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Gilead and Kite Continue to Advance Next Generation Cancer Therapies at 2020 American Society of Clinical Oncology Annual Meeting
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Gilead Sciences (GILD) Confirms Approval of Remdesivir in Japan for Patients With Severe COVID-19
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Gilead Announces Approval of Veklury® (remdesivir) in Japan for Patients With Severe COVID-19
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Gilead (GILD) sets goal of producing at least 500,000 treatment courses of remdesivir by October
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Gilead’s Investigational Antiviral Remdesivir Receives U.S. Food and Drug Administration Emergency Use Authorization for the Treatment of COVID-19
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Gilead Sciences Announces Second Quarter 2020 Dividend
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Gilead Sciences (GILD) Phase 3 Trial of Remdesivir in Severe COVID-19 Patients Shows Improvement
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Gilead Announces Results From Phase 3 Trial of Investigational Antiviral Remdesivir in Patients With Severe COVID-19
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Gilead Sciences to Release First Quarter 2020 Financial Results on Thursday, April 30, 2020
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Gilead Provides Additional Information Regarding 2020 Annual Meeting of Stockholders Due to COVID-19 Precautions
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Gilead Sciences (GILD) Remdesivir Study Shows Two-Third of Severe COVID-19 Patients Improved
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Data on 53 Patients Treated With Investigational Antiviral Remdesivir Through the Compassionate Use Program Published in New England Journal of Medicine
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Gilead Announces $20 Million Philanthropic Fund to Support Nonprofit Organizations Impacted by the COVID-19 Crisis
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Gilead Sciences (GILD) Completes Forty Seven (FTSV) Acquisition
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Gilead Completes Acquisition of Forty Seven, Inc.
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Gilead Sciences (GILD) Announces Expiration of Hart-Scott-Rodino Waiting Period for Forty Seven Tender Offer
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Gilead Announces Expiration of Hart-Scott-Rodino Waiting Period for Forty Seven Tender Offer
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Gilead (GILD) Announces FDA Approval for Epclusa for Children Ages 6 and Older with HCV
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U.S. Food And Drug Administration Approves Epclusa® (Sofosbuvir/Velpatasvir) for Children Ages 6 and Older or Weighing at Least 17 kg with Chronic Hepatitis C Infection
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Gilead Sciences (GILD) Announces New Clinical Study Data for its Investigational HIV-1 Capsid Inhibitor GS-6207 Presented at CROI 2020
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New Clinical Study Data for Gilead’s Investigational HIV-1 Capsid Inhibitor GS-6207 Presented at CROI 2020
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Gilead (GILD) Announces Treatment With its Vesatolimod is Evaluated for Safety and Virologic and Immunologic Response Versus Placebo in Phase 1B HIV Functional Cure Study
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Treatment With Gilead’s Vesatolimod Is Evaluated for Safety and Virologic and Immunologic Response Versus Placebo in Phase 1B HIV Functional Cure Study
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Gilead Sciences (GILD) Presents 96-week DISCOVER Trial Data Demonstrating Favorable Renal and Bone Safety Profile of Descovy® for HIV PrEP in At-Risk Populations
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Gilead Presents 96-week DISCOVER Trial Data Demonstrating Favorable Renal and Bone Safety Profile of Descovy® for HIV PrEP in At-Risk Populations
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New Data on Gilead’s Biktarvy® Presented at CROI 2020, Including Data in Black Americans and Older Adults
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Press release Biocartis Group NV: BIOCARTIS ANNOUNCES 2019 RESULTS AND 2020 OUTLOOK
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Pre-Open Stock Movers 03/02: (FTSV) (TRIL) (TWTR) Higher; (BIOC) (ENLV) (NVAX) Lower (more...)
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Gilead Sciences (GILD) Initiates Two Phase 3 Studies of Remdesivir for Treatment of COVID-19
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Gilead Sciences Initiates Two Phase 3 Studies of Investigational Antiviral Remdesivir for the Treatment of COVID-19
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U.S. health officials urge Americans to prepare for spread of coronavirus
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Gilead Appoints Michael Quigley to Lead Research Biology Group and Names Linda Higgins as Head of Company’s External Innovation Center
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Gilead Sciences to Present at the Cowen and Company 40th Annual Health Care Conference on Monday, March 2, 2020
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Gilead Sciences (GILD) Announces FDA Grants Priority Review for Kite's KTE-X19 BLA in R/R Mantle Cell Lymphoma
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U.S. FDA Grants Priority Review for Kite’s KTE-X19 Biologics License Application (BLA) in Relapsed or Refractory Mantle Cell Lymphoma
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Gilead Sciences Announces 8 Percent Increase In First Quarter 2020 Dividend
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Sandra Horning, MD, Joins Gilead Sciences’ Board of Directors
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European Medicines Agency Validates Kite’s Marketing Application for Company’s Second CAR T Cell Therapy
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Gilead Sciences to Release Fourth Quarter and Full Year 2019 Financial Results on Tuesday, February 4, 2020
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Kyverna Therapeutics Secures $25 Million Series A Funding from Key Investors and Enters into Strategic Collaboration with Gilead Sciences
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Gilead Sciences (GILD) Licenses Portfolio of HIV Antibodies From The Rockefeller University
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Gilead Sciences Licenses Portfolio of HIV Antibodies From The Rockefeller University
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Scholar Rock Holding Corp. (SRRK) Reports $25M Milestone Payment from Strategic Fibrosis Collaboration with Gilead Sciences (GILD)
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Scholar Rock Achieves First Milestone in Strategic Fibrosis Collaboration with Gilead Sciences
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Gilead Sciences to Present at the 38th Annual J.P. Morgan Healthcare Conference on Monday, January 13, 2020
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Gilead Sciences (GILD) Announces China NMPA Approves Vosevi for People With Chronic Hepatitis C Infection Who Require Re-Treatment
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China National Medical Products Administration Approves Vosevi® (Sofosbuvir, Velpatasvir and Voxilaprevir) for People With Chronic Hepatitis C Infection Who Require Re-Treatment
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Gilead Sciences (GILD) Submits Filgotinib NDA to FDA Under Priority Review for Rheumatoid Arthritis Treatment
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Gilead Submits Filgotinib New Drug Application to U.S. Food and Drug Administration Under Priority Review for Rheumatoid Arthritis Treatment
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Gilead Sciences (GILD) Announces Topline Results From Phase 2 ATLAS Study in Patients With Bridging Fibrosis and Compensated Cirrhosis Due to NASH

