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Articles published by Gilead Sciences, Inc.

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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
From Gilead Sciences, Inc.
Via Business Wire
Tickers GILD
Daiichi Sankyo Authorizes the First YESCARTA® (Axicabtagene Ciloleucel) CAR T-cell Therapy Treatment Site in Japan
From Gilead Sciences, Inc.
Via Business Wire
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Yescarta® ZUMA-12 Study Demonstrates 78% Complete Response Rate as Part of First-Line Treatment in Newly Diagnosed High-Risk Large B-Cell Lymphoma
From Gilead Sciences, Inc.
Via Business Wire
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Yescarta® Demonstrates Durable Two-Year Clinical Benefit in Adults With Relapsed or Refractory Indolent Non-Hodgkin Lymphoma Including Follicular Lymphoma
From Gilead Sciences, Inc.
Via Business Wire
Tickers GILD
Yescarta® Is First CAR T-cell Therapy to Report Five-Year Survival Data From Pivotal Study Showing Durable Long-Term Survival in Patients With Refractory Large B-cell Lymphoma
From Gilead Sciences, Inc.
Via Business Wire
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Yescarta® CAR T-Cell Therapy Quadruples Median Event-Free Survival Duration Over Standard of Care in Second-Line Relapsed or Refractory Large B-Cell Lymphoma
From Gilead Sciences, Inc.
Via Business Wire
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Trodelvy® Demonstrates Clinical Benefit for Black Patients Consistent with Full Metastatic Triple-Negative Breast Cancer Population in ASCENT Study
From Gilead Sciences, Inc.
Via Business Wire
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Gilead’s Bold Ambition of Transforming Triple-Negative Breast Cancer Treatment to Be Highlighted With New Data at SABCS
From Gilead Sciences, Inc.
Via Business Wire
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Trodelvy® (sacituzumab govitecan) Granted European Commission Marketing Authorization for Treatment of Metastatic Triple-Negative Breast Cancer in Second Line
From Gilead Sciences, Inc.
Via Business Wire
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Gilead Submits Biologics License Application to U.S. Food and Drug Administration for Bulevirtide, an Investigational Treatment for People Living With Chronic Hepatitis Delta
From Gilead Sciences, Inc.
Via Business Wire
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Gilead Sciences to Present at Upcoming Investor Conference
From Gilead Sciences, Inc.
Via Business Wire
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Gilead Exercises Options to Three Arcus Biosciences Clinical-Stage Programs and Adds Research Collaboration
From Gilead Sciences, Inc.
Via Business Wire
Tickers GILD RCUS
Everest Medicines and Gilead Sciences Jointly Announce Phase 2b Study of Sacituzumab Govitecan Conducted in China of Patients With Metastatic Triple-Negative Breast Cancer Meets Primary Overall Response Rate Endpoint
From Gilead Sciences, Inc.
Via Business Wire
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Gilead to Present Data From Liver Disease Development Programs at The Liver Meeting®
From Gilead Sciences, Inc.
Via Business Wire
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Gilead and Kite Oncology Demonstrate Broad Leadership in Cell Therapy and Expanding Blood Cancer Pipeline
From Gilead Sciences, Inc.
Via Business Wire
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Clinical and Patient-Reported Outcomes in People Living With HIV on Biktarvy® in Observational BICSTaR Study Demonstrate Consistent Efficacy Profile in Real-World Setting
From Gilead Sciences, Inc.
Via Business Wire
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Gilead Announces Clinical Trial Collaboration With Merck to Evaluate Trodelvy® (sacituzumab govitecan-hziy) in Combination With KEYTRUDA® (pembrolizumab) in Patients With First-Line Metastatic Triple-Negative Breast Cancer
From Gilead Sciences, Inc.
Via Business Wire
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Gilead Sciences Announces Third Quarter 2021 Financial Results
From Gilead Sciences, Inc.
Via Business Wire
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Gilead and Merck Initiate Phase 2 Study Evaluating an Oral Weekly Combination Regimen of Investigational Lenacapavir and Investigational Islatravir for HIV-1 Treatment in Virologically Suppressed Adults
From Gilead Sciences, Inc.
Via Business Wire
Tickers GILD MRK
Gilead Presents Long-Term Switch Data Reinforcing Biktarvy® as a Treatment Option for a Broad Range of People Living With HIV
From Gilead Sciences, Inc.
Via Business Wire
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Gilead Sciences Announces Veklury® Donations to Help Address the Ongoing COVID-19 Crisis in Indonesia and Armenia
From Gilead Sciences, Inc.
Via Business Wire
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U.S. Food and Drug Administration Approves Expanded Indication of Gilead’s Biktarvy® for Treatment of HIV-1 in Pediatric Populations
From Gilead Sciences, Inc.
Via Business Wire
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Sacituzumab Govitecan Receives Positive CHMP Opinion as 2L Treatment for Adult Patients With Metastatic Triple-Negative Breast Cancer
From Gilead Sciences, Inc.
Via Business Wire
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Gilead Sciences to Release Third Quarter 2021 Financial Results on Thursday, October 28, 2021
From Gilead Sciences, Inc.
Via Business Wire
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U.S. FDA Approves Kite’s Tecartus® as the First and Only Car T for Adults With Relapsed or Refractory B-cell Acute Lymphoblastic Leukemia
From Gilead Sciences, Inc.
Via Business Wire
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Gilead Marks Fifth Approval for Trodelvy® in Metastatic Triple-Negative Breast Cancer Under Project Orbis Initiative with Health Canada Authorization
From Gilead Sciences, Inc.
Via Business Wire
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Veklury® (Remdesivir) Significantly Reduced Risk of Hospitalization in High-Risk Patients with COVID-19
From Gilead Sciences, Inc.
Via Business Wire
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Gilead to Present Latest Antiviral Research Data Addressing Urgent Global Needs in Infectious Disease at IDWeek 2021
From Gilead Sciences, Inc.
Via Business Wire
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New Data Demonstrate Trodelvy® Survival Benefit in Metastatic Triple-Negative Breast Cancer Patients Regardless of Initial HR/HER2 Status
From Gilead Sciences, Inc.
Via Business Wire
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Trodelvy® Significantly Improved Quality of Life Over Standard of Care in 2L+ Metastatic Triple-Negative Breast Cancer in Phase 3 ASCENT Study
From Gilead Sciences, Inc.
Via Business Wire
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