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US FDA requires Lilly to conduct post-marketing studies for obesity pill

US FDA requires Lilly to conduct post-marketing studies for obesity pill

ReutersTue, April 14, 2026 at 12:42 PM UTC

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FILE PHOTO: A bottle of Eli Lilly’s Foundayo weight-loss pills in this undated illustration. Eli Lilly/Handout via REUTERS

April 14 (Reuters) - The U.S. ‌Food ‌and Drug Administration ​said Eli Lilly is required ‌to ⁠conduct post-marketing trials ⁠to gauge risks ​for ​liver ​injury, cardiovascular ‌events, gastric emptying and a milk-only lactation ‌study ​related ​to ​its ‌newly approved obesity ​pill.

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(Reporting ​by Sriparna Roy ​in ‌Bengaluru; Editing ​by Tasim ​Zahid)

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