Semaglutide: The Weekly GLP-1 That Redefined Obesity Care
FDA-approved GLP-1 receptor agonist marketed as Ozempic, Wegovy and Rybelsus. ~15% mean weight loss in adults with obesity at 68 weeks.
Injectable GLP-1 agonists and their successors dominate modern obesity medicine. This category covers approved drugs (liraglutide, dulaglutide, orforglipron [Foundayo, April 2026]), next-generation dual/triple agonists (tirzepatide, retatrutide, survodutide), late-stage candidates (CagriSema β NDA filed Dec 2025, MariTide, amycretin), the muscle-sparing antibody bimagrumab, the rare-disease MC4R agonist setmelanotide, and failed or fringe agents (adipotide, AOD-9604).
FDA-approved GLP-1 receptor agonist marketed as Ozempic, Wegovy and Rybelsus. ~15% mean weight loss in adults with obesity at 68 weeks.
First approved dual incretin β GIP + GLP-1. ~21% mean weight loss at 72 weeks (SURMOUNT-1).
Once-daily GLP-1 agonist. Victoza (T2D, 2010), Saxenda (obesity, 2014). ~5β8% mean weight loss at one year.
GLP-1 agonist fused to an IgG4-Fc fragment. Once-weekly, FDA-approved for T2D and CV risk reduction.
Weekly GCGR/GLP-1 dual agonist in Phase 3 for obesity, MASH, T2D. ~19% weight loss at 46 weeks in Phase 2.
Eli Lilly's triple GIP/GLP-1/glucagon receptor agonist β the most impressive Phase 2 weight-loss numbers published so far, in a drug that remains strictly investigational
Non-peptide GLP-1 agonist in Phase 3. Daily oral pill, no food/water restrictions. ~15% weight loss in Phase 2.
Dual therapy combining a GLP-1 agonist and an amylin analogue. ~23% weight loss at 68 weeks in Phase 3 REDEFINE-1.
Amgenβs bispecific peptide-antibody conjugate combining GLP-1 agonism with GIP receptor blockade. Monthly dosing, Phase 3 ongoing.
Novo Nordisk investigational peptide combining GLP-1 and amylin agonism in a single molecule. Early-phase results show rapid weight loss.
Monoclonal antibody blocking ActRII receptors. Originally for sarcopenia; repurposed for obesity β loses fat while preserving or increasing muscle.
Cyclic peptide agonist of the melanocortin-4 receptor. FDA-approved for specific rare genetic obesity syndromes.
Modified fragment of human growth hormone marketed as a fat-loss peptide. Human trials did not support efficacy; widely sold in grey market.
Experimental peptide that selectively destroys blood vessels feeding white fat. Dramatic rodent and monkey results; never advanced in humans for obesity.
Unmodified C-terminal fragment of human growth hormone. Rodent lipolysis data; no approved human use. Closely related to AOD-9604.