FDA Approves Merck's KEYTRUDA® (pembrolizumab) Plus Platinum- and Fluoropyrimidine-Based Chemotherapy for Treatment of Certain Patients With Locally Advanced or Metastatic Esophageal or Gastroesophageal Junction (GEJ) CarcinomaBusiness Wire • 03/23/21
Merck' Keytruda Plus Eisai's Lenvima Cuts Risk Of Death By 38% In Endometrial Cancer Trial Compared To ChemoBenzinga • 03/19/21
KEYTRUDA® (pembrolizumab) Plus LENVIMA® (lenvatinib) Significantly Improved Progression-Free Survival and Overall Survival Versus Chemotherapy in Patients With Advanced Endometrial Cancer Following Prior Platinum-Based Chemotherapy in Phase 3 StudyBusiness Wire • 03/19/21
Merck Announces Filing of Form 10 Registration Statement in Connection with Planned Spinoff of Organon & Co.Business Wire • 03/17/21
Amathus Therapeutics, Merck In Agreement For Neurodegenerative Disease-Targeted TherapiesBenzinga • 03/17/21
European Commission Approves Expanded Indication for Merck's KEYTRUDA® (pembrolizumab) in Adult and Pediatric Patients With Relapsed or Refractory Classical Hodgkin Lymphoma (cHL)Business Wire • 03/17/21
4 Pharma Stocks That Could Be Losers With the $1.9 Trillion Stimulus PackageThe Motley Fool • 03/17/21
Immutep's Lead Candidate To Be Tested In Combination With Keytruda In Second Head & Neck Cancer StudyBenzinga • 03/16/21