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In the dosing conditions trial, AUC 024h,semaglutide,day10 (primary endpoint), C max,semaglutide,day10 , AUC 06h,SNAC,day10 and C max,SNAC,day10 were log-transformed and analysed in linear normal models with post-dose fasting period, water volume and an interaction between post-dose fasting period and water volume as fixed factors
Serious AEs were reported by 3.6% of participants receiving survodutide ( n =11: DG1, n =1
Madsen AS et al
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