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Amgen Preclinical Study Demonstrated Anti-Tumor Activity in Mammary Tumor Model

April 19, 2010

THOUSAND OAKS, Calif., April 19 /PRNewswire-FirstCall/ — Amgen (Nasdaq: AMGN) today announced results of a preclinical study demonstrating a positive response to administration of RANK-Fc against mammary tumor formation in mouse models. OPG-Fc and RANK-Fc bind to and block the action of RANKL. These molecules have a comparable mechanism of action to denosumab. The study was presented today in a late-breaking abstract at the American Association for Cancer Research (AACR) 101st Annual Meeting 2010 in Washington, D.C.

As denosumab does not recognize rodent RANKL and the pharmacodynamic mechanism of denosumab is aligned with that of OPG-Fc or RANK-Fc, investigations conducted with these molecules in rodents are deemed appropriate to gain further understanding of the mechanism of action of RANKL in cancer.

Using a hormone (MPA) and carcinogen (DMBA)-induced mammary tumor model in wild-type (WT) mice, the study showed that treatment with RANK-Fc at the initiation of DMBA treatment delayed the time to mammary tumor formation vs. control-treated mice (P<0.0001). RANK-Fc treatment also decreased the incidence of palpable mammary tumors at 32 weeks post last DMBA (22 percent in RANK-Fc treated mice vs. 94 percent in control-treated mice).

The study also tested three different doses of zoledronic acid (0.025, 0.2 and 0.5 mg/kg weekly at DMBA initiation) in WT mice for anti-tumor activity. Zoledronic acid had no effect at any dose on time to tumor formation compared to the control. Additionally, zoledronic acid had no effect at any dose on mammary tumor incidence at 32 weeks post last DMBA (92,100 and 95 percent mammary tumor incidence for 0.5 mg/kg, 0.2 mg/kg and 0.025 mg/kg treated groups respectively).

“In this preclinical study, RANKL inhibition reduced mammary tumor formation in hormone-dependent mouse models,” said Roger M. Perlmutter, M.D., Ph.D., executive vice president of Research and Development at Amgen. “These studies suggest that RANKL inhibition might also prove effective in the treatment of human malignancy. We are encouraged by these results, which could ultimately prove important for patients with breast cancer.”

In previous preclinical studies, RANKL inhibition has been shown to reduce skeletal tumor progression and improve survival of tumor-bearing animals. The current study demonstrates the additional ability of RANKL inhibition to reduce the development of tumors outside the skeleton in hormone-dependent mammary tumor models.

RANKL and its target receptor RANK are key factors in bone remodeling and bone destruction associated with bone metastasis. Denosumab, a fully human monoclonal antibody that specifically inhibits RANKL, inhibits osteoclastogenesis and osteoclast-mediated bone destruction.

About Denosumab and Amgen’s Research in Bone Biology

Denosumab is the first fully human monoclonal antibody in late stage clinical development that specifically targets RANK Ligand, the essential regulator of osteoclasts (the cells that break down bone). With more than 19,000 patients in trials across indications worldwide, the denosumab development program is the largest ever initiated by Amgen. This broad and deep development program demonstrates Amgen’s commitment to researching and delivering pioneering medicines to patients with unmet medical needs. Amgen is studying denosumab in numerous tumor types across the spectrum of cancer-induced bone disease. Over 11,000 patients have been enrolled in the denosumab oncology clinical trials testing the drug for the amelioration of treatment-induced bone loss in patients with breast or prostate cancers, for the prevention of skeletal related events due to the spread of cancer to the bone in patients with multiple myeloma or those suffering from a variety of solid tumors or those suffering from multiple myeloma, and for its potential to delay bone metastases in prostate cancer.

About Amgen

Amgen discovers, develops, manufactures and delivers innovative human therapeutics. A biotechnology pioneer since 1980, Amgen was one of the first companies to realize the new science’s promise by bringing safe and effective medicines from lab, to manufacturing plant, to patient. Amgen therapeutics have changed the practice of medicine, helping millions of people around the world in the fight against cancer, kidney disease, rheumatoid arthritis, and other serious illnesses. With a deep and broad pipeline of potential new medicines, Amgen remains committed to advancing science to dramatically improve people’s lives. To learn more about our pioneering science and our vital medicines, visit www.amgen.com.

Forward-Looking Statements

This news release contains forward-looking statements that are based on management’s current expectations and beliefs and are subject to a number of risks, uncertainties and assumptions that could cause actual results to differ materially from those described. All statements, other than statements of historical fact, are statements that could be deemed forward-looking statements, including estimates of revenues, operating margins, capital expenditures, cash, other financial metrics, expected legal, arbitration, political, regulatory or clinical results or practices, customer and prescriber patterns or practices, reimbursement activities and outcomes and other such estimates and results. Forward-looking statements involve significant risks and uncertainties, including those discussed below and more fully described in the Securities and Exchange Commission (SEC) reports filed by Amgen, including Amgen’s most recent annual report on Form 10-K and most recent periodic reports on Form 10-Q and Form 8-K. Please refer to Amgen’s most recent Forms 10-K, 10-Q and 8-K for additional information on the uncertainties and risk factors related to our business. Unless otherwise noted, Amgen is providing this information as of April 19, 2010 and expressly disclaims any duty to update information contained in this news release.

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    CONTACT: Amgen, Thousand Oaks
    Christine Regan: +1 (805) 447-5476 (media)
    Arvind Sood: +1 (805) 447-1060 (investors)

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