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PC-030 · GLP-1 · survodutide

Survodutide

BI 456906

Also: Dual GLP-1/GCGR

human trial

A dual GLP-1 and glucagon receptor agonist developed by Boehringer Ingelheim. Survodutide represents a different approach to metabolic disease by combining GLP-1 effects with glucagon's ability to increase energy expenditure and reduce liver fat. Showing strong results in NASH/MASH clinical trials.

Dual agonism of GLP-1 receptor (appetite suppression, glucose control) and glucagon receptor (energy expenditure increase, hepatic fat reduction, amino acid metabolism). The glucagon component specifically targets liver fat, making it promising for NASH/MASH.

  • NASH/MASH treatment
  • Weight loss
  • Type 2 diabetes
  • Liver fat reduction
  • · Nausea
  • · Diarrhea
  • · Vomiting
  • · Decreased appetite
  • · Constipation

Mechanism of Action

Dual agonism of GLP-1 receptor (appetite suppression, glucose control) and glucagon receptor (energy expenditure increase, hepatic fat reduction, amino acid metabolism). The glucagon component specifically targets liver fat, making it promising for NASH/MASH.

Common Uses

NASH/MASH treatmentWeight lossType 2 diabetesLiver fat reduction

Dosage & Pharmacology

DOSAGE RANGE: 0.6-4.8 mg weekly (subcutaneous) — clinical trial doses
HALF-LIFE: ~5 days
Dosage information is for research reference only. Not a recommendation.

Known Side Effects

  • Nausea
  • Diarrhea
  • Vomiting
  • Decreased appetite
  • Constipation

Legal Status

US:Not yet FDA-approved (Phase 3 trials — Boehringer Ingelheim)
UK:Not approved
EU:Not approved
AU:Not approved
View all Survodutide research on PubMed