The FDA granted priority review to pembrolizumab for neoadjuvant and adjuvant use in head and neck squamous cell carcinoma, ...
The FDA accepted for priority review a supplemental Biologics License Application for Keytruda for resectable locally ...
Keytruda demonstrated a statistically significant and clinically meaningful improvement in event-free survival and major ...
The US Food and Drug Administration (FDA) has accepted for priority review a new supplemental Biologics License Application ...
Among those with a chronic condition, concern of getting shingles is low with only 12% highly concerned and 37% somewhat concerned Over 80% of those with a chronic condition have not been informed by ...
Merck (MRK) announced the FDA has accepted for priority review a new supplemental Biologics License Application seeking approval for keytruda – ...
The US Food and Drug Administration (FDA) has accepted Bristol Myers Squibb’s (BMS) supplemental biologics licence ...