Weight LossIn Clinical TrialsClinical Trials

Survodutide

Also known as BI 456906

A dual GLP-1/glucagon receptor agonist being developed for obesity and metabolic dysfunction-associated fatty liver disease (MASH). Phase 2 showed 83% MASH resolution vs 18% placebo.

Phase 3 Clinical Trials - FDA Breakthrough Therapy Designation for MASH

Regulatory Pathway

Preclinical
Phase I
Phase II
Phase III
Phase IV
Approved

Dosing Protocol

Typical Dose

Research protocols only

Frequency

Weekly injection

Duration

Long-term use expected

Community-reported dosing. Individual results vary. Not a medical recommendation.
Typical community protocol: Research protocols only via Subcutaneous injection weekly, Weekly injection. Dose range: Variable (Phase 3 ongoing). Duration: Long-term use expected.

Timing & Administration

Administer via Subcutaneous injection weekly. Frequency: Weekly injection.

Mechanism of Action

Activates both GLP-1 receptors (appetite suppression, glucose control) and glucagon receptors (increased energy expenditure, reduced liver fat). Glucagon component provides additional metabolic benefits beyond standard GLP-1 agonists.

Research Summary

Evidence level: clinical trials. Clinical status: Phase 3 Clinical Trials - FDA Breakthrough Therapy Designation for MASH.

Side Effects & Safety

Important Warnings

  • Phase 3 obesity trials expected completion early 2026
Nausea (55-75%)
vomiting (41%)
diarrhea (49%)
constipation
GI effects during dose escalation

References

No references available.