Posts

Merck & Co.'s Keytruda Posts $8B in Q1 2026 as Qlex Picks Up Steam

Merck Wins FDA Approval for Subcutaneous Keytruda as Exclusivity Challenges Approach

Eisai Secures FDA Approval for Leqembi Autoinjector for Maintenance Dosing in Alzheimer’s Patients

FDA Approves CSL's Andembry, Directly Competing With Takeda's Takhzyro in HAE