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Investigational and not approved by the FDA. This page is educational information only. It is not medical advice and not a recommendation to use anything.
IndexedBuilt automatically from public databases on 2026-09-30. Not yet hand-reviewed by PLOBT.How this works →

Survodutide

Investigational

Glucagon/GLP-1 dual agonist

Also known as: BI 456906, BI-456906, GLXC-27923

Evidence score
63/ 100
Moderate evidence

A real evidence base, with gaps

  • Regulatory standing. In clinical trials, not yet approved
  • Limited human data. Some human data exists, not conclusive
  • Registered human trials. 29 registered studies on ClinicalTrials.gov, most advanced Phase 3
  • 1 cited source. Includes primary / regulatory sources

Computed with the same four public criteria as every profile. The human-evidence grade on an indexed profile is set automatically and may change when it is hand-reviewed. It is not a safety score, not a purity rating, and not medical advice, and not a claim that this compound treats, cures, or prevents any condition.

What it is

Survodutide, also known as BI 456906, is an investigational injectable peptide developed by Boehringer Ingelheim. It activates both the glucagon receptor and the GLP-1 receptor, which is thought to reduce appetite while also increasing energy expenditure and fat processing in the liver.

What the evidence shows

Automatic summaryLimited human data

Survodutide is not FDA-approved. Phase 2 trials reported weight loss and improvements in fatty liver disease, and it has reached Phase 3 among 28 registered human trials, but those later-stage results are not yet conclusive and long-term safety is not established.

Key facts

Molecular formula
C192H289N47O61
Molecular weight
4232 g/mol

Registered human trials

Published literature

Sources

Risks, side effects and study doses are only published on hand-reviewed profiles. Want this one reviewed, or spotted something wrong? Tell us.