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Merck to Present New Data on ZEPATIER™ (elbasvir and grazoprevir) and Chronic Hepatitis C Clinical Development Programs at The Liver Meeting® 2016
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Merck Congratulates Guatemala as Fourth Country in Latin America to Achieve WHO Verification of Elimination of River Blindness
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Merck (MRK) Says Extensive KEYTRUDA Data Accepted for Presentation at ESMO
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Two New Trials of Merck’s KEYTRUDA® (pembrolizumab) as Monotherapy and in Combination with Chemotherapy for First-Line Treatment of Patients with Advanced Non-Small Cell Lung Cancer to be Presented
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Incyte (INCY) Announces Publication of Updated Phase 1 Data on Epacadostat + Keytruda in Advanced Melanoma (MRK)
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Merck to Hold Third-Quarter 2016 Sales and Earnings Conference Call on October 25
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Merck to Host Investor Teleconference to Discuss ESMO 2016 Highlights
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Pfizer (PFE), Merck (MRK) Announce Ertugliflozin Phase 3 Met Primary Endpoint in T2D
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Merck and Pfizer Announce Investigational Ertugliflozin Met Primary Endpoint of A1C Reduction When Added to Sitagliptin and Metformin in People with Type 2 Diabetes
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Merck Publishes 2015/2016 Global Corporate Responsibility Report
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Merck to Participate at the Morgan Stanley Global Healthcare Conference
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Merck (MRK) Announces FDA Accepts BLA with Priority Review and Grants Breakthrough Therapy Designation for KEYTRUDA for NSCLC
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Merck's (MRK) KEYTRUDA sBLA in NSCLC Accepted for FDA Priority Review
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FDA Accepts Supplemental Biologics License Application, Assigns Priority Review and Grants Breakthrough Therapy Designation to Merck’s KEYTRUDA® (pembrolizumab) for First-Line Treatment of Patients
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Merck (MRK) to Discontinue Development of Odanacatib for Osteoporosis
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Merck Provides Update on Odanacatib Development Program
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Merck (MRK) Announces Publication of Strong ZEPATIER Phase 3 Data as HCV Treatment
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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

