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Merck (MRK) Announces EU Approval of KEYTRUDA Plus Chemotherapy for NSCLC

Merck (MRK) Announces EU Approval of KEYTRUDA Plus Chemotherapy for NSCLC
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United statesJulie cunninghamDamini chokshiSolange petersPeter dannenbaumMerck research laboratoriesStatement of merck co incCentre hospitalier universitaire vaudoisEuropean commissionExchange commissionCommittee for medicinal products humanMerck co incMedicinal productsHuman useMarjorie greenMerck research

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

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
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United statesSolange petersExchange commissionEuropean commissionEuropean commission approves merckProduct serviceMerck co incCommittee for medicinal products humanStatement of merck co incCentre hospitalier universitaire vaudoisMerck research laboratoriesNeoadjuvant treatmentThen continuedAdjuvant treatmentResectable non small cell lung cancerHigh risk

Merck Receives Positive EU CHMP Opinion for KEYTRUDA® (pembrolizumab) in Combination With Chemotherapy as Neoadjuvant Treatment, Then Continued as Monotherapy as Adjuvant Treatment, for the Treatment of Resectable NSCLC at High Risk of Recurrence

Opinion granted based on positive overall survival and event-free survival results from the Phase 3 KEYNOTE-671 trial First opinion to be granted for an anti-PD-1/L1 therapy in resectable non-small.

United statesStatement of merck co incEuropean commissionEuropean unionAmerican joint committee on cancerMerck research laboratoriesExchange commissionMerck co incEuropean medicines agencyMedicinal productsHuman useAmerican joint committeeMarjorie greenMerck researchSelected important safetyImportant safety information

FDA Grants Priority Review to Merck s Application for KEYTRUDA® (pembrolizumab) Plus Chemotherapy as Treatment for Primary Advanced or Recurrent Endometrial Carcinoma

FDA Grants Priority Review to Merck s Application for KEYTRUDA® (pembrolizumab) Plus Chemotherapy as Treatment for Primary Advanced or Recurrent Endometrial Carcinoma
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United statesDamini chokshiGursel aktanJohn infantiPeter dannenbaumJulie cunninghamRamez eskanderSociety of gynecologic oncologyStatement of merck co incMerck research laboratoriesMoores cancer centerOncology centerDrug administrationUs national cancer instituteNational institutes of healthDevelopment agreement

Merck s KEYTRUDA® (pembrolizumab) Reduced the Risk of Death by 38% Versus Placebo as Adjuvant Therapy for Patients With Renal Cell Carcinoma (RCC) at an Increased Risk of Recurrence Following Nephrectomy -January 27, 2024 at 10:01 am EST

KEYNOTE-564 is the first Phase 3 trial to demonstrate superior overall survival with adjuvant therapy compared to placebo in patients with RCC Late-breaking OS results selected for the official.

United statesTonik choueiriNancy kohlbergHarvard medical schoolExchange commissionAsco gu press programDana farber cancer instituteLank centerAmerican society of clinical oncologyStatement of merck co incMerck research laboratoriesEuropean unionAkeso incMerck co incClinical oncologyCancers symposium