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The U.S. Food and Drug Administration approved the expanded use of GSK's respiratory syncytial virus vaccine on Friday in adults aged between 50 and 59, making it the first shot endorsed for that age...
A U.S. Food and Drug Administration advisory panel on Tuesday voted against a therapy based on the party drug MDMA for patients with post-traumatic stress disorder, marking a setback to the nascent... -June 04, 2024 at 05:39 pm EDT - MarketScreener
By Sriparna Roy and Pratik Jain (Reuters) - A panel of advisers to the U.S. Food and Drug Administration will meet on Tuesday to discuss a therapy based on the psychedelic drug MDMA for patients with post-traumatic stress disorder (PTSD). The meet...
(Reuters) - Catalent said on Wednesday its stockholders have voted to approve Novo Nordisk parent's $16.5 billion bid to take over the contract manufacturer. In February, Novo Holdings had agreed to buy Catalent, a key manufacturing subcontractor o...
By Sriparna Roy (Reuters) - The U.S. Food and Drug Administration has approved Elanco Animal Health's methane-reducing feed ingredient for lactating dairy cows, the company said on Tuesday. WHY IT'S IMPORTANT One tablespoon of Bovaer per lactating...