Clicky

Merck & Company, Inc.(MRK) News

Date Title
Dec 21 KEYTRUDA® (pembrolizumab) Plus LENVIMA® (lenvatinib) Receive Public Listing for Patients with Advanced Endometrial Carcinoma (EC) that is not MSI-H or dMMR
Dec 20 Merck Provides U.S. Regulatory Update on Gefapixant
Dec 20 FDA Accepts Merck's (MRK) BLA for 21-Valent Pneumococcal Jab
Dec 20 Merck to Participate in the Goldman Sachs Healthcare C-Suite Unscripted Conference
Dec 19 13 Most Promising Growth Stocks According to Analysts
Dec 19 Merck (MRK) Gets EU Nod for Expanded Use in Gastric Cancer
Dec 19 Merck gets FDA decision date for new pneumococcal vaccine
Dec 19 FDA Grants Priority Review to Merck’s New Biologics License Application for V116, an Investigational, 21-valent Pneumococcal Conjugate Vaccine Specifically Designed to Protect Adults
Dec 18 European Commission Approves Merck’s KEYTRUDA® (pembrolizumab) Plus Chemotherapy for New First-Line Indications in Advanced HER2-Negative Gastric or GEJ Adenocarcinoma in Tumors Expressing PD-L1 (CPS ≥1) and Advanced Biliary Tract Cancer
Dec 18 13 Most Profitable Pharmaceutical Stocks Now
Dec 10 12 Dow Stocks Billionaires Like The Most
Dec 10 12 Healthcare Stocks Billionaires Like the Most
Dec 9 Income Investors Should Know That Merck & Co., Inc. (NYSE:MRK) Goes Ex-Dividend Soon
Dec 8 Merck's (MRK) Keytruda-Lynparza Combo Fails Lung Cancer Study
Dec 8 Company News for Dec 8, 2023
Dec 8 Merck and Eisai Provide Update on Phase 3 LEAP-001 Trial Evaluating (pembrolizumab) Plus LENVIMA® (lenvatinib) as First-Line Treatment for Patients with Advanced or Recurrent Endometrial Carcinoma
Dec 8 Merck suffers bad week as 3 Keytruda combination trials fail
Dec 7 13 Best S&P 500 Dividend Stocks To Buy
Dec 7 Merck Scraps Phase 3 Keytruda-Lynparza Lung Cancer Study
Dec 7 Merck Announces KEYLYNK-008 Trial Evaluating KEYTRUDA® (pembrolizumab) Plus LYNPARZA® (olaparib) for Patients With Metastatic Squamous Non-Small Cell Lung Cancer to Stop for Futility