Merck wins FDA priority review for KEYTRUDA bladder cancer combo expansion
If approved, the move would significantly broaden the use of KEYTRUDA and KEYTRUDA QLEX in combination with Padcev
If approved, the move would significantly broaden the use of KEYTRUDA and KEYTRUDA QLEX in combination with Padcev
A decision is expected by August 17, 2026 under the Prescription Drug User Fee Act timeline
The new facility is expected to significantly improve access to high-quality medical services for patients across Gujarat and neighbouring regions
The Clinical Trial Application (CTA) approval clears the way for the company to launch trial locations in France and Romania
PMDA is regarded among the most stringent regulatory bodies globally
The move aims to accelerate the development, commercialization, and global rollout of advanced AI-powered mammography tools
The aim is to bolster healthcare delivery in a region increasingly burdened by chronic disease
The event marks a significant push into South Korea’s rapidly expanding bio-health ecosystem
TheraNym will set up a greenfield large-scale mammalian drug substance manufacturing facility
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