Pemvidutide
Altimmune (investigational)
Pemvidutide (ALT-801) is an investigational dual-agonist peptide that activates both the GLP-1 and glucagon receptors, developed by Altimmune specifically for metabolic dysfunction-associated steatohepatitis (MASH) and obesity. Like survodutide, pemvidutide exploits the glucagon receptor's ability to drive hepatic fatty acid oxidation and increase energy expenditure, while the GLP-1 component provides appetite suppression, insulin secretion, and glycemic counterbalance. The molecule was engineered with a specific GLP-1-to-glucagon potency ratio optimized for liver fat reduction — a design choice that distinguishes it from other dual agonists in the space. In the MOMENTUM phase 2 trial in adults with overweight or obesity, pemvidutide achieved approximately 15.6% body weight reduction at 48 weeks at the 2.4 mg dose, with significant reductions in liver fat content assessed by MRI-PDFF. The MASH-focused ATLAS trial demonstrated meaningful histological improvement. The tolerability profile follows the expected incretin-class pattern: nausea, vomiting, and diarrhea were the most common adverse events, predominantly during dose escalation. Altimmune has progressed pemvidutide into late-stage development, positioning it as a competitor to survodutide in the GLP-1/glucagon dual-agonist category. The molecule's differentiation rests on its specific receptor-potency balance and its emerging liver-fat data, which suggest glucagon-containing dual agonists may offer mechanistic advantages over GLP-1 monoagonists for hepatic steatosis.
Specifications
| Origin / Manufacturer | Synthetic |
| Regulatory Status | Phase 2b/3 investigational (no approvals as of 2026) |
| Active Components | Pemvidutide (investigational) |
| Storage | Refrigerate 2–8°C (clinical supply) |
| Shelf Life | Per clinical protocol |
| Form Factor | Investigational subcutaneous injectable |
Clinical Evidence
Clinical report reference
Frequently Asked Questions
Sources & References
Every clinical claim on this page traces to a primary peer-reviewed source.
- 1Altimmune Inc.. Pemvidutide (ALT-801) Phase 2 MOMENTUM Trial Results. Company Clinical Data Presentation. 2024.
- 2Day JW, Ottaway N, Patterson JT, et al.. A new glucagon and GLP-1 co-agonist eliminates obesity in rodents. Nature Chemical Biology. 2009;5(10):749-757. doi:10.1038/nchembio.209 PMID:19597507
- 3Boland ML, Laker RC, Mather K, et al.. Resolution of NASH and hepatic fibrosis by the GLP-1R/GcgR dual-agonist cotadutide via modulating mitochondrial function and lipogenesis. Nature Metabolism. 2020;2:413-431. doi:10.1038/s42255-020-0209-6 PMID:32694734
Reviewed by
Peptides Academy Editorial
Editorial Team
All clinical claims cross-checked against primary sources. Read our editorial policy →
Related Peptides
Liraglutide
Saxenda / Victoza
The first GLP-1 receptor agonist approved for chronic weight management (Saxenda, 2014) — an acylated human GLP-1 analog with ~13-hour half-life dosed once daily.
Retatrutide
Eli Lilly (investigational)
An investigational triple GIP / GLP-1 / glucagon receptor agonist from Eli Lilly, showing the largest weight-loss effect sizes yet reported in obesity trials (up to ~24% at 48 weeks in phase-2).
Semaglutide
Ozempic / Wegovy / Rybelsus
Long-acting GLP-1 receptor agonist — FDA-approved for type-2 diabetes and chronic weight management, landmark for its ~15% mean weight reduction in STEP trials.
Survodutide
Boehringer Ingelheim (investigational)
A dual GLP-1/glucagon receptor agonist in phase 3 development by Boehringer Ingelheim for MASH (metabolic dysfunction-associated steatohepatitis) and obesity, with strong liver-directed efficacy signals.
Tirzepatide
Mounjaro / Zepbound
First-in-class dual GIP/GLP-1 receptor agonist — SURMOUNT trials showed ~20% mean weight reduction and superior A1c control versus semaglutide.