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Veklury® Significantly Reduced Risk of Hospitalization in High-Risk Patients with COVID-19

Veklury® Significantly Reduced Risk of Hospitalization in High-Risk Patients with COVID-19
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United statesFoster cityJacquie rossNicole rodriguezRobertl gottliebMerdad parseyGilead sciencesDrug administrationGilead sciences incExchange commissionGilead on twitter sciencesGilead public affairsBaylor scott white research institutePrincipal investigator at baylor university medical centerDouble blind placebo controlled study evaluatedYearly use

Gilead to Present Latest Antiviral Research Data Addressing Urgent Global Needs in Infectious Disease at IDWeek 2021

Gilead to Present Latest Antiviral Research Data Addressing Urgent Global Needs in Infectious Disease at IDWeek 2021
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United statesFoster cityJacquie rossBrian plummerNicole rodriguezFrank duffPrevention researchGilead sciencesGilead sciences incPrevention research lenacapavirExchange commissionUs food drug administrationGilead on twitter sciencesGilead public affairsEuropean medicines agencyTreatment research

Trodelvy® Significantly Improved Quality of Life Over Standard of Care in 2L+ Metastatic Triple-Negative Breast Cancer in Phase 3 ASCENT Study

Trodelvy® Significantly Improved Quality of Life Over Standard of Care in 2L+ Metastatic Triple-Negative Breast Cancer in Phase 3 ASCENT Study
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United statesUnited kingdomFoster cityJacquie rossCentre for hematologyEuropean organization for researchGilead sciencesOncology clinical researchGilead sciences incExchange commissionTnbc severely impacts patient healthGilead public affairsImpacts patient health related qualityPoorer outcomesMetastatic diseaseBreast cancer subtypes

New Data Demonstrate Trodelvy® Survival Benefit in Metastatic Triple-Negative Breast Cancer Patients Regardless of Initial HR/HER2 Status

New Data Demonstrate Trodelvy® Survival Benefit in Metastatic Triple-Negative Breast Cancer Patients Regardless of Initial HR/HER2 Status
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United statesUnited kingdomFoster cityComunidad autonoma de catalunaJacquie rossJavier cortGilead sciencesEuropean society of medical oncologyGilead sciences incExchange commissionHead of the international breast cancer centerGilead public affairsPatients whose disease changedTriple negative had similar positive outcomesOverall metastaticFirst treatment

European Medicines Agency Validates Gilead s Marketing Authorization Application for Lenacapavir, an Investigational, Long-Acting Capsid Inhibitor for the Treatment of HIV-1 in People With Limited Therapy Options

EMA MAA Validation Follows Submission of NDA for Lenacapavir to the U.S. FDA – – If Authorized, Lenacapavir Would be the First Capsid Inhibitor and the Only HIV-1 Treatment Option Administered Twice Yearly – Gilead Sciences, Inc. today announced that the company’s Marketing Authorization Application for lenacapavir, an investigational, long-acting HIV-1 capsid inhibitor, has been fully validated and is now .

United statesFoster cityJacquie rossBrian plummerMerdad parseyGilead sciencesGilead sciences incExchange commissionUs food drug administrationEuropean unionGilead public affairsGilead on twitter sciencesEuropean medicines agencyCommittee for medicinal products human useFollows submissionLenacapavir would