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Merck Receives FDA Approval of PREVYMIS™ (letermovir) for Prevention of Cytomegalovirus (CMV) Infection and Disease in Adult Allogeneic Stem Cell Transplant Patients
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Merck's Consumer Health Leads Debate on Preparing Gen Z for 100 Healthy Years
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Merck Animal Health Introduces Care & Control of Pet Diabetes To Help Pet Owners Deal with the Disease
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Merck Announces Any and All Tender Offers
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Merck Publishes Annual Corporate Responsibility Report
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Merck Animal Health Introduces Care & Control of Pet Diabetes To Help Pet Owners Deal with the Disease
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Merck (MRK) Withdraws European Application for KEYTRUDA in Combination with Pemetrexed and Carboplatin for First-Line Treatment of NSCLC
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Merck Provides Update on European Application for KEYTRUDA® (pembrolizumab) in Combination with Pemetrexed and Carboplatin for First-Line Treatment of Nonsquamous Non-Small Cell Lung Cancer (NSCLC)
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Merck Announces Third-Quarter 2017 Financial Results
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Corning to Showcase Latest in Pharmaceutical Glass Technologies at CPhI Worldwide in Frankfurt, Germany
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Merck (MRK) & AstraZeneca PLC (AZN) Report Second Regulatory Submission to Rapidly Advance LYNPARZA (olaparib) in Japan
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AstraZeneca and Merck Rapidly Advance LYNPARZA® (olaparib) in Japan With a Second Regulatory Submission
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Merck (MRK) Announces Data from Real-World Study Shows ZEPATIER (Elbasvir and Grazoprevir)
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Real-World Study Shows ZEPATIER® (Elbasvir and Grazoprevir) Resulted in High Rates of Sustained Virologic Response in Patients with Chronic Hepatitis C Infection Who Have Chronic Kidney Disease
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Merck (MRK) and AstraZeneca (AZN) Granted FDA Acceptance of Regulatory Submission for LYNPARZA (Olaparib)
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U.S. FDA Accepts Regulatory Submission for LYNPARZA® (olaparib) in Metastatic Breast Cancer and Grants Priority Review
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Merck (MRK) Says KEYTRUDA More Than Doubled Median Overall Survival Compared to Chemotherapy After Two Years of Follow Up in First-Line Treatment of Patients with Metastatic NSCLC with High Levels of
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Merck’s KEYTRUDA® (pembrolizumab) More Than Doubled Median Overall Survival Compared to Chemotherapy After Two Years of Follow Up in First-Line Treatment of Patients with Metastatic Non-Small Cell
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Merck Makes $3 Million Charitable Donation to Support Swim Across America
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Merck Joins with the American Liver Foundation to Educate U.S. Veterans on Chronic Hepatitis C Virus (HCV) Infection
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Merck (MRK) Says it Won't Submit Applications for Regulatory Approval for Anacetrapib
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Merck Provides Update on Anacetrapib Development Program
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Merck (MRK) Announces Six-year Efficacy Data for GARDASIL 9 Presented at EUROGIN 2017 Congress
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Six-year Efficacy Data for GARDASIL® 9 Presented at EUROGIN 2017 Congress
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Merck (MRK) Reports 40 Data Presentations at ID Week 2017
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Merck Highlights Ongoing Commitment to Fighting Infectious Diseases With 40 Data Presentations at ID Week 2017
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Merck (MRK) to Present New Data on ZEPATIER for Treatment of Chronic HCV Infection at The Liver Meeting
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Merck to Present New Data on ZEPATIER® (elbasvir and grazoprevir) for the Treatment of Chronic Hepatitis C Virus Infection at The Liver Meeting® 2017
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Merck (MRK) to Discontinue MK-3682B and MK-3682C Development Programs for HCV
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Merck (MRK) Says New and Updated Data on KEYTRUDA to Be Presented at WCLC
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Merck Discontinues MK-3682B and MK-3682C Development Programs
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New and Updated Clinical Data on Merck’s KEYTRUDA® (pembrolizumab) to Be Presented at 18th World Conference on Lung Cancer
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Merck Animal Health Extends Commitment to Fighting Rabies in the World’s Most At-Risk Regions
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Merck to Hold Third-Quarter 2017 Sales and Earnings Conference Call on October 27
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Merck (MRK) Says FDA Approves KEYTRUDA for Recurrent Metastatic Gastric or GEJ Cancer Whose Tumors Express PD-L1
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FDA Approves Merck’s KEYTRUDA® (pembrolizumab) for Previously Treated Patients with Recurrent Locally Advanced or Metastatic Gastric or Gastroesophageal Junction Cancer Whose Tumors Express PD-L1 (
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Merck KGaA, Pfizer (PFE) Report European Commission Approval for Bavencio (avelumab) for Metastatic Merkel Cell Carcinoma
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European Commission Approves Bavencio (avelumab) for Metastatic Merkel Cell Carcinoma
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Pro Baseball Hall of Famer and Cancer Survivor Mike Schmidt Joins Merck, Jim Kelly and Leading Cancer Organizations To Expand Your Cancer Game Plan To Help More People Impacted by Cancer
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Merck (MRK) Says Phase 3 Study of KEYTRUDA Compared to Standard of Care in Patients with Previously Treated HNSCC Didn't Meet Primary Endpoint
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Merck Announces Findings from Phase 3 Study of KEYTRUDA® (pembrolizumab), Compared to Standard of Care, in Patients with Previously Treated Recurrent or Metastatic Head and Neck Squamous Cell Carcino
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Merck KGaA, Darmstadt, Germany, Set to Join Forces with Project Data Sphere to Pioneer Global Oncology Big Data Alliance
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Incyte (INCY) Reports Progression-Free Survival Data from ECHO-202 Trial of Epacadostat in Combination with Merck (MRK) KEYTRUDA (pembrolizumab)
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Merck’s KEYTRUDA® (pembrolizumab) Continues to Show Overall Survival Benefit Over Chemotherapy with Nearly Two Years Follow-Up in Previously Treated Patients with Advanced Urothelial Carcinoma, Pos
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Progression-Free Survival Data from ECHO-202 Trial of Incyte’s Epacadostat in Combination with Merck’s KEYTRUDA® (pembrolizumab) Underscore Durability of Response in Patients with Advanced Melano
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Merck (MRK) Reports KEYTRUDA (pembrolizumab) plus Pemetrexed & Carboplatin (pem/carbo) Demonstrated Continued Benefit
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Merck’s KEYTRUDA® (pembrolizumab) Plus Pemetrexed and Carboplatin (pem/carbo) Demonstrated Continued Benefit in Overall Response Rates and Progression-Free Survival Compared to Pem/Carbo Alone in P
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Merck (MRK) Says Updated Data for KEYTRUDA in Patients with Advanced Gastric Cancer Across Treatment Settings to Be Presented at ESMO
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Updated Data for Merck’s KEYTRUDA® (pembrolizumab) in Patients with Advanced Gastric Cancer Across Treatment Settings to Be Presented at ESMO 2017 Congress
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Dr. Sam Bozzette Joins Premier Inc. to Lead Its Research Division

