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Merck and Daiichi Sankyo withdraw lung cancer drug application
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Ifinatamab Deruxtecan Biologics License Application for Certain Patients with Previously Treated Extensive-Stage Small Cell Lung Cancer Voluntarily Withdrawn
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FDA approves Merck and Eisai kidney cancer combination therapy
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U.S. FDA Approves WELIREG® (belzutifan) Plus LENVIMA® (lenvatinib) for Certain Previously Treated Adult Patients With Advanced Renal Cell Carcinoma With a Clear Cell Component (ccRCC)
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Merck's remigromig meets primary endpoint in DME phase 2b/3 trial
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Merck’s Remigromig, a Tri-specific Agonist of the Wingless-related Integration Site (Wnt) Pathway, Met Primary Endpoint in the Pivotal Phase 2b/3 BRUNELLO Study of Adults with Diabetic Macular Edema
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FDA updates Merck's Winrevair label with early PAH trial data
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U.S. FDA Approves Update to the Label for WINREVAIR™ (sotatercept-csrk) to Include Data from the Phase 3 HYPERION Trial Evaluating Adults Recently Diagnosed with Pulmonary Arterial Hypertension (PAH
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Japan approves Merck's subcutaneous pembrolizumab for all Keytruda uses
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Merck’s KEYTRUDA QLEX™ (pembrolizumab and berahyaluronidase alfa-pmph) Approved in Japan for Subcutaneous Administration for All KEYTRUDA® (pembrolizumab) Indications Approved in Japan
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EU panel backs Merck's Keytruda plus Padcev for bladder cancer
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Merck Receives Positive EU CHMP Opinion for KEYTRUDA® (pembrolizumab) Plus Padcev® (enfortumab vedotin-ejfv) as Perioperative Treatment for Adults With Resectable Muscle-Invasive Bladder Cancer (MIB
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Merck Launches Your Hive of Whole Health to Support Whole Person Care for People Living With HIV
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Merck to Participate in the Morgan Stanley 24th Annual Global Healthcare Conference
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Merck to Participate in the Wells Fargo 21st Annual Healthcare Conference
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Merck and Moderna's melanoma drug combo beats Keytruda alone in trial
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Merck and Moderna Announce Phase 3 INTerpath-001 Trial of Intismeran Autogene Plus KEYTRUDA® Met Endpoints of Recurrence-Free Survival (RFS) and Distant Metastasis-Free Survival (DMFS) in Patients Wi
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FDA accepts Merck's sBLA for Enflonsia to cover second RSV season
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U.S. FDA Accepts sBLA for ENFLONSIA™ (clesrovimab-cfor) to Update its Respiratory Syncytial Virus (RSV) Lower Respiratory Tract Disease Indication to Include Children Under Two Years at Increased Ri
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Merck Announces Fourth-Quarter 2026 Dividend
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Merck signs HIV prevention drug licenses covering 129 countries
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Merck Announces Initial Access Plans for Alimatravir, an Investigational Once-Monthly Oral HIV Pre-Exposure Prophylaxis in Phase 3 Development
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Gilead and Merck HIV pill shows strong results in Phase 3 trials
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Investigational Once-Weekly Oral HIV Treatment Regimen of Islatravir and Lenacapavir Maintained Virological Suppression in Adults With HIV Who Switched Antiretroviral Therapy
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MilliporeSigma Announces Opening of BioReliance® Testing Facility in Darmstadt, Germany to Support Drug Product Release in Europe
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FDA approves Merck's Lipfendra as first oral PCSK9 inhibitor
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Merck’s LIPFENDRA® (enlicitide) is the First and Only Once-Daily Oral PCSK9 Inhibitor Approved by the U.S. FDA to Reduce LDL-C in Adults with Hypercholesterolemia
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Merck to present HIV pipeline data at AIDS 2026 conference
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Merck to Present New Data on Daily, Weekly, and Monthly Options Across its HIV Treatment and Prevention Pipeline at AIDS 2026
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Merck's Keytruda meets PFS endpoint in endometrial cancer trial
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KEYTRUDA® (pembrolizumab) as Monotherapy Significantly Improved Progression-Free Survival (PFS) in Certain Patients With Advanced or Recurrent Endometrial Cancer With Mismatch Repair Deficient (dMMR)
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FDA clears Merck's Keytruda combo for muscle-invasive bladder cancer
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FDA Approves KEYTRUDA® (pembrolizumab) and KEYTRUDA QLEX™ (pembrolizumab and berahyaluronidase alfa-pmph), Each With Padcev® (enfortumab vedotin-ejfv), as Treatment Before and After Surgery for Ad
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Merck to Hold Second-Quarter 2026 Sales and Earnings Conference Call Aug. 4
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Merck reaches deal to expand HIV drug access via ADAP programs
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Merck Announces New Agreement with ADAP Crisis Task Force to Improve Access and Care for People Living with HIV
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FDA approves Merck's Keytruda combo with Trodelvy for TNBC
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FDA Approves KEYTRUDA® (pembrolizumab) and KEYTRUDA QLEX™ (pembrolizumab and berahyaluronidase alfa-pmph), each with Trodelvy® (sacituzumab govitecan-hziy) as First-Line Treatment of PD-L1+ (CPS �
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EU approves Merck's Keytruda plus Padcev for bladder cancer
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European Commission Approves KEYTRUDA® (pembrolizumab) Plus Padcev® (enfortumab vedotin-ejfv) as First PD-1 Inhibitor Plus Antibody-Drug Conjugate Regimen for Adults With Cisplatin-Ineligible Resect
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Merck's tulisokibart meets Phase 3 endpoints in ulcerative colitis trial
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Merck’s Tulisokibart Met Primary and Key Secondary Endpoints in the Phase 3 ATLAS-UC Induction-only Study in Patients With Moderately to Severely Active Ulcerative Colitis (UC)
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FDA approves Merck's Capvaxive for children at higher pneumonia risk
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U.S. FDA Approves an Additional Indication for CAPVAXIVE® (Pneumococcal 21-valent Conjugate Vaccine) in Children and Adolescents Aged 2 through 17 at Increased Risk for Pneumococcal Disease
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Study Reveals Dog Owners and Veterinarians See Challenges in Treating Allergic Skin Disease, Highlighting a Need for a Targeted Rapid Onset Treatment for Dogs of All Ages
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FDA approves Merck's KEYTRUDA and WELIREG combination for kidney cancer
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FDA Approves KEYTRUDA® (pembrolizumab) and KEYTRUDA QLEX™ (pembrolizumab and berahyaluronidase alfa-pmph), Each With WELIREG® (belzutifan), for Adjuvant Treatment of Certain Patients With Clear Ce
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Merck Animal Health to acquire poultry technology firm TARGAN
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Merck Animal Health to Acquire TARGAN
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Gilead and Merck announce successful HIV treatment trial results
