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Evidence: AWeight LossMetabolic Health

Survodutide: Benefits, Dosage & FDA Status

Survodutide (BI 456906)

A dual GLP-1 / glucagon receptor agonist with strong Phase 2 weight-loss and MASH data. Resolution of MASH in 83% of participants at the highest dose at week 48.

FDA Status

Not FDA-approved — Phase 3 trials for obesity and MASH

Typical Dose

Trial range: 0.6–6 mg weekly (subcutaneous)

Evidence Grade

AStrong RCT or FDA-approved evidence

Half-Life

~6 days

Routes of Administration

subcutaneous

First Synthesized

2020

Clinics Indexed

6 providers have offered Survodutide in our tracked directory.

Mechanism of Action

Dual GLP-1 / glucagon receptor agonist; combines incretin appetite control with glucagon-driven energy expenditure and hepatic fat reduction.

Key Reported Benefits

Benefits listed reflect commonly reported effects from clinical trials and practitioner use. Individual response varies. Evidence-grade A indicates strong rct or fda-approved evidence.

Reported Side Effects

  • Nausea
  • Vomiting
  • GI symptoms

Contraindications

  • Personal/family history of medullary thyroid carcinoma
  • Pregnancy

Regulatory & Safety Context

FDA status: Not FDA-approved — Phase 3 trials for obesity and MASH

This page is for educational purposes only and does not constitute medical advice. Peptide use outside of an FDA-approved indication should be discussed with a licensed medical professional. Source quality, cold-chain storage, and injection hygiene all materially affect safety outcomes.

See state-by-state legality: US peptide legality by state →

References

Selected primary literature on Survodutide. Full PubMed records linked. Additional citations are available on request.

  1. PubMed PMID 38924765

Last reviewed: 2026-04-30

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