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Kite Announces New Data Analyses for CAR T Therapy in Patients with Blood Cancers at the 2018 American Society of Clinical Oncology Meeting
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Kite Announces Initial Results From a Phase 1 Study of T Cell Receptor (TCR) Cell Therapy in HPV-16-Positive Solid Tumors
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Gilead Sciences to Present at the Goldman Sachs 39th Annual Global Healthcare Conference on Wednesday, June 13
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Gilead Sciences (GILD) Reports Chinese Approval of Epclusa (Sofosbuvir/Velpatasvir)
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China Drug Administration Approves Epclusa® (Sofosbuvir/Velpatasvir), Gilead’s Pan-Genotypic Treatment for Chronic Hepatitis C Virus Infection
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Gilead Sciences to Present at the Jefferies 2018 Healthcare Conference on Wednesday, June 6
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Gilead Sciences (GILD) Says FDA Approves Expanded Indication for Truvada for Reducing the Risk of Acquiring HIV-1 in Adolescents
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U.S. Food and Drug Administration Approves Expanded Indication for Truvada® (Emtricitabine and Tenofovir Disoproxil Fumarate) for Reducing the Risk of Acquiring HIV-1 in Adolescents
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Kite Announces New Worldwide Facilities and Expanded Collaboration With National Cancer Institute to Support Cell Therapy Pipeline
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Gilead Sciences (GILD) Appoints Harish M. Manwani to Board
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Harish Manwani Joins Gilead Sciences’ Board of Directors
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Gilead Sciences to Present at the Bank of America Merrill Lynch Healthcare Conference on Wednesday, May 16
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Gilead Sciences Announces Second Quarter 2018 Dividend
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Gilead and Verily Announce Scientific Collaboration to Identify and Understand Immunological and Molecular Drivers of Inflammatory Diseases
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Gilead Sciences (GILD) Reports European CHMP Adopts Positive Opinion for Biktarvy (Bictegravir, Emtricitabine, Tenofovir Alafenamide)
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European CHMP Adopts Positive Opinion for Gilead’s Biktarvy® (Bictegravir, Emtricitabine, Tenofovir Alafenamide)
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Gilead Sciences to Release First Quarter 2018 Financial Results on Tuesday, May 1, 2018
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Gilead (GILD) Presents Data on Multiple Investigational Regimens for Treatment of NASH and Advanced Fibrosis at The International Liver Congress
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Gilead Presents Data on Multiple Investigational Regimens for the Treatment of Patients With Nonalcoholic Steatohepatitis (NASH) and Advanced Fibrosis at The International Liver Congress™ 2018
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Gilead (GILD) Says Norbert Bischofberger, PhD, to Step Down; John McHutchison, MD, Appointed Chief Scientific Officer and Andrew Cheng, MD, PhD, Appointed Chief Medical Officer
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Gilead (GILD) Says Norbert Bischofberger, PhD, to Step Down; John McHutchison, MD, Appointed Chief Scientific Officer and Andrew Cheng, MD, PhD, Appointed Chief Medical Officer
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Gilead Sciences’ Norbert Bischofberger, PhD, to Step Down; John McHutchison, MD, Appointed Chief Scientific Officer and Andrew Cheng, MD, PhD, Appointed Chief Medical Officer
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Gilead Sciences (GILD) Presents Data From Phase 3 Study Evaluating Women Who Switched to Biktarvy From Boosted Protease Inhibitor-Based Regimen
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Gilead Presents Data From Phase 3 Study Evaluating Women Who Switched to Biktarvy® (Bictegravir, Emtricitabine and Tenofovir Alafenamide) From a Boosted Protease Inhibitor-Based Regimen or Boosted El
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Gilead (GILD) Presents Results from Phase 3 Study Evaluating Patients Who Switched to Biktarvy from Regimen Containing Abacavir, Dolutegravir and Lamivudine
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Gilead Presents Results from Phase 3 Study Evaluating Patients Who Switched to Biktarvy® (Bictegravir, Emtricitabine and Tenofovir Alafenamide) from Regimen Containing Abacavir, Dolutegravir and Lami
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Gilead Sciences (GILD) Reports Preclinical Data on Study Evaluating Combination of GS-9620 and PGT121
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Gilead Announces Data from New Preclinical Study Evaluating a Combination of an Investigational TLR7 Agonist and an Investigational HIV Envelope Targeting Antibody in SHIV-Infected, Virally Suppressed
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Gilead Sciences (GILD) Says James Meyers, EVP, Commercial Operations, Will Retire
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Gilead Sciences Announces Senior Management Change
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Gilead Sciences to Present at the RBC Capital Markets 2018 Global Healthcare Conference on Wednesday, February 21
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Gilead Sciences (GILD) Announces FDA Approval for Biktarvy for Treatment of HIV-1 Infection
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U.S. Food and Drug Administration Approves Gilead’s Biktarvy® (Bictegravir, Emtricitabine, Tenofovir Alafenamide) for Treatment of HIV-1 Infection
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Gilead Sciences Announces 10 Percent Increase in First Quarter 2018 Dividend
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Jacqueline K. Barton, Ph.D., Joins Gilead Sciences’ Board of Directors
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Gilead Sciences to Release Fourth Quarter and Full Year 2017 Financial Results on Tuesday, February 6, 2018
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Gilead's (GILD) Kite Announces Clinical Collaboration to Evaluate Investigational Combination of Yescarta and Pfizer's (PFE) Utomilumab in Large B-Cell Lymphoma
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Kite Announces Clinical Collaboration to Evaluate Investigational Combination of Yescarta™ (Axicabtagene Ciloleucel) and Pfizer’s Utomilumab in Large B-Cell Lymphoma
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Gilead Sciences to Present at the 36th Annual J.P. Morgan Healthcare Conference on Monday, January 8
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Gilead Sciences (GILD) Says John C. Martin to Transition From Executive Chairman to Chairman
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Gilead Sciences Announces That John C. Martin, PhD Will Transition From Executive Chairman to Chairman of the Board of Directors
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Gilead Sciences (GILD) Company, Kite, Reports Data From ZUMA-3 Study of KTE-C19
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Kite Announces Data From ZUMA-3 Study of KTE-C19 in Adult Patients with Relapsed or Refractory Acute Lymphoblastic Leukemia
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Gilead Sciences' (GILD) Kite LT Pivotal ZUMA-1 Study of Yescarta Shows 42% of Patients Remained in Response, Including 40% in Complete Remission
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Kite Announces Long-Term Data From Pivotal ZUMA-1 Study of Yescarta™ (Axicabtagene Ciloleucel) in Patients With Refractory Large B-cell Lymphoma
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Gilead Sciences (GILD) and Kite to Acquire Cell Design Labs for up to $567M
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Gilead Sciences and Kite to Acquire Cell Design Labs
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Gilead Announces 10-Year, $100 Million Commitment to Address the HIV/AIDS Epidemic in the Southern United States
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Gilead Sciences to Present at the Nasdaq 37th Investor Program on Wednesday, December 6
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Gilead Sciences Announces Fourth Quarter 2017 Dividend

