ORANGEMetabolic / Weight Management

Survodutide

Research compound1 SKU available18 clinical trials562 papers

Research Hub — Aggregated Studies

MedTech Research Group aggregates published research from peer-reviewed journals, clinical trials, and academic institutions. We do not conduct original research. All studies cited below are the work of their respective authors and institutions. Sources are linked for verification.

This product is designated FOR RESEARCH USE ONLY (RUO). These compounds have not been approved or cleared under 21 U.S.C. § 505 and have not been evaluated by the FDA for safety, efficacy, or labeling for clinical, diagnostic, or therapeutic use in humans or animals.

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Purchaser Restrictions

  • Purchaser must be a qualified researcher at an accredited institution or licensed research facility
  • This product may not be sold or redistributed to individual consumers, wellness clinics, health food stores, or retail establishments
  • Not intended for human or animal consumption, diagnostic use, or therapeutic application
  • Institutional affiliation and research purpose will be verified prior to order fulfillment

Distribution is limited to qualified research use in compliance with applicable federal and state law. These products bear the "For Research Use Only" designation per FDA labeling requirements (minimum 10 pt. font). Ref: 21 U.S.C. § 505; FD&C Act § 201(p) (unapproved new drug definition).

Compound Overview
Risk TierORANGE
CategoryMetabolic / Weight Management
SubcategoryDual-Action Glycemic and Hepatic Regulation
Pharmacological ClassDual Peptide Hormone Analog
SubclassGLP-1 / Glucagon Dual Receptor Agonist
Molecular TypeModified Peptide (dual-agonist, oxyntomodulin-based)
OriginSynthetic analog inspired by endogenous oxyntomodulin, which naturally activates both GLP-1 and glucagon receptors
Regulatory StatusInvestigational. Phase 3 trials by Boehringer Ingelheim for MASH (metabolic dysfunction-associated steatohepatitis) and obesity. Not FDA-approved.
Route of AdministrationSubcutaneous injection
ReconstitutionLyophilized powder; reconstitute with bacteriostatic water
StorageRefrigerate (2-8°C)

Chemical Properties

Molecular FormulaC192H289N47O61
Molecular Weight4232 g/mol
Exact Mass4231.1024139 Da
InChI KeyMEDXQFAHWBMVIM-PCLHIQTFSA-N
Synonyms
  • Survodutide
  • 2805997-46-8
  • BI-456906
  • GLXC-27923
PubChemView full record

Source: NCBI PubChem — public domain data

Molecular Structure

PubChem CID 171378821Sourced from PubChem

Loading molecular data from PubChem...

2D structure diagram from NCBI PubChem. This is the actual molecular structure of Survodutide.

Detailed Research

Description

Survodutide (BI 456906) is a dual GLP-1 and glucagon receptor agonist developed by Boehringer Ingelheim in collaboration with Zealand Pharma. Unlike tirzepatide (which targets GLP-1 and GIP receptors), survodutide activates GLP-1 and glucagon receptors simultaneously. This is a pharmacologically distinct approach based on the biology of oxyntomodulin, a naturally occurring gut hormone released from intestinal L-cells after meals that activates both receptor types at moderate potency.

The GLP-1 receptor agonism component provides the expected benefits: appetite suppression, improved insulin secretion, and glycemic control. The glucagon receptor agonism component — which might seem counterintuitive given that glucagon raises blood sugar — provides powerful metabolic effects including increased hepatic fat oxidation, elevated energy expenditure (thermogenesis), reduced hepatic lipogenesis, and mobilization of glycogen stores. In carefully titrated doses where the GLP-1 component offsets the hyperglycemic effect of glucagon agonism, the net result is significant weight loss AND liver fat reduction. Phase 2 trials demonstrated up to 19% weight loss at 46 weeks and — critically — up to 87% relative reduction in liver fat content, which has positioned survodutide as a leading candidate for MASH (formerly NASH) treatment.

Clinical Context

MASH/NASH is a growing epidemic with limited approved therapies. The liver fat reduction observed with survodutide far exceeds what has been seen with GLP-1 agonists alone. Boehringer Ingelheim is running Phase 3 trials for both MASH and obesity indications. If approved, survodutide would occupy a unique niche as a metabolic agent that addresses both obesity and fatty liver disease simultaneously.

Research Applications
MASH / NASH and hepatic steatosis research
Obesity and weight management studies
Glucagon receptor signaling and energy expenditure research
Dual-agonist pharmacology studies
Hepatic lipid metabolism research
Comparison studies vs. GLP-1-only and GLP-1/GIP agonists
Clinician Notes
Important Notes for Clinicians
  • Glucagon receptor agonism may transiently increase blood glucose; careful titration is essential
  • GI side effects (nausea, vomiting, diarrhea) are common and dose-dependent
  • Liver enzyme elevations (ALT/AST) have been observed and require monitoring
  • Contraindications likely similar to other GLP-1 agonists (MTC history, MEN 2, pancreatitis history)
  • No established dosing protocol for compounded versions; clinical trial doses ranged from 0.3mg to 6.0mg weekly with slow titration

Published Research

Published Research & Clinical Data

Peer-reviewed studies and clinical trial data related to Survodutide

All research below is conducted by independent institutions. MedTech Research Group provides these references for informational purposes only.

Research citations are being compiled for this compound.

Check back soon — our team is curating peer-reviewed sources.

Clinical Trials

18 Registered Clinical Trials

Research data sourced from ClinicalTrials.gov. Public domain (U.S. National Library of Medicine).

MedTech Research Group provides these references for informational purposes. We do not conduct original research. All studies are the work of their respective authors and institutions.

18

Total Trials

4

Recruiting

4

Active

9

Completed

CompletedPhase 1NCT06772532
A Study in Healthy People to Compare How 3 Different Formulations of Survodutide Are Taken up in the Body

Sponsor: Boehringer Ingelheim · Completed: 2025-06-10

CompletedPhase 1NCT07071974
A Study in Healthy People to Compare How 2 Different Formulations of Survodutide Are Taken up in the Body

Sponsor: Boehringer Ingelheim · Completed: 2025-10-28

CompletedPhase 3NCT06176365
A Study to Test Whether Survodutide Helps Japanese People Living With Obesity Disease

Sponsor: Boehringer Ingelheim · Completed: 2025-12-03

Scholarly Research

Research Library — 562 Papers

Research data sourced from OpenAlex. CC0 public domain. Articles are the work of their respective authors.

MedTech Research Group provides these references for informational purposes. We do not conduct original research. All studies are the work of their respective authors and institutions.

562 papers found23 open access2 paywalledSorted by citation count (most-cited first)
#1 Open Access427 citations · 2024

Type 2 diabetes mellitus in adults: pathogenesis, prevention and therapy

Xi Lu, Qingxing Xie, Xiaohui Pan, et al. · Signal Transduction and Targeted Therapy

Research by Xi Lu et al., published in Signal Transduction and Targeted Therapy. Not conducted by MedTech Research Group.

#2 Paywalled389 citations · 2024

A Phase 2 Randomized Trial of Survodutide in MASH and Fibrosis

Arun J. Sanyal, Pierre Bédossa, Mandy Fraessdorf, et al. · New England Journal of Medicine

Research by Arun J. Sanyal et al., published in New England Journal of Medicine. Not conducted by MedTech Research Group.

#3 Open Access286 citations · 2024

Efficacy and Safety of GLP-1 Medicines for Type 2 Diabetes and Obesity

Daniel J. Drucker · Diabetes Care

Research by Daniel J. Drucker, published in Diabetes Care. Not conducted by MedTech Research Group.

#4 Open Access275 citations · 2024

What is the pipeline for future medications for obesity?

Eka Melson, Uzma Ashraf, Dimitris Papamargaritis, et al. · International Journal of Obesity

Research by Eka Melson et al., published in International Journal of Obesity. Not conducted by MedTech Research Group.

#5 Open Access223 citations · 2024

Metabolic dysfunction-associated steatotic liver disease: heterogeneous pathomechanisms and effectiveness of metabolism-based treatment

Norbert Stefan, Hannele Yki‐Järvinen, Brent A. Neuschwander‐Tetri · The Lancet Diabetes & Endocrinology

Research by Norbert Stefan et al., published in The Lancet Diabetes & Endocrinology. Not conducted by MedTech Research Group.

#6 Open Access210 citations · 2024

Diabetes mellitus—Progress and opportunities in the evolving epidemic

E. Dale Abel, Anna L. Gloyn, Carmella Evans‐Molina, et al. · Cell

Research by E. Dale Abel et al., published in Cell. Not conducted by MedTech Research Group.

#7 Paywalled172 citations · 2024

Glucagon and GLP-1 receptor dual agonist survodutide for obesity: a randomised, double-blind, placebo-controlled, dose-finding phase 2 trial

Carel W. le Roux, Oren Steen, Kathryn Jean Lucas, et al. · The Lancet Diabetes & Endocrinology

Research by Carel W. le Roux et al., published in The Lancet Diabetes & Endocrinology. Not conducted by MedTech Research Group.

#8 Open Access163 citations · 2024

4. Comprehensive Medical Evaluation and Assessment of Comorbidities: Standards of Care in Diabetes—2025

Nuha A. ElSayed, Rozalina G. McCoy, Grazia Aleppo, et al. · Diabetes Care

Research by Nuha A. ElSayed et al., published in Diabetes Care. Not conducted by MedTech Research Group.

#9 Open Access156 citations · 2023

Incretins (GLP-1 receptor agonists and dual/triple agonists) and the liver

Philip N. Newsome, Phil Ambery · Journal of Hepatology

Research by Philip N. Newsome et al., published in Journal of Hepatology. Not conducted by MedTech Research Group.

#10 Open Access149 citations · 2025

Metabolic Dysfunction–Associated Steatotic Liver Disease (MASLD) in People With Diabetes: The Need for Screening and Early Intervention. A Consensus Report of the American Diabetes Association

Kenneth Cusi, Manal F. Abdelmalek, Caroline M. Apovian, et al. · Diabetes Care

Research by Kenneth Cusi et al., published in Diabetes Care. Not conducted by MedTech Research Group.