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Merck (MRK) Plans KEYTRUDA, KEYNOTE-006 and KEYNOTE-001 Presentations at ASCO 2016
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New KEYTRUDA® (pembrolizumab) Data from KEYNOTE-006 and KEYNOTE-001 in Advanced Melanoma, Including Updated Survival Data, To Be Presented at 2016 ASCO Annual Meeting
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Merck (MRK) Will Present New KEYTRUDA Data in Head and Neck Cancer, NSCLC
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New KEYTRUDA® (pembrolizumab) Data at 2016 ASCO Annual Meeting Includes Three-Year Overall Survival Data in Melanoma and Updated Overall Survival Data in Non-Small Cell Lung Cancer As Well As Updated
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Merck (MRK) Will Present JANUVIA, Diabetes Pipeline, Other Data at 76th Scientific Sessions of the ADA
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Merck to Present Phase 3 Data on Investigational Medicines Ertugliflozin and MK-1293 at the 76th Scientific Sessions of the American Diabetes Association
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Merck Announces First-Quarter 2016 Financial Results
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Merck to Present at the Deutsche Bank 41st Annual Health Care Conference
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Christina Applegate and Merck Urge Insomnia Sufferers to Learn "Why They're So Awake"
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Merck, the American Diabetes Association and America's Diabetes Challenge Celebrity Voices Unite to Take on National Health Epidemic
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Journal of the American Medical Association Publishes Phase III Data from Allergic Asthma Trial with ALK's House Dust Mite SLIT-tablet, ACARIZAX®
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Merck (MRK) Animal Health Enters Agreement to Acquire Whisper Veterinary Stethoscope System
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Merck Animal Health to Acquire Worldwide Rights to Whisper® Veterinary Stethoscope System
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Merck (MRK) Comments on Blueprint PD-L1 Assay Comparison Project; Encouraged by Findings
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Merck Statement on Blueprint Project Findings Presented at the American Association for Cancer Research 2016 Annual Meeting
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Merck (MRK) Receives FDA Breakthrough Therapy Designation for KEYTRUDA in cHL
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Merck Receives Breakthrough Therapy Designation from U.S. Food and Drug Administration for KEYTRUDA® (pembrolizumab) in Classical Hodgkin Lymphoma (cHL)
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Merck (MRK) Preents Data from Two ZEPATIER Phase 3s; High SVR Demonstrated
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Merck Announces Results From Phase 3 Studies of ZEPATIER™ (Elbasvir and Grazoprevir) in Chronic Hepatitis C Patient Populations at The International Liver Congress™
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Merck (MRK) Announces Strong Data from C-EDGE Head-to-Head Study
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Merck’s ZEPATIER™ (Elbasvir and Grazoprevir) Showed Superiority on Efficacy and Safety Endpoints Compared to Sofosbuvir Plus Peginterferon and Ribavirin Treatment Regimen in Phase 3 Trial
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Merck (MRK) Announces FDA Acceptance of KEYTRUDA sBLA; Priority Review Granted
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FDA Accepts Supplemental Biologics License Application (sBLA) for KEYTRUDA® (pembrolizumab) in Recurrent or Metastatic Head and Neck Cancer, and Grants Priority Review
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Merck to Hold First-Quarter 2016 Sales and Earnings Conference Call on May 5
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Merck Highlights Ongoing Commitment to Fighting Infectious Diseases with More Than 30 Data Presentations at ECCMID 2016
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Merck (MRK) Will Present New KEYTRUDA Data at AACR Annual Meeting
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Merck to Present New Data for KEYTRUDA® (pembrolizumab) at the American Association for Cancer Research 2016 Annual Meeting
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Pfizer (PFE), Merck (MRK) Treat First Patient in Avelumab Phase 3
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Advaxis (ADXS), Merck (MRK) Complete First Two Dose Escalations in KEYNOTE-046 Trial
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Advaxis Combination Trial with Merck Completes First Two Dose-Escalation Cohorts
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Merck Receives 2016 ENERGY STAR Sustained Excellence Award From U.S. Environmental Protection Agency
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Merck to Present New Findings from Chronic Hepatitis C Clinical Development Programs at The International Liver CongressTM 2016
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Merck Applauds the U.S. Department of Veterans Affairs (VA) for Broadening Treatment Access for Veterans with Chronic Hepatitis C Infection
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Sanofi Pasteur (SNY) and Merck (MRK) to End Joint Vaccines Operations in Europe
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Sanofi Pasteur and Merck (Known as MSD Outside the United States and Canada) Announce Intent to End Joint Vaccines Operations in Europe, Sanofi Pasteur MSD, to Pursue Their Own Distinct Growth Strateg
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Merck Names Sanat Chattopadhyay President of Merck Manufacturing Division; Will Succeed Willie A. Deese Who Will Retire
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Merck (MRK) Annnounces FDA Acceptance of KEYTRUDA sBLA
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FDA Accepts Supplemental Biologics License Application (sBLA) for KEYTRUDA® (pembrolizumab) in Advanced Non-Small Cell Lung Cancer
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Merck and the Mectizan Donation Program Donate $1 Million to the END Fund for Efforts to Help Eliminate River Blindness in Africa
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Merck Announces Second-Quarter 2016 Dividend
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Merck Puts Spotlight on Women's Health and Well-being
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Merck (MRK) Announces ISENTRESS Phase 3 Met Primary Efficacy Endpoint in HIV-1
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Merck’s Investigational Once-Daily Formulation of ISENTRESS® (raltegravir) Meets Primary and Secondary Endpoints in Pivotal Phase 3 Study
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Diplomat Pharmacy (DPLO) Begins Filling Prescriptions for ZEPATIER as HCV Treatment (MRK)
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Merck (MRK) Announces Receipt of CRL for ZETIA and VYTORIN NDA
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Merck Receives Complete Response Letter from the U.S. FDA for ZETIA® (ezetimibe) and VYTORIN® (ezetimibe and simvastatin)
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FDA Approves Merck’s Single-Dose EMEND® (fosaprepitant dimeglumine) for Injection, in Combination with Other Antiemetic Agents, for the Prevention of Delayed Nausea and Vomiting in Adults Receiving
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Merck Announces Fourth-Quarter and Full-Year 2015 Financial Results
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Merck (MRK) Announces FDA Approval of ZEPATIER as Genotype 1, 4 HCV Treatment
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Merck Receives FDA Approval of ZEPATIER™ (elbasvir and grazoprevir) for the Treatment of Chronic Hepatitis C Virus Genotype 1 or 4 Infection in Adults Following Priority Review

