FDA Approves Merck’s KEYTRUDA® (pembrolizumab) for Patients With MSI‑H/dMMR Advanced Endometrial Carcinoma, Who Have Disease Progression Following Prior Systemic Therapy in Any Setting and Are Not Candidates for Curative Surgery or Radiation
Based on KEYNOTE-158 Trial, Patients Receiving KEYTRUDA Demonstrated an Objective Response Rate of 46% Approval Marks Fourth Gynecologic Cancer Indication for KEYTRUDA KENILWORTH, N.J.– Merck (NYSE: MRK), known as MSD… Read More




