Friday, July 31, 2009
Amgen Statement on the House Energy & Commerce Committee’s Approval of an Amendment to Create a Biosimilars Pathway
The following statement was issued today by Amgen on the passage of the Eshoo-Inslee-Barton amendment to the House Energy & Commerce Committee’s health care reform legislation.
The strong bipartisan support in the Energy and Commerce Committee for a fair and balanced pathway for the approval of biosimilars is a win for patients. The amendment introduced by Representatives Eshoo, Inslee and Barton and overwhelmingly approved by the Committee strikes a necessary balance in allowing access to safe and effective biosimilar medicines for patients, and providing fair incentives for the discovery of new medicines for serious diseases.
Read the rest of this entryPosted in Company Statements
Monday, July 27, 2009
Amgen to Collaborate With GlaxoSmithKline to Commercialize Denosumab in Europe for Postmenopausal Osteoporosis (PMO)
THOUSAND OAKS, Calif. and
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Posted in Press Releases, Pipeline News
Monday, July 27, 2009
Amgen's Second Quarter 2009 Adjusted Earnings Per Share Increased 13 Percent To $1.29
Second Quarter 2009 Revenue Decreased 1 Percent to THOUSAND OAKS, Calif. –
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Posted in Press Releases
Monday, July 20, 2009
Amgen Scholars Discover Their Potential During Summer Science Research Program and National Symposium
THOUSAND OAKS, Calif. – July 20, 2009 – From July 18-20, more than 260 of the country’s brightest undergraduate students met at UCLA for the third annual Amgen Scholars U.S. Symposium designed to bring together program participants and help them apply their science research experiences into future science careers.
Read the rest of this entryPosted in Philanthropy, Press Releases
Friday, July 17, 2009
Amgen Announces KRAS Safety Update to U.S. Prescribing Information for Vectibix(R) (Panitumumab)
Class Labeling Recognizes KRAS as a Predictive Biomarker for anti-EGFr Antibody Monotherapy in Metastatic Colorectal Cancer
Results from First Pivotal Trials Prospectively Evaluating KRAS Utility in Combination Therapy Expected In Third Quarter 2009
THOUSAND OAKS, Calif., July 17 /PRNewswire-FirstCall/—Amgen Inc. (Nasdaq: AMGN) today announced the U.S. Food and Drug Administration (FDA) has approved revisions to the U.S. prescribing information for the epidermal growth factor receptor (EGFr) class of antibodies, including Vectibix (panitumumab). This decision follows the FDA’s December 2008 Oncologics Drugs Advisory Committee (ODAC) meeting where the clinical utility of the KRAS gene as a predictive biomarker in patients with metastatic colorectal cancer (mCRC) treated with anti-EGFr antibody was discussed.
Read the rest of this entryPosted in Press Releases, Product News
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