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Gilead Sciences Announces 10 Percent Increase in First Quarter 2017 Dividend
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Gilead Sciences to Release Fourth Quarter and Full Year 2016 Financial Results on Tuesday, February 7, 2017
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Gilead Sciences (GILD) MMA for Sofosbuvir/Velpatasvir/Voxilaprevir Full Validated in EU
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European Medicines Agency Validates Gilead’s Marketing Authorization Application for Investigational Chronic Hepatitis C Therapy Sofosbuvir/Velpatasvir/Voxilaprevir (SOF/VEL/VOX)
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Gilead Awards More Than $22 Million in Grants to Support HIV Cure Research
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Alessandro Riva, MD, to Join Gilead as Senior Vice President, Hematology and Oncology Therapeutic Area Head
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Gilead Sciences to Present at the 35th Annual J.P. Morgan Healthcare Conference on Monday, January 9
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Japan’s Ministry of Health, Labour and Welfare Approves Gilead’s Vemlidy® for Patients With Chronic Hepatitis B Virus Infection
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Gilead Submits New Drug Application to U.S. Food and Drug Administration for the Investigational Single Tablet Regimen Sofosbuvir/Velpatasvir/Voxilaprevir
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Gilead Sciences Announces Promotion of James R. Meyers to Executive Vice President, Worldwide Commercial Operations
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Gilead Sciences (GILD) Announces Momelotinib Phase 3 Met Primary Endpoint in Myelofibrosis; Secondary Endpoint Missed
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Gilead Announces Top-Line Results From Two Phase 3 Studies Evaluating Momelotinib for Patients With Myelofibrosis
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Gilead Sciences to Present at the Annual Piper Jaffray Healthcare Conference on Tuesday, November 29
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Gilead Sciences (GILD) Says Phase 2 Data for Selonsertib in NASH Presented at The Liver Meeting
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Phase 2 Data for Selonsertib in Nonalcoholic Steatohepatitis (NASH) Presented at The Liver Meeting® 2016
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Gilead Sciences' (GILD) Vemlidy Approved by FDA for Treatment of Chronic Hepatitis B
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U.S. Food and Drug Administration Approves Gilead’s Vemlidy® (Tenofovir Alafenamide) for the Treatment of Chronic Hepatitis B Virus Infection
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Gilead Sciences Announces Fourth Quarter 2016 Dividend
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Gilead Sciences to Release Third Quarter 2016 Financial Results on Tuesday, November 1, 2016
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Gilead Sciences to Present at the Credit Suisse 25th Annual Healthcare Conference on Monday, November 7
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Gilead Sciences (GILD) Announces Results from Studies of Switching HIV-1 Patients to Descovy; Results Statistically non-Inferior
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Gilead Presents Results from Phase 3 Studies Evaluating Switching to Descovy® (FTC/TAF)-Based Regimens from Truvada® (FTC/TDF)-Based Regimens
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Gilead Sciences (GILD) Announces Tipline Data from Four Sofosbuvir , Velpatasvir, Voxilaprevir Phase 3s in Genotype 1 - 6 HCV
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Gilead Announces SVR12 Rates From Four Phase 3 Studies of a Once-Daily, Fixed-Dose Combination of Sofosbuvir, Velpatasvir and Voxilaprevir in Treatment-Naïve and Treatment-Experienced Genotype 1-6 Ch
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Gilead Sciences (GILD) Announces Topline Selonsertib Phase 2 Data in NASH; Anti-Fibrotic Activity Noted
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Gilead Announces Top-Line Phase 2 Results for GS-4997 (Selonsertib) in Nonalcoholic Steatohepatitis (NASH), Pulmonary Arterial Hypertension (PAH) and Diabetic Kidney Disease (DKD)
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Gilead Sciences (GILD), WHO Enter Five-Year Visceral Leishmaniasis Collaboration
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Gilead Sciences and the World Health Organization Announce Five-Year Visceral Leishmaniasis Collaboration
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Gilead (GILD) Terminates Phase 2/3 Study of GS-5745 in Ulcerative Colitis Due to Futility
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Gilead Terminates Phase 2/3 Study of GS-5745 in Patients With Ulcerative Colitis
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Gilead Prices $5 Billion of Senior Unsecured Notes
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Gilead Sciences to Present at Three Upcoming Investor Conferences in September
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Gilead Sciences (GILD) Adds Cisco Systems' Kramer as Director
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Kelly A. Kramer Joins Gilead Sciences’ Board of Directors
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Gilead Sciences (GILD) Receives EC Marketing Approval for Truvada in HIV-1 Risk Reduction
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European Commission Grants Marketing Authorization for Gilead’s Once-Daily Truvada® For Reducing the Risk of Sexually Acquired HIV-1
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Portola Pharma (PTLA) Says IndexXa MAA Accepted for Review in Europe
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Gilead Sciences Announces Third Quarter 2016 Dividend
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European CHMP Adopts Positive Opinion on Gilead’s Type II Variation Application for Truvada® for Reducing the Risk of Sexually Acquired HIV
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Gilead Sciences (GILD) Announces Two Odefsey Phase 3b Studies Met Primary Objectives
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Gilead’s Odefsey® (Emtricitabine, Rilpivirine, Tenofovir Alafenamide) Meets Primary 48-Week Objective in Two Phase 3b Studies
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Gilead Sciences to Release Second Quarter 2016 Financial Results on Monday, July 25, 2016
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Ligand Pharma (LGND) Enters OmniAb Licensing Agreement with Gilead (GILD)
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Gilead Sciences (GILD) Receives FDA Approval for Epclusa as HCV Treatment in All Genotypes
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U.S. Food and Drug Administration Approves Gilead’s Epclusa® (Sofosbuvir/Velpatasvir) for the Treatment of All Genotypes of Chronic Hepatitis C
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Gilead Sciences (GILD) Granted EC Marketing Approval for Odefsey STR
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European Commission Grants Marketing Authorization for Gilead’s Single Tablet Regimen Odefsey® (Emtricitabine, Rilpivirine, Tenofovir Alafenamide) for the Treatment of HIV
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Gilead Sciences (GILD) Presents Prelim. Data from Bictegravir Phase 1
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Gilead Presents Preliminary Data on Bictegravir, an Investigational Integrase Strand Transfer Inhibitor for the Treatment of HIV
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Gilead Sciences to Present at the 36th Annual William Blair Growth Stock Conference on Tuesday, June 14

