
Safety data sheet
Standardized safety protocols and material specifications for professional use.
Certificate of Analysis
Purity verified via High-Performance Liquid Chromatography (HPLC) for #myo-survodutide-10mg
Survodutide (10mg)
Research Grade >99.2% Purity
Authorized Resellers
Available through our trusted partners
123peptide.com
Netherlands · Europe
local_shipping2-3 Business Days
Depeptidenwinkel.com
Netherlands · Europe
local_shipping2-3 Business Days
Scientific Background
Survodutide (BI 456906) is an investigational long-acting dual agonist of the GLP-1 receptor and glucagon receptor (GCGR) — a mechanistic combination that addresses two complementary aspects of energy balance simultaneously. While GLP-1 receptor agonism is well-established for appetite suppression, glycaemic control, and satiety enhancement, glucagon receptor co-activation provides the additional metabolic dimension of increased energy expenditure through hepatic gluconeogenesis suppression, thermogenesis, and hepatic fat mobilisation.
The dual GLP-1/GCGR mechanism is particularly compelling for non-alcoholic steatohepatitis (NASH) and metabolic liver disease research, where glucagon receptor activation drives preferential hepatic fat reduction and liver enzyme normalisation in addition to systemic weight reduction. Phase 2 clinical data demonstrates 12.5–14.9% body weight reduction at 46 weeks with survodutide, alongside significant liver fat content reduction.
Compared to GLP-1 monotherapy (semaglutide), survodutide's glucagon co-activation provides stronger liver-specific metabolic effects. Against tirzepatide (GLP-1 + GIP), survodutide replaces GIP with glucagon, producing different metabolic profiles particularly relevant in hepatic steatosis models. Against retatrutide (triple GLP-1/GIP/glucagon agonist), survodutide offers a potentially more balanced efficacy-tolerability profile.
Intended Research Use
- Dual GLP-1/GCGR pharmacology and receptor co-agonism studies
- Non-alcoholic steatohepatitis (NASH) and liver fat reduction research
- Body weight reduction through complementary appetite and thermogenesis mechanisms
- Comparative metabolic agonist research (vs. semaglutide, tirzepatide, retatrutide)
- Hepatic gluconeogenesis modulation and glycaemic control studies
- Energy expenditure and brown adipose thermogenesis research
menu_bookScientific Publications
Nature Medicine (2023)
Survodutide (BI 456906) for metabolic dysfunction-associated steatohepatitis — Phase 2 trial
open_in_newhttps://pubmed.ncbi.nlm.nih.gov/37488397/
Lancet Diabetes & Endocrinology (2023)
Survodutide in overweight and obesity: dose-dependent weight reduction and metabolic improvements
open_in_newhttps://pubmed.ncbi.nlm.nih.gov/37717591/
FOR RESEARCH USE ONLY. This product is intended for laboratory research purposes only and is not for human consumption, medical, or diagnostic use.
Possible stacks with other peptides
Synergistic combinations for enhanced research outcomes
Survodutide's unique GLP-1/glucagon dual mechanism positions it in specific metabolic research stacks focused on liver health and weight management.

Semaglutide 5mg (5mg vial)
arrow_forwardmyo-semaglutide-5mg
GLP-1 intensification comparison — semaglutide monotherapy research provides a direct comparator for survodutide's dual-agonist effects, helping quantify the glucagon receptor contribution to weight and liver endpoints.

Cagrilintide 5mg (5mg vial)
arrow_forwardmyo-cagrilintide-5mg
Amylin pathway addition — cagrilintide adds a third satiety mechanism (amylin receptor) to survodutide's GLP-1/glucagon framework for comprehensive multi-receptor appetite and metabolic research.

MOTS-C (10mg vial)
arrow_forwardmyo-mots-c-10mg
Mitochondrial support adjunct — MOTS-C's AMPK activation supports cellular energy efficiency during the caloric restriction achieved through survodutide-driven appetite suppression.

Mazdutide 5mg (5mg vial)
arrow_forwardmyo-mazdutide-5mg
Dual GLP-1/glucagon agonist with a similar metabolic mechanism — studied alongside Survodutide for comparative dual receptor activation and hepatic fat research.

Tirzepatide 10mg (10mg vial)
arrow_forwardmyo-tirzepatide-10mg
Dual GLP-1/GIP agonist for weight control — compared with Survodutide's GLP-1/glucagon profile in studies evaluating different dual agonist receptor combinations.
Cycling Note: Survodutide is used as continuous once-weekly maintenance — not cycled. Titrate to maximum tolerated dose and maintain for the full protocol duration (minimum 16 weeks for meaningful metabolic endpoints).