Overview
Survodutide is an investigational dual agonist of the glucagon and GLP-1 receptors developed by Boehringer Ingelheim in collaboration with Zealand Pharma. It is an acylated peptide with a long half-life suitable for once-weekly regimens in clinical trials, and its design reflects the hypothesis that adding glucagon-receptor activity to GLP-1 agonism can increase energy expenditure and directly reduce liver fat.
A phase 2 trial in people with metabolic dysfunction-associated steatohepatitis (MASH) and fibrosis, published in 2024, reported improvement in MASH without worsening fibrosis in a large majority of participants receiving the compound. Phase 2 obesity studies also reported meaningful weight reductions. Phase 3 programmes in obesity (SYNCHRONIZE) and MASH are ongoing. Survodutide is not approved anywhere. Our product is a research-grade reference compound for studies of hepatic metabolism and dual-receptor pharmacology.
Mechanism studied
- Survodutide
- GLP-1R + GCGR
- Hepatic lipid oxidation
- Liver & weight endpoints
Survodutide activates the glucagon receptor, abundant in the liver, and the GLP-1 receptor, found in the pancreas, gut and brain. Hepatic glucagon-receptor signalling increases fatty-acid oxidation and reduces lipogenesis, lowering liver fat, and may raise energy expenditure. GLP-1 receptor signalling reduces appetite, slows gastric emptying and enhances glucose-dependent insulin release, offsetting the glucose-raising potential of glucagon agonism. The relative balance between the two activities is a key design parameter studied across this drug class.
Research highlights
- 01Dual glucagon and GLP-1 receptor agonist from Boehringer Ingelheim and Zealand
- 02Phase 2 MASH trial published in the New England Journal of Medicine (2024)
- 03Glucagon-receptor activity targets hepatic lipid metabolism
- 04Phase 3 programmes in obesity and MASH are ongoing
- 05Not approved by any regulator
Latest published research
93 papers on PubMed →Interpreting Survodutide Renoprotection in a Hyperfiltration Model
Ye T et al. · Diabetes, obesity & metabolism · 2026 Oct 19 · PMID 42897119
From pathophysiology to therapy: dual and triple agonists as a new frontier in metabolic dysfunction-associated steatotic liver disease
Argano C et al. · Frontiers in pharmacology · 2026 · PMID 42947668
Does Survodutide Provide Renoprotection Beyond Its Metabolic and Haemodynamic Effects in Diabetic Kidney Disease?
He J et al. · Diabetes, obesity & metabolism · 2026 Oct 12 · PMID 42864267
The Power of Two: Harnessing Dual Glucagon and Incretin Signaling for Treatment of Obesity and Metabolic Dysfunction-Associated Steatohepatitis-A Narrative Review with a Translational Focus
Ard JD et al. · Obesity reviews : an official journal of the International Association for the Study of Obesity · 2026 Oct 11 · PMID 42860310
Development and validation of a multiplexed LC-HRMS method for nine GLP-1 receptor agonists and its pharmaceutical application
Tong LH et al. · Journal of chromatography. A · 2026 Oct 11 · PMID 42603384
Survodutide for the treatment of obesity: Mechanistic rationale, clinical evidence, and remaining uncertainties
Sergi CM et al. · Contemporary clinical trials · 2026 Oct 2 · PMID 42822760
Nephroprotective Effects of the Dual GCGR/GLP-1R Agonist Survodutide in Hypertension-Accelerated Diabetic Kidney Disease
Hamilton A et al. · Diabetes, obesity & metabolism · 2026 Oct 1 · PMID 42823075
Survodutide Once Weekly in Adults with Obesity and Type 2 Diabetes
Wharton S et al. · The New England journal of medicine · 2026 Oct 1 · PMID 42820639
Live feed from PubMed (NCBI) for “Survodutide”, updated 2026-10-30. Listing a paper is not an endorsement of its findings.
Registered studies
29 on ClinicalTrials.gov →- CompletedPhase 3
A Study to Test the Effect of Survodutide (BI 456906) on Cardiovascular Safety in People With Overweight or Obesity (SYNCHRONIZE™ - CVOT)
NCT06077864 · Boehringer Ingelheim · 2023-11-20
- RecruitingPhase 3
A Study to Test Whether Survodutide Helps People With Type 2 Diabetes Control Their Blood Sugar
NCT07754461 · Boehringer Ingelheim · 2026-08-24
- Active not recruitingPhase 1
A Study to Compare How 2 Different Formulations of Survodutide Are Taken up in the Body When Given by Injection in Healthy Men and Women With and Without Overweight or Obesity
NCT07768813 · Boehringer Ingelheim · 2026-09-02
- RecruitingPhase 3
LIVERAGE™: A Study to Test Whether Survodutide Helps People With a Liver Disease Called NASH/MASH Who Have Moderate or Advanced Liver Fibrosis
NCT06632444 · Boehringer Ingelheim · 2024-10-14
- RecruitingPhase 3
LIVERAGE™ - Cirrhosis: A Study to Test Whether Survodutide Helps People With a Liver Disease Called NASH/MASH Who Have Cirrhosis
NCT06632457 · Boehringer Ingelheim · 2024-11-12
- Not yet recruitingPhase 3
SYNCHRONIZE®-START- A Study to Test Whether Survodutide Helps People Living With Overweight or Obesity Who do Not Have Diabetes to Lose Weight
NCT07855900 · Boehringer Ingelheim · 2026-11-07
- CompletedPhase 1
A Study in Healthy People to Compare How 2 Different Formulations of Survodutide Are Taken up by the Body
NCT07221591 · Boehringer Ingelheim · 2025-11-05
- Not yet recruitingPhase 3
ELEVATE-LIVER: A Study to Test Whether Survodutide Helps Improve Heart Structure and Function in People With Overweight or Obesity and Fatty Liver Disease
NCT07850063 · Boehringer Ingelheim · 2026-10-23
From the public ClinicalTrials.gov registry for “Survodutide”, updated 2026-10-30. Shown for research context only; Purity Peptides products are not for human use.
Key references
- [1]Sanyal et al., 2024 — N Engl J Med (MASH)
- [2]PubMed — reviews on survodutide
FAQ
Glucagon receptors are highly expressed in the liver, and activating them increases fat oxidation in hepatocytes. Combining this with GLP-1 agonism has made survodutide a candidate in MASH research, where reductions in liver fat and inflammation are key endpoints in clinical and preclinical studies.
Lyophilized Survodutide is normally kept sealed at −20 °C, protected from light and moisture. Once reconstituted for laboratory work, aliquots are held at 2–8 °C for short-term use or frozen, avoiding repeated freeze–thaw. Follow the lot-specific guidance on the certificate of analysis.
Every lot of Survodutide ships with a certificate of analysis reporting HPLC purity, mass-spectrometry identity against the expected molecular weight, appearance and lot number. Match the COA lot to the vial label and keep it with your experimental records.
FOR RESEARCH USE ONLY.Not for human or veterinary use. Not intended to diagnose, treat, cure, or prevent any disease.



