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Pemvidutide
GLP-1 Analogs

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 / ManufacturerSynthetic
Regulatory Status
Phase 2b/3 investigational (no approvals as of 2026)
Active Components
Pemvidutide (investigational)
StorageRefrigerate 2–8°C (clinical supply)
Shelf LifePer clinical protocol
Form FactorInvestigational subcutaneous injectable

Clinical Evidence

MOMENTUM phase 2 trial: approximately 15.6% weight reduction at 2.4 mg weekly dose over 48 weeks in adults with overweight or obesity. Significant liver fat reduction by MRI-PDFF demonstrated across dose groups. ATLAS trial evaluating MASH histological endpoints. Safety profile consistent with incretin class; GI adverse events most common.

Clinical report reference

Frequently Asked Questions

Sources & References

Every clinical claim on this page traces to a primary peer-reviewed source.

  1. 1Altimmune Inc.. Pemvidutide (ALT-801) Phase 2 MOMENTUM Trial Results. Company Clinical Data Presentation. 2024.
  2. 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
  3. 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

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