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Results from Merck’s Phase 3 Study Evaluating ZEPATIER™ (elbasvir and grazoprevir) in Patients with Chronic Hepatitis C Receiving Treatment for Opioid Dependence Published in Annals of Internal Me
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REPEAT/FDA Approves Merck’s KEYTRUDA® (pembrolizumab) for Patients with Recurrent or Metastatic Head and Neck Squamous Cell Carcinoma with Disease Progression on or After Platinum-Containing Chemot
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Merck (MRK) Announces FDA Approval of KEYTRUDA as HNSCC Treatment
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FDA Approves Merck’s KEYTRUDA® (pembrolizumab) for Patients with Recurrent or Metastatic Head and Neck Squamous Cell Carcinoma with Disease Progression on or After Platinum-Containing Chemotherapy
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Merck (MRK) Announces FDA Filing Acceptance of NDA for MK-1293
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Merck Announces U.S. FDA Filing Acceptance of New Drug Application (NDA) for MK-1293, an Investigational Follow-On Biologic Insulin Glargine
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Merck’s KEYTRUDA® (pembrolizumab) Approved by the European Commission for Patients with Advanced Non-Small Cell Lung Cancer (NSCLC) Whose Tumors Express PD-L1
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Merck Announces Second-Quarter 2016 Financial Results
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Merck Announces Fourth-Quarter 2016 Dividend
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Merck Receives Breakthrough Therapy Designation from FDA and PRIME Status from EMA for Investigational Ebola Zaire Vaccine (V920)
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Merck (MRK) Reports Statistically non-Inferior Data from ISENTRESS Phase 3 in HIV-1
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Data for Merck's Investigational Once-Daily Formulation of ISENTRESS® (raltegravir) Show That at Week 48, a Regimen Containing the Once-Daily Dosing Formulation...
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Merck (MRK) Animal Health Announces FDA Approval of BRAVECTO
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Merck Animal Health Receives FDA Approval of BRAVECTO® (fluralaner topical solution) for Cats and Dogs
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Merck (MRK) Provides Regulatory Update on BLA for Bezlotoxumab; Says FDA Requested Submission of New Data and Analyses from MODIFY Trials
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Merck Provides Regulatory Update on Biologics Licensing Application for Investigational Agent Bezlotoxumab
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Pfizer (PFE), Merck (MRK) Commence Aveluma Combo Phase 3 in Ovarian Cancer
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Merck Animal Health to Acquire Controlling Vallée S.A. Stake in $400M Deal (MRK)
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Merck Animal Health Announces Agreement to Acquire Controlling Interest In Brazilian Animal Health Company Vallée S.A.
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Premier (PINC), Merck (MRK) Enter Osteoporosis-Focused Collaboration
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Merck and Premier Inc. Collaborate to Prevent Fractures for Osteoporosis Patients
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Merck and Moderna Announce Strategic Collaboration to Advance Novel mRNA-Based Personalized Cancer Vaccines with KEYTRUDA® (pembrolizumab) for the Treatment of Multiple Types of Cancer
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Merck (MRK) Announces Receipt of Positive CHMP Opinion on KEYTRUDA as NSCLC Treatment
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Merck Receives CHMP Positive Opinion for KEYTRUDA® (pembrolizumab) for the Treatment of Advanced Non-Small Cell Lung Cancer (NSCLC)
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Merck to Hold Second-Quarter 2016 Sales and Earnings Conference Call on July 29
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Incyte (INCY) Treats First Patient in ECHO-301 Combo Phase 3 (MRK)
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Merck (MRK) Announces Relebactam Combo Phase 2 Met Primary Endpoint
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Results of Phase 2 Study of Merck’s Investigational Beta-Lactamase Inhibitor Relebactam in Combination with Imipenem/Cilastatin Presented at ASM Microbe
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Systematic Review of 58 Publications of Real-World Use of GARDASIL® Presented at EUROGIN Congress
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Merck (MRK) Announces Superior Data on KEYTRUDA vs. Chemotherapy in Untreated NSCLC
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Merck’s KEYTRUDA® (pembrolizumab) Demonstrates Superior Progression-Free and Overall Survival Compared to Chemotherapy as First-Line Treatment in Patients with Advanced Non-Small Cell Lung Cancer
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Merck Highlights Ongoing Commitment to Fighting Infectious Diseases with More than 30 Data Presentations at ASM Microbe 2016
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Merck (MRK) Announces MK-1293 Met Primary Endpoint in Two Phase 3 Studies
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Merck’s Investigational Insulin Glargine, MK-1293, Met Primary Endpoint in Two Phase 3 Studies, Showing Non-Inferiority to Lantus®
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Merck and Pfizer Announce Two Pivotal Phase 3 Studies for Ertugliflozin, an Investigational SGLT-2 Inhibitor, Met Primary Endpoints, Showing Significant A1C Reductions in Patients with Type 2 Diabetes
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Merck to Acquire Afferent Pharmaceuticals
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Merck (MRK) Enters Agreement to Acquire Afferent Pharma in ~$1.25B Deal
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Merck to Acquire Afferent Pharmaceuticals
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KEYTRUDA® (pembrolizumab) Shows Overall Response Rates of 73 to 83 Percent, with Complete Response Rates of 27 to 30 Percent, in Heavily Pre-treated Patients with cHL, in Update to Study KN-087
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Updated Findings from KEYNOTE-012 for KEYTRUDA® (pembrolizumab) Show Continued Benefit in Response Rates and Duration of Response Lasting Up to 30 Months in Patients with Previously Treated Recurrent
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Merck (MRK) Announces Presentation of New KEYTRUDA Data in NSCLC
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New Data from Phase 2 Study Evaluating KEYTRUDA® (pembrolizumab) for the Treatment of Cancers Deficient in DNA Mismatch Repair Show Durable Responses Across a Range of Cancers
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New Data for KEYTRUDA® (pembrolizumab) in Combination with Talimogene Laherparepvec, Dabrafenib Plus Trametinib, or Low-Dose Ipilimumab in Advanced Melanoma Presented at 2016 ASCO Annual Meeting
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New KEYTRUDA® (pembrolizumab) Data from KEYNOTE-010 and KEYNOTE-001 in Advanced Non-Small Cell Lung Cancer, Including Survival Data, To Be Presented at 2016 ASCO Annual Meeting
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New Data Evaluating KEYTRUDA® (pembrolizumab) in Combination with Chemotherapy for First-Line Treatment of Non-Small Cell Lung Cancer Demonstrate Response Rates Ranging from 48 to 71 Percent
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Merck to Hold Investor Briefing at 2016 ASCO Annual Meeting
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Merck (MRK) Announces Positive CHMP Opinion for ZEPATIER
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Merck Receives Positive CHMP Opinion for ZEPATIER™ (elbasvir and grazoprevir) in the European Union
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Merck Announces Third-Quarter 2016 Dividend
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Merck to Present at the UBS Global Healthcare Conference

