Merck and Eisai Receive Positive EU CHMP Opinions for KEYTRUDA® (pembrolizumab) Plus LENVIMA® (lenvatinib) in Two Different Types of CancerBusiness Wire • 10/15/21
Merck Receives Positive CHMP Opinion for VAXNEUVANCE™ (Pneumococcal 15-valent Conjugate Vaccine) in Individuals 18 Years of Age and OlderBusiness Wire • 10/15/21
The success of Merck's antiviral—and other COVID-19 pills in development—may depend on how quickly people start taking themMarket Watch • 10/14/21
Holocene Advisors Believes Merck's Proposed Offer of $180 Per Share for Acceleron Significantly Undervalues CompanyBusiness Wire • 10/13/21
FDA Approves Merck's KEYTRUDA® (pembrolizumab) Plus Chemotherapy, With or Without Bevacizumab, as Treatment for Patients With Persistent, Recurrent or Metastatic Cervical Cancer Whose Tumors Express PD-L1 (CPS ≥1)Business Wire • 10/13/21
Merck's Covid-19 Antiviral Can Still Get FDA Authorization, Despite Safety Concerns, Analyst SaysBarrons • 10/13/21
Merck Reportedly Plans To Double Production Of New Covid-Fighting Pill As Wealthy Countries Corner Scarce SuppliesForbes • 10/12/21
Should you buy Merck shares as it files with FDA for emergency use of its covid pill?Invezz • 10/11/21
Coronavirus Update: Merck seeks authorization for what would be first pill to treat COVID-19, and AstraZeneca reports positive results for antibody treatmentMarket Watch • 10/11/21
Merck requests FDA authorization for its anti-COVID-19 pill, the next step towards rolling it outBusiness Insider • 10/11/21