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  • Pipeline in the News
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In the News

ESAs in the News
Aug. 7, 2008
Amgen Posts Updated ESA Labeling
Jul. 30, 2008
Amgen Issues Statement in Response to Revised ESA Labeling from the FDA
May 8, 2008
Amgen Statement on Aranesp ‘145 Manuscript’ In the Journal of Clinical Oncology
May 6, 2008
Amgen Statement on U.S. Food and Drug Administration approval of Aranesp® Q2W dosing for de novo correction of anemia in patients with chronic renal failure (CRF)
Mar. 13, 2008
Amgen Discusses Benefits and Risks of ESA Treatment for Cancer Patients with Anemia Due to Chemotherapy at FDA ODAC Meeting
Mar. 11, 2008
Amgen Statement on Briefing Materials Prepared for March 13, 2008 ODAC Meeting
Mar. 7, 2008
Letter to Healthcare Professionals
Mar. 7, 2008
Amgen Announces Update to U.S. Prescribing Information for Aranesp® and EPOGEN®
Dec. 4, 2007
Amgen statement on the Gynecologic Oncology Group study on Epoetin Alfa
Nov. 13, 2007
Amgen New Evidence Reconsideration Request
Nov. 8 , 2007
Amgen to Provide New Evidence as Part of a Formal Reconsideration of CMS' National Coverage Determination on ESAs
Oct. 23, 2007
Amgen’s Ongoing Commitment to the Safety of its ESA Products: New Pharmacovigilance Program Proposed
Oct. 23, 2007
Jury Rules Roche Infringes Amgen's EPO Patents
Sept. 11, 2007
Press Release: Amgen to Review Benefits, Risks of ESA Therapy in Chronic Renal Failure Patients at FDA Advisory Committee
Sept. 7, 2007
Amgen to Present at FDA CRDAC Meeting Sept. 11
July 31, 2007
Press Release: Amgen Responds to Final CMS National Coverage Determination on Use of Erythropoiesis-Stimulating Agents in Oncology
June 26, 2007
Press Release: Amgen Submits Testimony to House Ways & Means Committee
June 26, 2007
Summary of Amgen Testimony to House Ways & Means Committee
June 26, 2007
Amgen Submission to House Ways & Means Committeee
June 19, 2007
Amgen’s Further Response to Senator Charles Grassley Regarding ESA Safety
June 12, 2007
Amgen’s Response to Senator Charles Grassley Regarding ESA Safety
June 2, 2007
Amgen’s Response to CMS Proposed Decision Memorandum for ESAs for Non-Renal Disease Indications
May 31, 2007
Amgen’s Policy on Sharing Our Clinical Trial Results
May 31, 2007
Amgen’s Position on Ethical Marketing of ESAs
May 21, 2007
Amgen CEO Kevin Sharer’s Letter to the Editor of the New York Times Regarding the Use of ESAs

Background Documents

Prescribing information for Aranesp®
Prescribing information for EPOGEN®

 

Enbrel® (etanercept) in the News
Jun. 18, 2008
Amgen and Wyeth Statement on Outcome of Dermatologic and Ophthalmic Drugs Advisory Committee (DODAC) Meeting
Jun. 18, 2008
Enbrel® (etanercept) Application for the Treatment of Pediatric Psoriasis to be Discussed at FDA Dermatologic and Ophthalmic Drugs Advisory Committee (DODAC) Meeting
Jun. 16, 2008
Amgen Statement on Briefing Materials Prepared for June 18, 2008 DODAC Meeting
Jun. 4, 2008
Amgen and Wyeth Statement on the FDA Early Communication About Tumor Necrosis Factor (TNF) Blockers
May 1, 2008
Amgen to Participate in Dermatologic and Ophthalmic Drugs Advisory Committee Meeting in June
Apr. 16, 2008
Amgen Statement on Alzheimer's Case Study
Mar. 17, 2008
Press Release: Amgen Announces Update to U.S. Prescribing Information for Enbrel®
Mar. 17, 2008
Letter to Healthcare Professionals

Background Documents

Prescribing information for Enbrel®

 

Pipeline in the News
Jul. 24 , 2008
Amgen Statement on Business Wire® Erroneous Release of Nplate™ (romiplostim) News
Jun. 4 , 2008
Amgen Presents New Data at ASCO
Apr. 21 , 2008
Amgen Issues Statement in Response  to Sheffield Telegraph Story on Denosumab
Apr. 8 , 2008
Amgen Statement on Romiplostim PDUFA Date
Apr. 3 , 2008
Amgen's Oncology Pipeline Data Highlighted at Upcoming Scientific Meeting
Apr. 2, 2008
Pivotal Phase 3 Data Show Denosumab Increased Bone Density at Multiple Skeletal Sites in Early and Later Stage Postmenopausal Women
Mar. 12 , 2008
Amgen to Discuss Romiplostim Application at FDA ODAC Meeting
Mar. 10 , 2008
Amgen Statement on Briefing Materials Prepared for March 12, 2008 ODAC Meeting

 

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