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Merck Announces Phase 3 KEYNOTE-522 Trial Met its Overall Survival (OS) Endpoint in Patients With High-Risk Early-Stage Triple Negative Breast Cancer (TNBC)

Merck Announces Phase 3 KEYNOTE-522 Trial Met its Overall Survival (OS) Endpoint in Patients With High-Risk Early-Stage Triple Negative Breast Cancer (TNBC)
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United statesGursel aktanData monitoring committeeMerck co incStatement of merck co incMerck research laboratoriesExchange commissionMerck researchAmong merckSelected important safetyImportant safety informationFatal immune mediated adverseWhich can present with diabeticNervous systemConnective tissuePatients with multiple

Merck to Present New Data at 2024 ASCO Annual Meeting Demonstrating Advancements in Novel Oncology Treatment Approaches Across Broad Portfolio and Diverse Pipeline

Merck to Present New Data at 2024 ASCO Annual Meeting Demonstrating Advancements in Novel Oncology Treatment Approaches Across Broad Portfolio and Diverse Pipeline
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United statesKristen drakeDaiichi sankyoJulie cunninghamSeagen padcevDamini chokshiPeter dannenbaumBioxcel therapeutics incExchange commissionMerck research laboratoriesAmerican society of clinical oncologyGeorgetown universityAgensys incPfizer incStatement of merck co incMerck co inc

Merck Provides Update on Phase 3 KeyVibe-010 Trial Evaluating an Investigational Coformulation of Vibostolimab and Pembrolizumab as Adjuvant Treatment for Patients With Resected High-Risk Melanoma

Merck Provides Update on Phase 3 KeyVibe-010 Trial Evaluating an Investigational Coformulation of Vibostolimab and Pembrolizumab as Adjuvant Treatment for Patients With Resected High-Risk Melanoma
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United statesData monitoring committeeMerck co incExchange commissionStatement of merck co incMerck research laboratoriesMarjorie greenMerck researchSelected important safetyImportant safety informationFatal immune mediated adverseWhich can present with diabeticNervous systemConnective tissuePatients with multipleNeck squamous cell

Merck Initiates Phase 3 Clinical Trial of MK-1084, an Investigational Oral KRAS G12C Inhibitor, in Combination with KEYTRUDA® (pembrolizumab) for First-Line Treatment of Certain Patients With Metastatic Non-Small Cell Lung Cancer

Merck , known as MSD outside of the United States and Canada, today announced it has initiated a Phase 3 clinical trial evaluating MK-1084, an investigational oral selective KRAS G12C inhibitor, in.

United statesMerck research laboratoriesEuropean society for medical oncologyExchange commissionStatement of merck co incTaiho pharmaceutical coMerck co incAstex pharmaceuticals united kingdomOtsuka pharmaceutical co ltdMarjorie greenMerck researchEuropean societyMedical oncologyTaiho pharmaceuticalAstex pharmaceuticalsUnited kingdom

European Commission Approves Merck s KEYTRUDA® (pembrolizumab) Plus Chemotherapy as Neoadjuvant Treatment, Then Continued as Monotherapy as Adjuvant Treatment, for Resectable Non-Small Cell Lung Cancer (NSCLC) at High Risk of Recurrence in Adults -March 28, 2024 at 06:46 am EDT

Decision marks the first approval in Europe for an anti-PD-1/L1 therapy in resectable NSCLC based on positive overall survival results and represents the sixth approval for KEYTRUDA in lung cancer in.

United statesSolange petersExchange commissionMerck research laboratoriesStatement of merck co incCentre hospitalier universitaire vaudoisCommittee for medicinal products humanMerck co incEuropean commissionMedicinal productsHuman useMarjorie greenMerck researchAmerican joint committeeCancer staging manualSelected important safety