GLP-1
GLP-1 signalling affects satiety, gastric emptying and glucose-dependent insulin response.
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.
Phase 3 development

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.
GLP-1 signalling affects satiety, gastric emptying and glucose-dependent insulin response.
Glucagon-receptor signalling affects liver metabolism and energy expenditure.
Phase 2 and reported phase 3. Educational information. Not diagnosis, treatment or use advice.
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.
Checked identity data for this research compound or blend.
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 ↗This module only converts concentration and volume. Inputs are not recommendations or individual dosing advice.
Once weekly in clinical trials

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

Disinfect the rubber closures of both vials and allow them to dry.
Withdraw only the diluent validated for the specific compound.
Let the liquid run slowly down the inside wall of the vial.
Do not shake; rotate gently until the material has dissolved.
Follow the product label, COA and validated stability data.
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.
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.
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.
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 examples, not a product-specific protocol. The chosen volume determines concentration; always check the label, COA and calculator.
| Vial strength | Commonly listed volume |
|---|---|
| 2 mg | 1–2 mL |
| 5 mg | 2–3 mL |
| 6 mg | 2–3 mL |
| 10 mg | 2–4 mL |
| 15 mg | 3–5 mL |
| 20 mg | 4–8 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.
Research route, formulation and population determine what a result actually means.