Overview
Activates GLP-1 receptors in pancreas, brain, and gut to regulate glucose and hunger.
Proposed mechanism
Mimics endogenous glucagon-like peptide-1 (GLP-1), binding to GLP-1 receptors in the pancreas, brain, and gut. Increases insulin secretion in a glucose-dependent manner, suppresses glucagon, slows gastric emptying, and reduces appetite via hypothalamic signaling.
What the evidence supports
Randomised controlled trial data in humans exists and supports use in specific contexts.
Graded Clinical
Findings supported by randomised, controlled trials in humans, with pre-registered endpoints and published results.
Key citations
Representative primary sources, including results that did not favour the compound.
- [1]
Semaglutide for weight loss
· DOI:10.1056/NEJMoa2032183 · 2021
- [2]
GLP-1 receptor agonists
· DOI:10.2337/dci19-0034 · 2019
- [3]
Wilding et al. — Semaglutide 2.4 mg for obesity (STEP 1 trial)
· · 0
- [4]
Marso et al. — Semaglutide cardiovascular outcomes (SUSTAIN-6)
· · 0
- [5]
Rubino et al. — STEP 4 trial: sustained weight loss
· · 0
Citation records in this build are illustrative placeholders for the design.
Reference information for research purposes. Not medical advice, and not a recommendation to use any compound. Many entries describe substances that are not approved for human use.