European Commission Approves KEYTRUDA® (pembrolizumab) Plus LENVIMA® (lenvatinib) for Patients With Certain Types of Endometrial CarcinomaBusiness Wire • 11/29/21
European Commission Approves KEYTRUDA® (pembrolizumab) Plus LENVIMA® (lenvatinib) as First-Line Treatment for Adult Patients With Advanced Renal Cell CarcinomaBusiness Wire • 11/29/21
Updated Data Shows Merck's Oral COVID-19 Antiviral Cuts Hospitalization, Death Risk By 30%Benzinga • 11/26/21
Merck and Ridgeback Biotherapeutics says COVID antiviral reduced risk of hospitalization or death in at-risk adultsMarket Watch • 11/26/21
Merck and Ridgeback Biotherapeutics Provide Update on Results from MOVe-OUT Study of Molnupiravir, an Investigational Oral Antiviral Medicine, in At Risk Adults With Mild-to-Moderate COVID-19Business Wire • 11/26/21
Merck's Keytruda Conditionally Approved In Canada For Triple-Negative Breast CancerBenzinga • 11/23/21
Merck KGaA, Darmstadt, Germany Highlights Novel Mechanisms with the Potential to Transform Standards of Care in Several Cancers, MS, and LupusBusiness Wire • 11/22/21
Merck Highlights Novel Mechanisms with the Potential to Transform Standards of Care in Several Cancers, MS, and LupusBusiness Wire • 11/22/21