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The FDA stated in January 2024 that their preliminary evaluation does not find that GLP-1 medicines cause suicidal thoughts or actions, though they continue monitoring and cannot definitively rule out a small risk

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References The original post is taken from Food and Drug Administration (FDA) Product Label Zepbound Food and Drug Administration (FDA) Product Label Mounjaro Tirzepatide Once Weekly for the Treatment of Obesity 4.

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The updated regulatory timeline: May 21, 2026: TRIUMPH-1 top-line data released June 2026: Detailed data presented at the 86th ADA Scientific Sessions Q4 2026: NDA submission to FDA (obesity indication) 2027: FDA review period (6-10 months standard