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Merck Announces Phase 3 KEYNOTE-A18 Trial Met Primary Endpoint of Progression-Free Survival (PFS) in Patients With Newly Diagnosed High-Risk Locally Advanced Cervical Cancer

KEYTRUDA® (pembrolizumab) plus concurrent chemoradiotherapy demonstrated statistically significant and clinically meaningful improvement in PFS versus concurrent chemoradiotherapy alone in these patients

United statesDomenica lorussoGursel aktanEuropean network for gynaecological oncology trialFoundation incExchange commissionCatholic university of romeStatement of merck co incData monitoring committeeMerck co incMerck research laboratoriesMerck researchCatholic universityEuropean networkGynaecological oncology trialSelected important safety

Merck Provides Update on Phase 3 KEYNOTE-585 Trial in Locally Advanced Resectable Gastric and Gastroesophageal Junction (GEJ) Adenocarcinoma

Merck Provides Update on Phase 3 KEYNOTE-585 Trial in Locally Advanced Resectable Gastric and Gastroesophageal Junction (GEJ) Adenocarcinoma
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United statesJulie cunninghamChrissy trankScot ebbinghausDamini chokshiPeter dannenbaumExchange commissionMerck co incMerck research laboratoriesData monitoring committeeStatement of merck co incMerck researchSelected important safetyImportant safety informationFatal immune mediated adverse reactionsImmune mediated hepatitis

Merck (MRK) Provides Update on Phase 3 KEYNOTE-585 Trial

Merck (MRK) Provides Update on Phase 3 KEYNOTE-585 Trial
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United statesChrissy trankPeter dannenbaumJulie cunninghamDamini chokshiScot ebbinghausExchange commissionMerck co incData monitoring committeeStatement of merck co incMerck research laboratoriesMerck researchSelected important safetyImportant safety informationFatal immune mediated adverse reactionsSingle agent

Merck s KEYTRUDA® (pembrolizumab) Plus Chemotherapy Significantly Improved Overall Survival Compared to Chemotherapy Alone in Patients With Advanced or Unresectable Biliary Tract Cancer

Results from Phase 3 KEYNOTE-966 to be presented at AACR 2023 Annual Meeting during Clinical Trials Plenary Session, included in official meeting press program and published simultaneously in The. | April 16, 2023

United statesSan franciscoRobin kate kelleyMerck co incStatement of merck co incExchange commissionUniversity of californiaAmerican association for cancer researchClinical trials plenary sessionAmerican associationCancer researchSelected important safetyImportant safety informationFatal immune mediated adverseSingle agentThyroid disorders

Merck (MRK) Announces Phase 3 KEYNOTE-671 Trial Met Primary Endpoint of Event-Free Survival (EFS)

Merck (MRK) Announces Phase 3 KEYNOTE-671 Trial Met Primary Endpoint of Event-Free Survival (EFS)
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United statesJulie cunninghamNikki sullivanPeter dannenbaumEliav barrDamini chokshiMerck research laboratoriesMerck access programPatient support programDrug administrationData monitoring committeeStatement of merck co incMerck patient support programExchange commissionMerck co incBiologics license application