   1ST FLR   BUFFALO   NY   14209

1747

  Affiliated   5673   Orchard Park Dialysis   ACQ-5673-NY   3801 TAYLOR RD     ORCHARD PARK   NY   14127

1748

  Affiliated   2420   TC Jester   DNVO-TC Jester-TX   1800 W 26TH ST   STE 11   HOUSTON   TX   77008-1419

1749

  Affiliated   4436   Champions   DNVO-Champions Dialysis (Houston)-TX   4427 FM 1960 W   STE D   HOUSTON   TX   77068-3409

1750

  Affiliated   5083   Magic City Dialysis MMC   DNVO-Magic City Dialysis (Birmingham)-AL   300 22ND ST SO     BIRMINGHAM   AL   35233-2209

1751

  Affiliated   5084   Steel City Dialysis   DNVO-Steel City Dialysis (Birmingham)-AL   1809 AVE H (ENSLEY)     BIRMINGHAM   AL   35218

1752

  Affiliated   5081   Jewel Dialysis   DNVO-Jewel Dialysis (Camellia, Birmingham)-AL   514 WEST TOWN PLAZA     BESSEMER   AL   35020

1753

  Affiliated   660   Crystal River   Crystal River Dialysis   7435 W GULF TO LAKE HWY     CRYSTAL RIVER   FL   34429-7834

1754

  Affiliated   1936   Southwest Kidney   Estrella Dialysis Center   8410 W THOMAS RD   STE 1 BLDG 1   PHOENIX   AZ   85037-3356

1755

  Affiliated   1937   Gilbert Dialysis   Gilbert Dialysis Center   5222 E BASELINE RD   STE 14   GILBERT   AZ   85234-2963

1756

  Affiliated   1938   Tempe Dialysis   Tempe Dialysis Center   2149 E WARNER RD   STE 11   TEMPE   AZ   85284-3496

1757

  Affiliated   1939   Phoenix Dialysis   Phoenix Dialysis Center   337 E CORONADO RD   STE 11   PHOENIX   AZ   85004-1582

1758

  Affiliated   1949   Arrowhead Lakes Dialysis   Arrowhead Lakes Dialysis   20325 N 51ST AVE   BLDG 11, STE 186   GLENDALE   AZ   85308-4625

1759

  Affiliated   1952   Mountain Vista Dialysis   Mountain Vista Dialysis Center of Arizona   10238 E HAMPTON AVE   STE 18   MESA   AZ   85209-3317

1760

  Affiliated   1977   South Meadows Dialysis Center   South Meadows Dialysis Center   10085 DOUBLE R BLVD   STE 16   RENO   NV   89521-4867

1761

  Affiliated   1978   Reno Dialysis Center   Reno Dialysis Center   1500 E 2ND ST   STE 11   RENO   NV   89502-1189

1762

  Affiliated   1979   Carson City Dialysis Center   Carson City Dialysis Center   3246 N. CARSON ST   STE 11   CARSON CITY   NV   89706-0248

1763

  Affiliated   844   Sparks   Sparks Dialysis Center   4860 VISTA BLVD   STE 1   SPARKS   NV   89436-2817

1764

  Affiliated   2015   Sierra Rose Dialysis   Sierra Rose Dialysis Center   685 SIERRA ROSE DR     RENO   NV   89511-2060

1765

  Affiliated   2325   Northwest Tucson   Northwest Tucson Dialysis   2945 W INA RD   STE 15   TUCSON   AZ   85741-2366

1766

  Affiliated   4355   Mesa   Central Mesa Dialysis Center   1134 E UNIVERSITY DR   STE 11   MESA   AZ   85203-8048

1767

  Affiliated   4371   Raven   Raven Dialysis Center   3540 E BASELINE RD   STE 11   PHOENIX   AZ   85042-9628

1768

  Affiliated   4374   Brookwood   Brookwood Dialysis Center   8910 N 43RD AVE   STE 17   GLENDALE   AZ   85302-5340

1769

  Affiliated   4405   Ocotillo   Ocotillo Dialysis   975 W CHANDLER HEIGHTS RD   UNIT 11   CHANDLER   AZ   85248-5724

1770

  Affiliated   4364   Maryvale   Maryvale Dialysis Center   4845 W MCDOWELL RD   STE 1A, 2A, 3A   PHOENIX   AZ   85035-4076

1771

  Administrative Services   181   Childrens Hospital   MGD-Children’s National Medical Center   111 MICHIGAN AVE NW     WASHINGTON   DC   20010-2916

1772

  Administrative Services   1624   Renal Care Seat Pleasant   MGD-Renal Care of Seat Pleasant   6274 CENTRAL AVE     SEAT PLEASANT   MD   20743

1773

  Administrative Services   1715   Moses Taylor Hospital Renal Unit   Moses Taylor Hospital Renal Unit   700 QUINCY AVE     SCRANTON   PA   18510-1724

1774

  Administrative Services   3330   Aurora Medical Group - Fond du Lac   Aurora Medical Group-Fond du Lac   210 WISCONSIN AMERICAN DR   ATTN DAVITA DIALYSIS (WEST END OF BLDG)   FOND DU LAC   WI   54937-2999

1775

  Administrative Services   3331   Aurora Medical Group - Sheboygan   Aurora Medical Group-Sheboygan   2414 KOHLER MEMORIAL DR     SHEBOYGAN   WI   53081-3129

1776

  Administrative Services   3338   Aurora Medical Group - Lake Geneva   Aurora Medical Group-Lake Geneva   146 E GENEVA SQ     LAKE GENEVA   WI   53147-9694

1777

  Administrative Services   3555   Aurora Medical Group - Marinette Dialysis   Aurora Medical Group-Marinette Dialysis   4061 OLD PESHTIGO RD     MARINETTE   WI   54143

 

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1778

  Administrative Services   3607   Aurora Medical Group - Brown County Dialysis   Aurora Medical Group-Brown County Dialysis   1751 DECKNER AVE     GREEN BAY   WI   54302-2630

1779

  Administrative Services   3641   Aurora Medical Group - Sturgeon Bay Dialysis   Aurora Medical Group-Sturgeon Bay Dialysis   108 S 10TH AVE     STURGEON BAY   WI   54235-1802

1780

  Administrative Services   3653   Aurora Medical Group - Oshkosh West Dialysis   Aurora Medical Group-Oshkosh West Dialysis   855 N WESTHAVEN DR     OSHKOSH   WI   54904-7668

1781

  Administrative Services   3665   Aurora Medical Group - Manitowoc Dialysis   Aurora Medical Group-Manitowoc Dialysis   601 REED AVE     MANITOWOC   WI   54220-2026

1782

  Administrative Services   3672   Aurora Medical Group - Wautoma Dialysis   Aurora Medical Group-Wautoma Dialysis   900 EAST DIVISION ST     WAUTOMA   WI   54982-6944

1783

  Administrative Services   1868   Maize Dialysis   Maize Dialysis Center   10001 GRADY AVE     MAIZE   KS   67101

1784

  Administrative Services   1912   Kidney Dialysis Center   MGD-Kidney Dialysis Center, LLC (MMG Macon)   640 MARTIN LUTHER KING JR BLVD     MACON   GA   31201-3206
  Administrative Services   6079   MAGNOLIA WEST AT HOME   Magnolia West At Home   11161 MAGNOLIA AVE   STE B   RIVERSIDE   CA   92505-3605
  Administrative Services   1903   Riverside PD Central NAMG   Riverside PD Central   3660 PARK SIERRA DR   STE 18   RIVERSIDE   CA   92505-3071
  Affiliated   1995   Winter Park Home PD Dialysis   Winter Park Home PD Dialysis   4100 METRIC DR   STE 2   WINTER PARK   FL   32792-6832
  Affiliated   4302   Lockport HHD PD At Home   Lockport Home Dialysis-PD   16626 W 159TH ST   STE 73   LOCKPORT   IL   60441-8019
  Affiliated   1972   HHD 6183 and PD 1972 in Shreveport   Shreveport Home Dialysis PD   1560 IRVING PL     SHREVEPORT   LA   71101-4604
  Affiliated   5618   Home Dialysis of Dayton – South   Home Dialysis of Dayton-South   4700 SPRINGBORO PIKE   STE 3   MORAINE   OH   45439-1964
  Affiliated   5619   Home Dialysis of Dayton   Home Dialysis of Dayton   627 S EDWIN C MOSES BLVD   STE 2B   DAYTON   OH   45417-3474
  Affiliated   144   Timpanogos Dialysis Center   Timpanogos Dialysis   1055 N 500 W   STE 222   PROVO   UT   84604-3329
  Affiliated   216   HOME DIALYSIS UNIT   Home Dialysis /CAPD Unit   825 S 8TH ST STE 1202     MINNEAPOLIS   MN   55404
  Affiliated   284   MANZANITA HOME TRAINING CENTER   Manzanita Home Training Center (fka North CAPD)   4005 MANZANITA AVE   STE 18   CARMICHAEL   CA   95608-1779
  Affiliated   408   WICHITA DIALYSIS CENTER   Wichita Dialysis Center-PD Program   909 N TOPEKA ST     WICHITA   KS   67214-3620
  Affiliated   978   CENTRAL TULSA DIALYSIS CENTER   Central Tulsa PD   1124 S SAINT LOUIS AVE     TULSA   OK   74120-5413
  Affiliated   1748   ST PAUL CAPITAL PD   St. Paul Capital Dialysis at Home-PD (fka Capital PD Program)   555 PARK ST   STE 110   SAINT PAUL   MN   55103-2110
  Affiliated   1787   ASH TREE PD   Ash Tree PD   2666 N GROVE INDUSTRIAL DR     FRESNO   CA   93727-1552
  Affiliated   1821   EMERALD DIALYSIS   Emerald Dialysis PD (fka Hyde Park PD)   710 W 43RD ST     CHICAGO   IL   60609-3435
  Affiliated   1822   OLYMPIA FIELDS DIALYSIS   Olympia Fields PD   4557B LINCOLN HWY   STE B   MATTESON   IL   60443-2385
  Affiliated   1823   LAKE COUNTY DIALYSIS   Lake County PD   918 S MILWAUKEE AVE     LIBERTYVILLE   IL   60048-3229
  Affiliated   1825   COMPREHENSIVE RENAL CARE-GARY   CRC-Gary PD   4802 BROADWAY     GARY   IN   46408-4509
  Affiliated   1826   COMPREHENSIVE RENAL CARE-HAMMOND   CRC-Hammond PD   222 DOUGLAS ST     HAMMOND   IN   46320-1960
  Affiliated   1827   COMPREHENSIVE RENAL CARE-VALPARAISO   CRC-Valparaiso PD   606 E LINCOLNWAY     VALPARAISO   IN   46383-5728
  Affiliated   1828   COMPREHENSIVE RENAL CARE-MICHIGAN CITY   CRC-Michigan City PD   9836 WEST 400 NORTH     MICHIGAN CITY   IN   46360-2910
  Affiliated   1829   MERRILLVILLE PD   Merrillville Dialysis PD   9223 TAFT ST     MERRILLVILLE   IN   46410-6911
  Affiliated   1833   NAMPA DIALYSIS CENTER   Nampa Dialysis PD   846 PARKCENTRE WAY     NAMPA   ID   83651-1790
  Affiliated   1834   TABLE ROCK DIALYSIS CENTER   Table Rock Dialysis PD   5610 W GAGE ST     BOISE   ID   83706
  Affiliated   1835   TWIN FALLS DIALYSIS CENTER   Twin Falls Dialysis PD   1840 CANYON CREST DR     TWIN FALLS   ID   83301-3007
  Affiliated   1836   TREASURE VALLEY DIALYSIS CENTER   Treasure Valley Dialysis PD & Home   3525 E LOUISE DR   STE 155   MERIDIAN   ID   83642-6303
  Affiliated   1837   GATE CITY DIALYSIS CENTER   Gate City Dialysis PD   2001 BENCH RD     POCATELLO   ID   83201-2033
  Affiliated   1838   FOUR RIVERS DIALYSIS CENTER   Four Rivers Dialysis PD   515 EAST LN     ONTARIO   OR   97914-3953
  Affiliated   1869   LOWRY DIALYSIS CENTER   Lowry Dialysis PD   7465 E 1ST AVE   STE A   DENVER   CO   80230-6877
  Affiliated   1905   BURLEY DIALYSIS CENTER   Burley Dialysis PD   741 N OVERLAND AVE     BURLEY   ID   83318-3440
  Affiliated   1909   TURFWAY PD DIALYSIS   Turfway PD Training   11 SPIRAL DR   STE 15A   FLORENCE   KY   41042-1394
  Affiliated   1910   MARYVILLE DIALYSIS   Maryville Dialysis PD   2136B VADALABENE DR     MARYVILLE   IL   62062-5632
  Affiliated   1917   PDL ANNEX-PD   PDL Annex-PD (PDL=Physician Dialysis Lancaster)   2110 HARRISBURG PIKE   STE 310   LANCASTER   PA   17601-2644
  Affiliated   1924   KANKAKEE COUNTY DIALYSIS   Kankakee County Dialysis PD   581 WILLIAM R LATHAM SR DR   STE 104   BOURBONNAIS   IL   60914-2439
  Affiliated   1946   SNAKE RIVER DIALYSIS PD   DNVO-Snake River Dialysis PD (fka Blackfoot)-ID   1491 PARKWAY DR     BLACKFOOT   ID   83221-1667
  Affiliated   1953   NORTH HIGHLANDS DIALYSIS CENTER   North Highlands Dialysis Center PD   4986 WATT AVE   STE C   NORTH HIGHLANDS   CA   95660-5182
  Affiliated   1966   AMERY DIALYSIS   Amery Dialysis PD   970 ELDEN AVE     AMERY   WI   54001-1448
  Affiliated   1975   KIDNEY HOME CENTER   Kidney HOME (Home Operations & Medical Education) Center PD   2245 ROLLING RUN DR   STE 4   WINDSOR MILL   MD   21244-1858
  Affiliated   1988   MEMPHIS DOWNTOWN DIALYSIS   Memphis Downtown Dialysis PD   2076 UNION AVE   FL 2   MEMPHIS   TN   38104-4138
  Affiliated   1989   PGH HOME MODALITY COE   Pittsburgh Home Modality Center of Excellence PD   5171 LIBERTY AVE   STE A   PITTSBURGH   PA   15224-2254
  Affiliated   2223   LAKE VILLA DIALYSIS   Lake Villa Dialysis PD   37809 N IL RTE 59     LAKE VILLA   IL   60046-7332
  Affiliated   2232   RICHFIELD DIALYSIS   Richfield PD Program   6601 LYNDALE AVE S   STE 150   RICHFIELD   MN   55423-2490
  Affiliated   2297   TOKAY HOME DIALYSIS CENTER   Tokay Home Dialysis-PD   777 S HAM LN   STE L   LODI   CA   95242-3593
  Affiliated   2302   SPIVEY PERITONEAL AND HOME DIALYSIS CENTER   Spivey Peritoneal Dialysis and Home Dialysis Center   1423 STOCKBRIDGE RD   STE B   JONESBORO   GA   30236-3740
  Affiliated   2326   WARRENSVILLE HEIGHTS PD DIALYSIS   Warrensville Heights PD Dialysis   4200 WARRENSVILLE CENTER RD   STE 210   WARRENSVILLE HEIGHTS   OH   44122-7000
  Affiliated   2340   EASTGATE HOME   Eastgate Home Training   4435 AICHOLTZ RD   STE 800B   CINCINNATI   OH   45245-1692
  Affiliated   2366   WESLEY CHAPEL DIALYSIS   Wesley Chapel Dialysis (PD ONLY)   2255 GREEN HEDGES WAY     WESLEY CHAPEL   FL   33544-8183

 

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  Affiliated   2400   FRESNO PD   Fresno At Home Center-PD Only   568 E HERNDON AVE   STE 301   FRESNO   CA   93720-2989
  Affiliated   2456   GRAND HOME DIALYSIS PD/HHD   Grand Home Dialysis (PD only)   14674 W MOUNTAIN VIEW BLVD   STE 204   SURPRISE   AZ   85374-2708
  Affiliated   2458   WASHINGTON COUNTY DIALYSIS   Washington County Dialysis PD Only (fka Hagerstown)   1136 OPAL CT     HAGERSTOWN   MD   21740-5940
  Affiliated   2477   SAN JOSE PD   San Jose At Home-PD Only (Freestanding)   4400 STEVENS CREEK BLVD   STE 50   SAN JOSE   CA   95129-1104
  Affiliated   2483   FREMONT HOME TRAINING JV   DNVO-Fremont At Home PD/HHD-CA   39355 CALIFORNIA AVE     FREMONT   CA   94538
  Affiliated   2490   HOME DIALYSIS OPTIONS OF BALDWIN COUNTY   Home Dialysis Options of Baldwin County-PD Only   27880 N MAIN ST   STE A   DAPHNE   AL   36526-7080
  Affiliated   3299   TRI COUNTIES HOME TRAINING   Tri Counties Home Dialysis   433 S BRIDGE ST     VISALIA   CA   93277-2801
  Affiliated   3640   WHITE OAK HOME TRAINING DIALYSIS   White Oak Home Training   5520 CHEVIOT RD   STE B   CINCINNATI   OH   45247-7069
  Affiliated   3683   BUTLER COUNTY HOME TRAINING DIALYSIS   Butler County Home Training   3497 S DIXIE HWY     FRANKLIN   OH   45005-5717
  Affiliated   3727   HANFORD AT HOME DIALYSIS   Hanford Home Dialysis PD   900 N DOUTY ST     HANFORD   CA   93230-3918
  Affiliated   3735   HIOAKS DIALYSIS PD   Hioaks Dialysis PD   681 HIOAKS RD   STE B   RICHMOND   VA   23225-4043
  Affiliated   3891   MEMPHIS EAST DIALYSIS PD   Memphis East Dialysis PD   50 HUMPHREYS CTR   STE 28B   MEMPHIS   TN   38120-2369
  Affiliated   3892   NASHVILLE HOME TRAINING DIALYSIS PD   Nashville Home Training Dialysis PD   1919 CHARLOTTE AVE   STE 200   NASHVILLE   TN   37203-2245
  Affiliated   3989   DEARBORN HOME DIALYSIS   Dearborn Home Dialysis-PD   22030 PARK ST     DEARBORN   MI   48124-2854
  Affiliated   4308   GALLERIA HOME TRAINING DIALYSIS   Galleria Home Training Dialysis PD (aka SW Tennessee)   9045 HIGHWAY 64   STE 102   LAKELAND   TN   38002-8394
  Affiliated   4310   GREATER TAMPA AT HOME   Greater Tampa At Home PD   4204 N MACDILL AVE   STE 1B NORTH BLDG   TAMPA   FL   33607-6364
  Affiliated   4315   LORAIN COUNTY HOME DIALYSIS   DNVO-Lorain County Home Dialysis HHD/PD-OH   824 E BROAD ST     ELYRIA   OH   44035-6557
  Affiliated   4375   GARFIELD HOME PROGRAM   Garfield Home Program (PD Only)   228 N GARFIELD AVE   STE 301   MONTEREY PARK   CA   91754-1709
  Affiliated   4453   BINZ HOME TRAINING   Binz Home Training - PD only   1213 HERMANN DR   STE 180   HOUSTON   TX   77004-7018
  Affiliated   5021   FRANKLIN AT HOME PD   Franklin At Home PD   301 CALLOWHILL ST     PHILADELPHIA   PA   19123-4117
  Affiliated   5028   CALDWELL DIALYSIS CENTER PD   Caldwell Dialysis Center   821 S SMEED PKWY     CALDWELL   ID   83605-5130
  Affiliated   5170   FORT WAYNE HOME DIALYSIS   DNVO-Fort Wayne Home Dialysis (PD-HHD)-IN   3124 E STATE BLVD   STE 5B   FORT WAYNE   IN   46805-4763
  Affiliated   5556   VISALIA AT HOME   Visalia At Home PD   1120 N CHINOWTH ST     VISALIA   CA   93291-7896
  Affiliated   5569   BLUEMOUND PD   Bluemound PD   601 N 99TH ST STE 300     WAUWATOSA   WI   53226-4362
  Affiliated   5581   WOODLAWN HOME PROGRAM PD   Woodlawn Home Program PD Only   5841 S MARYLAND AVE   RM L-026   CHICAGO   IL   60637-1447
  Affiliated   5599   BEVERLY DIALYSIS PD   Beverly PD   8109 S WESTERN AVE     CHICAGO   IL   60620-5939
  Affiliated   5600   WOODLAWN PEDIATRIC HOME PROGRAM   Woodlawn Pediatrics Home Program PD Only   5841 S MARYLAND AVE L026     CHICAGO   IL   60615
  Affiliated   5616   SPRINGHILL HOME TRAINING DIALYSIS   Springhill Home Training (PD Only)   3401 SPRINGHILL DR   STE 330   NORTH LITTLE ROCK   AR   72117-2945
  Affiliated   5647   FIRST COLONIAL DAVITA PD   First Colonial DaVita PD   1157 FIRST COLONIAL RD   STE 200   VIRGINIA BEACH   VA   23454-2432
  Affiliated   5898   AMHERST AT HOME   Amherst At Home   3200 COOPER FOSTER PRK RD W     LORAIN   OH   44053-3654
  Affiliated   5900   CATHERDRAL CITY AT HOME   DNVO JV-Cathedral City At Home-CA   30-885 DATE PALM DR     CATHEDRAL CITY   CA   92234-2958
  Affiliated   5904   ROBBINSDALE AT HOME   Robbinsdale At Home   3461 WEST BROADWAY AVE     ROBBINSDALE   MN   55422-2955
  Affiliated   5905   NORTH PALM BEACH AT HOME   North Palm Beach At Home   2841 PGA BLVD     PALM BEACH GARDENS   FL   33410-2910
  Affiliated   5907   SOUTHTOWNS AT HOME   Southtowns At Home (Hamburg)   4910 CAMP RD   STE 100   HAMBURG   NY   14075-2617
  Affiliated   5909   FORT WAYNE HOME AT HOME   DNVO-Fort Wayne Home At Home   3124 E STATE BLVD   STE 5B   FORT WAYNE   IN   46805-4763
  Affiliated   5910   FORT WAYNE WEST AT HOME   DNVO JV-Fort Wayne West At Home   4916 ILLINOIS RD   STE 118   FORT WAYNE   IN   46804-5116
  Affiliated   5913   WINCHESTER AT HOME   Winchester At Home   2301 VALOR DR     WINCHESTER   VA   22601-6111
  Affiliated   5914   MARSHFIELD AT HOME   Marshfield At Home   123 NORTHRIDGE ST     MARSHFIELD   WI   54449-8341
  Affiliated   5915   MOSCOW AT HOME   Moscow At Home   212 RODEO DR   STE 110   MOSCOW   ID   83843-9791
  Affiliated   5919   AVON AT HOME   Avon At Home   9210 ROCKVILLE RD   STE D   INDIANAPOLIS   IN   46234-2670
  Affiliated   5923   NORTHSIDE AT HOME   Northside At Home   320 E NORTH AVE   4TH FLOOR SOUTH TOWER   PITTSBURGH   PA   15212-4756
  Affiliated   5926   PANAMA CITY AT HOME   Panama City At Home   615 HIGHWAY 231     PANAMA CITY   FL   32405-4704
  Affiliated   5927   MAGNOLIA OAKS AT HOME   Magnolia Oaks At Home (aka Hinesville, Satilla River)   2377 HIGHWAY 196 W   BLDG A MAGNOLIA OAKS   HINESVILLE   GA   31313-8036
  Affiliated   5928   WESTBANK AT HOME   Westbank At Home   3631 BEHRMAN PL     NEW ORLEANS   LA   70114-0906
  Affiliated   5931   ROCKSIDE AT HOME   Rockside At Home   4801 ACORN DR     INDEPENDENCE   OH   44131-2566
  Affiliated   5932   WADSWORTH AT HOME   Wadsworth At Home   195 WADSWORTH RD STE 302   FOUNDERS HALL 3RD FLOOR   WADSWORTH   OH   44281-9504
  Affiliated   5933   WOODLAWN AT HOME HHD   Woodlawn Home Program At Home   5841 S MARYLAND AVE   RM L-026   CHICAGO   IL   60637-1447
  Affiliated   5934   WESLEY CHAPEL AT HOME   Wesley Chapel At Home   2255 GREEN HEDGES WAY     WESLEY CHAPEL   FL   33544-8183
  Affiliated   5935   THOUSAND OAKS AT HOME   Thousand Oaks At Home   375 ROLLING OAKS DR   STE 100   THOUSAND OAKS   CA   91361-1024
  Affiliated   5936   SIMI VALLEY AT HOME   Simi Valley At Home   2950 SYCAMORE DR   STE 100   SIMI VALLEY   CA   93065-1210
  Affiliated   5937   MIDWEST FAIRBORN AT HOME   Midwest Fairborn At Home   1266 N BROAD ST     FAIRBORN   OH   45324
  Affiliated   5938   NORTH ST LOUIS COUNTY AT HOME   North St. Louis County At Home   13119 NEW HALLS FERRY RD     FLORISSANT   MO   63033-3228
  Affiliated   5939   BLUEMOUND AT HOME   Bluemound At Home   601 N 99TH ST   STE 110   WAUWATOSA   WI   53226
  Affiliated   5940   MESA COUNTY AT HOME   Mesa County At Home (Grand Junction)   561 25 RD   STE D   GRAND JUNCTION   CO   81505-1303

 

Page 124 of 136


  Affiliated   5942   PLANO AT HOME   Plano At Home   481 SHILOH RD   STE 100   PLANO   TX   75074-7231
  Affiliated   5943   WEST BLOOMFIELD AT HOME   West Bloomfield At Home   6010 W MAPLE RD STE 215     WEST BLOOMFIELD   MI   48322-4406
  Affiliated   5945   BINZ HOME TRAINING AT HOME   Binz Home Training At Home   1213 HERMANN DR STE 180     HOUSTON   TX   77004-7070
  Affiliated   5947   HANNIBAL AT HOME   Hannibal At Home   3140 PALMYRA RD     HANNIBAL   MO   63401-2204
  Affiliated   5949   BEVERLY AT HOME   Beverly At Home   8109 SOUTH WESTERN AVE     CHICAGO   IL   60620-5939
  Affiliated   5950   NORTH JACKSON AT HOME   North Jackson At Home (fka Stonegate)   217 STERLING FARM DR     JACKSON   TN   38305-5727
  Affiliated   5951   PORTAGE AT HOME   Portage At Home   5823 US HIGHWAY 6     PORTAGE   IN   46368-4851
  Affiliated   5952   ROGUE VALLEY AT HOME   Rogue Valley At Home   760 GOLF VIEW DR UNIT 100     MEDFORD   OR   97504-9685
  Affiliated   5953   EVERETT AT HOME   Everett At Home   8130 EVERGREEN WAY STE C     EVERETT   WA   98203-6419
  Affiliated   5954   OLYMPIA AT HOME   Olympia At Home   335 COOPER POINT ROAD NW   SUITE 105   OLYMPIA   WA   98502-4436
  Affiliated   5955   LORAIN COUNTY HOME AT HOME   DNVO-Lorain County Home At Home   824 EAST BROAD ST     ELYRIA   OH   44035-6559
  Affiliated   5956   RENAISSANCE AT HOME   Renaissance At Home   1840 DARBY DR     FLORENCE   AL   35630-2623
  Affiliated   5957   POOLER AT HOME   Pooler At Home   54 TRADERS WAY   LIVE OAK PLAZA   POOLER   GA   31322-4158
  Affiliated   5958   GULF SHORES AT HOME   Gulf Shores At Home   3947 GULF SHORES PKWY   UNIT 150   GULF SHORES   AL   36542-2735
  Affiliated   5959   FRANKLIN AT HOME   Franklin At Home   301 CALLOWHILL ST     PHILADELPHIA   PA   19123-4117
  Affiliated   5961   RENO AT HOME   Reno At Home   1500 EAST 2ND STREET   STE 101, 106   RENO   NV   89502-1189
  Affiliated   5963   JACKSONVILLE SOUTH AT HOME   Jacksonville South At Home   14965 OLD SAINT AUGUSTINE RD   UNIT 114   JACKSONVILLE   FL   32258-9481
  Affiliated   5964   LAKE ST LOUIS AT HOME   Lake St. Louis At Home   200 BREVCO PLZ   STE 202   LAKE ST LOUIS   MO   63367-2950
  Affiliated   5965   UNION CITY AT HOME (GA)   Union City At Home (GA)   6851 SHANNON PARKWAY   STE 200   UNION CITY   GA   30291-2049
  Affiliated   5966   WEBER VALLEY AT HOME   Weber Valley At Home   1920 W 250TH N     MARRIOTT-SLATERVILLE   UT   84404-9233
  Affiliated   5968   PARKER DIALYSIS CENTER   Parker At Home   10371 S PARK GLENN WAY   STE 180   PARKER   CO   80138-3871
  Affiliated   5971   KENNESTONE AT HOME   Kennestone At Home   200 COBB PKWY N   STE 318   MARIETTA   GA   30062-3558
  Affiliated   5973   NORTH COLORADO SPRINGS AT HOME   North Colorado Springs At Home   6071 E WOODMEN RD   STE 100   COLORADO SPRINGS   CO   80923-2610
  Affiliated   5974   PGH HOME MODALITY COD/HHD   Pittsburgh Home Modality Center of Excellence At Home   5171 LIBERTY AVE   STE A   PITTSBURGH   PA   15224-2254
  Affiliated   5977   FRESNO AT HOME CENTER   Fresno At Home Center-HHD Only   568 E HERNDON AVE   STE 301   FRESNO   CA   93720-2989
  Affiliated   5978   BLUFF CITY AT HOME   Bluff City At Home   2400 LUCY LEE PKWY   STE E   POPLAR BLUFF   MO   63901-2427
  Affiliated   5979   NORTH METRO AT HOME   North Metro At Home   12365 HURON ST   STE 500   WESTMINSTER   CO   80234-3498
  Affiliated   5980   FIVE STAR AT HOME   Five Star At Home (fka Las Vegas Multi-Care)   2400 TECH CENTER CT     LAS VEGAS   NV   89128-0804
  Affiliated   5981   KIDNEY HOME AT HOME   Kidney HOME (Home Operations & Medical Education) At Home   2245 ROLLING RUN DR   STE 3   WINDSOR MILL   MD   21244-1858
  Affiliated   5982   FARGO AT HOME   Fargo At Home   4474 23RD AVE S   STE M   FARGO   ND   58104-8795
  Affiliated   5983   GALLERIA HOME TRAINING AT HOME   Galleria Home Training At Home   9045 HIGHWAY 64   STE 102   LAKELAND   TN   38002-8394
  Affiliated   5986   BELDEN COMMUNITY AT HOME   Belden Community At Home   4685 FULTON DR NW     CANTON   OH   44718-2379
  Affiliated   5987   MAINPLACE AT HOME   Mainplace At Home   972 W TOWN AND COUNTRY RD     ORANGE   CA   92868-4714
  Affiliated   5988   PENNSAUKEN AT HOME   Pennsauken At Home   7024 KAIGHNS AVE     PENNSAUKEN   NJ   08109-4417
  Affiliated   5989   JEDBURG AT HOME   Jedburg At Home   2897 W 5TH NORTH ST     SUMMERVILLE   SC   29483-9674
  Affiliated   5993   CAPE CORAL SOUTH AT HOME   Cape Coral South At Home   3046 DEL PRADO BLVD S   STE 4A   CAPE CORAL   FL   33904-7232
  Affiliated   5994   GREATER TAMPA HOME AT HOME   Greater Tampa At Home   4204 N MACDILL AVE   STE 1B NORTH BLDG   TAMPA   FL   33607-6364
  Affiliated   5995   ATHENS EAST AT HOME   Athens East At Home   2026 S MILLEDGE AVE   STE A2   ATHENS   GA   30605-6480
  Affiliated   5996   UNIVERSITY UNIT RIVERSIDE AT HOME   University Unit Riverside At Home   1045 WESTGATE DR   STE 90   SAINT PAUL   MN   55114-1079
  Affiliated   5997   WOODRIDGE AT HOME   Woodridge Home At Home   7425 JANES AVE   STE 103   WOODRIDGE   IL   60517-2356
  Affiliated   5998   INDY SOUTH AT HOME   Indy South At Home   972 EMERSON PKWY   STE E   GREENWOOD   IN   46143-6202
  Affiliated   5999   LOCKPORT HOME AT HOME   Lockport Home Dialysis At Home   16626 W 159TH ST   STE 703   LOCKPORT   IL   60441-8019
  Affiliated   6000   CAMELBACK AT HOME HEMO   Camelback Dialysis At Home   7321 E OSBORN DR     SCOTTSDALE   AZ   85251-6418
  Affiliated   6002   WEST BOUNTIFUL DIALYSIS AT HOME   West Bountiful Dialysis At Home   724 W 500 S   STE 300   WEST BOUNTIFUL   UT   84087-1471
  Affiliated   6002   WEST BOUNTIFUL DIALYSIS AT HOME   West Bountiful Dialysis At Home   724 W 500 S   STE 300   WEST BOUNTIFUL   UT   84087-1471
  Affiliated   6004   CORNERSTONE DIALYSIS AT HOME   Cornerstone Dialysis At Home   23857 GREENFIELD RD     SOUTHFIELD   MI   48075-3122
  Affiliated   6006   DIALYSIS CARE OF MOORE COUNTY AT HOME   Dialysis Care of Moore County At Home (aka Pinehurst)   16 REGIONAL DR     PINEHURST   NC   28374-8850
  Affiliated   6007   HOME DIALYSIS AT HOME   Home Dialysis At Home (Minneapolis)   825 S 8TH ST   STE 1224   MINNEAPOLIS   MN   55404-1223
  Affiliated   6009   ST PAUL CAPITOL DIALYSIS AT HOME   St Paul Capital Dialysis At Home   555 PARK ST   STE 210   SAINT PAUL   MN   55103-2193
  Affiliated   6011   BALLENGER PT AT HOME   Ballenger Pt. At Home   2262 S BALLENGER HWY     FLINT   MI   48503-3447
  Affiliated   6012   LAKEWOOD AT HOME   Lakewood At Home   1750 PIERCE ST     LAKEWOOD   CO   80214-1434
  Affiliated   6013   MED-CENTER AT HOME   Med-Center at Home   7580 FANNIN ST   STE 230   HOUSTON   TX   77054-1939
  Affiliated   6014   UTAH VALLEY DIALYSIS AT HOME   Utah Valley Dialysis At Home   1055 N 500 W   STE 221   PROVO   UT   84604-3305
  Affiliated   6015   LOWRY AT HOME   Lowry At Home   7465 E 1ST AVE   STE A   DENVER   CO   80230-6877

 

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  Affiliated   6016   MANZANITA AT HOME   Manzanita At Home   4005 MANZANITA AVE   STE 17   CARMICHAEL   CA   95608-1779
  Affiliated   6017   FIRST COLONIAL DAVITA AT HOME   First Colonial DaVita At Home   1157 FIRST COLONIAL RD   STE 200   VIRGINIA BEACH   VA   23454-2432
  Affiliated   6019   LAKEWOOD WASHINGTON AT HOME   Lakewood Washington At Home   5919 LAKEWOOD TOWNE CENTER BLVD SW   STE A   LAKEWOOD   WA   98499-6513
  Affiliated   6020   GRAPEVINE AT HOME   Grapevine At Home   1600 W NORTHWEST HWY   STE 100   GRAPEVINE   TX   76051-8131
  Affiliated   6021   GRAND RAPIDS AT HOME (CHERRY STREET)   Grand Rapids At Home (Cherry Street)   801 CHERRY ST SE     GRAND RAPIDS   MI   49506-1440
  Affiliated   6022   FEDERAL WAY AT HOME   Federal Way At Home   1015 S 348TH ST     FEDERAL WAY   WA   98003-7078
  Affiliated   6023   CENTURY CITY AT HOME   Century City At Home   10630 SANTA MONICA BLVD     LOS ANGELES   CA   90025
  Affiliated   6024   REDDING AT HOME   Redding At Home   1876 PARK MARINA DR     REDDING   CA   96001-0913
  Affiliated   6025   OLYMPIA FIELDS AT HOME   Olympia Fields At Home   4557B LINCOLN HWY   STE B   MATTESON   IL   60443-2318
  Affiliated   6026   MT VERNON AT HOME   Mount Vernon At Home   1800 JEFFERSON AVE     MOUNT VERNON   IL   62864-4300
  Affiliated   6028   YAKIMA AT HOME   Yakima At Home   1221 N 16TH AVE     YAKIMA   WA   98902-1347
  Affiliated   6029   MID-COLUMBIA AT HOME   Mid Columbia At Home   6825 BURDEN BLVD   STE A   PASCO   WA   99301-9584
  Affiliated   6030   GEORGETOWN ON THE POTOMAC AT HOME   Georgetown on the Potomac At Home   3323 K STREET NW   SUITE 110   WASHINGTON   DC   20007
  Affiliated   6031   SIOUX FALLS AT HOME   Sioux Falls At Home   800 E 21ST ST     SIOUX FALLS   SD   57105-1016
  Affiliated   6032   HILLSBORO AT HOME   Hillsboro At Home   2500 NW 229TH AVE   STE 300 BLDG E   HILLSBORO   OR   97124-7516
  Affiliated   6033   PIKES PEAK AT HOME   Pikes Peak At Home   2002 LELARAY ST   STE 130   COLORADO SPRINGS   CO   80909-2804
  Affiliated   6034   WALNUT CREEK AT HOME   Walnut Creek At Home   400 N WIGET LN     WALNUT CREEK   CA   94598-2408
  Affiliated   6035   SAN ANTONIO AT HOME   San Antonio At Home   5284 MEDICAL DR   STE 100   SAN ANTONIO   TX   78229-4849
  Affiliated   6036   SANTA ROSA AT HOME   Santa Rosa At Home   5819 HIGHWAY 90     MILTON   FL   32583-1763
  Affiliated   6037   DUNMORE AT HOME   Dunmore At Home   1212 ONEILL HWY     DUNMORE   PA   18512-1717
  Affiliated   6038   PALMERTON AT HOME   Palmerton At Home   185 DELAWARE AVE   STE C   PALMERTON   PA   18071-1716
  Affiliated   6039   LONGVIEW AT HOME   Longview At Home   425 N FREDONIA ST     LONGVIEW   TX   75601-6464
  Affiliated   6040   JB ZACHARY AT HOME   JB Zachary At Home   333 CASSELL DR   STE 2300   BALTIMORE   MD   21224-6815
  Affiliated   6041   MEMPHIS EAST AT HOME   Memphis East At Home   50 HUMPHREYS CTR   STE 28B   MEMPHIS   TN   38120-2369
  Affiliated   6042   PLAINFIELD AT HOME   Plainfield At Home   1200 RANDOLPH RD   KENYAN HOUSE   PLAINFIELD   NJ   07060-3361
  Affiliated   6045   CHARLOTTE AT HOME   Charlotte (NC) At Home   2321 W MOREHEAD ST   STE 102   CHARLOTTE   NC   28208-5145
  Affiliated   6046   DALY CITY AT HOME   Daly City At Home   1498 SOUTHGATE AVE   STE 101   DALY CITY   CA   94015-4015
  Affiliated   6047   SALEM AT HOME   Salem At Home (OR)   3550 LIBERTY RD S   STE 100   SALEM   OR   97302-5700
  Affiliated   6048   OMAHA WEST AT HOME   Omaha West At Home   13014 W DODGE RD     OMAHA   NE   68154-2148
  Affiliated   6049   TUCSON EAST AT HOME   Tucson East At Home   6420 E BROADWAY BLVD   STE C300   TUCSON   AZ   85710-3512
  Affiliated   6050   WHITE OAK AT HOME   White Oak At Home   5520 CHEVIOT RD   STE B   CINCINNATI   OH   45247-7069
  Affiliated   6051   BELPRE AT HOME   Belpre At Home   2906 WASHINGTON BLVD     BELPRE   OH   45714-1848
  Affiliated   6052   BIRMINGHAM AT HOME   Birmingham At Home   2101 7TH AVE S     BIRMINGHAM   AL   35233-3105
  Affiliated   6053   STAMFORD AT HOME   Stamford At Home   30 COMMERCE RD     STAMFORD   CT   06902-4506
  Affiliated   6054   WHITEBRIDGE AT HOME   Whitebridge At Home   103 WHITE BRIDGE PIKE   STE 6   NASHVILLE   TN   37209-4539
  Affiliated   6055   ZANESVILLE AT HOME   Zanesville At Home   3120 NEWARK RD     ZANESVILLE   OH   43701-9659
  Affiliated   6056   TYSON'S CORNER AT HOME   Tyson's Corner At Home   8391 OLD COURTHOUSE RD   STE 160   VIENNA   VA   22182-3819
  Affiliated   6057   BRADFORD AT HOME   Bradford At Home   665 E MAIN ST     BRADFORD   PA   16701-1869
  Affiliated   6059   NORTHLAND AT HOME   Northland At Home   2750 CLAY EDWARDS DR   STE 515   N KANSAS CITY   MO   64116-3258
  Affiliated   6060   LAKE WORTH AT HOME   Lake Worth At Home   2459 S CONGRESS AVE   STE 100   PALM SPRINGS   FL   33406-7616
  Affiliated   6061   MEADVILLE AT HOME   Meadville At Home   19050 PARK AVENUE PLZ     MEADVILLE   PA   16335-4012
  Affiliated   6063   WILLINGBORO AT HOME   Willingboro At Home   230 VAN SCIVER PKWY     WILLINGBORO   NJ   08046-1131
  Affiliated   6064   DERENNE AT HOME   DeRenne At Home   5303 MONTGOMERY ST     SAVANNAH   GA   31405-5138
  Affiliated   6065   BRUNSWICK AT HOME   Brunswick At Home   53 SCRANTON CONNECTOR     BRUNSWICK   GA   31525-1862
  Affiliated   6067   AIKEN AT HOME   Aiken At Home   775 MEDICAL PARK DR     AIKEN   SC   29801-6306
  Affiliated   6068   BRIDGEPORT AT HOME   Bridgeport At Home   900 MADISON AVE     BRIDGEPORT   CT   06606-5534
  Affiliated   6069   ST PETERSBURG AT HOME   St Petersburg At Home   2850 34TH ST S     ST PETERSBURG   FL   33711-3817
  Affiliated   6070   DENISON AT HOME   Denison At Home   1220 REBA MACENTIRE LN     DENISON   TX   75020-9057
  Affiliated   6072   ATLANTIC AT HOME   Atlantic At Home   6 INDUSTRIAL WAY W   STE B   EATONTOWN   NJ   07724-2258
  Affiliated   6073   NEWTOWN AT HOME   Newtown At Home (fka St. Mary)   60 BLACKSMITH RD     NEWTOWN   PA   18940-1847
  Affiliated   6075   FOX RIVER AT HOME   Fox River At Home   1910 RIVERSIDE DR     GREEN BAY   WI   54301-2319
  Affiliated   6076   TOKAY AT HOME   Tokay At Home   777 S HAM LN   STE L   LODI   CA   95242-3593
  Affiliated   6077   CAPITAL CITY AT HOME   Capital City At Home   307 N 46TH ST     LINCOLN   NE   68503-3714
  Affiliated   6081   GREATER MIAMI AT HOME   Greater Miami At Home   160 NW 176TH ST   STE 100   MIAMI   FL   33169-5023

 

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  Affiliated   6083   EFFINGHAM AT HOME   Effingham At Home   904 MEDICAL PARK DR   STE 1   EFFINGHAM   IL   62401-2193
  Affiliated   6084   SPRINGFIELD CENTRAL AT HOME   Springfield Central At Home   932 N RUTLEDGE ST     SPRINGFIELD   IL   62702-3721
  Affiliated   6085   DECATUR EAST WOOD AT HOME   Decatur East Wood At Home   794 E WOOD ST     DECATUR   IL   62523-1155
  Affiliated   6086   ILLINI AT HOME   Illini At Home   507 E UNIVERSITY AVE     CHAMPAIGN   IL   61820-3828
  Affiliated   6087   JANESVILLE AT HOME   Janesville At Home   1305 WOODMAN RD     JANESVILLE   WI   53545-1068
  Affiliated   6088   NEW HAVEN AT HOME   New Haven At Home   100 CHURCH ST S   STE C   NEW HAVEN   CT   06519-1703
  Affiliated   6089   NASHUA AT HOME   Nashua At Home   38 TYLER ST   STE 100   NASHUA   NH   03060-2912
  Affiliated   6090   EAST EVANSVILLE AT HOME   East Evansville At Home   1312 PROFESSIONAL BLVD     EVANSVILLE   IN   47714-8007
  Affiliated   6095   BROOKRIVER AT HOME   Brookriver At Home   8101 BROOKRIVER DR     DALLAS   TX   75247-4003
  Affiliated   6098   METRO EAST AT HOME   Metro East At Home   5105 W MAIN ST     BELLEVILLE   IL   62226-4728
  Affiliated   6099   MARION AT HOME   Marion At Home   324 S 4TH ST     MARION   IL   62959-1241
  Affiliated   6100   ROXBURY AT HOME   Roxbury At Home   622 ROXBURY RD     ROCKFORD   IL   61107-5089
  Affiliated   6101   SYCAMORE AT HOME   Sycamore At Home   2200 GATEWAY DR     SYCAMORE   IL   60178-3113
  Affiliated   6103   WESTVIEW AT HOME   Westview At Home   3749 COMMERCIAL DR   STE B   INDIANAPOLIS   IN   46222-1676
  Affiliated   6105   OCALA AT HOME   Ocala At Home   2860 SE 1ST AVE     OCALA   FL   34471-0406
  Affiliated   6106   COMPLETE CARE AT HOME   Complete Care At Home   7850 W SAMPLE RD     MARGATE   FL   33065-4710
  Affiliated   6107   INTERAMERICAN AT HOME   InterAmerican At Home   7815 CORAL WAY   STE 115   MIAMI   FL   33155-6541
  Affiliated   6109   PURCELLVILLE AT HOME   Purcellville At Home   280 N HATCHER AVE     PURCELLVILLE   VA   20132-3193
  Affiliated   6110   TABLE ROCK AT HOME   Table Rock At Home   5610 GAGE ST   STE B   BOISE   ID   83706
  Affiliated   6111   TWIN FALLS AT HOME   Twin Falls At Home   1840 CANYON CREST DR     TWIN FALLS   ID   83301-3007
  Affiliated   6113   FOUR RIVERS AT HOME   Four Rivers At Home   515 EAST LN     ONTARIO   OR   97914-3953
  Affiliated   6114   OLYMPIC VIEW AT HOME   Olympic View At Home   125 16TH AVE E   FL 5   SEATTLE   WA   98112-5211
  Affiliated   6115   SPIVEY AT HOME   Spivey At Home   1423 STOCKBRIDGE RD   STE B   JONESBORO   GA   30236-3740
  Affiliated   6116   EAST DES MOINES AT HOME   East Des Moines At Home   1301 PENNSYLVANIA AVE   STE 208   DES MOINES   IA   50316-2365
  Affiliated   6118   KETTERING AT HOME   Kettering At Home   5721 BIGGER RD     KETTERING   OH   45440-2752
  Affiliated   6119   CITRUS VALLEY AT HOME   Citrus Valley At Home   894 HARDT ST     SAN BERNARDINO   CA   92408-2854
  Affiliated   6124   MERIDIAN PARK AT HOME   Meridian Park At Home   19255 SW 65TH AVE   STE 100   TUALATIN   OR   97062-9712
  Affiliated   6125   MARYVILLE AT HOME   Maryville At Home   2136B VADALABENE DR     MARYVILLE   IL   62062-5632
  Affiliated   6128   PDI-WORCESTER AT HOME   PDI-Worcester At Home   19 GLENNIE ST   STE A   WORCESTER   MA   01605-3918
  Affiliated   6129   PDI-ROCKY HILL AT HOME   PDI-Rocky Hill At Home   30 WATERCHASE DR     ROCKY HILL   CT   06067-2110
  Affiliated   6133   WICHITA AT HOME   Wichita At Home   909 N TOPEKA ST     WICHITA   KS   67214-3620
  Affiliated   6134   ASHEVILLE KIDNEY AT HOME   Asheville Kidney At Home   1600 CENTERPARK DR     ASHEVILLE   NC   28805-6206
  Affiliated   6136   STRONGSVILLE AT HOME   Strongsville At Home   17792 PEARL RD     STRONGSVILLE   OH   44136-6909
  Affiliated   6137   BATON ROUGE AT HOME   DSI Divest-Baton Rouge At Home   3888 NORTH BLVD   STE 101   BATON ROUGE   LA   70806-3824
  Affiliated   6138   WEST BROADWAY DIALYSIS AT HOME   West Broadway At Home   720 W BROADWAY   STE 200   LOUISVILLE   KY   40202-3245
  Affiliated   6140   BRONX AT HOME   Bronx At Home   1615 EASTCHESTER RD     BRONX   NY   10461-2603
  Affiliated   6142   CLEVE HILL AT HOME   Cleve Hill At Home   1461 KENSINGTON AVE     BUFFALO   NY   14215-1436
  Affiliated   6144   WHITE PLAINS AT HOME   White Plains At Home   200 HAMILTON AVE   STE 13B   WHITE PLAINS   NY   10601-1859
  Affiliated   6146   LAKE VILLA AT HOME   Lake Villa At Home   37809 N IL ROUTE 59     LAKE VILLA   IL   60046-7332
  Affiliated   6148   TULSA AT HOME   Tulsa At Home   4436 S HARVARD AVE     TULSA   OK   74135-2605
  Affiliated   6151   LITHONIA AT HOME   Lithonia At Home   2485 PARK CENTRAL BLVD     DECATUR   GA   30035-3902
  Affiliated   6152   LANHAM AT HOME   Lanham At Home   8855 ANNAPOLIS RD   STE 200   LANHAM   MD   20706-2919
  Affiliated   6153   HAMMOND AT HOME   Hammond At Home   222 DOUGLAS ST     HAMMOND   IN   46320-1960
  Affiliated   6156   UNION CITY CENTER AT HOME (CA)   Union City Center At Home (CA)   32930 ALVARADO NILES RD   STE 300   UNION CITY   CA   94587-8101
  Affiliated   6157   CHICO AT HOME   Chico At Home   530 COHASSET RD     CHICO   CA   95926-2212
  Affiliated   6158   MONTCLAIR AT HOME   Montclair At Home   5050 PALO VERDE ST   STE 100   MONTCLAIR   CA   91763-2333
  Affiliated   6161   PDI - LANCASTER AT HOME   PDI-Lancaster At Home   1412 E KING ST     LANCASTER   PA   17602-3240
  Affiliated   6162   PDI JOHNSTOWN AT HOME   PDI-Johnstown At Home   344 BUDFIELD ST     JOHNSTOWN   PA   15904-3214
  Affiliated   6163   CAMP HILL AT HOME   Camp Hill At Home   425 N 21ST ST   PLAZA 21 BLDG 1ST FL   CAMP HILL   PA   17011-2202
  Affiliated   6164   PDI MONTGOMERY AT HOME   PDI-Montgomery At Home   1001 FOREST AVE     MONTGOMERY   AL   36106-1181
  Affiliated   6165   FAIRFAX AT HOME   Fairfax At Home   8501 ARLINGTON BLVD   STE 100   FAIRFAX   VA   22031-4625
  Affiliated   6170   WEST SACRAMENTO AT HOME   West Sacramento At Home   3450 INDUSTRIAL BLVD   STE 100   WEST SACRAMENTO   CA   95691-5003
  Affiliated   6171   EAST MACON AT HOME   East Macon At Home   165 EMERY HWY   STE 101   MACON   GA   31217-3666
  Affiliated   6178   GERMANTOWN AT HOME   Germantown At Home   20111 CENTURY BLVD   STE C   GERMANTOWN   MD   20874-9165

 

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  Affiliated   6180   SEDC-WILMINGTON AT HOME   SEDC-Wilmington (NC) At Home   2215 YAUPON DR     WILMINGTON   NC   28401-7334
  Affiliated   6182   HERMISTON COMMUNITY AT HOME   Hermiston Community At Home   1155 W LINDA AVE     HERMISTON   OR   97838-9601
  Affiliated   6183   SHREVEPORT HHD LA   Shreveport Home Dialysis At Home   1560 IRVING PL     SHREVEPORT   LA   71101-4604
  Affiliated   6184   DOWNTOWN SAN ANTONIO AT HOME   Downtown San Antonio At Home   615 E QUINCY ST     SAN ANTONIO   TX   78212
  Affiliated   6186   COLUMBIA MO AT HOME   RTC-Columbia (MO) At Home   1701 E BROADWAY   STE G102   COLUMBIA   MO   65201-8029
  Affiliated   6188   REGENCY AT HOME   Regency At Home (fka Jacksonville)   9535 REGENCY SQUARE BLVD N     JACKSONVILLE   FL   32225-8128
  Affiliated   6193   WEST GEORGIA AT HOME   West Georgia At Home (fka Columbus (GA))   1216 STARK AVE     COLUMBUS   GA   31906-2500
  Affiliated   6194   BUFORD AT HOME   Buford At Home   1550 BUFORD HWY   STE 1E   BUFORD   GA   30518-3666
  Affiliated   6195   KALAMAZOO WEST AT HOME   Kalamazoo West At Home   1040 N 10TH ST     KALAMAZOO   MI   49009-6149
  Affiliated   6196   SOUTH VALLEY AT HOME   South Valley At Home   17815 VENTURA BLVD   STE 100   ENCINO   CA   91316-3600
  Affiliated   6204   QUEENS VILLAGE AT HOME   Queens Village At Home   22202 HEMPSTEAD AVE   STE 170   QUEENS VILLAGE   NY   11429-2123
  Affiliated   6207   LANSING AT HOME-MI   Lansing Home Hemodialysis At Home   1675 WATERTOWER PL   STE 700   EAST LANSING   MI   48823-6397
  Affiliated   6208   SOUTH COUNTY AT HOME   South County At Home (Deaconess)   4145 UNION RD     SAINT LOUIS   MO   63129-1064
  Affiliated   6211   TACOMA AT HOME   Tacoma At Home   3401 S 19TH ST     TACOMA   WA   98405-1909
  Affiliated   6213   CEDAR PARK AT HOME   Cedar Park At Home (fka North Austin)   1720 E WHITESTONE BLVD     CEDAR PARK   TX   78613-7640
  Affiliated   6214   SOUTH FORT WORTH DIALYSIS AT HOME   South Fort Worth At Home   6260 SOUTHWEST BLVD     BENBROOK   TX   76109-6906
  Affiliated   6215   THE WOODLANDS AT HOME   DNVO-The Woodlands At Home   9301 PINECROFT DR     SHENANDOAH   TX   77380-3179
  Affiliated   6218   ARROWHEAD LAKES AT HOME   Arrowhead Lakes At Home   20325 N 51ST AVE   STE 184 BLDG 11   GLENDALE   AZ   85308-4625
  Affiliated   6220   COLUMBUS WEST HOME TRAINING   Columbus West Home Training At Home   1391 GEORGESVILLE RD     COLUMBUS   OH   43228-3611
  Affiliated   6221   RICHMOND KIDNEY CENTER AT HOME   Richmond Kidney Center At Home (Staten Island)   1366 VICTORY BLVD     STATEN ISLAND   NY   10301-3907
  Affiliated   6225   DIALYSIS CARE OF KANNAPOLIS AT HOME   Dialysis Care of Kannapolis At Home   1607 N MAIN ST     KANNAPOLIS   NC   28081-2317
  Affiliated   6226   BUTLER-FARM AT HOME   Butler Farm At Home   501 BUTLER FARM RD   STE A   HAMPTON   VA   23666-1777
  Affiliated   6228   NEW PORT RICHEY AT HOME   New Port Richey Kidney At Home   7421 RIDGE RD     PORT RICHEY   FL   34668-6933
  Affiliated   6229   GRAND HOME AT HOME   Grand Home At Home   14674 W MOUNTAIN VIEW BLVD   STE 204   SURPRISE   AZ   85374-2708
  Affiliated   6230   WILLIAMSBURG AT HOME   Williamsburg At Home (fka Yorktown)   500 SENTARA CIR   STE 103   WILLIAMSBURG   VA   23188-5727
  Affiliated   6231   BALDWIN COUNTY AT HOME   Home Dialysis Options of Baldwin County At Home   27880 N MAIN ST   STE A   DAPHNE   AL   36526-7080
  Affiliated   6232   CLINTON TOWNSHIP AT HOME   Clinton Township at Home   15918 19 MILE RD   STE 110   CLINTON TOWNSHIP   MI   48038-1101
  Affiliated   6233   GROSSE POINTE AT HOME   Grosse Pointe At Home   18000 E WARREN AVE   STE 100   DETROIT   MI   48224-1336
  Affiliated   6234   GREENSBURG AT HOME   Greensburg At Home   1531 N COMMERCE EAST DR   STE 6   GREENSBURG   IN   47240-3259
  Affiliated   6236   GULF BREEZE AT HOME   Gulf Breeze At Home   1519 MAIN ST     DUNEDIN   FL   34698-4650
  Affiliated   6237   JACKSONVILLE CENTRAL AT HOME   Jacksonville Central At Home   400 T P WHITE DR     JACKSONVILLE   AR   72076-3287
  Affiliated   6238   SAN JOSE AT HOME   San Jose At Home (Freestanding)   4400 STEVENS CREEK BLVD   STE 50   SAN JOSE   CA   95129-1104
  Affiliated   6243   ORLANDO AT HOME   Orlando At Home (0178)   14050 TOWN LOOP BLVD   STE 104B   ORLANDO   FL   32837-6190
  Affiliated   6244   KENNEDY HOME DIALYSIS-AT HOME   Kennedy Home Dialysis-At Home   5509 N CUMBERLAND AVE   STE 515   CHICAGO   IL   60656-4702
  Affiliated   6245   YPSILANTI AT HOME   Ypsilanti At Home   2762 WASHTENAW RD     YPSILANTI   MI   48197-1506
  Affiliated   6246   JACKSONVILLE AT HOME   SEDC (NC II) Jacksonville At Home   14 OFFICE PARK DR     JACKSONVILLE   NC   28546-7325
  Affiliated   6247   LEBANON AT HOME   Lebanon At Home   918 COLUMBUS AVE   STE 2 UNIT B   LEBANON   OH   45036-1402
  Affiliated   6248   SLIDELL KIDNEY CARE AT HOME   Slidell Kidney Care At Home   1150 ROBERT BLVD   STE 240   SLIDELL   LA   70458-2005
  Affiliated   6249   WATERBURY AT HOME   Waterbury At Home   150 MATTATUCK HEIGHTS RD     WATERBURY   CT   06705-3893
  Affiliated   6251   WHITE LANE AT HOME   White Lane At Home   7701 WHITE LN   STE D   BAKERSFIELD   CA   93309-0201
  Affiliated   6253   HANFORD AT HOME   Hanford At Home   900 N DOUTY ST     HANFORD   CA   93230-3918
  Affiliated   6254   ANAHEIM AT HOME   Anaheim At Home   1107 W LA PALMA AVE     ANAHEIM   CA   92801-2804
  Affiliated   6255   MERCED AT HOME   Merced At Home   3150 NORTH G ST   STE B   MERCED   CA   95340-1346
  Affiliated   6257   ST JOSEPH AT HOME   St. Joseph At Home   5514 CORPORATE DR   STE 100   SAINT JOSEPH   MO   64507-7752
  Affiliated   6258   CENTRAL LITTLE ROCK AT HOME   Central Little Rock At Home   5800 W 10TH ST   STE 510   LITTLE ROCK   AR   72204-1760
  Affiliated   6260   DURHAM WEST AT HOME   Durham West At Home   4307 WESTERN PARK PL   STE 101   DURHAM   NC   27705-1204
  Affiliated   6262   TOLEDO AT HOME   Toledo At Home   1614 S BYRNE RD     TOLEDO   OH   43614-3464
  Affiliated   6263   HIOAKS AT HOME   Hioaks At Home   681 HIOAKS RD   STE D   RICHMOND   VA   23225-4043
  Affiliated   6264   ELIZABETH AT HOME   Elizabeth At Home   201 MCKEESPORT RD     ELIZABETH   PA   15037-1623
  Affiliated   6265   ABINGTON AT HOME   Abington At Home   3940A COMMERCE AVE     WILLOW GROVE   PA   19090-1705
  Affiliated   6267   NORTH ORANGEBURG AT HOME   North Orangeburg At Home   124 FIRE TOWER RD     ORANGEBURG   SC   29118-1401
  Affiliated   6268   DEARBORN HOME DIALYSIS - AT HOME   Dearborn Home Dialysis-At Home   22030 PARK ST     DEARBORN   MI   48124-2854
  Affiliated   6269   OCEAN SPRINGS AT HOME   Ocean Springs At Home   13150 PONCE DEL LEON     OCEAN SPRINGS   MS   39564-2460
  Affiliated   6270   HAKC - HUNTINGTON AT HOME   HAKC-Huntington At Home   256 BROADWAY     HUNTINGTON STATION   NY   11746-1403

 

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  Affiliated   6271   42ND ST AT HOME   Philadelphia 42nd Street At Home   4126 WALNUT ST     PHILADELPHIA   PA   19104-3511
  Affiliated   6275   CHARLOTTESVILLE NORTH AT HOME   Charlottesville North At Home   1800 TIMBERWOOD BLVD   STE C   CHARLOTTESVILLE   VA   22911-7544
  Affiliated   6276   HEARTLAND AT HOME   Heartland At Home   925 NE 8TH ST     OKLAHOMA CITY   OK   73104-5800
  Affiliated   6278   LAKELAND SOUTH AT HOME   Lakeland South At Home   5050 S FLORIDA AVE   STE 1   LAKELAND   FL   33813-2501
  Affiliated   6282   RAINBOW CITY AT HOME   Rainbow City At Home   2800 RAINBOW DR     RAINBOW CITY   AL   35906-5811
  Affiliated   6283   ATHENS AT HOME   Athens At Home   15953 ATHENS LIMESTONE DR   STE 15   ATHENS   AL   35613-2214
  Affiliated   6284   SYLACAUGA AT HOME   Sylacauga At Home   331 JAMES PAYTON BLVD     SYLACAUGA   AL   35150
  Affiliated   6287   PITTSBURGH AT HOME   Pittsburgh At Home   4312 PENN AVE     PITTSBURGH   PA   15224-1310
  Affiliated   6289   RADNOR AT HOME   Radnor At Home   250 KING OF PRUSSIA RD     RADNOR   PA   19087-5220
  Affiliated   6291   RADFORD AT HOME   Radford At Home   600 E MAIN ST   STE B   RADFORD   VA   24141-1826
  Affiliated   6292   HARRISONBURG AT HOME   Harrisonburg At Home   871 CANTRELL AVE   STE 100   HARRISONBURG   VA   22801-4323
  Affiliated   6293   KERRVILLE AT HOME   Kerrville At Home   515 GRANADA PL     KERRVILLE   TX   78028-5992
  Affiliated   6294   WEST TALLAHASSEE AT HOME   West Tallahassee At Home   2645 W TENNESSEE ST   STE 8   TALLAHASSEE   FL   32304-2521
  Affiliated   6295   ROME AT HOME   Rome At Home   15 JOHN MADDOX DR NW     ROME   GA   30165-1413
  Affiliated   6297   ST LOUIS WEST AT HOME   St. Louis West At Home   450 N LINDBERGH BLVD   STE 100C   CREVE COEUR   MO   63141-7858
  Affiliated   6298   COOKEVILLE AT HOME   Cookeville At Home   140 W 7TH ST     COOKEVILLE   TN   38501-1726
  Affiliated   6300   DOTHAN AT HOME   Dothan At Home   216 GRACELAND DR     DOTHAN   AL   36305-7346
  Affiliated   6302   HENRICO COUNTY AT HOME   Henrico County At Home   5270 CHAMBERLAYNE RD     RICHMOND   VA   23227-2950
  Affiliated   6303   WEYMOUTH CLINIC AT HOME   Weymouth At Home   330 LIBBEY INDUSTRIAL PKWY   STE 900   WEYMOUTH   MA   02189-3122
  Affiliated   6304   ERIE AT HOME   Erie At Home   350 E BAYFRONT PKWY   STE A   ERIE   PA   16507-2410
  Affiliated   6305   WILSON AT HOME   Wilson At Home   1605 MEDICAL PARK DR W     WILSON   NC   27893-2799
  Affiliated   6306   NORTH FULTON AT HOME   North Fulton At Home   1250 NORTHMEADOW PKWY   STE 120   ROSWELL   GA   30076-4914
  Affiliated   6311   BRADENTON AT HOME   Bradenton At Home   3501 CORTEZ RD W   STE 104   BRADENTON   FL   34210-3104
  Affiliated   6312   COLUMBIA UNIVERSITY AT HOME   Columbia University At Home   60 HAVEN AVENUE     NEW YORK   NY   10032-2604
  Affiliated   6313   NEW BEDFORD AT HOME   New Bedford At Home   524 UNION ST     NEW BEDFORD   MA   02740-3546
  Affiliated   6314   MUSKEGON AT HOME   Muskegon At Home   1277 MERCY DR     MUSKEGON   MI   49444-4605
  Affiliated   6315   WELLINGTON CIRCLE AT HOME   Wellington Circle At Home   10 CABOT RD   STE 103B   MEDFORD   MA   02155-5173
  Affiliated   6316   FREDERICK AT HOME   Frederick At Home   140 THOMAS JOHNSON DR   STE 100   FREDERICK   MD   21702-4475
  Affiliated   6317   SELINSGROVE AT HOME   Selinsgrove At Home   1030 N SUSQUEHANNA TRL     SELINSGROVE   PA   17870-7767
  Affiliated   6318   LAKE CHARLES SOUTHWEST AT HOME   Lake Charles Southwest At Home   300 18th ST     LAKE CHARLES   LA   70601-7342
  Affiliated   6319   LENEXA AT HOME   Lenexa At Home   8630 HALSEY ST     LENEXA   KS   66215-2880
  Affiliated   6321   NASHVILLE HOME TRAINING AT HOME   Nashville Home Training At Home   1919 CHARLOTTE AVE   STE 200   NASHVILLE   TN   37203-2245
  Affiliated   6322   GOLDSBORO AT HOME   Goldsboro At Home   2609 HOSPITAL RD     GOLDSBORO   NC   27534-9424
  Affiliated   6323   MIAMI CAMPUS AT HOME   Miami Campus At Home   1500 NW 12TH AVE   STE 106   MIAMI   FL   33136-1028
  Affiliated   6324   DAYTONA BEACH AT HOME   Daytona Beach At Home   578 HEALTH BLVD     DAYTONA BEACH   FL   32114-1492
  Affiliated   6325   GRASS VALLEY AT HOME   Grass Valley At Home   360 CROWN POINT CIR   STE 210   GRASS VALLEY   CA   95945-2543
  Affiliated   6326   POMONA AT HOME   Pomona At Home   2111 NORTH GAREY AVENUE     POMONA   CA   91767
  Affiliated   6327   MID ATLANTA HOME AT HOME   MidAtlanta Home At Home   418 DECATUR ST SE   SUITE B   ATLANTA   GA   30312-1801
  Affiliated   6328   MARTINSVILLE AT HOME   Martinsville Dialysis   33 BRIDGE ST S     MARTINSVILLE   VA   24112-6214
  Affiliated   6329   HUBBARD ROAD AT HOME   Hubbard Road At Home   1963 HUBBARD RD     MADISON   OH   44057
  Affiliated   6350   PLAINFIELD RENAL CENTER AT HOME   Plainfield Renal At Home (P278)   8110 NETWORK DR     PLAINFIELD   IN   46168-9024
  Affiliated   6351   NORTH ANDOVER RENAL CENTER AT HOME   North Andover Renal At Home (P178)   201 SUTTON ST     NORTH ANDOVER   MA   1845
  Affiliated   6352   JACKSON NORTH DIALYSIS AT HOME   Jackson North At Home (P181)   571 BEASLEY RD   STE B   JACKSON   MS   39206-3042
  Affiliated   6353   SUMMIT RENAL AT HOME   Summit Renal At Home (P186)   73 MASSILLON RD     AKRON   OH   44312-1028
  Affiliated   6354   MARLTON DIALYSIS AT HOME   Marlton At Home (P200)   769 E RTE 70     MARLTON   NJ   08053-2341
  Affiliated   6355   CENTRAL FORT WAYNE DIALYSIS AT HOME   Central Fort Wayne At Home (P223)   1940 BLUFTON RD     FORT WAYNE   IN   46809-1307
  Affiliated   6356   LAS CRUCES RENAL CENTER AT HOME   Las Cruces Renal At Home (P237)   3961 E LOHMAN AVE   STE 29   LAS CRUCES   NM   88011-8272
  Affiliated   6357   NORTHEAST PORTLAND RENAL CENTER AT HOME   Northeast Portland Renal At Home (P240)   703 NE HANCOCK ST     PORTLAND   OR   97212-3955
  Affiliated   6358   KANSAS CITY RENAL CENTER AT HOME   Kansas City Renal At Home (P264)   4333 MADISON AVE     KANSAS CITY   MO   64111-3429
  Affiliated   6359   COASTAL DIALYSIS AT HOME   South Texas Renal At Home (P257)   4300 S PADRE ISLAND DR     CORPUS CHRISTI   TX   78411-4433
  Affiliated   6360   NORTH SPOKANE RENAL CENTER AT HOME   North Spokane Renal At Home (P262)   12610 E MARIBEAU PRKWY   STE 100   SPOKANE   WA   99216
  Affiliated   5659   TEMPE DIALYSIS PD   Tempe Dialysis Center PD   2149 EAST WARNER RD   STE 109   TEMPE   AZ   85284-3496
  Affiliated   5660   ARROWHEAD LAKES DIALYSIS PD   Arrowhead Lakes Dialysis PD   20325 N 51ST AVE   BLDG 11, STE 184   GLENDALE   AZ   85308-4625
  Affiliated   5916   SHAKER SQUARE AT HOME   Shaker Square At Home   12800 SHAKER BLVD   STE 1   CLEVELAND   OH   44120-2004

 

Page 129 of 136


  Affiliated   6130   SIERRA ROSE AT HOME   Sierra Rose At Home   685 SIERRA ROSE DR     RENO   NV   89511-2060
  Affiliated   6217   TEMPE AT HOME   Tempe At Home   2149 E WARNER RD   STE 109   TEMPE   AZ   85284-3496
  Affiliated   6281   TUSCALOOSA AT HOME   Tuscaloosa At Home   805 OLD MILL ST     TUSCALOOSA   AL   35401-7132

TEMPORARY CLOSURES

(Included above are several centers that have temporarily suspended operations for a variety of reasons, but are scheduled to resume operations within the coming few months)

    614   Lynwood            
    643   Vidalia            
    3518   Huntingdon Valley Dialysis            
    626   Tuba City            
    903   Littleton            

 

Page 130 of 136


Exhibit SR-1

Purchase Data Submission Form

Contract #:    «Contract»    Dialysis Center:    DaVita Inc.

 

 

1. Purchase Data For Measurement Period: [Enter Measurement Period (for example, Q4 2013)]

ESA 1: [Product NameX]

ESA 2: [Product NameY]

ESA 3: [Product NameZ]

[Example 1 for illustration purposes only]

 

Dialysis Center Committed Purchasers

ESA

  

Total Number of [*] Purchased

ESA 1

   1,000 [*]

ESA 2

   XX mcg

ESA 3

   2,000 [*]

[Example 2 for illustration purposes only]

 

Dialysis Center Purchasers

ESA

  

Total Number of [*] Purchased

ESA 1

   1,000 [*]

ESA 2

   XX mcg

ESA 3

   2,000 [*]

 

2. Number of patients who received any and each ESA or combination from Dialysis Center Purchasers during the entire Measurement Period.

 

Page 131 of 136


[Example 1 for illustration purposes only]

 

ESA

  

Total Number of Patients

ESA 1

   50

ESA 2

   10

ESA 3

   5

[Example 2 for illustration purposes only]

 

ESA

  

Total Number of Patients

ESA 1

   60

ESA 2

  

[Example 3 for illustration purposes only]

 

ESA

  

Total Number of Patients

ESA 1

   100

ESA 3

  

[Example 4 for illustration purposes only]

 

ESA

  

Total Number of Patients

ESA 2

   100

ESA 3

  

Completed Purchase Data Submission Forms should be submitted electronically as an Excel file to Amgen by e-mail at [*], or as otherwise specified in writing by Amgen.

 

Page 132 of 136


Schedule 1

Data

 

Category

  

Data Element

  

Facility

  

Patient

Facility Reference

   Facility Name    ü   
   Address    ü   
   City, State, Zip    ü   
   Phone    ü   
   Facility ID (unique within account)    ü   
   Regional ID (unique within account)    ü   
   State in which facility is located    ü   

Patient Demographics

   De-identified Patient ID       ü
   Date of Service (Treatment Date)       ü
   Treatment Date/Date of Encounter (evaluated as treatment date)       ü
   [*] (in [*])       ü
   [*] Date       ü
   Date of [*] (month, day & year)       ü
   Date of [*]       ü
   [*] Date       ü
   [*] Date       ü
   [*]       By the end of Q4 2012
   [*] Type ([*],[*],[*])*       ü
   [*] Date*       ü
   Primary Payor (Govnt - Medicare, Medicaid, VA or Commercial - Medicare Advantage, MCO, HMO, PPO)      

By the end

of Q1 2012

   Secondary Payor (Govnt - Medicare, Medicaid, VA or Commercial - Medicare Advantage, MCO, HMO, PPO)      

By the end

of Q1 2012

Medications

   ESA Name       ü
   ESA Dose (EPOGEN / Aranesp)       ü
   EPOGEN Administration Frequency (On DVA offered Protocol)      

By the end

of Q1 2012

   Aranesp Administration Frequency*      

By the end

of Q1 2012

   ESA Route of Administration      

By the end

of Q1 2012

   ESA Start Date      

By the end

of Q1 2012

   ESA Stop Date (Missed dose due to held)*      

By the end

of Q1 2012

   [*] Name       ü
   [*]       ü

 

Page 133 of 136


   [*] Administration Frequency (Maintenance / Loading)*      

By the end

of Q1 2012

   [*] Order (Not administered, stop)*      

By the end

of Q1 2012

   Vitamin D Name       ü
   Vitamin D Dose       ü
   Vitamin D Order (Stop date)*      

By the end

of Q1 2012

Lab Measurements    Hemoglobin       ü
   [*]       ü
   [*]       ü
   [*] / [*]       ü
   [*]       ü
   [*] ([*] or [*])       ü
   [*]       ü
   Corrected [*]       ü
   Corrected [*] Product       ü
   Albumin       ü
Other Measurements    [*]       ü
   [*]       ü
   [*]       ü
   Kt/v       ü
   URR (until CMS no longer requires)       ü
   Modality       ü
   PD treatments (# pts per month)       ü
   Home HD treatments (# pts per month)*       ü
   Home HD treatments (# txs per month)      

By the end

of Q1 2012

 

* For designated fields, Dialysis Center will provide Amgen business rules to calculate value of the field based on the submitted Data.

Timing on providing Data with specific target date in the data column means Data or business rules will be delivered to Amgen by the end of the specified Quarter. For example: by end of Q1 2012 means deadline for delivery is March 31, 2012.

 

Page 134 of 136


Schedule 2

Compensation Data

Product Data Submission Requirements. Compensation Data shall be sent in either Excel or a tab-delimited text file to the following email address: [*]. The file naming convention shall include the Dialysis Center name, EPOGEN, and data month and year (i.e. DaVita_Epogen_January_2011). Dialysis Center must supply all of the information set forth in the table below.

 

ID

  

Data Field Name

  

Data Field Description

1

   Unique Account Identifier    DaVita’s numeric identifier for each account (PFac & OFac)

2

   Account Name    Account requesting EPOGEN

3

   Account Street Address    Account requesting EPOGEN

4

   Account City    Account requesting EPOGEN

5

   Account State    Account requesting EPOGEN

6

   Account zip    Account requesting EPOGEN

7

   Dispensing Pharmacy for EPOGEN    DaVita’s numeric identifier for location that has dispensed EPOGEN

8

   EPOGEN NDC Number   

9

   EPOGEN Description    Name of EPOGEN including strength (Label Name)

10

   Quantity Shipped   

11

   Unit Of Measure    Tabs, bottles, vials, etc.

12

   EPOGEN shipped/dispensed date   

 

Page 135 of 136


Schedule 3

Available EPOGEN SKU Schedule

EPOGEN® (Epoetin alfa):

 

VII. NDC

  

Description

55513-126-10

  

2,000 Unit, 1 mL (2,000 Units/mL) single-use vial

10 vials/pack, 10 packs/case

55513-267-10

  

3,000 Unit, 1 mL (3,000 Units/mL) single-use vial

10 vials/pack, 10 packs/case

55513-148-10

  

4,000 Unit, 1 mL (4,000 Units/mL) single-use vial

10 vials/pack, 10 packs/case

55513-144-10

  

10,000 Unit, 1 mL (10,000 Units/mL) single-use vial

10 vials/pack, 10 packs/case

55513-283-10

  

20,000 Unit, 2 mL (10,000 Units/mL) multi-use vial

10 vials/pack, 4 packs/case

55513-478-10

  

20,000 Unit, 1 mL (20,000 Units/mL) multi-use vial

10 vials/pack, 4 packs/case

 

Page 136 of 136

Subsidiaries of the Company

Exhibit 21

AMGEN INC.

 

 

SUBSIDIARY

(Name under which

subsidiary does business)

    

STATE OR OTHER

JURISDICTION OF

INCORPORATION

OR ORGANIZATION

  Immunex Corporation      Washington
  Amgen Manufacturing, Limited      Bermuda
  Amgen USA Inc.      Delaware
Rule 13a-14(a) Certifications

Exhibit 31

CERTIFICATIONS

I, Kevin W. Sharer, Chairman of the Board and Chief Executive Officer of Amgen Inc., certify that:

 

  1. I have reviewed this Annual Report on Form 10-K of Amgen Inc.;

 

  2. Based on my knowledge, this annual report does not contain any untrue statement of a material fact or omit to state a material fact necessary to make the statements made, in light of the circumstances under which such statements were made, not misleading with respect to the period covered by this annual report;

 

  3. Based on my knowledge, the financial statements, and other financial information included in this annual report, fairly present in all material respects the financial condition, results of operations and cash flows of the registrant as of, and for, the periods presented in this annual report;

 

  4. The registrant’s other certifying officer(s) and I are responsible for establishing and maintaining disclosure controls and procedures (as defined in Exchange Act Rules 13a-15(e) and 15d-15(e)) and internal control over financial reporting (as defined in Exchange Act Rules 13a-15(f) and 15d-15(f)) for the registrant and have:

 

  (a) Designed such disclosure controls and procedures, or caused such disclosure controls and procedures to be designed under our supervision, to ensure that material information relating to the registrant, including its consolidated subsidiaries, is made known to us by others within those entities, particularly during the period in which this annual report is being prepared;

 

  (b) Designed such internal control over financial reporting, or caused such internal control over financial reporting to be designed under our supervision, to provide reasonable assurance regarding the reliability of financial reporting and the preparation of financial statements for external purposes in accordance with generally accepted accounting principles;

 

  (c) Evaluated the effectiveness of the registrant’s disclosure controls and procedures and presented in this report our conclusions about the effectiveness of the disclosure controls and procedures, as of the end of the period covered by this annual report based on such evaluation; and

 

  (d) Disclosed in this annual report any change in the registrant’s internal control over financial reporting that occurred during the registrant’s most recent fiscal quarter (the registrant’s fourth fiscal quarter in the case of an annual report) that has materially affected, or is reasonably likely to materially affect, the registrant’s internal control over financial reporting; and

 

  5. The registrant’s other certifying officer(s) and I have disclosed, based on our most recent evaluation of internal control over financial reporting, to the registrant’s auditors and the audit committee of the registrant’s board of directors (or persons performing the equivalent functions):

 

  (a) All significant deficiencies and material weaknesses in the design or operation of internal control over financial reporting which are reasonably likely to adversely affect the registrant’s ability to record, process, summarize and report financial information; and

 

  (b) Any fraud, whether or not material, that involves management or other employees who have a significant role in the registrant’s internal control over financial reporting.

 

Date: February 29, 2012      

/s/ KEVIN W. SHARER

      Kevin W. Sharer
      Chairman of the Board and Chief Executive Officer


CERTIFICATIONS

I, Jonathan M. Peacock, Executive Vice President and Chief Financial Officer of Amgen Inc., certify that:

 

  1. I have reviewed this Annual Report on Form 10-K of Amgen Inc.;

 

  2. Based on my knowledge, this annual report does not contain any untrue statement of a material fact or omit to state a material fact necessary to make the statements made, in light of the circumstances under which such statements were made, not misleading with respect to the period covered by this annual report;

 

  3. Based on my knowledge, the financial statements, and other financial information included in this annual report, fairly present in all material respects the financial condition, results of operations and cash flows of the registrant as of, and for, the periods presented in this annual report;

 

  4. The registrant’s other certifying officer(s) and I are responsible for establishing and maintaining disclosure controls and procedures (as defined in Exchange Act Rules 13a-15(e) and 15d-15(e)) and internal control over financial reporting (as defined in Exchange Act Rules 13a-15(f) and 15d-15(f)) for the registrant and have:

 

  (a) Designed such disclosure controls and procedures, or caused such disclosure controls and procedures to be designed under our supervision, to ensure that material information relating to the registrant, including its consolidated subsidiaries, is made known to us by others within those entities, particularly during the period in which this annual report is being prepared;

 

  (b) Designed such internal control over financial reporting, or caused such internal control over financial reporting to be designed under our supervision, to provide reasonable assurance regarding the reliability of financial reporting and the preparation of financial statements for external purposes in accordance with generally accepted accounting principles;

 

  (c) Evaluated the effectiveness of the registrant’s disclosure controls and procedures and presented in this report our conclusions about the effectiveness of the disclosure controls and procedures, as of the end of the period covered by this annual report based on such evaluation; and

 

  (d) Disclosed in this annual report any change in the registrant’s internal control over financial reporting that occurred during the registrant’s most recent fiscal quarter (the registrant’s fourth fiscal quarter in the case of an annual report) that has materially affected, or is reasonably likely to materially affect, the registrant’s internal control over financial reporting; and

 

  5. The registrant’s other certifying officer(s) and I have disclosed, based on our most recent evaluation of internal control over financial reporting, to the registrant’s auditors and the audit committee of the registrant’s board of directors (or persons performing the equivalent functions):

 

  (a) All significant deficiencies and material weaknesses in the design or operation of internal control over financial reporting which are reasonably likely to adversely affect the registrant’s ability to record, process, summarize and report financial information; and

 

  (b) Any fraud, whether or not material, that involves management or other employees who have a significant role in the registrant’s internal control over financial reporting.

 

Date: February 29, 2012      

/s/ JONATHAN M. PEACOCK

      Jonathan M. Peacock
      Executive Vice President and Chief Financial Officer
Section 1350 Certifications

Exhibit 32

Certification of Chief Executive Officer

Pursuant to 18 U.S.C. § 1350, as created by Section 906 of the Sarbanes-Oxley Act of 2002, the undersigned officer of Amgen Inc. (the “Company”) hereby certifies that:

 

  (i) the accompanying Annual Report on Form 10-K of the Company for the period ended December 31, 2011 (the “Report”) fully complies with the requirements of Section 13(a) or Section 15(d), as applicable, of the Securities Exchange Act of 1934, as amended; and

 

  (ii) information contained in the Report fairly presents, in all material respects, the financial condition and results of operations of the Company.

 

Dated:      February 29, 2012    

/s/ KEVIN W. SHARER

         Kevin W. Sharer
         Chairman of the Board and Chief Executive Officer

A signed original of this written statement required by Section 906 of the Sarbanes-Oxley Act of 2002 (“Section 906”), or other document authenticating, acknowledging, or otherwise adopting the signature that appears in typed form within the electronic version of this written statement required by Section 906, has been provided to Amgen Inc. and will be retained by Amgen Inc. and furnished to the Securities and Exchange Commission or its staff upon request.


Certification of Chief Financial Officer

Pursuant to 18 U.S.C. § 1350, as created by Section 906 of the Sarbanes-Oxley Act of 2002, the undersigned officer of Amgen Inc. (the “Company”) hereby certifies that:

 

  (i) the accompanying Annual Report on Form 10-K of the Company for the period ended December 31, 2011 (the “Report”) fully complies with the requirements of Section 13(a) or Section 15(d), as applicable, of the Securities Exchange Act of 1934, as amended; and

 

  (ii) information contained in the Report fairly presents, in all material respects, the financial condition and results of operations of the Company.

 

Dated:      February 29, 2012    

/s/ JONATHAN M. PEACOCK

         Jonathan M. Peacock
         Executive Vice President and Chief Financial Officer

A signed original of this written statement required by Section 906 of the Sarbanes-Oxley Act of 2002 (“Section 906”), or other document authenticating, acknowledging, or otherwise adopting the signature that appears in typed form within the electronic version of this written statement required by Section 906, has been provided to Amgen Inc. and will be retained by Amgen Inc. and furnished to the Securities and Exchange Commission or its staff upon request.