GLP-1/glucagon receptor dual agonist

Survodutide

GLP-1 · Glucagon

Survodutide (BI 456906) combines GLP-1 and glucagon receptor agonism and is being studied for obesity and liver disease. The balance between weight reduction, liver effects and gastrointestinal tolerability is central to phase 3 development.

2Overview
1× / wkReference frequency
DataPhase 2 and reported phase 3
Research status

Phase 3 development

Velora Survodutide vial
SURVODUTIDE10 MG
01 · Overview

What is Survodutide?

Survodutide (BI 456906) combines GLP-1 and glucagon receptor agonism and is being studied for obesity and liver disease. The balance between weight reduction, liver effects and gastrointestinal tolerability is central to phase 3 development.

Research route, formulation and population determine what a result actually means.

01

GLP-1

GLP-1 signalling affects satiety, gastric emptying and glucose-dependent insulin response.

02

Glucagon

Glucagon-receptor signalling affects liver metabolism and energy expenditure.

02 · Research

What do the studies show?

Phase 2 and reported phase 3. Educational information. Not diagnosis, treatment or use advice.

18.7%
Phase 2

Obesity trial at week 46

In phase 2, the highest planned dose achieved large mean weight reduction; discontinuations and gastrointestinal adverse effects were relevant.

Phase 3
Phase 3

Larger confirmatory trials

Recent phase 3 publications confirm efficacy in obesity while also examining liver fat and metabolic complications.

03 · DATA

Peptide and product specifications

Checked identity data for this research compound or blend.

SurvodutidePeptide and product specifications
Development code
BI 456906
Developer
Boehringer Ingelheim / Zealand Pharma
Molecular formula
C₁₉₂H₂₈₉N₄₇O₆₁
Molecular weight
4231.69 Da
CAS number
2805997-46-8
Amino-acid sequence / components
His-1-aminocyclobutanecarboxyl-Gln-Gly-Thr-Phe-Thr-Ser-Asp-Tyr-Ser-Lys-Tyr-Leu-Asp-Glu-Arg-Ala-Ala-Lys-Asp-Phe-Ile-Lys(side-chain)-Trp-Leu-Glu-Ser-Ala-NH₂
Amino-acid count
29 in de hoofdketen + een 7-residu linker/zijtak
Modified residues
C18 diacid/γ-glutamate-Gly-Ser-Gly-Ser-Gly-Gly side chain at Lys²⁴; C-terminal alaninamide
Purity
Batch-specific — confirm identity and purity with the Velora COA
Reference diluent
Formulation- and batch-specific; there is no universal diluent for every research compound
Unreconstituted-material storage
Follow the accompanying COA, product label and validated stability data

These are compound references, not a batch certificate. Purity and identity of a specific Velora batch must be confirmed by its accompanying COA and laboratory report.

Official USAN identity document ↗
04 · Calculator

Reconstitution and U-100 conversion

This module only converts concentration and volume. Inputs are not recommendations or individual dosing advice.

Calculator

Once weekly in clinical trials

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Survodutide vial
SURVODUTIDE
10 MG
Concentration
Per unit
Complete amounts
Calculated duration
LAB · RECONSTITUTION

How to reconstitute Survodutide for laboratory research

A visual workflow for controlled laboratory reconstitution. Always follow the product label, COA and a validated protocol.

Five visual laboratory reconstitution steps: clean, measure diluent, add slowly, swirl gently and store according to protocol.
1

Clean

Disinfect the rubber closures of both vials and allow them to dry.

2

Measure diluent

Withdraw only the diluent validated for the specific compound.

3

Add slowly

Let the liquid run slowly down the inside wall of the vial.

4

Swirl gently

Do not shake; rotate gently until the material has dissolved.

5

Store per protocol

Follow the product label, COA and validated stability data.

Important checks before and after reconstitution

Check the product

First confirm that the product is a lyophilised vial. Prefilled pens and ready-to-use solutions do not require reconstitution. Check the label, COA and specified diluent.

Use clean, sterile technique

Wash your hands, clean the work surface and use new sterile equipment for every procedure. Clean both rubber closures with separate alcohol swabs and let them dry completely.

Concentration, not total amount

The volume of liquid added changes the concentration in mg per mL, but not the total amount of research compound in the vial. Use the calculator to check this in advance.

Inspect and label

Check for unexpected discoloration, cloudiness or visible particles. Record the compound, concentration and reconstitution date. Storage time and temperature are product-specific; a fixed 28-day rule does not apply to every compound.

General reconstitution volumes listed by the source

General examples, not a product-specific protocol. The chosen volume determines concentration; always check the label, COA and calculator.

Vial strengthCommonly listed volume
2 mg1–2 mL
5 mg2–3 mL
6 mg2–3 mL
10 mg2–4 mL
15 mg3–5 mL
20 mg4–8 mL

Practical background source: Free Medical Journals — Complete Step-by-Step Guide to Peptide Reconstitution, accessed July 2026. This is a secondary educational source; the product label, COA and validated stability data remain authoritative.

05 · Safety and limitations

Safety and limitations

Research route, formulation and population determine what a result actually means.

What is known

  • Visible research claims use primary or official sources.
  • The calculator is arithmetic and does not turn a study amount into medical advice.
  • A registered medicine and a research vial are not automatically equivalent.

What remains uncertain

  • Many products lack long-term safety data and independent replication.
  • Animal and cell findings do not predict a safe human dose.
  • Stability depends on formulation, pH, sterility, light, temperature and packaging.
Status: Phase 3 development. Educational information. Not diagnosis, treatment or use advice.
06 · FAQ

Frequently asked questions

Survodutide (BI 456906) combines GLP-1 and glucagon receptor agonism and is being studied for obesity and liver disease. The balance between weight reduction, liver effects and gastrointestinal tolerability is central to phase 3 development.
In phase 2, the highest planned dose achieved large mean weight reduction; discontinuations and gastrointestinal adverse effects were relevant. Recent phase 3 publications confirm efficacy in obesity while also examining liver fat and metabolic complications.
No. It performs arithmetic conversions only. Medical decisions belong with a licensed healthcare professional.
The curve follows the agreed storage model and is not a laboratory result.
2–8 °C. Protect from light and repeated freeze-thaw cycles.
07 · Sources

Primary research sources

Educational information. Not diagnosis, treatment or use advice.

Survodutide for obesity: randomised dose-finding phase 2 trial Lancet Diabetes & Endocrinology, 2024. Link
Survodutide once weekly for adults with obesity New England Journal of Medicine, 2026. Link