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Gilead's (GILD) Yescarta Shows Positive Results as a First-Line Treatment for Patients With High-Risk Large B-cell Lymphoma
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Gilead's (GILD) Magrolimab Demonstrates Clinical Responses in Ongoing Phase 1b Trial of Previously Untreated Acute Myeloid Leukemia Patients
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Yescarta® Shows Positive Results as a First-Line Treatment for Patients With High-Risk Large B-cell Lymphoma
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Magrolimab Demonstrates Clinical Responses in Ongoing Phase 1b Trial of Previously Untreated Acute Myeloid Leukemia Patients
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Yescarta® Is First CAR T-cell Therapy to Demonstrate High Response Rates and Durable Clinical Benefit in a Pivotal Indolent Non-Hodgkin Lymphoma Study
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New Data for TecartusTM Demonstrate Durable Responses at One Year Follow-Up in Relapsed or Refractory Mantle Cell Lymphoma
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New Four-Year Data Show Long-Term Survival in Patients With Large B-Cell Lymphoma Treated With Yescarta® in ZUMA-1 Trial
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Gilead Sciences to Present at the 3rd Annual Evercore ISI HealthCONx Conference on Wednesday, December 2, 2020
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Gilead Sciences' (GILD) Lenacapavir Achieves Primary Endpoint in Phase 2/3 Study in Heavily Treatment-Experienced People Living With HIV
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Gilead Announces Investigational Long-Acting HIV-1 Capsid Inhibitor, Lenacapavir, Achieves Primary Endpoint in Phase 2/3 Study in Heavily Treatment-Experienced People Living With HIV
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Gilead and Novo Nordisk Present New Data from Proof-of-Concept Trial in NASH
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Gilead and Kite to Share Latest Scientific Advances in Hematologic Malignancies at ASH 2020
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Gilead Sciences Announces Fourth Quarter 2020 Dividend
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Gilead Sciences (GILD) Completes Acquisition of Immunomedics (IMMU)
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Gilead Sciences Completes Acquisition of Immunomedics, Inc.
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Gilead Sciences (GILD) Confirms FDA Approved its Antiviral Veklury for Treatment of COVID-19
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U.S. Food and Drug Administration Approves Gilead’s Antiviral Veklury® (remdesivir) for Treatment of COVID-19
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Gilead Sciences (GILD) Announces Anthony Welters to Board
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Anthony Welters Joins Gilead Sciences’ Board of Directors
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Gilead Sciences (GILD) Presents New Data Showing Biktarvy Effective for the Treatment of HIV in Black Americans
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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

