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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
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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
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Merck (MRK) Announces FDA Acceptance of Bezlotoxumab BLA in C. difficile Prevention
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Merck Announces FDA Acceptance of Biologics License Application for Bezlotoxumab, an Investigational Antitoxin for Prevention of Clostridium Difficile Infection Recurrence
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Pre-Open Stock Movers 01/25: (AFMD) (GRUB) (SUNE) (TYC) Higher; (OMED) (NVAX) (TWTR) Lower (more...)
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Data for KEYTRUDA® (pembrolizumab) in a Range of Gastrointestinal Cancers to be Presented at 2016 Gastrointestinal Cancers Symposium
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Merck (MRK) Announces Resolation to Vioxx Securities Class Action; Will Pay $830M
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Merck Resolves Previously Disclosed Securities Class Action Lawsuit Related to Vioxx
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Merck (MRK) Announces Acquisition of IOmet
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Merck Acquires IOmet Pharma and Expands Immuno-Oncology Development Program
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Merck to Present at the 34th Annual J.P. Morgan Healthcare Conference
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Merck to Hold Fourth-Quarter and Full-Year 2015 Sales and Earnings Conference Call on February 3
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Merck to Present at Goldman Sachs Healthcare CEOs Unscripted: A View from the Top
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Merck (MRK) Announces WHO Acceptance of EUAL for Ebola Zaire Vaccine
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World Health Organization to Review Merck’s Investigational Ebola Vaccine for Emergency Use Assessment and Listing
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Merck’s KEYTRUDA® (pembrolizumab) Significantly Improves Survival Compared to Chemotherapy in Previously-Treated Patients with Non-Small Cell Lung Cancer Whose Tumors Express Any Level of PD-L1
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Merck (MRK) Announces Expanded Indication for KEYTRUDA
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FDA Approves Expanded Indication for Merck’s KEYTRUDA® (pembrolizumab) for the Treatment of Patients with Advanced Melanoma
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Merck's (MRK) Elbasvir/Grazoprevir MAA Will New Come Under EMA CHMP Standard Review
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Merck Provides Update on European Medicines Agency Marketing Authorization Application for Investigational Chronic Hepatitis C Therapy Elbasvir/Grazoprevir
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Merck (MRK) Says GARDASIL 9 Age Expanded in Males 16-26
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FDA Approves Expanded Age Indication for GARDASIL® 9 in Males
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Biothera Announces Clinical Study to Evaluate Combination Therapy of Imprime PGG and Merck's Checkpoint Inhibitor Keytruda in Patients with Non-Small Cell Lung Cancer
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Eli Lilly & Co. (LLY), Merck (MRK) Enter Collaboration for Abemaciclib Phase 1
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Lilly and Merck Expand Immuno-Oncology Collaboration Adding Abemaciclib and KEYTRUDA® Combination Trial
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Merck (MRK) Presents KEYTRUDA Data at ASH 2015
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Findings Across a Range of Hematological Cancers Add to The Growing Breadth of KEYTRUDA® (pembrolizumab) Data
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Merck (MRK) Announces Receipt of RENFLEXIS Approval in Korea
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Merck Announces Samsung Bioepis Receives Approval of RENFLEXIS™ (Infliximab), a Biosimilar of Remicade, in Korea
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Responses Observed in Three-Quarters of Heavily Pre-Treated Multiple Myeloma Patients Receiving KEYTRUDA® (pembrolizumab) Combined With Lenalidomide and Dexamethasone
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Amgen And Merck Announce Cancer Immunotherapy Collaboration For Patients With Non-Hodgkin Lymphoma
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New Survey Showed That Most People Living With HIV Were More Concerned About Their Other Chronic Health Conditions Than Their HIV
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Merck Announces Increased Quarterly Dividend
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Merck Announces Initial Results for KEYTRUDA® (pembrolizumab) with Novel Immunotherapy Combinations from Three Investigational Studies Presented at the Society for Melanoma Research International Con

