Survodutide

Weight Management & Metabolic Research
Dual GLP-1 / Glucagon Metabolic Research Peptide
GLP-1R · Glucagon Receptor · Metabolic Signaling
10mg

$119.99

Out of stock

For research purposes only.
Emma Lindsay research guide in a white lab coat with a steel blue blouse

Emma Lindsay

RESEARCH GUIDE

I’ve pulled together the key product details, research context, and supporting information so you can quickly decide whether this item lines up with your research goals.

Overview

Survodutide is a research peptide studied for weight management, appetite regulation, blood sugar control, liver fat, and overall metabolic health. In plain English, it is designed to affect two important metabolic signaling systems at the same time, which may help explain why researchers are interested in its effects on body weight, energy balance, and liver-related metabolic changes. Human studies have already shown meaningful reductions in body weight and promising changes in liver fat, making Survodutide an important compound in current metabolic research.

Scientifically, Survodutide is an investigational dual agonist of the GLP-1 receptor and glucagon receptor. GLP-1 receptor activation is associated with appetite suppression, delayed gastric emptying, and improved glucose-dependent insulin signaling, while glucagon receptor activity influences hepatic metabolism and may contribute to increased energy expenditure. Phase 2 human studies have reported substantial body-weight reductions and encouraging outcomes in MASH and liver-fat research, while larger Phase 3 clinical programs are continuing to evaluate its long-term metabolic effects.

The Science Behind Survodutide
Explore how Survodutide combines GLP-1 and glucagon receptor signaling in metabolic and liver research.

Survodutide, previously known as BI 456906, is a long-acting peptide designed to activate both the glucagon-like peptide-1 receptor and the glucagon receptor. This combination is scientifically interesting because the two receptors influence different but complementary aspects of metabolism. GLP-1 receptor activation is associated with reduced appetite, delayed gastric emptying, and improved glucose-dependent insulin signaling, while glucagon receptor activity influences hepatic energy metabolism and may contribute to increased energy expenditure.

The molecule was deliberately designed with greater relative activity at the GLP-1 receptor than at the glucagon receptor. The aim is to preserve the appetite and glycemic effects associated with GLP-1 signaling while adding glucagon-mediated effects on liver metabolism and energy balance. This distinguishes Survodutide from single GLP-1 agonists and from dual GIP/GLP-1 compounds such as Tirzepatide.

In a Phase 2 obesity trial, Survodutide produced clinically meaningful body-weight reductions across multiple dose groups compared with placebo. Separate Phase 2 research in biopsy-confirmed MASH also showed significant improvements in MASH without worsening of fibrosis, along with substantial reductions in liver fat. These findings have led to larger Phase 3 programs in both obesity and liver disease.

Is Survodutide Right for Your Research Goals?
Discover where Survodutide fits within body-weight, metabolic, liver-fat, and dual-receptor research.

Survodutide may be relevant to research focused on obesity biology, appetite regulation, energy expenditure, glucose metabolism, liver fat, MASH, and glucagon/GLP-1 receptor interactions. It is particularly useful when the research question involves whether adding glucagon receptor activity to GLP-1 signaling can produce metabolic effects beyond those seen with GLP-1 receptor agonism alone.

The liver is an especially important area of Survodutide research. In a 48-week Phase 2 trial involving 293 participants with biopsy-confirmed MASH and fibrosis, improvement in MASH without worsening of fibrosis occurred in 47% to 62% of participants across the Survodutide dose groups, compared with 14% receiving placebo. A reduction in liver fat of at least 30% occurred in 57% to 67% of treated participants, compared with 14% of the placebo group.

Research Use, Reconstitution & Storage
General research-context information on Survodutide preparation, handling, concentration, and storage.

Published Survodutide clinical trials have used structured, escalating study protocols designed for controlled clinical research. In the Phase 2 MASH trial, investigators studied once-weekly doses of 2.4 mg, 4.8 mg, and 6.0 mg after a dose-escalation period. These trial protocols were designed for supervised clinical investigation and should not be interpreted as personal-use recommendations.

For laboratory preparation, lyophilized Survodutide should be reconstituted according to the specific research protocol being followed. Avoid vigorous shaking; gentle swirling is preferable. Researchers should use validated concentration calculations and appropriate sterile laboratory technique.

Store refrigerated and protect from light, heat, contamination, and repeated temperature changes. Once reconstituted, maintain appropriate refrigerated conditions and minimize repeated freeze-thaw cycles where possible.

Use the SilverLeaf Reconstitution Calculator for concentration and volume calculations where appropriate. This information is provided for laboratory and research reference only.

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