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Merck to Present New Phase 3 Data on Investigational Ertugliflozin, Additional Analyses of Studies of JANUVIA® (sitagliptin), and Real-World Evidence Research at the 77th Scientific Sessions of the A
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Merck (MRK) Announces FDA Approval for KEYTRUDA as First-Line Combination Therapy with Pemetrexed and Carboplatin for Patients with Metastatic NSCLC
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FDA Approves Merck’s KEYTRUDA® (pembrolizumab) as First-Line Combination Therapy with Pemetrexed and Carboplatin for Patients with Metastatic Nonsquamous Non-Small Cell Lung Cancer (NSCLC), Irrespe
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Merck KGaA, Pfizer (PFE) Announce FDA Approval for BAVENCIO for Common Type of Advanced Bladder Cancer
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FDA Grants BAVENCIO® (avelumab) Approval for a Common Type of Advanced Bladder Cancer
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Merck (MRK) Announces EC Approval of KEYTRUDA for Patients with Relapsed/Refractory cHL
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European Commission Approves KEYTRUDA® (pembrolizumab) for Patients with Relapsed or Refractory Classical Hodgkin Lymphoma Who Failed Autologous Stem Cell Transplant and Brentuximab Vedotin (BV), or
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Merck to Present at the Deutsche Bank 42nd Annual Health Care Conference
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Merck Announces First-Quarter 2017 Financial Results
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America's Diabetes Challenge Unveils Common Challenges Affecting the Type 2 Diabetes Community
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Merck (MRK) Reports New Phase 2 Data on Investigational Triple Combination Therapy MK-3682B for Chronic Hepatitis C
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Merck Announces New Phase 2 Data on Investigational Triple Combination Therapy MK-3682B for Chronic Hepatitis C
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Real-World Observational Study in the U.S. Veterans Affairs System Evaluating Use of Merck’s ZEPATIER® (Elbasvir and Grazoprevir) Shows High Sustained Virologic Response Rates in Patients with Chro
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Merck Donates $300,000 to Support Neglected Tropical Disease Elimination Efforts in Africa
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Merck (MRK) Announces 25 Data Presentations at ECCMID
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Merck Underscores Continued Commitment to Fighting Infectious Diseases With More than 25 Data Presentations at ECCMID 2017
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Togo Becomes First Country in Africa to Validate the Elimination of Lymphatic Filariasis as a Public Health Problem
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Togo Becomes First Country in Africa to Validate the Elimination of Lymphatic Filariasis as a Public Health Problem
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Dr. John H. Noseworthy Nominated to Stand for Election to Merck Board of Directors
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Merck (MRK) Receives CRL from FDA for TECOS Study with Sitagliptin
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Merck Receives Complete Response Letter from the U.S. FDA for TECOS Study with Sitagliptin
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Merck Receives 2017 ENERGY STAR Sustained Excellence Award from U. S. Environmental Protection Agency
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Merck (MRK) to Present New Data on ZEPATIER and Investigational Combination Therapy MK-3682B at Liver Congress
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Merck to Present New Data on ZEPATIER® (elbasvir and grazoprevir) and Investigational Combination Therapy MK-3682B for the Treatment of Chronic Hepatitis C Infection at The International Liver Congre
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Ziopharm Oncology (ZIOP), Merck (MRK) & Intrexon (XON) Announce Development Update on CAR-T Therapy for Cancer
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Merck to Hold First-Quarter 2017 Sales and Earnings Conference Call on May 2
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Incyte (INCY), Merck (MRK) Provide Details on Pact to Investigate Epacadostat and KEYTRUDA
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Incyte and Merck Provide Additional Details on Previously Announced Collaboration Investigating Epacadostat and KEYTRUDA® (pembrolizumab)
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Merck (MRK) Announces EMA's CHMP Recommends Approval of KEYTRUDA to Treat Classical Hodgkin Lymphoma
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European Medicines Agency’s CHMP Recommends Approval of Merck’s KEYTRUDA® (pembrolizumab) for the Treatment of Patients with Relapsed or Refractory Classical Hodgkin Lymphoma
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Pfizer (PFE) and Merck (MRK) BioPharma Unit Get FDA Approval for BAVENCIO® (Avelumab), the 1st Immunotherapy Approved for Metastatic Merkel Cell Carcinoma
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FDA Grants Approval for BAVENCIO® (avelumab), the First Immunotherapy Approved for Metastatic Merkel Cell Carcinoma
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Merck Animal Health Completes Acquisition of Vallée S.A.
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Merck (MRK) Announces FDA Approval for KEYTRUDA to Treat Patients with Refractory cHL or Relapses
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FDA Approves Merck’s KEYTRUDA® (pembrolizumab) for Adult and Pediatric Patients with Classical Hodgkin Lymphoma (cHL) Refractory to Treatment, or Who Have Relapsed After Three or More Prior Lines o
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Merck (MRK) Provides Update on sBLA for KEYTRUDA in Previously Treated Advanced MSI-H
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Merck Provides Update on Supplemental Biologics License Application (sBLA) for KEYTRUDA® (pembrolizumab) in Previously Treated Advanced Microsatellite Instability-High Cancer
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'It's like kumbaya': Trump's genial private meetings with CEOs jar with public attacks
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Merck (MRK), Pfizer (PFE) Announce FDA and EMA Filing Acceptances of Three Marketing Applications for Ertugliflozin-Containing Medicines
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Merck and Pfizer Announce U.S. FDA and EMA Filing Acceptances of Three Marketing Applications for Ertugliflozin-Containing Medicines for Adults with Type 2 Diabetes
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Merck Announces Second-Quarter 2017 Dividend
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Recent Survey Finds Many Adults with Diabetes Unaware of Their Increased Risk for Certain Serious Illnesses
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Merck’s Letermovir, an Investigational Antiviral Medicine for Prevention of Cytomegalovirus (CMV) Infection in Bone Marrow Transplant Recipients, Highly Effective Through Week 24 Post-Transplant in
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Merck (MRK) Says V212 Reduced Incidence of Confirmed HZ Cases in First Phase 3 Trial
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In First Phase 3 Trial, Merck’s Investigational Inactivated Varicella Zoster Virus Vaccine (V212) Reduced the Incidence of Confirmed Herpes Zoster Cases by an Estimated 64 Percent in Immunocompromis
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Trump again vows to bring back U.S. jobs, but offers few details
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Aptus Health's RxStart(TM) Solution Launches with Electronic Health Record Partners to Engage Providers and Patients at the Point of Care
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Merck’s Fight Against Infectious Disease Goes Digital with Launch of ILÚM Health Solutions
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Merck (MRK) Stops EPOCH Study of Verubecestat in Mild to Moderate AD on Lack of Efficacy
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Merck Announces EPOCH Study of Verubecestat for the Treatment of People with Mild to Moderate Alzheimer’s Disease to Stop for Lack of Efficacy

