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FDA Approves KEYTRUDA® (pembrolizumab) for Treatment of Patients With Resectable (T?4 cm or N+) NSCLC in Combination With Chemotherapy as Neoadjuvant Treatment, Then Continued as a Single Agent as Adjuvant Treatment After Surgery

FDA Approves KEYTRUDA® (pembrolizumab) for Treatment of Patients With Resectable (T?4 cm or N+) NSCLC in Combination With Chemotherapy as Neoadjuvant Treatment, Then Continued as a Single Agent as Adjuvant Treatment After Surgery
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United statesHeather wakeleeStanford universityDrug administrationMerck co incEuropean society for medical oncologyProduct serviceMerck access programPatient support programStatement of merck co incExchange commissionMerck research laboratoriesAmerican joint committee on cancerMerck patient support programPatients with resectableNeoadjuvant treatment

European Commission Approves KEYTRUDA® (pembrolizumab) as Adjuvant Treatment for Adults With Non-Small Cell Lung Cancer at High Risk of Recurrence Following Complete Resection and Platinum-Based Chemotherapy

RAHWAY, N.J. (BUSINESS WIRE) Oct 16, 2023

United statesSolange petersGregory lubinieckiPeter dannenbaumDamini chokshiJulie cunninghamStatement of merck co incMerck research laboratoriesMerck co incEuropean organisation for researchCentre hospitalier universitaire vaudoisExchange commissionEuropean commissionAmerican joint committee on cancerCommittee for medicinal products humanMedicinal products

Merck & Co , Inc : FDA Approves KEYTRUDA (pembrolizumab) for Treatment of Patients With Resectable (T=4 cm or N+) NSCLC in Combination With Chemotherapy as Neoadjuvant Treatment, Then Continued as a Single Agent as Adjuvant Treatment After Surgery

Merck & Co , Inc : FDA Approves KEYTRUDA (pembrolizumab) for Treatment of Patients With Resectable (T=4 cm or N+) NSCLC in Combination With Chemotherapy as Neoadjuvant Treatment, Then Continued as a Single Agent as Adjuvant Treatment After Surgery
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United statesJulie cunninghamPeter dannenbaumIhre chancenIndiens wirtschaftDamini chokshiHeather wakeleeStanford universityDrug administrationStatement of merck co incMerck access programPatient support programMerck patient support programAmerican joint committee on cancerExchange commissionMerck co inc

Merck & Co , Inc : Merck Receives Positive EU CHMP Opinion for KEYTRUDA (pembrolizumab) Plus Chemotherapy as First-Line Treatment for HER2-Negative Advanced Gastric or Gastroesophageal Junction (GEJ) Adenocarcinoma Expressing PD-L1 (CPS =1)

Merck & Co , Inc : Merck Receives Positive EU CHMP Opinion for KEYTRUDA (pembrolizumab) Plus Chemotherapy as First-Line Treatment for HER2-Negative Advanced Gastric or Gastroesophageal Junction (GEJ) Adenocarcinoma Expressing PD-L1 (CPS =1)
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United statesMichael mcardlePeter dannenbaumDamini chokshiJulie cunninghamMerck research laboratoriesEuropean commissionExchange commissionStatement of merck co incEuropean unionMerck co incEuropean medicines agencyMedicinal productsHuman useCombined positive scoreMarjorie green

Merck Receives Positive EU CHMP Opinion for KEYTRUDA® (pembrolizumab) Plus Chemotherapy as First-Line Treatment for HER2-Negative Advanced Gastric or Gastroesophageal Junction (GEJ) Adenocarcinoma Expressing PD-L1 (CPS ≥1) -October 13, 2023 at 07:46 am EDT

Opinion granted based on positive overall survival results from the Phase 3 KEYNOTE-859 trial If approved, a KEYTRUDA combination would become an option in the EU for the treatment of both.

United statesMerck co incEuropean unionStatement of merck co incExchange commissionMerck research laboratoriesEuropean commissionEuropean medicines agencyMedicinal productsHuman useCombined positive scoreMarjorie greenMerck researchSelected important safetyImportant safety informationFatal immune mediated adverse