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Survodutide
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Safety data sheet

Standardized safety protocols and material specifications for professional use.

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Certificate of Analysis

Purity verified via High-Performance Liquid Chromatography (HPLC) for #myo-survodutide-10mg

Official Product Data Sheet

Survodutide (10mg)

Research Grade >99.2% Purity

Vial Contents
10 mg Survodutide (BI 456906, lyophilized powder)
Includes
2 ml bacteriostatic water for reconstitution
Form
Freeze-dried white powder
Purity
≥99%, third-party confirmed (COA available)
Sequence
Long-acting GLP-1/glucagon dual agonist (proprietary structure)
Molecular Formula
C192H289N47O61
Molecular Mass
4232 g/mol
CAS No.
2805997-46-8
Solubility
Reconstitutes readily in bacteriostatic water to 5 mg/mL
Storage
Lyophilized frozen at −20 °C; reconstituted refrigerated at 2–8 °C for up to 4 weeks

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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
warning

FOR RESEARCH USE ONLY. This product is intended for laboratory research purposes only and is not for human consumption, medical, or diagnostic use.

Myotrope

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.

schedule

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).