FDA approves additional dosage of KEYTRUDA across all adult indications
The approval is for the use of the KEYTRUDA dosage in both monotherapy and combination therapy. According to Merck, the FDA granted the accelerated approval of the new
The company’s AAVSmartLibrary and associated technology are said to be used for developing AAV capsids for enhanced tissue tropism, manufacturability, and pre-existing immunity. The collaboration will make use
The trial dubbed CheckMate -743 saw the Opdivo, Yervoy combination delivered a statistically significant and clinically meaningful improvement in overall survival (OS) compared to chemotherapy comprised of pemetrexed