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New TROPiCS-02 Data in HR+/HER2- Metastatic Breast Cancer Patients Demonstrates Progression-Free Survival Benefit of Trodelvy® Regardless of Their HER2 Status
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Gilead Sciences to Present at Upcoming Investor Conferences
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Gilead Sciences (GILD) Demonstrates Strength of Oncology Portfolio Across Diverse Tumor Types
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Gilead Demonstrates Strength of Oncology Portfolio Across Diverse Tumor Types at ESMO Congress 2022
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Gilead Sciences (GILD) Granted Approval of Sunlenca in EU
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Gilead Announces First Global Regulatory Approval of Sunlenca® (Lenacapavir), the Only Twice-Yearly HIV Treatment Option
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Gilead Sciences Announces Collaboration With Morehouse School of Medicine and Xavier University of Louisiana College of Pharmacy to Address Inequities in HIV Care
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Gilead Sciences (GILD) Acquires Remaining Worldwide Rights of Trodelvy
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Gilead to Acquire Remaining Worldwide Rights of Trodelvy®
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Gilead Sciences (GILD) Announces Trodelvy Significantly Improves OS in Pre-Treated HR+/HER2- Metastatic Breast Cancer Patients in the TROPiCS-02 Study
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Trodelvy® Significantly Improves Overall Survival in Pre-Treated HR+/HER2- Metastatic Breast Cancer Patients in the TROPiCS-02 Study
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Gilead Sciences and a Coalition of LGBTQ+ and Human Rights-Focused Organizations Mobilize to Address Monkeypox Public Health Emergency
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Gilead Sciences (GILD) Acquires MiroBio
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Gilead Sciences to Acquire MiroBio
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Biktarvy® Demonstrates High Efficacy for a Broad Range of People Initiating Treatment for HIV, Including Those With HBV Coinfection
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AlloVir Announces $126.6 Million Registered Direct Offering
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Gilead Sciences (GILD) Announces Kite’s CAR T-cell Therapy Tecartus Receives Positive CHMP Opinion in Relapsed or Refractory Acute Lymphoblastic Leukemia
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Kite’s CAR T-cell Therapy Tecartus® Receives Positive CHMP Opinion in Relapsed or Refractory Acute Lymphoblastic Leukemia (r/r ALL)
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Gilead Sciences (GILD) Receives Positive CHMP Opinion Recommending Veklury Receive Full Marketing Authorization
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CHMP Adopts Positive Opinion Recommending Veklury® (Remdesivir) Receive Full Marketing Authorization for the Treatment of Patients With COVID-19
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Scientific Innovation and Collaboration Highlighted at AIDS 2022 as Gilead Extends Leadership Efforts Toward Ending the Global HIV Epidemic
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Gilead Sciences Contributes Additional $85 Million to Its Foundation to Advance Health Equity
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Gilead Sciences (GILD) Enters Procurement Agreement with the European Commission for Veklury
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Gilead Sciences Signs New Joint Procurement Agreement with the European Commission for Veklury® (Remdesivir)
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Gilead Sciences to Release Second Quarter 2022 Financial Results on Tuesday, August 2, 2022
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Gilead Sciences Appoints Deborah Telman as Executive Vice President, Corporate Affairs and General Counsel
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Gilead Sciences (GILD) Granted EU Approval for Yescarta for Treatment of Relapsed or Refractory Follicular Lymphoma
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Kite’s CAR T-cell Therapy Yescarta® Granted European Marketing Authorization for the Treatment of Relapsed or Refractory Follicular Lymphoma
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Gilead Sciences (GILD) Resubmits NDA to FDA for Lenacapavir, an Investigational, Long-Acting HIV-1 Capsid Inhibitor
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Gilead Resubmits New Drug Application to U.S. Food and Drug Administration for Lenacapavir, an Investigational, Long-Acting HIV-1 Capsid Inhibitor
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Gilead Endorses The Kigali Declaration On Preventing, Controlling and Eliminating Neglected Tropical Diseases
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Gilead Sciences (GILD) Announces Lenacapavir Receives Positive CHMP Opinion for People With Multi-Drug Resistant HIV
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Investigational Lenacapavir Receives Positive CHMP Opinion for People With Multi-Drug Resistant HIV
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Gilead Sciences (GILD) Announces Treatment With Hepcludex Meets Primary Endpoint and Achieves Significant Response in Chronic Hepatitis Delta Virus at 48 Weeks
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Treatment With Hepcludex® (Bulevirtide) Meets Primary Endpoint and Achieves Significant Response in Chronic Hepatitis Delta Virus at 48 Weeks
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Gilead to Present Latest Data From Across Liver Disease Development Programs at the International Liver Congress™ 2022
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Gilead Sciences (GILD) Reports Final Data From Phase 3 ASCENT Study Showing Trodelvy Extends Overall Survival Over Chemotherapy in Second-Line Metastatic TNBC
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Final Data From Phase 3 ASCENT Study Demonstrates Trodelvy Extends Overall Survival Over Chemotherapy in Second-Line Metastatic TNBC
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Gilead Sciences (GILD) Reports Tecartus Car T-cell Therapy Demonstrates Strong Overall Survival Rates and Continued Durable Responses in Long-Term Follow-Up
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Tecartus® Car T-cell Therapy Demonstrates Strong Overall Survival Rates and Continued Durable Responses in Long-Term Follow-Up of Two Pivotal Studies Including Longest Ever Follow-Up of a CAR T-cell
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Gilead Sciences (GILD) Reports Trodelvy Improved Progression-Free Survival by 34% in Heavily Pre-Treated HR+/HER2- Metastatic Breast Cancer
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Sub-analyses of Landmark ZUMA-7 Trial Reinforce Yescarta® CAR T-cell Therapy Superiority Over Standard of Care (SOC) as Initial Treatment for Patients With Relapsed or Refractory Large B-cell Lymphom
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Trodelvy® Improved Progression-Free Survival by 34% in Heavily Pre-Treated HR+/HER2- Metastatic Breast Cancer Patients
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Gilead Sciences's (GILD) Kite Announces Yescarta CAR T-cell Therapy Demonstrates Consistent Survival Outcomes and Safety in Real-World Setting Regardless of Race and Ethnicity
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Yescarta® CAR T-cell Therapy Demonstrates Consistent Survival Outcomes and Safety in Real-World Setting Regardless of Race and Ethnicity
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Gilead Sciences Appoints Stacey Ma, PhD as Executive Vice President, Pharmaceutical Development and Manufacturing
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Gilead Reaches Number One Spot as Top Overall Philanthropic Funder of HIV-Related Programs, According to Funders Concerned About AIDS Report
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Gilead and Kite Oncology to Highlight Advances Supporting New Innovations in Cancer Care at the ASCO Annual Meeting
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Gilead Sciences (GILD) Announces FDA Lifts Clinical Hold on Investigational Lenacapavir for the Treatment and Prevention of HIV
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FDA Lifts Clinical Hold on Investigational Lenacapavir for the Treatment and Prevention of HIV

