Semaglutide
Semaglutide is a GLP-1 receptor agonist approved for type 2 diabetes (Ozempic, 0.5–2mg weekly SC; Rybelsus, 7–14mg oral daily) and chronic weight management (Wegovy, up to 2.4mg weekly SC). In the STEP trials, semaglutide 2.4mg produced ~15% average weight loss vs. 2.4% placebo over 68 weeks. Cardiovascular outcomes trials (SUSTAIN-6) show significant MACE reduction. Robust evidence base across type 2 diabetes, obesity, MASH, and cardiovascular risk reduction. One of the most impactful drugs of the 2020s.
Evidence
Strong evidence
Safety
Unknown safety profile
Clinical Status
Approved
Research Sync
Feb 19, 2026
Dosing
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Pharmacology
Evidence Score
Scores estimated from study counts. Exact breakdown computed after research sync.
Plain-English Snapshot
Semaglutide is currently categorized as a fat loss compound.
Evidence is strong (78/100) with a relatively mature body of research (495 indexed studies).
Safety scoring is incomplete. Start conservatively and monitor carefully.
Core mechanism
GLP-1 receptor agonist: delays gastric emptying, suppresses appetite via hypothalamic signaling, stimulates glucose-dependent insulin secretion
Practical Context
Strongest current signals
- Level B: Comparative Efficacy of Semaglutide versus Liraglutide on Weight Loss and Glycaemic Control.
- Level C: Efficacy and safety of once-weekly insulins in type 2 diabetes: A systematic review and meta-analysis.
- Level C: Semaglutide and tirzepatide in prediabetes: Evidence for diabetes prevention and cardiovascular protection.
Elevated caution signals
2 severe/high side effect flags