Merck and Eisai combination endometrial cancer treatment fails to meet goals in clinical trialMarket Watch • 12/08/23
Merck and Eisai Provide Update on Phase 3 LEAP-001 Trial Evaluating (pembrolizumab) Plus LENVIMA® (lenvatinib) as First-Line Treatment for Patients with Advanced or Recurrent Endometrial CarcinomaBusiness Wire • 12/08/23
Merck cancels Phase 3 lung cancer study on disappointing interim data as separate mid-stage trial failsProactive Investors • 12/07/23
Merck Announces KEYLYNK-008 Trial Evaluating KEYTRUDA® (pembrolizumab) Plus LYNPARZA® (olaparib) for Patients With Metastatic Squamous Non-Small Cell Lung Cancer to Stop for FutilityBusiness Wire • 12/07/23
Merck Announces Findings from Phase 2 KeyVibe-002 Trial Evaluating an Investigational Coformulation of Vibostolimab and Pembrolizumab in Previously Treated Patients with Metastatic Non-Small Cell Lung Cancer (NSCLC)Business Wire • 12/07/23
Merck Provides Update on Phase III Results for Evobrutinib in Relapsing Multiple SclerosisBusiness Wire • 12/05/23
Abbisko Therapeutics Announced the Entry into a Licensing Agreement for Pimicotinib (ABSK021) with MerckPRNewsWire • 12/04/23
Merck Strengthens Oncology Portfolio Through Commercialization Agreement With Abbisko for Phase III Asset, PimicotinibBusiness Wire • 12/04/23
FDA Grants Priority Review to Merck's Application for KEYTRUDA® (pembrolizumab) Plus Padcev® (enfortumab vedotin-ejfv) for the First-Line Treatment of Patients With Locally Advanced or Metastatic Urothelial CancerBusiness Wire • 11/30/23
Merck & Co., Inc. (MRK) Management Presents at 6th Annual Evercore ISI HealthCONx Conference (Transcript)Seeking Alpha • 11/30/23
Merck's V116, an Investigational, 21-valent Pneumococcal Conjugate Vaccine Specifically Designed to Protect Adults, Demonstrated Superior Immunogenicity for 10 of 11 Unique Serotypes Compared to PCV20 in Adults 50 Years of Age and OlderBusiness Wire • 11/28/23