metabolic research / GLP-1
Investigational
Survodutide
Also known as: BI 456906, BI456906, dual GLP-1/glucagon agonist
Dual glucagon and GLP-1 receptor agonist combining appetite suppression with increased energy expenditure. Shows promise for NASH/MASH.
Research overview
Survodutide, also known as BI 456906 or BI456906, is a dual agonist peptide that represents an innovative approach to metabolic research. This compound is classified as a dual agonist, specifically targeting both glucagon and GLP-1 receptors simultaneously.
The mechanism of action involves dual receptor activation that produces complementary metabolic effects in research models. Glucagon receptor activation promotes lipolysis and thermogenesis, whilst GLP-1 receptor activation enhances insulin secretion and satiety responses. This dual pathway approach creates a synergistic effect that researchers are investigating for its potential in metabolic studies.
Primary research effects observed in laboratory studies include appetite suppression, increased energy expenditure, improved insulin sensitivity, weight reduction, and reduction in liver fat content. These effects make Survodutide particularly valuable for researchers studying metabolic pathways, energy homeostasis, and hepatic metabolism.
The evidence grade is classified as B, indicating that whilst there are clinical trials demonstrating effectiveness in reducing body weight and liver fat content in research models with obesity and NASH, long-term safety and efficacy data remain limited. More extensive trials are needed to fully characterise the compound's research profile.
Survodutide's dual agonist classification distinguishes it from single-target compounds, offering researchers a unique tool for investigating the complex interplay between glucagon and GLP-1 pathways in metabolic regulation.
Mechanism of action
Survodutide works by activating both glucagon and GLP-1 receptors. This dual activation leads to reduced appetite and increased energy expenditure. The glucagon receptor activation promotes lipolysis and thermogenesis, while GLP-1 receptor activation enhances insulin secretion and satiety.
