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Top-line outcomes at the 72-week primary endpoint, by dose: Additional SURMOUNT programme results: SURMOUNT-2 (adults with T2D, 72 weeks) reported 15.7% mean loss at 15mg

Gastrointestinal adverse reactions can be intensified when semaglutide is taken with other oral medicines or oral medications

A review of obesity pharmacotherapy published on NCBI describes a 12-week AOD 9604 trial in which the treated group lost more body fat than placebo without altering glucose control

H., Stagge, A., & Smith, U

Kidney Medicine

Roundtable on Obesity Solutions, Food and Nutrition Board, Health and Medicine Division, National Academies of Sciences, Engineering, and Medicine