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Merck Enters Exclusive Worldwide License Agreement with Teijin Pharma for Investigational Antibody Candidate Targeting Tau
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Merck (MRK) Granted FDA Approval of KEYTRUDA (pembrolizumab) for Adult & Pediatric Patients with Unresectable or Metastatic, Microsatellite Instability-High (MSI-H) or Mismatch Repair Deficient Cancer
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FDA Approves Merck’s KEYTRUDA® (pembrolizumab) for Adult and Pediatric Patients with Unresectable or Metastatic, Microsatellite Instability-High (MSI-H) or Mismatch Repair Deficient Cancer
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Merck Announces Third-Quarter 2017 Dividend
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Merck's (MRK) sBLA for KEYTRUDA to Treat Recurrent or Advanced Gastric or Gastroesophageal Junction Adenocarcinoma Granted FDA Priority Review
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FDA Grants Priority Review to Merck’s Supplemental Biologics License Application (sBLA) for KEYTRUDA® (pembrolizumab) for Treatment of Recurrent or Advanced Gastric or Gastroesophageal Junction Ade
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Merck (MRK) Announces Presentation of Phase 2 Results for MK-7264
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Merck Announces Presentation of Phase 2 Results for MK-7264, an Investigational, P2X3 Receptor Antagonist, Being Evaluated for the Treatment of Chronic Cough
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Merck (MRK) Announces CHMP Opinion Recommending Approval of ISENTRESS 600 mg
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Merck Receives CHMP Positive Opinion Recommending Approval of ISENTRESS® (raltegravir) 600 mg in the European Union
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100 Healthy Years - Are Kids Prepared?
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Merck (MRK) Says FDA Approves KEYTRUDA for Two New Indications fo Types of Bladder Cancer
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FDA Approves Merck’s KEYTRUDA® (pembrolizumab) for Certain Patients with Locally Advanced or Metastatic Urothelial Carcinoma, a Type of Bladder Cancer
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Merck (MRK) Says Data for KEYTRUDA Across 16 Types of Cancer to Be Presented at ASCO
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Data for KEYTRUDA® (pembrolizumab) Across 16 Types of Cancer from Merck’s Industry-Leading Immuno-Oncology Program to Be Presented at the 2017 ASCO Annual Meeting
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Merck KGaA, Darmstadt, Germany, and Pfizer to Present Data Highlighting Potential of Avelumab in Challenging Cancers at ASCO 2017
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Merck (MRK) to Report New Phase 3 Data on Investigational Ertugliflozin, Additional Analyses of Studies of JANUVIA® (sitagliptin) & Real-World Evidence Research at ADA Meetings
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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.

