What the studies show
Gastrointestinal events were frequent, as with every drug in this class, and mostly resolved.
“The most common treatment-emergent adverse events were gastrointestinal, and the majority were mild to moderate in severity and resolved by the end of the study.”
A few small or poorly-controlled human studies. Enough to be interesting; not enough to count on. Most of what gets called “clinically proven” online lives here.
- 1Dahl K, et al. Amycretin, a novel, unimolecular GLP-1 and amylin receptor agonist administered subcutaneously: results from a phase 1b/2a randomised controlled study.Lancet, 2025;406:149–162125 participants; up to 36 weeks. NCT06064006.
In context
Amycretin is a single molecule that activates both the GLP-1 and the amylin receptor, combining the two mechanisms that CagriSema delivers as two drugs. Its international name is now zenagamtide. In the first published trial — a phase 1b/2a study in 125 people — the highest dose produced 24.3% weight loss at 36 weeks: the largest figure reported for any weight-loss drug at this stage, from a small, early trial in which many participants withdrew. Two phase 2 trials in type 2 diabetes, published in The Lancet in 2026, add a dose-dependent HbA1c reduction of up to 1.7 points; the weight-loss figure has not yet been repeated in a larger trial.
Amycretin is investigational (early phase). Legal status differs by country — see the regulation section or the jurisdiction pages.
Questions
Is Amycretin proven to cause GI side effects?
What studies are behind the grade?
Is Amycretin approved for this?
Other outcomes for Amycretin
- CBody weight1 phase 1b/2a RCT (n=125)
- BBlood glucose (HbA1c) in type 2 diabetes1 phase 2 RCT (n=262); oral companion trial
- CTrial retentionadverse1 phase 1b/2a RCT
Written and maintained by LYO Research — how pages are written and checked. Reviewed 23 September 2026. Grades count human evidence only; see how LYO grades. Not medical advice. Correct this page →