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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
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KEYTRUDA® (pembrolizumab) and KEYTRUDA QLEX™ (pembrolizumab and berahyaluronidase alfa-pmph), Plus Paclitaxel ± Bevacizumab, Approved for Certain Adults with PD-L1+ (CPS ≥1) Platinum-Resistant O
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Merck Announces Second-Quarter 2026 Dividend
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Merck starts phase 3 trial of KRAS G12C inhibitor with KEYTRUDA QLEX
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Merck Initiates Phase 3 KANDLELIT-007 Trial Evaluating Calderasib (MK-1084), an Investigational Oral KRAS G12C Inhibitor, in Combination With KEYTRUDA QLEX™ (pembrolizumab and berahyaluronidase alfa
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Merck to Complete Acquisition of Cidara Therapeutics
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Merck to Hold Fourth-Quarter and Full-Year 2025 Sales and Earnings Conference Call Feb. 3
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Merck to Participate in the 44th Annual J.P. Morgan Healthcare Conference
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Merck agrees with US government to expand medicine access and cut costs
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Merck Reaches Agreement With U.S. Government to Expand Access to Medicines and Lower Costs for Americans
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Merck reports positive results for KEYTRUDA plus Padcev in bladder cancer
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KEYTRUDA® (pembrolizumab) Plus Padcev® (enfortumab vedotin-ejfv) Significantly Improved Event-Free Survival, Overall Survival and Pathologic Complete Response Rates for Cisplatin-Eligible Patients w
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Merck gets EU committee backing for expanded WINREVAIR use in PAH
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Merck Receives Positive EU CHMP Opinion for Expanded Use of WINREVAIR™ (sotatercept) in Adults with Pulmonary Arterial Hypertension (PAH, WHO* Group 1 Pulmonary Hypertension)
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German court grants HALOZYME injunction against Merck's Keytruda SC
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FDA conditionally approves Merck's cattle parasite treatment product
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FDA Conditionally Approves Merck Animal Health's EXZOLT™ CATTLE-CA1 for the Prevention and Treatment of New World Screwworm (Cochliomyia hominivorax) Larvae (myiasis)
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Merck receives FDA fast track for Alzheimer's drug MK-2214
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Merck Showcases Data for Alzheimer's Disease Candidates MK-2214 and MK-1167 at CTAD 2025
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Merck to Participate in the Citi 2025 Global Healthcare Conference
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Merck to Participate in the 8th Annual Evercore ISI HealthCONx Conference
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MERCK to present hematology pipeline data at ASH 2025 meeting
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Merck Data to be Presented at ASH 2025 Annual Meeting Showcase Continued Advancements in Hematology Pipeline and Novel Therapeutic Approaches
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Merck Recommends Rejection of Tutanota’s “Mini-Tender” Offer
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FDA approves Merck's KEYTRUDA combinations for 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 Perioperative Treatment for Adults with C
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Merck HIV drug combo meets phase 3 trial goals for treatment-naive patients
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Merck Announces Positive Topline Results from the Pivotal Phase 3 Trial Evaluating Investigational, Once-Daily, Oral, Two-Drug, Single-Tablet Regimen of Doravirine/Islatravir (DOR/ISL) in Treatment-Na
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European Commission approves subcutaneous KEYTRUDA for all adult indications
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European Commission Approves Subcutaneous Administration of KEYTRUDA® (pembrolizumab) for All Adult Indications Approved in the European Union
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Merck Announces First-Quarter 2026 Dividend
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Merck's WINREVAIR meets primary endpoint in phase 2 heart failure study
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Merck’s WINREVAIR™ (sotatercept-csrk) Met Primary Endpoint in Phase 2 CADENCE Study in Adults With Combined Post- and Precapillary Pulmonary Hypertension (CpcPH) due to Heart Failure With Preserve
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Merck to acquire Cidara for $9.2 billion to gain influenza drug
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Merck to Acquire Cidara Therapeutics, Inc., Diversifying Its Portfolio to Include Late-Phase Antiviral Agent
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Merck to Participate in the Jefferies Global Healthcare Conference in London
