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Introduction: Glucagon-like-peptide-1 (GLP-1) agonists such as semaglutide and dulaglutide are increasingly used to treat type 2 diabetes mellitus (T2DM) and obesity as they lower blood glucose levels and help lose weight by delaying gastric emptying, reducing appetite and nutritional intake.(1) While these effects might have cardiovascular benefits, their impact on the progression of amyotrophic lateral sclerosis (ALS) is unknown

1 In vivo pharmacokinetic profile and in vitro activity of mGIPR-Ab

Cicero AF, Ertek S, Borghi C