SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549
FORM 8-K
CURRENT REPORT
PURSUANT TO SECTION 13 OR 15(d)
OF THE SECURITIES EXCHANGE ACT OF 1934
July 22, 2003
Date of Report (Date of earliest event reported)
AMGEN INC.
(Exact name of registrant as specified in its charter)
| Delaware | 000-12477 | 95-3540776 | ||
| (State or other Jurisdiction of Incorporation) |
(Commission File Number) | (IRS Employer Identification Number) |
| Amgen Inc. One Amgen Center Drive Thousand Oaks, CA |
91320-1799 | |
| (Address of principal executive offices) | (Zip Code) |
805-447-1000
(Registrant’s telephone number, including area code)
N/A
(Former Name or Former Address, if Changed Since Last Report)
| Item 7. | Financial Statements, Pro Forma Financial Information And Exhibits. |
(c) Exhibits.
Exhibit 99.1 – Press Release dated July 22, 2003 of the Company.
| Item 9. | Regulation FD Disclosure |
In accordance with the interim guidance of the Securities and Exchange Commission, Amgen Inc. (the “Company”) is furnishing the information required by Item 12 of Form 8-K under “Item 9 Regulation FD Disclosure” and information contained in this report (including exhibits hereto) shall not be deemed “filed” for purposes of Section 18 of the Exchange Act of 1934, as amended, or otherwise subject to the liability of that section and shall not be deemed incorporated by reference in any filing under the Securities Act of 1933, as amended, or the Exchange Act of 1934, as amended.
On July 22, 2003, the Company issued a press release announcing its results of operations and financial condition for the three and six months ended June 30, 2003. The full text of the press release is set forth in Exhibit 99.1 attached hereto.
In its press release the Company included certain historical non-GAAP financial measures with respect to the three and six months ended June 30, 2003, as defined in Regulation G promulgated by the Securities and Exchange Commission. The Company believes that its presentation of historical non-GAAP financial measures provides useful supplementary information to investors. These historical non-GAAP financial measures are in addition to, not a substitute for, or superior to, measures of financial performance prepared in accordance with GAAP.
For the three and six months ended June 30, 2003, the Company’s adjustments to GAAP financial measures relate to 1) amounts associated with the Company’s acquisition of Immunex Corporation (“Immunex”) in July 2002 (the “Acquisition”), 2) the recovery of certain cost and expenses associated with the Company’s arbitration with Johnson & Johnson for breach of the license agreement with the Company (the “Cost Recovery”) and 3) the Company’s cash contribution to the Amgen Foundation (the “Foundation Contribution”).
For the three and six months ended June 30, 2003, the Company reported non-GAAP financial results for the following operating expenses: cost of sales, research and development, and selling, general and administrative, which were each adjusted to exclude incremental compensation paid or payable to certain Immunex employees for a limited period, principally under the Immunex short-term retention plan. The Company believes that excluding such retention payments provides a supplemental measure that will facilitate comparisons between periods before, during and after such retention payments are made.
The Company also reported non-GAAP adjusted net income and adjusted earnings per share, excluding the foregoing operating expense amounts, as well as excluding amortization of
2
acquired intangible assets, the Cost Recovery and the Foundation Contribution, and tax-effected such amounts. The Company believes that excluding the ongoing, non-cash amortization of intangible assets acquired in the Acquisition (primarily ENBREL®) treats those assets as if the Company had developed them internally in the past, and thus provides a supplementary measure of profitability in which the Company’s acquired intellectual property is treated in a comparable manner to its internally developed intellectual property. The Company believes that excluding the Cost Recovery and the Foundation Contribution provides a supplementary measure that will facilitate comparisons between periods in which such items did not occur. The Company uses the foregoing non-GAAP financial measures in connection with its own budgeting and financial planning.
3
SIGNATURES
Pursuant to the requirements of the Securities Exchange Act of 1934, as amended, the Registrant has duly caused this report to be signed on its behalf by the undersigned hereunto duly authorized.
| AMGEN INC. | ||||||
| Date: | July 25, 2003 |
By: |
/s/ RICHARD NANULA | |||
| Name: |
Richard Nanula | |||||
| Title: |
Executive Vice President, Finance, Strategy and Communications, and Chief Financial Officer | |||||
4
EXHIBIT INDEX
| Exhibit Number |
Document Description | |
| 99.1 |
Press release dated July 22, 2003 |
5
Exhibit 99.1
AMGEN’S SECOND QUARTER 2003 ADJUSTED
EARNINGS PER SHARE INCREASES 29% TO 49 CENTS
—
SECOND QUARTER GAAP EARNINGS PER SHARE
INCREASES 18% TO 45 CENTS
—
Total Product Sales Increase 72%
From Recently Launched and Acquired Products
—
2003 Product Sales Guidance Raised $400 Million
to a Range of $7.5 – $8.0 Billion
—
2003 Adjusted Earnings Per Share Guidance Raised 5 Cents From
a Range of $1.80 – $1.90 to a Range of $1.85 – $1.95
THOUSAND OAKS, Calif., July 22—Amgen (Nasdaq:AMGN) today announced that adjusted earnings per share for the second quarter of 2003 was 49 cents versus 38 cents for the second quarter of 2002, an increase of 29%. Adjusted net income was $653 million in the second quarter of 2003 versus $412 million in the second quarter of 2002, a 58% increase.
Amgen now expects adjusted earnings per share to range between $1.85 – $1.95 for the full year of 2003, versus the previous estimate of $1.80 – $1.90.
Adjusted earnings per share and adjusted net income for the three months ended June 30, 2003 exclude certain expenses related to the acquisition of Immunex, a benefit of $74 million related to the recovery of the fees and costs associated with the Company’s arbitration with Johnson & Johnson and a charitable contribution of $50 million made to the Amgen Foundation. These items are itemized on the attached reconciliation tables.
On a reported basis, calculated in accordance with US generally accepted accounting principles (GAAP), Amgen reported earnings per share of 45 cents in the second quarter of 2003 versus 38 cents, an 18% increase versus the second
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quarter of 2002. Reported net income for the second quarter of 2003 was $607 million versus $412 million, a 47% increase versus the same period a year ago.
Total revenue increased 63% to $2.0 billion in the second quarter of 2003.
“We continue to deliver strong financial performance and for the first time in Amgen’s history have recorded quarterly revenue of $2 billion,” said Kevin Sharer, chairman and chief executive officer. “We’re pleased with our sales performance across all our products, in particular Aranesp®, which continues to gain global market share in a growing anemia market. In addition, we continued our efforts to obtain regulatory approval for use of ENBREL® in patients suffering from ankylosing spondylitis and psoriasis, and we’re preparing to submit a regulatory dossier for Cinacalcet HCl later this year. None of this would have been possible without the dedication of our employees and their commitment to patients,” Sharer said.
Product Sales Performance and Expenses
Total product sales in the quarter were $1.9 billion, an increase of 72% over the same period last year due to new and acquired products. Excluding ENBREL® (etanercept) total product sales grew 45%. US product sales were $1.7 billion, an increase of 64% versus the second quarter of last year, and accounted for 86% of total product sales. International sales were $259 million for the second quarter versus $107 million for the same quarter last year, an increase of 142%. Without the beneficial impact of foreign exchange in the second quarter, international sales would have grown 102%. Total product sales are now expected to grow to a range between $7.5 and $8.0 billion in 2003 versus previous guidance of a range between $7.1 and $7.6 billion. Total revenue is now projected to range between $8.0 and $8.5 billion versus the previous guidance of a range between $7.7 and $8.2 billion. Total revenues are increasing to a lesser degree due to lower projected royalty income as Aranesp® continues to gain market share in the US oncology market.
For the second quarter, combined worldwide sales of EPOGEN® (Epoetin alfa), Amgen’s anemia therapy for patients on dialysis, and Aranesp® (darbepoetin alfa), its latest anemia product for the treatment of anemia associated with chronic renal failure and anemia due to chemotherapy, increased 53% to $959 million from $626 million for the second quarter of 2002. This increase was primarily driven by worldwide Aranesp® sales. EPOGEN® sales were $611 million for the second quarter, an increase of 7% over the same quarter last year. The company indicated that substantially all of the growth was due to a favorable revised estimate of dialysis demand for prior quarters. This adjustment, which results from spillover, is due to the company’s contractual relationship with Johnson & Johnson. (Please refer to the Company’s 2002 Form10-K for a more detailed discussion of this relationship and a description of spillover.)
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EPOGEN® demand in the second quarter was up slightly compared to the prior year. For the full year 2003, the company continues to believe underlying dialysis patient growth in the range of 4% to 5% will principally drive EPOGEN® sales.
Worldwide Aranesp® sales in the second quarter were $348 million versus $56 million in the second quarter of last year. The company believes worldwide Aranesp® sales were primarily driven by demand and reflect the mid-year 2002 approval for the incremental indication for chemotherapy-induced anemia in oncology in the US and growth in Europe. Second quarter US Aranesp® sales were $217 million versus $33 million last year. International Aranesp® sales were $131 million versus $23 million in the second quarter last year. The growth in international Aranesp® sales was aided by $23 million in foreign exchange benefits due to a weaker US dollar.
Due to increased Aranesp® strength in the US and Europe, the company is raising combined 2003 worldwide sales guidance of EPOGEN® and Aranesp® to a range between $3.7 and $3.9 billion versus the previous range of $3.4 to $3.6 billion.
Combined worldwide sales of Neulasta™ (pegfilgrastim) and NEUPOGEN® (Filgrastim) increased 34% to $634 million from $473 million in the second quarter last year. Worldwide Neulasta™ sales were $304 million in the second quarter of 2003, $13 million of which were international sales. US Neulasta™ sales were $291 million in the second quarter versus $110 million for the second quarter last year. Worldwide NEUPOGEN® sales were $331 million for the second quarter of 2003, a 9% decrease from the second quarter of 2002, reflecting US conversion to Neulasta™, which the company indicated has slowed. Neulasta™ is Amgen’s once-per-cycle product for decreasing the risk of chemotherapy-related infections, and NEUPOGEN® is used to decrease the incidence of infection during many types of cancer-related chemotherapy.
On a geographic basis, second quarter NEUPOGEN® sales were $233 million in the US versus $281 million in the second quarter of 2002, and $98 million outside the US versus $83 million. International NEUPOGEN® sales growth was entirely due to a weaker US dollar.
The company has increased its forecast for 2003 combined worldwide NEUPOGEN® and Neulasta™ sales and now expects sales to range between $2.4 and $2.6 billion versus the previous range of $2.3 to $2.5 billion.
ENBREL®, Amgen’s leading inflammation biologic, recorded second quarter sales of $304 million, a 58% increase over second quarter 2002 sales by Immunex Corporation of $192 million. ENBREL® sales in the second quarter were driven by new patients in both rheumatology and dermatology. Second quarter 2002 ENBREL® sales by Immunex Corporation were adversely affected by supply shortages. Amgen continues to forecast that 2003 ENBREL® sales will range between $1.2 and $1.4 billion.
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Operating Expenses on an adjusted basis were as follows:
| • | Cost of sales increased to $324 million in the second quarter of 2003 from $132 million in the second quarter of 2002 primarily due to increased sales, which include ENBREL® for the 2003 period only. Cost of sales as a percentage of sales increased from 12% in the second quarter of 2002 to 17% in the second quarter of 2003. This increase principally reflects the inclusion of ENBREL®, which has significantly higher manufacturing costs and higher royalty expense as compared with Amgen’s other products. In addition, the manufacturing costs of Amgen’s ENBREL® production facility in Rhode Island are greater than those of Amgen’s contract manufacturer. |
| • | In the second quarter of 2003, R&D expense was $385 million versus $234 million in the second quarter of 2002. This increase was primarily due to the inclusion of headcount in Seattle, additional R&D headcount in other locations, higher clinical trial and clinical manufacturing activity, and higher licensing and milestone fees associated with collaborations. |
| • | SG&A expense was $450 million in the second quarter of 2003 versus $321 million for the prior year. This increase was primarily due to support of ENBREL®, the Wyeth profit share related to ENBREL® and higher staff-related expenses to support new product launches. |
For 2003, adjusted operating expenses are now expected to range between $4.6 to $4.8 billion versus the previous estimate of between $4.4 and $4.7 billion. The increased guidance is due, in part, to higher costs of sales associated with a higher sales forecast and further investment in R&D and SG&A.
In the second quarter of 2003, share repurchases were $449 million representing the repurchase of approximately 7 million shares. Capital expenditures in the second quarter were $276 million compared to $111 million for the same period a year ago. The increase was principally related to the company’s Puerto Rico manufacturing expansion, the construction of the company’s research center in Seattle, and the building of a new ENBREL® manufacturing plant in Rhode Island. The company’s cash and marketable securities were $5 billion at the end of the quarter.
Pipeline Update
Amgen reported the successful completion of three Phase 3 studies supporting the use of cinacalcet HCl for the treatment of secondary hyperparathyroidism. Cinacalcet HCl, Amgen’s first small molecule therapeutic, is an oral-acting modulator of the parathyroid gland calcium-sensing receptor that enables targeted control of hyperparathyroidism associated with end-stage kidney disease. In the three Phase 3 trials, statistically
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significant efficacy was seen as judged by metabolic endpoints. Cinacalcet was safe and well-tolerated. Amgen expects to file cinacalcet HCl for regulatory approval with the FDA for secondary hyperparathyroidism in the second half of 2003.
As announced previously, during the second quarter Amgen submitted a supplemental Biologics License Application for the use of ENBREL® in moderate to severe plaque psoriasis. The company also presented data demonstrating the significant symptom relief of combination treatment with ENBREL® and methotrexate in patients with rheumatoid arthritis compared with ENBREL® or methotrexate alone. On June 24, a Food and Drug Administration Arthritis Advisory Committee unanimously recommended the approval of ENBREL® in patients suffering from ankylosing spondylitis, a chronic inflammatory disease of the spine.
At the American Society of Oncology in June, the company presented data on several programs including:
| • | Interim phase 2 data demonstrating single agent antitumor activity with ABX-EGF, a fully human monoclonal antibody, in patients with advanced colorectal cancer, |
| • | Data suggesting that the risk of infection doubles with reduced NEUPOGEN® administration, and, |
| • | Data on Aranesp® dosed once every two weeks in the management of patients with chemotherapy-induced anemia increases hemoglobin levels, improves fatigue and reduces the need for transfusions. |
In the second quarter, Amgen also announced an agreement with Tularik to collaborate on the discovery, development and commercialization of therapeutics aimed at oncology targets.
FORWARD LOOKING STATEMENTS
This news release contains forward-looking statements that involve significant risks and uncertainties, including those discussed below and others that can be found in our Form 10-K for the year ended December 31, 2002, and in our periodic reports on Form 10-Q and Form 8-K. Amgen is providing this information as of the date of this news release and does not undertake any obligation to update any forward-looking statements contained in this document as a result of new information, future events or otherwise.
No forward-looking statement can be guaranteed and actual results may differ materially from those we project. The Company’s results may be affected by our ability to successfully market both new and existing products domestically and internationally, sales growth of recently launched products, difficulties or delays in manufacturing our products, and regulatory developments (domestic or foreign) involving current and future products and manufacturing facilities. In addition, sales of our products are affected by reimbursement policies imposed by third party payors, including governments, private insurance plans and managed care providers, and may be affected by domestic and international trends toward managed care and healthcare cost
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containment as well as possible US legislation affecting pharmaceutical pricing and reimbursement. Government regulations and reimbursement policies may affect the development, usage and pricing of our products. Furthermore, our research, testing, pricing, marketing and other operations are subject to extensive regulation by domestic and foreign government regulatory authorities. We, or others could identify side effects or manufacturing problems with our products after they are on the market. In addition, we compete with other companies with respect to some of our marketed products as well as for the discovery and development of new products. Discovery or identification of new product candidates cannot be guaranteed and movement from concept to product is uncertain; consequently, there can be no guarantee that any particular product candidate will be successful and become a commercial product. In addition, while we routinely obtain patents for our products and technology, the protection offered by our patents and patent applications may be challenged, invalidated or circumvented by our competitors. Further, some raw materials, medical devices, and component parts for our products are supplied by sole third party suppliers.
Amgen is a global biotechnology company that discovers, develops, manufactures and markets important human therapeutics based on advances in cellular and molecular biology.
| CONTACT: | Amgen, Thousand Oaks | |
| Sabrina Johnson, 805/447-9753 (Media) | ||
| Cary Rosansky, 805/447-4634 (Investors) |
# # #
EDITOR’S NOTE: An electronic version of this news release may be accessed via our web site at www.amgen.com. Visit the Corporate Center and click on Amgen News. Journalists and media representatives may sign up to receive all news releases electronically at time of announcement by filling out a short form in the Amgen News section of the web site.
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Appendix I
Amgen Inc.
Condensed Consolidated Statements of Operations and
Reconciliation of GAAP Earnings to “Adjusted” Earnings
(In millions, except per share data)
(Unaudited)
| Three Months Ended June 30, 2003 |
Three Months Ended June 30, 2002 |
|||||||||||||||
| GAAP |
Adjustments |
“Adjusted” |
GAAP/”Adjusted” (6) |
|||||||||||||
| Revenues: |
||||||||||||||||
| Product sales |
$ | 1,916.5 | $ | — | $ | 1,916.5 | $ | 1,115.2 | ||||||||
| Royalty income |
91.9 | — | 91.9 | 80.0 | ||||||||||||
| Corporate partner revenues |
32.7 | — | 32.7 | 53.9 | ||||||||||||
| Total revenues |
2,041.1 | — | 2,041.1 | 1,249.1 | ||||||||||||
| Operating expenses: |
||||||||||||||||
| Cost of sales |
329.1 | (4.9 | ) (1) | 324.2 | 131.9 | |||||||||||
| Research and development |
393.7 | (9.1 | ) (1) | 384.6 | 233.6 | |||||||||||
| Selling, general and administrative |
453.5 | (3.7 | ) (1) | 449.8 | 320.5 | |||||||||||
| Amortization of intangible assets |
84.0 | (84.0 | ) (2) | — | — | |||||||||||
| Earnings of affiliates, net |
(12.3 | ) | — | (12.3 | ) | (1.7 | ) | |||||||||
| Other items, net |
(24.0 | ) | 74.0 | (3) | — | — | ||||||||||
| (50.0 | ) (4) | |||||||||||||||
| Total operating expenses |
1,224.0 | (77.7 | ) | 1,146.3 | 684.3 | |||||||||||
| Operating income |
817.1 | 77.7 | 894.8 | 564.8 | ||||||||||||
| Other income (expense): |
||||||||||||||||
| Interest and other income, net |
40.4 | — | 40.4 | 45.5 | ||||||||||||
| Interest expense, net |
(8.8 | ) | — | (8.8 | ) | (12.7 | ) | |||||||||
| Total other income |
31.6 | — | 31.6 | 32.8 | ||||||||||||
| Income before income taxes |
848.7 | 77.7 | 926.4 | 597.6 | ||||||||||||
| Provision for income taxes |
241.5 | 31.8 | (5) | 273.3 | 185.2 | |||||||||||
| Net income |
$ | 607.2 | $ | 45.9 | $ | 653.1 | $ | 412.4 | ||||||||
| Earnings per share: |
||||||||||||||||
| Basic |
$ | 0.47 | $ | 0.51 | $ | 0.40 | ||||||||||
| Diluted (7) |
$ | 0.45 | $ | 0.49 | $ | 0.38 | ||||||||||
| Shares used in calculation of earnings per share: |
||||||||||||||||
| Basic |
1,287.9 | 1,287.9 | 1,038.6 | |||||||||||||
| Diluted (7) |
1,347.0 | 1,347.0 | 1,098.8 | |||||||||||||
(1) – (7) See explanatory notes
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Amgen Inc.
Condensed Consolidated Statements of Operations and
Reconciliation of GAAP Earnings to “Adjusted” Earnings
(In millions, except per share data)
(Unaudited)
| Six Months Ended June 30, 2003 |
Six Months Ended June 30, 2002 |
|||||||||||||||||
| GAAP |
Adjustments |
“Adjusted” |
GAAP/“Adjusted” (6) |
|||||||||||||||
| Revenues: |
||||||||||||||||||
| Product sales |
$ | 3,552.4 | $ | — | $ | 3,552.4 | $ | 2,023.8 | ||||||||||
| Royalty income |
183.3 | — | 183.3 | 148.4 | ||||||||||||||
| Corporate partner revenues |
66.6 | — | 66.6 | 85.4 | ||||||||||||||
| Total revenues |
3,802.3 | — | 3,802.3 | 2,257.6 | ||||||||||||||
| Operating expenses: |
||||||||||||||||||
| Cost of sales |
612.4 | (9.8 | ) | (1) | 602.6 | 235.5 | ||||||||||||
| Research and development |
745.0 | (18.8 | ) | (1) | 726.2 | 437.0 | ||||||||||||
| Selling, general and administrative |
843.6 | (8.5 | ) | (1) | 835.1 | 566.3 | ||||||||||||
| Amortization of intangible assets |
167.9 | (167.9 | ) | (2) | — | — | ||||||||||||
| Earnings of affiliates, net |
(21.9 | ) | — | (21.9 | ) | (3.4 | ) | |||||||||||
| Other items, net |
(24.0 | ) | 74.0 | (3) | — | — | ||||||||||||
| (50.0 | ) | (4) | ||||||||||||||||
| Total operating expenses |
2,323.0 | (181.0 | ) | 2,142.0 | 1,235.4 | |||||||||||||
| Operating income |
1,479.3 | 181.0 | 1,660.3 | 1,022.2 | ||||||||||||||
| Other income (expense): |
||||||||||||||||||
| Interest and other income, net |
73.2 | — | 73.2 | 89.2 | ||||||||||||||
| Interest expense, net |
(15.7 | ) | — | (15.7 | ) | (19.7 | ) | |||||||||||
| Total other income |
57.5 | — | 57.5 | 69.5 | ||||||||||||||
| Income before income taxes |
1,536.8 | 181.0 | 1,717.8 | 1,091.7 | ||||||||||||||
| Provision for income taxes |
436.3 | 70.5 | (5) | 506.8 | 338.4 | |||||||||||||
| Net income |
$ | 1,100.5 | $ | 110.5 | $ | 1,211.0 | $ | 753.3 | ||||||||||
| Earnings per share: |
||||||||||||||||||
| Basic |
$ | 0.85 | $ | 0.94 | $ | 0.72 | ||||||||||||
| Diluted (7) |
$ | 0.82 | $ | 0.91 | $ | 0.70 | ||||||||||||
| Shares used in calculation of earnings per share: |
||||||||||||||||||
| Basic |
1,289.3 | 1,289.3 | 1,041.2 | |||||||||||||||
| Diluted (7) |
1,348.5 | 1,348.5 | 1,092.4 | |||||||||||||||
(1) – (7) See explanatory notes
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Amgen Inc.
Notes to Reconciliation of GAAP Earnings to “Adjusted” Earnings
(In millions, except per share data)
(Unaudited)
| (1) | To exclude the incremental compensation payable to certain Immunex employees principally under the Immunex short-term retention plan. The total estimated remaining costs of such retention benefits is approximately $65 million, pre-tax, and will be incurred through the quarter ending June 30, 2004. |
| (2) | To exclude the ongoing, non-cash amortization of acquired intangible assets, primarily ENBREL®, related to the Immunex acquisition. The total annual non-cash charge is currently estimated to be approximately $340 million, pre-tax. |
| (3) | To exclude a benefit for the recovery of costs and expenses associated with a legal award related to an arbitration proceeding with Johnson & Johnson. |
| (4) | To exclude a cash contribution to the Amgen Foundation. |
| (5) | To reflect the tax effect of the above adjustments. |
| (6) | For the three and six months ended June 30, 2002, GAAP earnings were equal to “Adjusted” earnings. |
| (7) | The following tables present the computations for GAAP and “Adjusted” diluted earnings per share computed under the treasury stock and the “if-converted” methods: |
| Three Months Ended June 30, 2003 |
Three Months Ended June 30, 2002 | ||||||||
| GAAP |
“Adjusted” |
GAAP/“Adjusted” | |||||||
| Income (Numerator): |
|||||||||
| Net income for basic EPS |
$ | 607.2 | $ | 653.1 | $ | 412.4 | |||
| Adjustment for interest expense on Convertible Notes, net of tax |
5.2 | 5.2 | 5.2 | ||||||
| Income for diluted EPS, after assumed conversion of Convertible Notes |
$ | 612.4 | $ | 658.3 | $ | 417.6 | |||
| Shares (Denominator): |
|||||||||
| Weighted-average shares for basic EPS |
1,287.9 | 1,287.9 | 1,038.6 | ||||||
| Effect of Dilutive Securities |
24.1 | 24.1 | 25.2 | ||||||
| Effect of Convertible Notes, after assumed conversion of Convertible Notes |
35.0 | 35.0 | 35.0 | ||||||
| Adjusted weighted-average shares for diluted EPS |
1,347.0 | 1,347.0 | 1,098.8 | ||||||
| Diluted earnings per share |
$ | 0.45 | $ | 0.49 | $ | 0.38 | |||
| Six Months Ended June 30, 2003 |
Six Months Ended June 30, 2002 | ||||||||
| GAAP |
“Adjusted” |
GAAP/“Adjusted” | |||||||
| Income (Numerator): |
|||||||||
| Net income for basic EPS |
$ | 1,100.5 | $ | 1,211.0 | $ | 753.3 | |||
| Adjustment for interest expense on Convertible Notes, net of tax |
10.4 | 10.4 | 6.9 | ||||||
| Income for diluted EPS, after assumed conversion of Convertible Notes |
$ | 1,110.9 | $ | 1,221.4 | $ | 760.2 | |||
| Shares (Denominator): |
|||||||||
| Weighted-average shares for basic EPS |
1,289.3 | 1,289.3 | 1,041.2 | ||||||
| Effect of Dilutive Securities |
24.2 | 24.2 | 27.6 | ||||||
| Effect of Convertible Notes, after assumed conversion of Convertible Notes |
35.0 | 35.0 | 23.6 | ||||||
| Adjusted weighted-average shares for diluted EPS |
1,348.5 | 1,348.5 | 1,092.4 | ||||||
| Diluted earnings per share |
$ | 0.82 | $ | 0.91 | $ | 0.70 | |||
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Appendix II
Amgen Inc.
Condensed Consolidated Balance Sheets
(In millions)
(Unaudited)
| June 30, 2003 |
December 31, 2002 | |||||
| Assets |
||||||
| Current assets: |
||||||
| Cash and marketable securities |
$ | 4,985.4 | $ | 4,663.9 | ||
| Trade receivables, net |
960.7 | 752.4 | ||||
| Inventories |
638.7 | 544.9 | ||||
| Other current assets |
384.5 | 442.3 | ||||
| Total current assets |
6,969.3 | 6,403.5 | ||||
| Property, plant, and equipment, net |
3,152.7 | 2,813.5 | ||||
| Intangible assets, net |
4,628.8 | 4,801.9 | ||||
| Goodwill |
9,871.8 | 9,871.1 | ||||
| Other assets |
758.9 | 566.3 | ||||
| Total assets |
$ | 25,381.5 | $ | 24,456.3 | ||
| Liabilities and Stockholders’ Equity |
||||||
| Current liabilities |
$ | 1,687.3 | $ | 1,529.2 | ||
| Deferred tax liabilities |
1,685.8 | 1,593.4 | ||||
| Long-term debt |
3,063.7 | 3,047.7 | ||||
| Stockholders’ equity |
18,944.7 | 18,286.0 | ||||
| Total liabilities and stockholders’ equity |
$ | 25,381.5 | $ | 24,456.3 | ||
| Shares outstanding |
1,288.7 | 1,289.1 | ||||
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Second Quarter 2003 Adjusted Earnings Per Share Increases 29% to 49 Cents
Page 11
Appendix III
Amgen Inc.
Product Sales Detail by Product and Geographic Region
(In millions)
(Unaudited)
| Three Months Ended June 30, |
Six Months Ended June 30, | |||||||||||
| 2003 |
2002 |
2003 |
2002 | |||||||||
| EPOGEN®—U.S. |
$ | 611.1 | $ | 570.3 | $ | 1,158.2 | $ | 1,082.5 | ||||
| Aranesp®—U.S. |
216.6 | 33.0 | 374.5 | 57.5 | ||||||||
| Aranesp®—International |
131.1 | 22.7 | 228.0 | 37.4 | ||||||||
| NEUPOGEN®—U.S. |
233.3 | 280.5 | 427.3 | 561.2 | ||||||||
| NEUPOGEN®—International |
97.5 | 82.9 | 187.5 | 157.2 | ||||||||
| Neulasta™—U.S. |
291.0 | 109.8 | 543.4 | 109.8 | ||||||||
| Neulasta™—International |
12.5 | — | 18.0 | — | ||||||||
| ENBREL®—U.S. |
293.7 | — | 558.2 | — | ||||||||
| ENBREL®—International |
10.3 | — | 19.8 | — | ||||||||
| Other product sales |
19.4 | 16.0 | 37.5 | 18.2 | ||||||||
| Total product sales |
$ | 1,916.5 | $ | 1,115.2 | $ | 3,552.4 | $ | 2,023.8 | ||||
| U.S. |
$ | 1,657.3 | $ | 1,008.3 | $ | 3,084.8 | $ | 1,827.4 | ||||
| International |
259.2 | 106.9 | 467.6 | 196.4 | ||||||||
| $ | 1,916.5 | $ | 1,115.2 | $ | 3,552.4 | $ | 2,023.8 | |||||
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Second Quarter 2003 Adjusted Earnings Per Share Increases 29% to 49 Cents
Page 12
Appendix IV
Amgen Inc.
Reconciliation of “Adjusted” Earnings Guidance to GAAP Earnings Guidance
for the Year Ended December 31, 2003
| 2003 |
||||
| “Adjusted” earnings per share guidance |
$ | 1.85 – $ 1.95 | ||
| Known adjustments to arrive at GAAP earnings: |
||||
| Amortization of acquired intangible assets |
(0.16 | ) | ||
| Merger related retention expenses |
(0.03 | ) | ||
| Amgen Foundation contribution |
(0.02 | ) | ||
| J&J arbitration recovery |
0.03 | |||
| GAAP earnings per share guidance |
$ | 1.67 – $1.77 | ||
| “Adjusted” operating expense guidance |
$ | 4.6 to $4.8 Billion | ||
| Impact of known adjustments to arrive at GAAP operating expenses: |
||||
| Amortization of acquired intangible assets |
340 million | |||
| Merger related retention expenses |
70 million | |||
| Amgen Foundation contribution |
50 million | |||
| J&J arbitration recovery |
(74 million | ) | ||
| GAAP operating expense guidance |
$ | 5.0 to $5.2 Billion | ||