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Merck Provides Update on Phase 3 KEYNOTE-B21 Trial Evaluating KEYTRUDA® (pembrolizumab) Plus Chemotherapy, With or Without Radiotherapy, for Patients With Newly Diagnosed, High-Risk Endometrial Cancer After Surgery With Curative Intent

Merck Provides Update on Phase 3 KEYNOTE-B21 Trial Evaluating KEYTRUDA® (pembrolizumab) Plus Chemotherapy, With or Without Radiotherapy, for Patients With Newly Diagnosed, High-Risk Endometrial Cancer After Surgery With Curative Intent
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United statesGursel aktanData monitoring committeeDrug administrationStatement of merck co incEuropean network for gynecologic oncology trialMerck research laboratoriesFoundation incExchange commissionMerck co incMerck researchBiologics license applicationPrescription drug user fee actEuropean networkGynecologic oncology trialAmong merck

Merck Announces Phase 3 KEYNOTE-811 Trial Met Dual Primary Endpoint of Overall Survival (OS) as First-Line Treatment in Patients With HER2-Positive Advanced Gastric or Gastroesophageal Junction (GEJ) Adenocarcinoma

These OS results build on positive data previously reported from KEYNOTE-811 that supported its FDA-approved indication .

United statesMerck research laboratoriesDrug administrationMerck co incEuropean society for medical oncologyStatement of merck co incExchange commissionMarjorie greenMerck researchEuropean societyMedical oncologyImportant safety informationSelected important safetyFatal immune mediated adverseSingle agentThyroid disorders

Merck Announces Phase 3 Trial Initiations for Four Investigational Candidates From its Promising Hematology and Oncology Pipeline

Global Phase 3 studies started for bomedemstat , nemtabrutinib , MK-2870 and MK-5684 Comprehensive clinical development programs being initiated for each investigational candidate Demonstrates.

United statesDrug administrationExchange commissionMerck co incAmerican society for hematologyMerck research laboratoriesEuropean medicines agencyStatement of merck co incOrion corporationMarjorie greenMerck researchOrphan drugFast track designationOrphan drug designationPriority medicinesAmerican society

Merck & Co , Inc : Merck Receives Positive EU CHMP Opinion for 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

Merck & Co , Inc : Merck Receives Positive EU CHMP Opinion for 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
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United statesPeter dannenbaumGregory lubinieckiJulie cunninghamDamini chokshiExchange commissionMerck co incMerck research laboratoriesEuropean unionEuropean organisation for researchStatement of merck co incEuropean commissionEuropean medicines agencyMedicinal productsHuman useMerck research

Merck Receives Positive EU CHMP Opinion for 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

Opinion granted based on positive disease-free survival results from the Phase 3 KEYNOTE-091 trial .

United statesGregory lubinieckiMerck research laboratoriesEuropean unionEuropean organisation for researchMerck co incExchange commissionEuropean commissionStatement of merck co incEuropean medicines agencyMedicinal productsHuman useMerck researchEuropean organisationEuropean thoracic oncology platformSelected important safety