Merck Enters into Research and Development Funding Agreement with Blackstone Life Sciences for Sacituzumab Tirumotecan
Merck Signs Agreement with Dr. Falk Pharma GmbH for Certain Development and Commercialization Rights to MK-8690 an Investigational Anti-CD30 Ligand Monoclonal Antibody
Merck and Eisai Provide Update on Phase 3 LEAP-012 Trial in Unresectable, Non-Metastatic Hepatocellular Carcinoma
European Commission Approves KEYTRUDA® as Part of a Treatment Regimen for Adults with Resectable Locally Advanced Head and Neck Squamous Cell Carcinoma Expressing PD-L1
Merck Announces KEYTRUDA® Plus WELIREG® Met Primary Endpoint of Disease-Free Survival in Certain Patients With Clear Cell Renal Cell Carcinoma Following Nephrectomy
Merck and Eisai Announce WELIREG® Plus LENVIMA® Met Primary Endpoint of Progression-Free Survival in Certain Previously Treated Patients With Advanced Renal Cell Carcinoma
U.S. FDA Approves Updated Indication for WINREVAIR in Adults with Pulmonary Arterial Hypertension Based on Phase 3 ZENITH Study
eschbach's Shiftconnector® Helps Power Merck's Visual Factory to Drive Greater Transparency, Agility, and Supply Chain Resilience
Merck to Present New Data from Its Innovative Cardio-Pulmonary Pipeline and Portfolio at AHA Scientific Sessions 2025
FDA Grants Priority Review for KEYTRUDA® and KEYTRUDA QLEX , Each in Combination with Padcev® , for Certain Patients with Muscle-Invasive Bladder Cancer
Systematic Review of 15 Studies Focused on Epidemiology and Antimicrobial Resistance of Pneumococcal Serotypes Covered by CAPVAXIVE® in U.S. Adults
KEYTRUDA® Demonstrates Long-Term Survival Benefit in Certain Patients With Earlier or Advanced Stages of Non-Small Cell Lung Cancer
Cardiol Therapeutics' Phase II ARCHER Trial Results to be Presented at the European Society of Cardiology Scientific Meeting on Myocardial & Pericardial Diseases
