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Amgen And Arrowhead Pharmaceuticals Announce Two Cardiovascular Collaborations
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Amgen (AMGN) Announces Erenumab Phase 3 Met Primary Endpoint in Migraine Prevention
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Amgen Announces Erenumab Significantly Reduces Monthly Migraine Days In Patients With Episodic Migraine In First Phase 3 Study
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Amgen (AMGN) Announces KYPROLIS Phase 3 CLARION Trial Missed Primary Endpoint
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Amgen Announces Top-Line Results From Phase 3 KYPROLIS® (Carfilzomib) CLARION Study In Newly Diagnosed Multiple Myeloma Patients
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Amgen Opens Nomination Process For LabCentral Residency
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Amgen (AMGN), UCB Announce FDA Acceptance of BLA For Romosozumab
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Amgen And UCB Announce U.S. FDA Acceptance Of Biologics License Application For Romosozumab
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Amgen's (AMGN) AMJEVITA Approved by U.S. FDA
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FDA Approves Amgen's AMJEVITA™ (Adalimumab-Atto) For Treatment Of Seven Inflammatory Diseases
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Amgen (AMGN) Announces Repatha Phase 3 GLAGOV Trial Met Primary, Secondary Endpoints
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Amgen Announces Positive Top-Line Results From Phase 3 GLAGOV Imaging Study Of Repatha® (Evolocumab)
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Amgen (AMGN), UCB Announce Significant Data from Romosozumab Phase 3 in Osteoporosis
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Results From Phase 3 FRAME Study Of Romosozumab Showed Significant Reductions In Both New Vertebral And Clinical Fractures In Postmenopausal Women With Osteoporosis
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Amgen (AMGN) Affirms Receipt of Positive CHMP Opinion on Parsabiv for Secondary Hyperparathyroidism
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Amgen Receives Positive CHMP Opinion For Parsabiv™ (Etelcalcetide) For The Treatment Of Secondary Hyperparathyroidism In Adult Patients With Chronic Kidney Disease On Hemodialysis
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Amgen (AMGN) Says Phase 2 on Erenumab Shows Statistically Significant Reduction in Migraines
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Amgen Presents Positive Data At EHMTIC 2016 Demonstrating Erenumab Significantly Reduces Monthly Migraine Days In Patients With Chronic Migraine
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Amgen To Webcast Investor Call
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Amgen to Present at the Bank of America Merrill Lynch Global Healthcare Conference
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Amgen To Present At The Morgan Stanley Global Healthcare Conference
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Amgen To Present At The Morgan Stanley Global Healthcare Conference
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Amgen (AMGN) to Highlight 19 Abstracts at ASBMR Meeting
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Amgen to Highlight 19 Abstracts on Osteoporosis Disease State and Treatment at American Society for Bone and Mineral Research Annual Meeting
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Amgen to Highlight 19 Abstracts on Osteoporosis Disease State and Treatment at American Society for Bone and Mineral Research Annual Meeting
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Amgen (AMGN) Receives FDA Approval for BLINCYTO sBLA in Ph- r/r ALL
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FDA Approves BLINCYTO® (blinatumomab) For Use In Pediatric Patients With Philadelphia Chromosome-Negative Relapsed Or Refractory B-cell Precursor Acute Lymphoblastic Leukemia
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FDA Approves BLINCYTO® (blinatumomab) For Use In Pediatric Patients With Philadelphia Chromosome-Negative Relapsed Or Refractory B-cell Precursor Acute Lymphoblastic Leukemia
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Amgen (AMGN) Acquires Global AMG 420 Rights from Boehringer Ingelheim
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Amgen Obtains Global Development And Commercial Rights From Boehringer Ingelheim For Investigational BiTE® Immuno-Oncology Drug For Multiple Myeloma
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Amgen Obtains Global Development And Commercial Rights From Boehringer Ingelheim For Investigational BiTE® Immuno-Oncology Drug For Multiple Myeloma
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Amgen (AMGN) Announces Servier Exercises Option to Commercialize Omecamtiv Mecarbil in Europe
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Amgen And Servier Extend Omecamtiv Mecarbil Collaboration In Chronic Heart Failure
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Amgen And Servier Extend Omecamtiv Mecarbil Collaboration In Chronic Heart Failure
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Amgen (AMGN) Announces Prolia Phase 3 Met Primary, Secondary Endpoints in Glucocorticoid Therapy Patients
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Amgen Announces Positive Top-Line Results From Phase 3 Study Of Prolia® (Denosumab) In Patients Receiving Glucocorticoid Therapy
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Amgen Announces Positive Top-Line Results From Phase 3 Study Of Prolia® (Denosumab) In Patients Receiving Glucocorticoid Therapy
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New Repatha® (evolocumab) Analyses Show Efficacy And Safety Across Risk Groups In Results Presented At ESC Congress 2016
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New Repatha® (evolocumab) Analyses Show Efficacy And Safety Across Risk Groups In Results Presented At ESC Congress 2016
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Amgen (AMGN) Receives CRL from FDA on Parsabiv NDA
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Amgen Provides Update On Status Of Parsabiv™ (Etelcalcetide) New Drug Application (NDA) Submitted To The U.S. Food And Drug Administration (FDA)
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Amgen (AMGN) to Present 11 Abstracts at ESC, Including Data Evaluating Repatha
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New Data Add To Understanding Of Repatha® (Evolocumab) In Multiple Patient Populations
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Amgen (AMGN), Advaxis (ADXS) Enter ADXS-NEO Global Development, Commercialization Agreement
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Amgen And Advaxis Enter Global Cancer Immunotherapies Collaboration
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Amgen Reports Second Quarter 2016 Financial Results
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Amgen Announces Webcast Of 2016 Second Quarter Financial Results
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Amgen Announces 2016 Third Quarter Dividend
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Amgen (AMGN), UCB Submit Romosozumab BLA to U.S. FDA as Osteoporosis Treatment
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Amgen And UCB Submit Biologics License Application For Romosozumab To The FDA

