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FDA Approves Merck’s Once-Daily IDVYNSO™ (doravirine/islatravir)
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Merck and Eisai report failed kidney cancer drug trial results
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MilliporeSigma Launches First Bio-Based Solvent Portfolio for High-Performance Liquid Chromatography
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Merck and Eisai trial for kidney cancer combination therapy fails endpoints
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Merck and Eisai Provide Update on Phase 3 LITESPARK-012 Trial Evaluating First-Line Combination Treatments for Certain Patients With Advanced Renal Cell Carcinoma (RCC)
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FDA grants priority review for Merck's KEYTRUDA combinations in bladder cancer
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FDA Grants Priority Review for KEYTRUDA® (pembrolizumab) and KEYTRUDA QLEX™ (pembrolizumab and berahyaluronidase alfa-pmph), Each with Padcev® (enfortumab vedotin-ejfv), for Cisplatin-Eligible Pat
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European Commission approves Merck's ENFLONSIA for RSV prevention in infants
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European Commission Approves Merck’s ENFLONSIA™ (clesrovimab) for the Prevention of Respiratory Syncytial Virus (RSV) Lower Respiratory Tract Disease in Infants During Their First RSV Season
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FDA grants priority review to ifinatamab deruxtecan for lung cancer treatment
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Ifinatamab Deruxtecan Granted Priority Review in the U.S. for Adult Patients with Previously Treated Extensive-Stage Small Cell Lung Cancer who Experienced Disease Progression on or After Platinum-Bas
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Merck launches tender offer to acquire Terns Pharmaceuticals for $53 per share
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Merck Begins Tender Offer to Acquire Terns Pharmaceuticals, Inc.
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Merck starts phase 2b/3 trial for eye disease drug MK-8748
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Merck Announces Initiation of Pivotal Phase 2b/3 Trial Evaluating MK-8748 (Tiespectus), an Investigational Bispecific Tie2 Agonist/VEGF Inhibitor, for the Treatment of Neovascular Age-Related Macular
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European Commission approves KEYTRUDA plus paclitaxel for ovarian cancer
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European Commission Approves KEYTRUDA® (pembrolizumab) Plus Paclitaxel ± Bevacizumab for the Treatment of Adults With PD-L1 (CPS ≥1) Platinum-Resistant Recurrent Ovarian Carcinoma Who Have Receive
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Merck to Hold First-Quarter 2026 Sales and Earnings Conference Call April 30
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Merck drug shows superior cholesterol reduction in phase 3 trial
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Merck’s Enlicitide Decanoate, an Investigational Oral PCSK9 Inhibitor, Demonstrated Significantly Greater LDL-C Reductions at Eight Weeks Compared to Guideline-Recommended Oral Non-Statin Therapies
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Merck's WINREVAIR shows promise in heart failure trial
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Positive Data from Phase 2 CADENCE Trial Provides Definitive Proof-of-Concept for WINREVAIR™ (sotatercept-csrk) in Adults With the Syndrome of Combined Post- and Precapillary Pulmonary Hypertension
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Merck to acquire Terns Pharmaceuticals for $6.7 billion
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Merck to Acquire Terns Pharmaceuticals, Inc., Expanding Its Hematology Pipeline With TERN-701, a Novel Candidate for Chronic Myeloid Leukemia (CML)
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FDA expands BRAVECTO QUANTUM label to cover two additional tick species
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FDA Approves BRAVECTO® QUANTUM (fluralaner for extended-release injectable suspension) from Merck Animal Health to Treat and Control Asian Longhorned Tick and Gulf Coast Tick for 12 Months in Dogs
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Merck to present HPV vaccine data showing 14-18 year efficacy
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Merck to Present New Data Reinforcing Long-Term Efficacy of GARDASIL®9 and GARDASIL® at the EUROGIN International Multidisciplinary HPV Congress 2026
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Merck to present data on cholesterol and heart failure drugs at ACC.26
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Merck Highlights New Data from Cardio-Pulmonary Pipeline at ACC.26 Showcasing Commitment to Advance Innovative Research
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KEYTRUDA Plus WELIREG Shows 28% Reduction in Cancer Recurrence Risk
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KEYTRUDA® (pembrolizumab) Plus WELIREG® (belzutifan) Given as Adjuvant Therapy Reduced the Risk of Disease Recurrence or Death by 28% Compared to KEYTRUDA Monotherapy in Certain Patients With Earlie
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WELIREG® (belzutifan) Plus LENVIMA® (lenvatinib) Reduced the Risk of Disease Progression or Death by 30% Compared to Cabozantinib in Certain Previously Treated Patients With Advanced Renal Cell Carc
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KEYTRUDA® (pembrolizumab) Plus Paclitaxel With or Without Bevacizumab Significantly Improved Key Secondary Endpoint of Overall Survival (OS) Versus Paclitaxel With or Without Bevacizumab in Patients
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Merck's KEYTRUDA plus Padcev reduces bladder cancer risk in trial
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KEYTRUDA® (pembrolizumab) Plus Padcev® (enfortumab vedotin-ejfv) Reduced Risk of Event-Free Survival Events by 47% and Risk of Death by 35% for Cisplatin-Eligible Patients with Muscle-Invasive Bladd
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FDA approves Merck's NUMELVI for dog skin allergies
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FDA Approves NUMELVI™ (atinvicitinib tablets) for Dogs from Merck Animal Health – The First and Only Second-Generation Janus Kinase (JAK) Inhibitor for the Control of Pruritus Associated with Alle
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Merck shares data on two-drug HIV regimen at medical conference
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Merck Announces Late-Breaking Data from Three Phase 3 Trials Evaluating Doravirine/Islatravir (DOR/ISL), an Investigational, Once-Daily, Two-Drug Regimen for the Treatment of Adults Living with HIV-1
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Merck to Participate in the TD Cowen 46th Annual Health Care Conference
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Merck restructures human health division into two business units
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Merck Evolves Human Health Operating Structure to Support Portfolio Execution
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Merck reports positive second-season data for RSV drug in high-risk children
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Merck Announces Positive New Data for ENFLONSIA™ (clesrovimab) for Infants and Children Under 2 Years of Age at Increased Risk for Severe Respiratory Syncytial Virus (RSV) Disease Over Two RSV Seaso
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Merck and Mayo Clinic partner on AI drug discovery collaboration
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Merck and Mayo Clinic Announce New Research and Development Collaboration to Support AI-Enabled Drug Discovery and Precision Medicine
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Merck presents cancer treatment data at ASCO GU symposium
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Merck Advances Treatment of Bladder and Kidney Cancers with New Data at 2026 ASCO GU Cancers Symposium
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FDA approves Merck's KEYTRUDA and KEYTRUDA QLEX for ovarian cancer
