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Alnylam Pharma (ALNY) Announces FDA Acceptance NDA and Priority Review Status for Patisiran
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Alnylam Announces FDA Acceptance of New Drug Application (NDA) and Priority Review Status for Patisiran, an Investigational RNAi Therapeutic for the Treatment of Hereditary ATTR (hATTR) Amyloidosis
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Alnylam to Webcast Conference Call Discussing Fourth Quarter and Full Year 2017 Financial Results
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Alnylam Pharma (ALNY) Announces EMA Acceptance of MAA for Patisiran for hATTR Amyloidosis
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Alnylam Announces EMA Acceptance of Marketing Authorisation Application (MAA) for Patisiran for the Treatment of Hereditary ATTR (hATTR) Amyloidosis
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Alnylam Pharma (ALNY) Releases Corporate Goals for 2018
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Alnylam Pharma (ALNY) and Sanofi (SNY) Report Strategic Restructuring of RNAi Therapeutics Rare Disease Alliance
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Alnylam Announces 2018 Corporate Goals
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Sanofi and Alnylam enter into strategic restructuring of RNAi therapeutics rare disease alliance
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Sanofi and Alnylam enter into strategic restructuring of RNAi therapeutics rare disease alliance
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Alnylam and Sanofi Enter into Strategic Restructuring of RNAi Therapeutics Rare Disease Alliance
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Alnylam Expands Alnylam Actâ„¢ Program to Include No-Charge Third-Party Genetic Testing and Counseling for People at Risk for Acute Hepatic Porphyrias
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Alnylam to Webcast Presentation at 36th Annual J.P. Morgan Healthcare Conference
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Alnylam to Webcast Presentation at Goldman Sachs Healthcare CEOs Unscripted Conference
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Sanofi (SNY) and Alnylam (ALNY) Submit EU Marketing Authorization Application for Patisiran to Treat hATTR amyloidosis
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Alnylam Pharma (ALNY) & Sanofi (SNY) Announce Marketing Authorisation Application to EMA for Patisiran for Treatment of Hereditary ATTR Amyloidosis
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Sanofi and Alnylam submit Marketing Authorization Application to the European Medicines Agency for patisiran for the treatment of hereditary ATTR amyloidosis
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Sanofi and Alnylam submit Marketing Authorization Application to the European Medicines Agency for patisiran for the treatment of hereditary ATTR amyloidosis
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Alnylam and Sanofi Submit Marketing Authorisation Application (MAA) to the European Medicines Agency (EMA) for Patisiran for the Treatment of Hereditary ATTR (hATTR) Amyloidosis
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Alnylam Pharma (ALNY) and Sanofi Genzyme (SNY) Reports Lift of FDA Hold on Fitusiran
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Sanofi (SNY) and Alnylam (ALNY) Announce FDA Lifted Clinical hold on Fitusiran
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Sanofi: FDA lifts clinical hold on fitusiran
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Sanofi: FDA lifts clinical hold on fitusiran
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FDA Lifts Clinical Hold on Fitusiran
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Alnylam Pharma (ALNY) Completes Submission of NDA to FDA for Patisiran for Treatment of Hereditary ATTR (hATTR) Amyloidosis
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Alnylam Completes Submission of New Drug Application to U.S. Food and Drug Administration (FDA) for Patisiran for the Treatment of Hereditary ATTR (hATTR) Amyloidosis
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Alnylam Pharma (ALNY) Announces Expansion of U.S. Orphan Drug Designation for Patisiran to Treatment of ATTR Amyloidosis
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Alnylam Announces Expansion of U.S. Orphan Drug Designation for Patisiran to Treatment of Transthyretin-Mediated Amyloidosis
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Alnylam to Webcast Presentation at BMO Capital Markets Prescriptions for Success Healthcare Conference
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Alnylam Pharma (ALNY) Granted FDA Breakthrough Therapy Designation for Patisiran
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U.S. Food and Drug Administration (FDA) Grants Alnylam Breakthrough Therapy Designation (BTD) for Patisiran for the Treatment of Hereditary ATTR (hATTR) Amyloidosis with Polyneuropathy
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Alnylam Pharma (ALNY) Commences Rolling Submission of New Drug Application FDA for Patisiran
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Alnylam Initiates Rolling Submission of New Drug Application (NDA) to U.S. Food and Drug Administration (FDA) for Patisiran for the Treatment of Hereditary ATTR (hATTR) Amyloidosis
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Alnylam Pharma (ALNY) Granted Accelerated Assessment of Patisiran by EMA
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European Medicines Agency (EMA) Grants Alnylam Accelerated Assessment of Patisiran for Patients with Hereditary ATTR (hATTR) Amyloidosis
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Alnylam Pharma (ALNY) Announces Successful Outcome Following FDA Type A Meeting on Fitusiran Program
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Alnylam Announces Successful Outcome Following FDA Type A Meeting to Discuss Fitusiran Program in Hemophilia
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Alnylam Pharmaceuticals Reports Third Quarter 2017 Financial Results and Highlights Recent Period Activity
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Alnylam Pharma (ALNY) Initiates ENVISION Phase 3 Clinical Study with Givosiran to Treat AHPs
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Alnylam Initiates ENVISION Phase 3 Clinical Study with Givosiran, an Investigational RNAi Therapeutic for the Treatment of Acute Hepatic Porphyrias (AHPs)
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Medicines Co. (MDCO), Alnylam Pharmaceuticals (ALNY) Announce Initiation of Phase III Clinical Trials of Inclisiran
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The Medicines Company and Alnylam Pharmaceuticals Announce Initiation of Phase III Clinical Trials of Inclisiran
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Alnylam Reports Positive Preliminary Results from Ongoing Phase 1/2 Study of Lumasiran (ALN-GO1) in Patients with Primary Hyperoxaluria Type 1 (PH1)
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Alnylam Pharma (ALNY), Sanofi (SNY) Present Positive Complete Results from APOLLO Phase 3 Study of Investigational Patisiran in hATTR Amyloidosis Patients with Polyneuropathy
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Sanofi and Alnylam present positive complete results from APOLLO Phase 3 study of investigational patisiran in hereditary ATTR (hATTR) amyloidosis patients with polyneuropathy
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Sanofi and Alnylam present positive complete results from APOLLO Phase 3 study of investigational patisiran in hereditary ATTR (hATTR) amyloidosis patients with polyneuropathy
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Alnylam and Sanofi Present Positive Complete Results from APOLLO Phase 3 Study of Investigational Patisiran in Hereditary ATTR (hATTR) Amyloidosis Patients with Polyneuropathy
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Alnylam to Webcast Presentations at Upcoming November Investor Conferences
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Alnylam to Webcast Conference Call Discussing Third Quarter 2017 Financial Results
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Alnylam and Collaborators to Present APOLLO Phase 3 Study Results at 1st European ATTR Amyloidosis Meeting for Patients and Doctors

