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Amgen (AMGN) Says 19 Abstracts Will be Presented at ACC
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Amgen To Present Repatha® (Evolocumab) Data At ACC.16
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Amgen (AMGN), UCB Announce Romosozumab Phase 3 Met Primary Endpoint in Men With Osteoporosis
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Amgen And UCB Announce Positive Top-Line Results From Phase 3 Study Evaluating Romosozumab In Men With Osteoporosis
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Amgen (AMGN) Comments Following Repatha Patent Win
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Amgen Wins Patent Case On Repatha® (Evolocumab)
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Regeneron (REGN) and Sanofi Confirm Negative Praluent Ruling, 'Strongly Disagree' with Verdict (AMGN)
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Amgen (AMGN) sBLA for Exapnded Enbrel Use Accepted by FDA
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FDA Accepts Amgen's Supplemental Biologics License Application For The Expanded Use Of Enbrel® (Etanercept) To Treat Pediatric Patients With Chronic Severe Plaque Psoriasis
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Amgen To Present At The Cowen And Company 36th Annual Health Care Conference
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Amgen Announces 2016 Second Quarter Dividend
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Amgen (AMGN) Submits sBLA For BLINCYTO
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Amgen Submits Supplemental Biologics License Application For BLINCYTO® (Blinatumomab)
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Amgen (AMGN), UCB Announce FRAME Phase 3 Met co-Primary Endpoints; One Secondary Endpoint Missed
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Amgen And UCB Announce Positive Top-Line Results From The Phase 3 Study Of Romosozumab In Postmenopausal Women With Osteoporosis
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Amgen (AMGN) Announces Aranesp Phase 3 Met Primary Endpoint in MDS Red Blood Cell Transfusion Reduction
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Phase 3 Study Demonstrates Aranesp® (Darbepoetin Alfa) Reduces Red Blood Cell Transfusions In Patients With Myelodysplastic Syndrome (MDS)
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Amgen To Present At The Leerink Partners 5th Annual Global Healthcare Conference
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Amgen (AMGN) Announces BLINCYTO Phase 3 TOWER Met Primary Endpoint in r/r B-Cell Precursor ALL
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Phase 3 Study of BLINCYTO® (Blinatumomab) Met Primary Endpoint Of Overall Survival In Patients With B-Cell Precursor Acute Lymphoblastic Leukemia
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Amgen (AMGN) Says Repatha Phase 3 GAUSS-3 Met co-Primary Endpoints
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Amgen Announces Positive Top-Line Results From Phase 3 GAUSS-3 Trial Of Repatha® (Evolocumab) In Statin-Intolerant Patients With High Cholesterol
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Amgen's 2015 Revenues Increased 8 Percent To $21.7 Billion And Adjusted Earnings Per Share (EPS) Increased 19 Percent To $10.38
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Amgen (AMGN) BLA for ABP 501 Accepted by FDA
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FDA Accepts Amgen's Biosimilar Biologics License Application For ABP 501
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Amgen Announces Webcast of 2015 Fourth Quarter and Full Year Financial Results
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Amgen (AMGN) Announces Vectibix + BSC Phase 3 Met Primary Endpoint
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Vectibix® (panitumumab) And Best Supportive Care Improves Overall Survival Compared To Best Supportive Care In Chemorefractory KRAS And RAS Wild-Type Metastatic Colorectal Cancer
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Amgen (AMGN) Announces Japanese Approval of Repatha as PCSK9 Inhibitor
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Amgen's Repatha® (Evolocumab) Approved As First PCSK9 Inhibitor In Japan For The Treatment Of High Cholesterol
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Amgen (AMGN) Announces FDA Approval of Supplemental Kyprolis Combo NDA in r/r Multiple Myeloma
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FDA Approves New Kyprolis® (Carfilzomib) Combination Therapy For The Treatment Of Patients With Relapsed Or Refractory Multiple Myeloma
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Amgen To Present At The 34th Annual J.P. Morgan Healthcare Conference
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Harris & Harris Group (TINY) Announces Receipt of BioVex Group-Related Milestone Payment
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Amgen (AMGN) Announces EC Approval of IMLYGIC for Unresectable Melanoma
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European Commission Approves Amgen's IMLYGIC™ (talimogene laherparepvec) As First Oncolytic Immunotherapy In Europe
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Amgen Announces 27 Percent Increase In 2016 First Quarter Dividend
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Pre-Open Stock Movers 12/15: (KTOV) (LL) (VRX) Higher; (NEOT) (KMT) (ZOES) Lower (more...)
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Amgen (AMGN) Will Reacquire All Prolia, XGEVA, and Vectibix Rights (GSK)
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Amgen Reacquires All Product Rights To Prolia® (denosumab), XGEVA® (denosumab) And Vectibix® (panitumumab) From GSK In 48 Countries
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Amgen (AMGN) Announces Presentation of Data from Three BLINCYTO Phase 2s at ASH 2015
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Amgen Presents Data From Three Trials Evaluating BLINCYTO® (blinatumomab) In Acute Lymphoblastic Leukemia At ASH 2015
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New Analyses Presented At ASH 2015 Demonstrate The Potential Of Kyprolis® (Carfilzomib) As Backbone Therapy In Multiple Myeloma
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Pivotal Head-To-Head ENDEAVOR Study Results Published in The Lancet Oncology Demonstrate Superiority of Kyprolis® (carfilzomib) Combination Over Velcade® (bortezomib) Combination
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Amgen Submits Application In Europe To Expand Indication Of Kyprolis® (carfilzomib) For The Treatment Of Relapsed Multiple Myeloma
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Amgen And Merck Announce Cancer Immunotherapy Collaboration For Patients With Non-Hodgkin Lymphoma
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Amgen's First Biosimilar Marketing Authorization Application Submitted To European Medicines Agency For ABP 501
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Amgen's First Biosimilar Biologics License Application For ABP 501 Submitted To U.S. Food And Drug Administration
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European Commission Approves Amgen's BLINCYTO® (blinatumomab) for the Treatment of Adults with Philadelphia Chromosome-Negative Relapsed or Refractory B-precursor Acute Lymphoblastic Leukemia
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Amgen Announces Repatha® Preferred Position On CVS Health Commercial Formularies

