What the studies show
The class profile — nausea, vomiting, diarrhoea concentrated in dose escalation. Nothing in the phase 2b separates it from the other incretin agonists on tolerability.
Human trials exist and mostly agree, but there are too few of them, they are too small, or one big one is still reading out. Expect the grade to move.
In context
Pemvidutide is a once-weekly peptide agonist at both the GLP-1 and glucagon receptors, developed by Altimmune for metabolic dysfunction-associated steatohepatitis (MASH). In IMPACT, a 212-patient phase 2b published in The Lancet in 2025, MASH resolved without worsening of fibrosis in 52–58% of treated patients against 20% on placebo at 24 weeks. The second endpoint — fibrosis improvement — was not met at either dose. It is not approved anywhere.
Pemvidutide is investigational (phase 2b). Legal status differs by country — see the regulation section or the jurisdiction pages.
Questions
Is Pemvidutide proven to cause GI side effects?
What studies are behind the grade?
Is Pemvidutide approved for this?
Other outcomes for Pemvidutide
- BMASH resolution without worsening fibrosis1 phase 2b RCT (n=212, 24 wk)
- BFibrosis improvement1 phase 2b RCT (n=212, 24 wk)
- CWeight lossPhase 2 programme
Written and maintained by LYO Research — how pages are written and checked. Reviewed 29 October 2026. Grades count human evidence only; see how LYO grades. Not medical advice. Correct this page →