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It occurred in 13.4% of the lixisenatide group vs 13.2% of the placebo group: hazard ratio=1.02

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Details of the FDA Ruling The FDA's decision, detailed in a March 10, 2025, update, specifies enforcement discretion periods for compounding Semaglutide: For 503A pharmacies (state-licensed), the FDA will not take action for violations related to Semaglutide's shortage list inclusion until April 22, 2025, or until the district court's decision on the preliminary injunction motion in Outsourcing Facilities Association (OFA) v