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Also known as: Triple agonist, GIP/GLP-1/Glucagon agonist
Investigational triple agonist targeting GIP, GLP-1, and glucagon receptors for maximal metabolic benefit and weight loss.
Benefits
6
Conditions
4
Evidence
Phase 2 trials published in NEJM 2023+ studies
Source
Synthetic triple receptor agonist
Gabriel Brain Score
Strong
Investigational triple agonist targeting GIP, GLP-1, and glucagon receptors for maximal metabolic benefit and weight loss.
Tri-agonist activating GIP, GLP-1, and glucagon receptors simultaneously, enhances insulin secretion and suppresses appetite (GIP/GLP-1), increases energy expenditure and fat oxidation (glucagon), synergistic metabolic optimization across multiple pathways.
* Dosing should be individualized. Always consult with a qualified healthcare practitioner.
Phase 2 trials published in NEJM 2023
Phase 2 trial showed 24% weight loss at 48 weeks (12 mg dose), superior to any approved agent. Excellent tolerability profile. Phase 3 trials ongoing. Represents next frontier in metabolic pharmacotherapy.
Dual GIP and GLP-1 receptor agonist that produces superior weight loss and glycemic control compared to GLP-1 agonists alone.
Long-acting GLP-1 receptor agonist that reduces appetite, improves glycemic control, and promotes significant weight loss.
Investigational dual glucagon and GLP-1 receptor agonist for obesity and metabolic dysfunction-associated steatohepatitis (MASH).