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These mechanisms are similar in that both induce the transition in the conformation of GLP-1 receptor through van der Waals interactions and hydrogen bonding of Trp33 ECD with extracellular loop (ECL) 1 and ECL2, instead of direct interaction of the peptide with ECL2 [43]

Therefore, there is no officially approved dosing guidance for general clinical use at this time

These effects were dose-dependent and particularly pronounced at higher doses

Survodutide, a glucagon/GLP-1 dual agonist, met its primary endpoint of histological improvement in MASH at 48 weeks and also demonstrated a statistically significant improvement in fibrosis, a secondary endpoint