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    Merck & Co (NY:MRK)

    111.17 -2.23 (-1.97%)
    Streaming Delayed Price Updated: 11:54 AM EDT, May 15, 2026 Add to My Watchlist
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    Press Releases about Merck & Co

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    Next-Generation GLP-1 Innovation Could Unlock Massive Metabolic Healthcare Market Opportunities
    Via Investor Brand Network
    InvestorNewsBreaks – SureNano Science Ltd. (CSE: SURE) (OTCQB: SURNF) Featured in BioMedWire Editorial on Next-Generation GLP-1 Innovation
    Via Investor Brand Network
    News headline image
    Merck Highlights New Long-Term Data and Advancements Across Broad Oncology Portfolio and Pipeline Research at ASCO 2026
    From Merck & Co., Inc.
    Via Business Wire
    News headline image
    Next-Generation GLP-1 Innovation Could Unlock Massive Metabolic Healthcare Market Opportunities
    From BioMedWire
    Via GlobeNewswire
    News headline image
    Merck Scientists Publish Landmark Paper on Novel Method for Large-Scale Biocatalytic Synthesis of Investigational Oral PCSK9 Inhibitor, Enlicitide Decanoate
    From Merck & Co., Inc.
    Via Business Wire
    News headline image
    Merck Animal Health Selects Salesforce’s Agentforce Life Sciences for Customer Engagement to Transform Animal Care and Enhance Support Experiences for Employees
    From Salesforce
    Via Business Wire
    News headline image
    Merck Completes Acquisition of Terns Pharmaceuticals, Inc.
    From Merck & Co., Inc.
    Via Business Wire
    News headline image
    Merck & Co., Inc., Rahway, N.J., USA Announces First-Quarter 2026 Financial Results; Highlights Significant Regulatory Approvals and Clinical Milestones
    From Merck & Co., Inc.
    Via Business Wire
    News headline image
    Merck’s Playing with Heart Program Teams Up With Professional Baseball Clubs and Baseball Legends to Help Raise Awareness About LDL-C, Called “Bad” Cholesterol, and How It May Impact the Risk of Heart Attack or Stroke
    From Merck & Co., Inc.
    Via Business Wire
    News headline image
    Merck Announces Expiration of Hart-Scott-Rodino Act Waiting Period to Acquire Terns Pharmaceuticals, Inc.
    From Merck & Co., Inc.
    Via Business Wire
    News headline image
    FDA Approves Merck’s Once-Daily IDVYNSO™ (doravirine/islatravir)
    From Merck & Co., Inc.
    Via Business Wire
    News headline image
    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)
    From Merck & Co., Inc.
    Via Business Wire
    News headline image
    FDA Grants Priority Review for KEYTRUDA® (pembrolizumab) and KEYTRUDA QLEX™ (pembrolizumab and berahyaluronidase alfa-pmph), Each with Padcev® (enfortumab vedotin-ejfv), for Cisplatin-Eligible Patients with Muscle-Invasive Bladder Cancer
    From Merck Sharp & Dohme
    Via Business Wire
    News headline image
    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
    From Merck & Co., Inc.
    Via Business Wire
    News headline image
    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-Based Chemotherapy
    From Daiichi Sankyo
    Via Business Wire
    News headline image
    BRODSKY & SMITH SHAREHOLDER UPDATE: Notifying Investors of the Following Investigations: Terns Therapeutics, Inc. (Nasdaq – TERN), Whitestone REIT (NYSE – WSR), Rallybio Corporation (Nasdaq – RLYB), Day One Biopharmaceuticals, Inc. (Nasdaq - DAWN)
    From Brodsky & Smith LLC
    Via GlobeNewswire
    News headline image
    Merck Begins Tender Offer to Acquire Terns Pharmaceuticals, Inc.
    From Merck & Co., Inc.
    Via Business Wire
    News headline image
    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 Degeneration
    From Merck & Co., Inc.
    Via Business Wire
    News headline image
    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 Received One or Two Prior Systemic Treatment Regimens
    From Merck & Co., Inc.
    Via Business Wire
    News headline image
    Merck to Hold First-Quarter 2026 Sales and Earnings Conference Call April 30
    From Merck & Co., Inc.
    Via Business Wire
    News headline image
    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 When Added to Background Statins
    From Merck & Co., Inc.
    Via Business Wire
    News headline image
    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 and Heart Failure With Preserved Ejection Fraction
    From Merck & Co., Inc.
    Via Business Wire
    News headline image
    Merck to Acquire Terns Pharmaceuticals, Inc., Expanding Its Hematology Pipeline With TERN-701, a Novel Candidate for Chronic Myeloid Leukemia (CML)
    From Terns Pharmaceuticals, Inc.
    Via GlobeNewswire
    News headline image
    Merck to Acquire Terns Pharmaceuticals, Inc., Expanding Its Hematology Pipeline With TERN-701, a Novel Candidate for Chronic Myeloid Leukemia (CML)
    From Merck & Co., Inc.
    Via Business Wire
    News headline image
    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
    From Merck & Co., Inc.
    Via Business Wire
    News headline image
    Merck to Present New Data Reinforcing Long-Term Efficacy of GARDASIL®9 and GARDASIL® at the EUROGIN International Multidisciplinary HPV Congress 2026
    From Merck Sharp & Dohme
    Via Business Wire
    News headline image
    Merck Highlights New Data from Cardio-Pulmonary Pipeline at ACC.26 Showcasing Commitment to Advance Innovative Research
    From Merck & Co., Inc.
    Via Business Wire
    News headline image
    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 Earlier-Stage Renal Cell Carcinoma (RCC)
    From Merck & Co., Inc
    Via Business Wire
    News headline image
    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 Carcinoma (RCC)
    From Merck & Co., Inc.
    Via Business Wire
    News headline image
    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 With Platinum-Resistant Recurrent Ovarian Cancer
    From Merck & Co., Inc.
    Via Business Wire
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