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Eikon Therapeutics Announces the Election of Robin L. Washington to Its Board of Directors
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Gilead Sciences (GILD) and Dragonfly Announce Strategic Research Collaboration to Develop Natural Killer Cell Engagers in Oncology and Inflammation
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Gilead and Dragonfly Announce Strategic Research Collaboration to Develop Natural Killer Cell Engagers in Oncology and Inflammation
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Gilead Sciences to Present at Upcoming Investor Conferences
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Gilead Sciences (GILD) Announces Veklury (Remdesivir) is First and Only Approved Treatment for Pediatric Patients Under 12 Years of Age with COVID-19
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Veklury® (Remdesivir) is First and Only Approved Treatment for Pediatric Patients Under 12 Years of Age with COVID-19
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Gilead Sciences (GILD) Reports New Findings Confirming Veklury Activity in Treating COVID-19
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Several New Studies Presented at ECCMIC 2022 Confirm Veklury® (Remdesivir) Activity in Treating COVID-19
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Gilead Sciences' (GILD) Kite Receives U.S. FDA Approval of New State-of-the-Art CAR T-Cell Therapy Manufacturing Facility in Maryland
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Kite Receives U.S. FDA Approval of New State-of-the-Art CAR T-Cell Therapy Manufacturing Facility in Maryland
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Gilead Sciences to Release First Quarter 2022 Financial Results on Thursday, April 28, 2022
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Gilead Sciences (GILD) Announces FDA Lifts Partial Clinical Hold on MDS and AML Magrolimab Studies
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FDA Lifts Partial Clinical Hold on MDS and AML Magrolimab Studies
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Yescarta® Receives U.S. FDA Approval as First CAR T-cell Therapy for Initial Treatment of Relapsed or Refractory Large B-cell Lymphoma (LBCL)
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Gilead Sciences Announces $24 Million in Grants to Help End the HIV Epidemic for Everyone, Everywhere
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Gilead Sciences (GILD) Reports Phase 3 TROPiCS-02 Study Met the Primary Endpoint of Progression-Free Survival
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Phase 3 TROPiCS-02 Study Met the Primary Endpoint of Progression-Free Survival in Late-Line HR+/HER2- Metastatic Breast Cancer
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Gilead Sciences (GILD) Receives CRL from FDA for Investigational Lenacapavir Due to Vial Compatability Issues
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Gilead Receives Complete Response Letter From U.S. FDA for Investigational Lenacapavir Due to Vial Compatability Issues
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Gilead Sciences (GILD) Announces New Clinical Data Support the Sustained Efficacy of Long-acting Lenacapavir, Gilead’s Investigational HIV-1 Capsid Inhibitor
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New Clinical Data Support the Sustained Efficacy of Long-acting Lenacapavir, Gilead’s Investigational HIV-1 Capsid Inhibitor
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Gilead Sciences (GILD) to Present New Phase 2/3 Interim Data of Veklury in Pediatric Patients With COVID-19 Presented at CROI 2022
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Phase 2/3 Interim Data Evaluating the Safety, Tolerability and Clinical Outcomes of Veklury® (Remdesivir) in Pediatric Patients With COVID-19 Presented at CROI 2022
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Biktarvy® Demonstrates High Efficacy and Durable Viral Suppression at Five Years, in Treatment-Naïve Adults
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Gilead Sciences (GILD) Announces Veklury Retains Antiviral Activity Against Omicron, Delta and Other Emergent SARS-CoV-2 Variants in Multiple In Vitro Studies
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Veklury® (Remdesivir) Retains Antiviral Activity Against Omicron, Delta and Other Emergent SARS-CoV-2 Variants in Multiple In Vitro Studies
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Gilead Sciences (GILD) to Present Latest Antiviral Research and Development Data at CROI
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Gilead to Present Latest Antiviral Research and Development Data at CROI 2022 Addressing Urgent Global Needs
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Gilead Sciences to Present at Upcoming Investor Conferences
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Gilead Sciences Announces 2.8 Percent Increase in First Quarter 2022 Dividend
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Gilead Sciences (GILD) Announces U.S. FDA Approves New Label Update for CAR T-Cell Therapy Yescarta Showing Prophylactic Steriod Use Improves Management of Cytokine Release Syndrome
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U.S. FDA Approves New Label Update for CAR T-Cell Therapy Yescarta® Showing Prophylactic Steriod Use Improves Management of Cytokine Release Syndrome
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Gilead Sciences (GILD) Announces FDA Clinical Hold on Studies Evaluating Magrolimab in Combination With Azacitidine
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Gilead Announces Partial Clinical Hold for Studies Evaluating Magrolimab in Combination With Azacitidine
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Gilead Sciences (GILD) Announces FDA Approval of Veklury for Treatment of Non-Hospitalized Patients at High Risk for COVID-19
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FDA Approves Veklury® (Remdesivir) for the Treatment of Non-Hospitalized Patients at High Risk for COVID-19 Disease Progression
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Gilead Sciences to Release Fourth Quarter & Full Year 2021 Financial Results on Tuesday, February 1, 2022
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Gilead Sciences (GILD) Enters Clinical Collaboration with Merck (MRK) to Evaluate Trodelvy in Combination With KEYTRUDA
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Gilead Announces Clinical Trial Collaborations With Merck to Evaluate Trodelvy® in Combination With KEYTRUDA® in First-Line Metastatic Non-Small Cell Lung Cancer
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Gilead Sciences (GILD) Announces NEJM Publication of Data Demonstrating Veklury (Remdesivir) Significantly Reduced Risk of Hospitalization in High-Risk Patients With COVID-19
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Gilead Announces New England Journal of Medicine Publication of Data Demonstrating Veklury® (Remdesivir) Significantly Reduced Risk of Hospitalization in High-Risk Patients With COVID-19
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Gilead Sciences (GILD) Announces Clinical Hold on Studies Evaluating Injectable Lenacapavir for HIV Treatment and Prevention Due to Vial Quality Concerns
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Gilead Announces Clinical Hold on Studies Evaluating Injectable Lenacapavir for HIV Treatment and Prevention Due to Vial Quality Concerns
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Gilead and Arcus Biosciences Complete Closing of Option Exercise for Three Clinical-stage Programs and New Research Collaboration
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Gilead and Arcus Biosciences Complete Closing of Option Exercise for Three Clinical-Stage Programs and New Research Collaboration
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Gilead Sciences to Present at Upcoming Investor Conference
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Gilead Sciences (GILD) Granted Expanded Indication for Veklury in Europe for Treatment of Adults Not on Supplemental Oxygen and Considered High Risk for COVID-19 Disease Progression
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European Commission Expands Indication for Veklury (Remdesivir) for the Treatment of Adults Not on Supplemental Oxygen and Considered High Risk for COVID-19 Disease Progression
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Daiichi Sankyo Authorizes the First YESCARTA® (Axicabtagene Ciloleucel) CAR T-cell Therapy Treatment Site in Japan
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Gilead Sciences (GILD) Announces Yescarta ZUMA-12 Study Demonstrates 78% Complete Response Rate as Part of First-Line Treatment in Newly Diagnosed High-Risk Large B-Cell Lymphoma

