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AstraZeneca furthers ambition to transform outcomes in early lung cancer and redefine metastatic breast cancer treatment at ASCO 2024

AstraZeneca furthers ambition to transform outcomes in early lung cancer and redefine metastatic breast cancer treatment at ASCO 2024
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United kingdomUnited statesSusan galbraithDave fredricksonDaiichi sankyo incDaiichi sankyo companyMerck co incAbelzeta pharmaceuticals incAmerican society of clinical oncologyAmerican societyClinical oncologyAnnual meetingRapid oral abstractExecutive vice presidentOncology business unitAbelzeta pharmaceuticals

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

European Medicines Agency Validates Bristol Myers Squibb s Application for Opdivo (nivolumab) Plus Yervoy (ipilimumab) for the First-Line Treatment of Adult Patients with Microsatellite

Application based on results from the CheckMate -8HW study, in which Opdivo plus Yervoy demonstrated statistically significant and clinically meaningful improvement in progression-free survival.

United statesSouth koreaYervoy opdivoBristol myers squibbDana walkerAmerican society of clinical oncologyCompany opdivoExchange commissionDrug administrationOno pharmaceutical coEuropean unionEuropean medicines agencyPlus yervoyFirst line treatmentAdult patientsMicrosatellite instability

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