Eli Lilly plans to submit a Biologics License Application (BLA) for Retatrutide to the U.S. Food and Drug Administration (FDA) in the first quarter of 2027. Eli Lilly stated that Retatrutide achieved significant weight loss results and met its primary endpoint in phase III trials. (Bloomberg)
Eli Lilly plans to submit a Biologics License Application (BLA) for Retatrutide to the U.S. Food and Drug Administration (FDA) in the first quarter of 2027. Eli Lilly stated that Retatrutide achieved significant weight loss results and met its primary endpoint in phase III trials. (Bloomberg)
智通财经2026/07/23 11:46Show original
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Eli Lilly plans to submit a Biologics License Application (BLA) for Retatrutide to the U.S. Food and Drug Administration (FDA) in the first quarter of 2027. Eli Lilly stated that Retatrutide achieved significant weight loss effects and reached its primary endpoint in Phase III trials. (Bloomberg).
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