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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
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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

