Dec 21
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KEYTRUDA® (pembrolizumab) Plus LENVIMA® (lenvatinib) Receive Public Listing for Patients with Advanced Endometrial Carcinoma (EC) that is not MSI-H or dMMR
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Dec 20
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Merck Provides U.S. Regulatory Update on Gefapixant
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Dec 20
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FDA Accepts Merck's (MRK) BLA for 21-Valent Pneumococcal Jab
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Dec 20
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Merck to Participate in the Goldman Sachs Healthcare C-Suite Unscripted Conference
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Dec 19
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13 Most Promising Growth Stocks According to Analysts
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Dec 19
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Merck (MRK) Gets EU Nod for Expanded Use in Gastric Cancer
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Dec 19
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Merck gets FDA decision date for new pneumococcal vaccine
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Dec 19
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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
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Dec 18
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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
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Dec 18
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13 Most Profitable Pharmaceutical Stocks Now
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Dec 10
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12 Dow Stocks Billionaires Like The Most
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Dec 10
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12 Healthcare Stocks Billionaires Like the Most
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Dec 9
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Income Investors Should Know That Merck & Co., Inc. (NYSE:MRK) Goes Ex-Dividend Soon
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Dec 8
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Merck's (MRK) Keytruda-Lynparza Combo Fails Lung Cancer Study
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Dec 8
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Company News for Dec 8, 2023
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Dec 8
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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
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Dec 8
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Merck suffers bad week as 3 Keytruda combination trials fail
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Dec 7
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13 Best S&P 500 Dividend Stocks To Buy
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Dec 7
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Merck Scraps Phase 3 Keytruda-Lynparza Lung Cancer Study
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Dec 7
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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
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