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Samples were collected under a University of Colorado institutional review board (IRB)-approved protocol (COMIRB #17-7788)
An adjusted indirect treatment comparison (aITC) was conducted using data from the SURPASS-2 and SUSTAIN FORTE trials
Part 2 also included two additional dose groups (intravenous and subcutaneous semaglutide) in order to investigate the absolute and relative bioavailability of oral semaglutide
NLY01, a long-acting pegylated exenatide form failed to show efficacy in a 36-week phase 2 study despite good tolerability [58]
Medscape (2026) 12
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