FDA Approves KEYTRUDA® (pembrolizumab) Plus LENVIMA® (lenvatinib) Combination for Patients With Certain Types of Advanced Endometrial CarcinomaBusiness Wire • 07/22/21
Merck Discloses New Islatravir Data Supporting Safety Profile For PrEP Regime For HIV InfectionBenzinga • 07/20/21
Merck Presents New Data from Ongoing Phase 2a Clinical Trial Evaluating the Safety, Tolerability and Pharmacokinetics of Investigational, Once-Monthly, Oral Islatravir for HIV-1 Prevention at IAS 2021Business Wire • 07/20/21
Week 29 MDA Breakout Stocks - July 2021: Short-Term Stocks And Funds To Give You An EdgeSeeking Alpha • 07/19/21
Merck Announces U.S. FDA Approval of VAXNEUVANCE™ (Pneumococcal 15-valent Conjugate Vaccine) for the Prevention of Invasive Pneumococcal Disease in Adults 18 Years and Older Caused by 15 SerotypesBusiness Wire • 07/16/21
Merck Touts Encouraging Event-Free Survival For Keytruda Regime Over Placebo-Chemo Regime In Breast CancerBenzinga • 07/15/21
KEYTRUDA® (pembrolizumab) Plus Chemotherapy Before Surgery and Continued as a Single Agent After Surgery Showed Statistically Significant Event-Free Survival (EFS) Result Versus Neoadjuvant Chemotherapy Alone in High-Risk Early-Stage TNBCBusiness Wire • 07/15/21
Merck, Ridgeback Highlight Interim Molnupiravir Data In Non-Hospitalized COVID-19 PatientsBenzinga • 07/12/21
Barron's 100 Top ESG Equities Show 77 With Dividends And 2 With Ideal ReturnsSeeking Alpha • 07/12/21
Interim Results from Phase 2/3 Studies of Molnupiravir, an Investigational Oral Antiviral Therapeutic for Mild to Moderate COVID-19, Presented at the European Congress of Clinical Microbiology & Infectious Diseases (ECCMID)Business Wire • 07/12/21