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and received advisory/consulting fees and/or other support from AbbVie, Altimmune, AstraZeneca, Bayer, Betagenon AB, BIOIO, Biomea Fusion, Boehringer Ingelheim, Carmot Therapeutics, Cytoki Pharma, Eli Lilly, Intercept, Janssen/Johnson & Johnson, Juvena Therapeutics, Keros Therapeutics, Mediflix, Merck, Metsera, Novo Nordisk, PharmaVentures, Pfizer, Regeneron Pharmaceuticals, Sanofi, Shionogi, Structure Therapeutics, Target RWE, Terns Pharmaceuticals, The Comm Group, WebMD, and Zealand Pharma

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The FDA’s decision followed results from the first phase of Novo Nordisk’s ESSENCE trial