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Merck presents new HIV drug trial data on weight and lipid effects
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Merck Announces New Data from Phase 3 Trials Evaluating the Investigational, Once-Daily, Oral, Two-Drug Regimen of Doravirine/Islatravir (DOR/ISL) in Adults with Virologically Suppressed HIV-1 Infecti
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Merck to Present New Data from HIV Treatment and Prevention Pipeline at European AIDS Conference 2025
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Merck presents cancer research data at ESMO 2025 congress
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Merck Advances Oncology Innovation, Highlighting Progress in New Tumor Types and Earlier Stages of Disease at ESMO 2025
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Merck completes $10 billion acquisition of Verona Pharma
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Merck Completes Acquisition of Verona Pharma
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Merck starts phase 2b trials for tulisokibart in three new conditions
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Merck Expands Tulisokibart Clinical Development Program With Initiation of Phase 2b Trials in Three Additional Immune-Mediated Inflammatory Diseases
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Merck to Hold Third-Quarter 2025 Sales and Earnings Conference Call Oct. 30
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Merck's WINREVAIR reduces clinical worsening events by 76% in early PAH patients
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WINREVAIR™ (sotatercept-csrk) Reduced the Risk of Clinical Worsening Events by 76% Compared to Placebo in Patients Recently Diagnosed With PAH on Background Therapy in Phase 3 HYPERION Trial
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FDA approves Merck's subcutaneous KEYTRUDA QLEX across 38 cancer indications
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FDA Approves Merck’s KEYTRUDA QLEX™ (pembrolizumab and berahyaluronidase alfa-pmph) Injection for Subcutaneous Use in Adults Across Most Solid Tumor Indications for KEYTRUDA® (pembrolizumab)
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Merck receives positive EU opinion for RSV prevention drug ENFLONSIA
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Merck Receives Positive EU CHMP Opinion for ENFLONSIA™ (clesrovimab) for the Prevention of Respiratory Syncytial Virus (RSV) in Infants During Their First RSV Season
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Merck receives positive EU opinions for KEYTRUDA subcutaneous form and head cancer use
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Merck Receives Two Positive EU CHMP Opinions for KEYTRUDA® (pembrolizumab), for Subcutaneous (SC) Administration and for New Indication for Earlier-Stage Head and Neck Cancer
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Daiichi Sankyo and Merck receive FDA breakthrough designation for ovarian cancer drug
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Raludotatug Deruxtecan Granted Breakthrough Therapy Designation by U.S. FDA for Patients with CDH6 Expressing Platinum-Resistant Ovarian, Primary Peritoneal or Fallopian Tube Cancers Previously Treate
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Merck reports positive trial results for pneumonia vaccine in children
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CAPVAXIVE® (Pneumococcal 21-valent Conjugate Vaccine) Demonstrates Positive Immune Responses in Children and Adolescents at Increased Risk of Pneumococcal Disease
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Daiichi Sankyo and Merck report phase 2 trial results for lung cancer drug
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Ifinatamab Deruxtecan Demonstrated Clinically Meaningful Response Rates in Patients with Extensive-Stage Small Cell Lung Cancer in IDeate-Lung01 Phase 2 Trial
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Merck's oral cholesterol drug meets key goals in phase 3 trial
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Merck’s Investigational Oral PCSK9 Inhibitor Enlicitide Decanoate Met All Primary and Key Secondary Endpoints in Adults with Hypercholesterolemia in Pivotal CORALreef Lipids Study
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Merck to Participate in the Morgan Stanley 23rd Annual Global Healthcare Conference
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Merck Provides New Results for VERQUVO® (vericiguat) in Patients with Chronic Heart Failure and Reduced Ejection Fraction
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Merck to Participate in the 2025 Wells Fargo Healthcare Conference
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Daiichi Sankyo and Merck begin phase 3 breast cancer trial
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HERTHENA-Breast04 Phase 3 Trial of Patritumab Deruxtecan Initiated in Patients with Metastatic Hormone Receptor Positive, HER2 Negative Breast Cancer Previously Treated with Endocrine Therapy
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Merck to present cardiovascular disease research at ESC Congress
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Merck Demonstrates Ongoing Commitment to Advancing Cardiovascular Disease Management and Patient Care with New Data at the European Society of Cardiology Congress 2025
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Vets and Pet-Owners See Gaps in Flea and Tick Prevention, Highlighting Need for Year-Round Care, New Merck Animal Health Global Survey Finds
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Ifinatamab Deruxtecan Granted Breakthrough Therapy Designation by U.S. FDA for Patients with Pretreated Extensive-Stage Small Cell Lung Cancer
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KEYTRUDA plus Padcev improves survival for bladder cancer patients
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KEYTRUDA® (pembrolizumab) plus Padcev® (enfortumab vedotin-ejfv) Significantly Improved Event-Free and Overall Survival and Pathologic Complete Response Rate for Certain Patients with Muscle-Invasiv
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MilliporeSigma and Washington University in St. Louis Sign MoU to Advance Scientific Collaboration
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Merck Announces Fourth-Quarter 2025 Dividend
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MilliporeSigma Launches AAW™ Workstation to Advance Lab Automation
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Merck launches phase 3 trials for monthly HIV prevention pill
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Merck to Initiate Phase 3 Trials for Investigational Once-Monthly HIV Prevention Pill
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FDA approves Merck's BRAVECTO QUANTUM for year-long flea and tick protection
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FDA Approves BRAVECTO® QUANTUM (Fluralaner for Extended-Release Injectable Suspension) from Merck Animal Health
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FDA accepts Merck's application for HIV two-drug regimen
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U.S. FDA Accepts New Drug Application for Merck’s Doravirine/Islatravir, an Investigational, Once-Daily, Oral, Two-Drug Regimen for Treatment of Adults with Virologically Suppressed HIV-1 Infection
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Merck to acquire Verona Pharma for $10 billion to add COPD treatment
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Merck to Acquire Verona Pharma, Expanding its Portfolio to Include Ohtuvayre® (ensifentrine), a First-In-Class COPD Maintenance Treatment for Adults and Expected to Drive Growth into the Next Decade
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Merck to present HIV research data at IAS 2025 conference
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Merck to Present New Data Highlighting Research Advancements Across its HIV Prevention and Treatment Pipeline at IAS 2025
