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Gilead Announces New Data on Biktarvy® for the Treatment of HIV in Black Americans
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Gilead (GILD) Presents New Data from Antiviral Development Programs at IDWeek 2020
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Gilead Presents New Data from Antiviral Development Programs at IDWeek 2020
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Gilead (GILD) Announces European CHMP Adopts Positive Opinion for Kite's KTE-X19 for the Treatment of R/R Mantle Cell Lymphoma
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European CHMP Adopts Positive Opinion for Kite’s KTE-X19 for the Treatment of Relapsed or Refractory Mantle Cell Lymphoma
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Gilead Sciences to Release Third Quarter 2020 Financial Results on Wednesday, October 28, 2020
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Gilead Sciences (GILD) Announces Expiration of HSR Waiting Period for Immunomedics (IMMU) Tender Offer
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Gilead Sciences Announces Expiration of Hart-Scott-Rodino Waiting Period for Immunomedics Tender Offer
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Gilead Sciences (GILD) Reports Final Results of NIAID ACTT-1 Trial Published in NEJM Expand Clinical Benefits of Veklury for Treatment of COVID-19
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Final Results of National Institute of Allergy and Infectious Diseases’ ACTT-1 Trial Published in New England Journal of Medicine Expand Clinical Benefits of Veklury® (remdesivir) for the Treatment
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Gilead Sciences (GILD) Presents Biktarvy Findings From Switch Studies & Analysis of Real-World BICSTaR Study At HIV Glasgow 2020
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Gilead Presents Biktarvy® Findings From Switch Studies & Analysis of Real-World BICSTaR Study At HIV Glasgow 2020
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Gilead Sciences (GILD) Presents Data From HIV Research and Development Programs at HIV Glasgow 2020
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Gilead Sciences Presents Data From HIV Research and Development Programs at HIV Glasgow 2020
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Eli Lilly (LLY) Said Baricitinib in Combination with Remdesivir Reduces Time to Recovery in Hospitalized Patients with COVID-19
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Gilead Sciences (GILD) Receives FDA Breakthrough Therapy Designation for Treatment of Myelodysplastic Syndrome
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Gilead’s Magrolimab, an Investigational Anti-CD47 Monoclonal Antibody, Receives FDA Breakthrough Therapy Designation for Treatment of Myelodysplastic Syndrome
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Gilead Sciences (GILD) to Acquire Immunomedics (IMMU) for $21 Billion
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Gilead Sciences to Acquire Immunomedics
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Gilead's(GILD) Kite Submits sBLA to FDA for Yescarta in Relapsed or Refractory Indolent Non-Hodgkin Lymphomas
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Kite Submits Supplemental Biologics License Application to U.S. Food and Drug Administration for Yescarta® in Relapsed or Refractory Indolent Non-Hodgkin Lymphomas
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Gilead Announces Presentation of More Than 40 Abstracts From Extensive Liver Disease Programs at the Digital International Liver Congress™ 2020
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Gilead Sciences (GILD) Receives CRL for Filgotinib for Treatment of Moderately to Severely Active Rheumatoid Arthritis
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Gilead Receives Complete Response Letter for Filgotinib for the Treatment of Moderately to Severely Active Rheumatoid Arthritis
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Gilead Sciences (GILD) Announces China National Medical Products Administration Approves Truvada for HIV Pre-Exposure Prophylaxis
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China National Medical Products Administration Approves Truvada® for HIV Pre-Exposure Prophylaxis (PrEP)
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Gilead Sciences (GILD) Submits NDA to U.S. FDA for Veklury (Remdesivir) for Treatment of COVID-19
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Gilead Submits New Drug Application to U.S. Food and Drug Administration for Veklury® (Remdesivir) for the Treatment of COVID-19
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Pfizer (PFE) Announces Agreement with Gilead (GILD) to Manufacture Remdesivir for Treatment of COVID-19
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Gilead Sciences Announces Third Quarter 2020 Dividend
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Gilead Sciences (GILD) Kite Announced FDA Accelerated Approval of Tecartus to Treat MCL
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U.S. FDA Approves Kite’s Tecartus™, the First and Only CAR T Treatment for Relapsed or Refractory Mantle Cell Lymphoma
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Gilead Sciences to Release Second Quarter 2020 Financial Results on Thursday, July 30, 2020
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Gilead Sciences (GILD) Presents Additional Data on Remdesivir for Treatment of COVID-19
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Gilead Presents Additional Data on Investigational Antiviral Remdesivir for the Treatment of COVID-19
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Gilead Sciences Presents Survey Findings on PrEP Access and Utilization in the U.S. During COVID-19 Shelter-in-Place Orders
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New Findings on Gilead’s Biktarvy® Presented at AIDS 2020: Virtual Include Positive Switch Data in Older Adults
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Gilead Sciences Presents Data Supporting a Potential Six-Month Dosing Interval for Investigational HIV-1 Capsid Inhibitor Lenacapavir (GS-6207)
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European Commission Grants Conditional Marketing Authorization for Gilead’s Veklury® (remdesivir) for the Treatment of COVID-19
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Gilead Sciences Demonstrates Commitment to Scientific Innovation In HIV With New Prevention, Treatment and Cure Research Data Presented At AIDS 2020: Virtual
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Gilead Sciences (GILD) Company, Kite, Granted European Medicines Agency Approval for CAR T Cell Therapy Manufacturing Facility in Europe
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Kite Receives European Medicines Agency Approval for CAR T Cell Therapy Manufacturing Facility in Europe
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Chinese and Iranian hackers targeted Biden and Trump campaigns, Google says
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Mark Genovese Joins Gilead to Lead Clinical Development of Company’s Inflammation Programs
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Gilead Sciences (GILD) Remdesivir Moderate COVID-19 Study Shows 65% More Likely to have Clinical Improvement at Day 11
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Gilead Announces Results From Phase 3 Trial of Remdesivir in Patients With Moderate COVID-19
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Gilead Sciences (GILD) Announces Yescarta Demonstrates High Rates of Response in Relapsed or Refractory Indolent Non-Hodgkin Lymphoma
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Gilead Sciences (GILD) Announces Investigational Magrolimab in Combination With Azacitidine Demonstrates Durable Activity in Previously-Untreated Myelodysplastic Syndrome and AML
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Investigational Magrolimab in Combination With Azacitidine Demonstrates Durable Activity in Previously-Untreated Myelodysplastic Syndrome and Acute Myeloid Leukemia
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Yescarta® (Axicabtagene Ciloleucel) Demonstrates High Rates of Response in Relapsed or Refractory Indolent Non-Hodgkin Lymphoma

