Educational reference only — not medical advice. Nothing is sold on this site. Research compounds are not for human use.
Home>>Peptides>>Survodutide
Clinical-stageGLP-1 / incretin

Survodutide

An investigational GLP-1/glucagon dual agonist (also known as BI 456906) under development for obesity, metabolic dysfunction-associated steatohepatitis, and type 2 diabetes.

CompoundSurvodutide
CategoryGLP-1 / glucagon dual agonist
ClassGLP-1 and Incretin Therapies
Evidence tierClinical-stage
WADA statusNot individually listed; verify current status if subject to testing
Sold on this siteNo — this is a reference database

Overview

Survodutide is catalogued here as a glp-1 / glucagon dual agonist and graded at the "Clinical-stage" evidence tier. This compound has completed or is undergoing formal human trials. Human safety and efficacy are being characterized, but no universal approval exists and results may still fail or be withdrawn.

An investigational GLP-1/glucagon dual agonist (also known as BI 456906) under development for obesity, metabolic dysfunction-associated steatohepatitis, and type 2 diabetes.

Mechanism of Action

The molecule combines GLP-1 receptor agonism — the dominant driver of appetite and glycemic effects — with glucagon receptor agonism, which is studied for potential contributions to energy expenditure and hepatic fat reduction.

Research and Evidence

Phase 2 obesity results reported roughly 19% mean weight reduction at the highest tested dose over 46 weeks, and a phase 2 program in MASH has reported histological improvement. Phase 3 trials are ongoing.

Evidence in context: the GLP-1 and Incretin Therapies class page collects the shared evidence themes and study-reading guidance for this category.

Safety and Side Effects

Dose-related gastrointestinal effects have been the most prominent adverse events reported to date; the full safety profile is still being characterized in ongoing trials.

Educational notice: this entry describes published research and, where they exist, regulator labels. It is not medical advice and not a recommendation for use. Research-grade compounds have no verified human-safety data.

Frequently Asked Questions

What is the evidence tier of Survodutide?

Survodutide is graded "Clinical-stage" on this site. This compound has completed or is undergoing formal human trials. Human safety and efficacy are being characterized, but no universal approval exists and results may still fail or be withdrawn.

Is Survodutide an approved medicine?

No. Clinical-stage means the compound has not reached universal regulatory approval; the tier description above explains exactly what level of evidence exists.

Where can I read the primary studies for Survodutide?

The references section at the end of this entry links the key primary sources — regulator labels, trial registrations, and peer-reviewed papers. Our "How to Read a Peptide Study" guide explains how to evaluate them.

References

  1. ClinicalTrials.gov — registered survodutide studies. [source]
EM
Dr. Elena Marsh, PhDMolecular Pharmacology · Lead Editor

Written and maintained by the editorial team. Medically reviewed by Dr. James Okafor, MD (Internal Medicine).

Evidence tier: Clinical-stage · Last reviewed: 2026-09-05 · Sources cited below.

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