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Merck’s Gefapixant (45 mg Twice Daily) Significantly Decreased Cough Frequency Compared to Placebo at Week 12 and 24 in Patients with Refractory or Unexplained Chronic Cough
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Vaccine makers announce pledge, outlining united commitment to uphold integrity of scientific process
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Biopharma Leaders Unite to Stand With Science
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Biopharma Leaders Unite to Stand with Science
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Biopharma Leaders Unite To Stand With Science
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Biopharma Leaders Unite to Stand with Science
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Biopharma Leaders Unite to Stand with Science
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Merck to Present at the Citi 15th Annual BioPharma Virtual Conference
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Merck (MRK) Says New Scientific Data at the ESMO Virtual Congress 2020 Reflect its Commitment to Advancing Cancer Research and Care
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New Scientific Data at the ESMO Virtual Congress 2020 Reflect Merck’s Commitment to Advancing Cancer Research and Care
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Merck's (MRK) KEYTRUDA Receives Two New Approvals in Japan
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Merck’s KEYTRUDA® (pembrolizumab) Receives Two New Approvals in Japan
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Merck's (MRK) KEYTRUDA in Combination With Chemotherapy Significantly Improved OS and PFS Compared With Chemotherapy in Locally Advanced or First-Line Metastatic Esophageal Cancer
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Merck’s KEYTRUDA® (pembrolizumab) in Combination With Chemotherapy Significantly Improved Overall Survival and Progression-Free Survival Compared With Chemotherapy in Locally Advanced or First-Line
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Merck Animal Health Completes Acquisition of IdentiGEN
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Merck and Hanmi Pharmaceutical Enter into Licensing Agreement to Develop Efinopegdutide, an Investigational Once-Weekly Therapy for Nonalcoholic Steatohepatitis (NASH)
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Merck (MRK) Animal Health Completes Acquisition of Worldwide Rights to VECOXAN Brand of Parasiticides for Ruminant Portfolio
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Merck Animal Health Completes Acquisition of Worldwide Rights to VECOXAN® Brand of Parasiticides for Ruminant Portfolio
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Merck Announces Second-Quarter 2020 Financial Results
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Merck (MRK) Announces Two US Regulatory Milestones for KEYTRUDA in Triple-Negative Breast Cancer
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Merck Announces Two US Regulatory Milestones for KEYTRUDA® (pembrolizumab) in Triple-Negative Breast Cancer (TNBC)
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Merck (MRK) Announces FDA Grants Breakthrough Therapy Designation to Novel HIF-2α Inhibitor MK-6482 for Treatment of Certain Patients With VHL- Associated RCC
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FDA Grants Breakthrough Therapy Designation to Merck’s Novel HIF-2α Inhibitor MK-6482 for Treatment of Certain Patients With Von Hippel-Lindau Disease- Associated Renal Cell Carcinoma
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Merck Announces Fourth-Quarter 2020 Dividend
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Factbox: More companies join Facebook ad boycott bandwagon
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Merck (MRK) Announces FDA Grants Priority Review to its NDA for Vericiguat
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FDA Grants Priority Review to Merck’s New Drug Application for Vericiguat
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MilliporeSigma Opens its Largest M Lab™ Collaboration Center in Shanghai
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Merck (MRK) Animal Health Receives U.S. FDA Approval of BRAVECTO Monthly Chews
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Merck Animal Health Receives U.S. FDA Approval of BRAVECTO® (fluralaner) Monthly Chews
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Merck (MRK) Announces FDA Grants Priority Review to its sBLA for KEYTRUDA for Second-Line Treatment of Patients With R/R Classical Hodgkin Lymphoma
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FDA Grants Priority Review to Merck’s Supplemental Biologics License Application for KEYTRUDA® (pembrolizumab) for Second-Line Treatment of Patients With Relapsed or Refractory Classical Hodgkin Ly
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Merck Announces Appointment of Organon & Co. General Counsel
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AstraZeneca (AZN), Merck (MRK) Announce LYNPARZA Approved in EU for Germline BRCA-mutated Metastatic Pancreatic Cancer
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LYNPARZA® (olaparib) Approved in the EU for Germline BRCA-mutated Metastatic Pancreatic Cancer
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Merck (MRK) and Eisai Receive CRL for KEYTRUDA plus LENVIMA Combination as First-Line Treatment for Unresectable HCC
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Merck and Eisai Receive Complete Response Letter for KEYTRUDA® (pembrolizumab) plus LENVIMA® (lenvatinib) Combination as First-Line Treatment for Unresectable Hepatocellular Carcinoma
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Merck (MRK) Reports New Analyses Showing Additional Safety & Efficacy Data for Investigational Islatravir in Combination with Doravirine in Adults with HIV-1 Infection
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Merck Announces New Analyses Showing Additional Safety and Efficacy Data for Investigational Islatravir in Combination with Doravirine in Adults with HIV-1 Infection
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Virbac completes divestment of U.S. Rights to SENTINEL® brands to MSD Animal Health
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Merck Animal Health Completes Acquisition of U.S. Rights to SENTINEL® Brand of Combination Parasiticides for Companion Animals
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Merck and Ridgeback Bio Announce Closing of Collaboration and Licensing Transaction
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Merck to Hold Second-Quarter 2020 Sales and Earnings Conference Call on July 31
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FDA Approves BAVENCIO as First-Line Maintenance Treatment for Patients with Locally Advanced or Metastatic Urothelial Carcinoma
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Merck (MRK) Announces FDA Approves its KEYTRUDA for First-Line Treatment of Patients With Unresectable or Metastatic MSI-H or dMMR Colorectal Cancer
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FDA Approves Merck’s KEYTRUDA® (pembrolizumab) for First-Line Treatment of Patients With Unresectable or Metastatic MSI-H or dMMR Colorectal Cancer
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Merck (MRK) Announces FDA Approves KEYTRUDA for Treatment of Patients with Recurrent or Metastatic cSCC that is Not Curable by Surgery or Radiation
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FDA Approves Merck’s KEYTRUDA® (pembrolizumab) for the Treatment of Patients with Recurrent or Metastatic Cutaneous Squamous Cell Carcinoma (cSCC) that is Not Curable by Surgery or Radiation
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Merck (MRK) Underscores Commitment to HIV with New Data Analyses to be Presented at AIDS 2020: Virtual
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Merck Underscores Commitment to HIV with New Data Analyses to be Presented at AIDS 2020: Virtual
