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FDA Accepts New Drug Applications for Merck’s Doravirine, the Company’s Investigational Non-Nucleoside Reverse Transcriptase Inhibitor (NNRTI), for Treatment of HIV-1 Infection
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Merck to Participate at the 36th Annual J.P. Morgan Healthcare Conference
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Merck to Hold Fourth-Quarter and Full-Year 2017 Sales and Earnings Conference Call on February 2
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Merck (MRK) Reports KEYTRUDA Approval in Japan for Use in Treatment of Patients with Urothelial Carcinoma That is Unresectable with Radical Surgery
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Merck’s KEYTRUDA® (pembrolizumab) Approved in Japan for Use in the Treatment of Patients with Urothelial Carcinoma That is Unresectable with Radical Surgery Who Have Progressed Following Cancer Che
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Merck (MRK) and Pfizer (PFE) Announce FDA Approval of SGLT2 Inhibitor STEGLATRO and Fixed-Dose Combination STEGLUJAN for Adults with Type 2 Diabetes
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FDA Approves SGLT2 Inhibitor STEGLATRO™ (ertugliflozin) and Fixed-Dose Combination STEGLUJAN™ (ertugliflozin and sitagliptin) for Adults with Type 2 Diabetes
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Merck (MRK) and Pfizer (PFE) Granted FDA Breakthrough Therapy Designation for Avelumab, INLYTA Combo in Advanced Renal Cell Carcinom
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FDA Grants Breakthrough Therapy Designation for Avelumab in Combination with INLYTA® in Advanced Renal Cell Carcinoma
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FDA Grants Breakthrough Therapy Designation for Avelumab in Combination with INLYTA® in Advanced Renal Cell Carcinoma
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Merck (MRK) Provides Update on Phase 3 Study of KEYTRUDA in Previously Treated Patients with GEJ
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Merck Provides Update on KEYNOTE-061, a Phase 3 Study of KEYTRUDA® (pembrolizumab) in Previously Treated Patients with Gastric or Gastroesophageal Junction Adenocarcinoma
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Merck (MRK) Announces FDA Accepts sBLA, Assigns Priority Review to its KEYTRUDA for Treatment of Relapsed or Refractory PMBCL
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FDA Accepts Supplemental Biologics License Application (sBLA), Assigns Priority Review to Merck’s KEYTRUDA® (pembrolizumab) for Treatment of Relapsed or Refractory Primary Mediastinal Large B-Cell
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Merck (MRK) Announces NEJM Publishes Phase 3 Clinical Study of PREVYMIS, Its New CMV Prophylaxis Medicine
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New England Journal of Medicine Publishes Phase 3 Clinical Study of PREVYMIS™ (letermovir), Merck’s New CMV Prophylaxis Medicine
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Merck Commemorates 30 Years of MECTIZAN® Donation Program Progress
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Merck (MRK) Announces New, Updated Data for its KEYTRUDA and Updated Data on LYNPARZA in Multiple Breast Cancer Subtypes to Be Presented at SABCS
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New and Updated Data for Merck’s KEYTRUDA® (pembrolizumab) and Updated Data on LYNPARZA® (olaparib) in Multiple Breast Cancer Subtypes to Be Presented at the 2017 San Antonio Breast Cancer Symposi
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Impassioned Lung Cancer Survivors Join Your Cancer Game Plan, Merck to Advocate for Others Facing This Highly Stigmatized Disease
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Merck Announces Increased Quarterly Dividend and $10 Billion Share Repurchase Authorization
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Merck KGaA, Darmstadt, Germany, and Pfizer Provide Update on Phase III JAVELIN Gastric 300 Study in Patients with Pre-Treated Advanced Gastric Cancer
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Merck (MRK) and Pfizer (PFE) Announce Phase III JAVELIN Gastric 300 Study in Patients With Pre-Treated Advanced Gastric Cancer Did Not Meet Primary Endpoint
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Merck and Pfizer Provide Update on Phase III JAVELIN Gastric 300 Study in Patients With Pre-Treated Advanced Gastric Cancer
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Merck Announces Final Results of Any and All Tender Offers
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Merck Announces Pricing of Any and All Tender Offers
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Trump taps ex-pharma executive Azar as U.S. health secretary
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Merck (MRK) Receives Positive CHMP Opinion for PREVYMIS in European Union
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Merck Receives Positive CHMP Opinion for PREVYMIS™ (letermovir) in the European Union
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Merck (MRK) Announces FDA Approval of PREVYMIS for Prevention of CMV Infection and Disease in Adult Allogeneic Stem Cell Transplant Patients
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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

