Investigational (Phase 3)GLP-1 Weight Loss

Survodutide

Also known as: BI 456906

A dual GLP-1 and glucagon receptor agonist developed by Boehringer Ingelheim. It has shown strong results for both weight loss and fatty liver disease (MASH), and received FDA Breakthrough Therapy designation for MASH. Phase 3 results expected in 2026.

How it works

Survodutide activates both GLP-1 and glucagon receptors. The GLP-1 action reduces appetite and improves blood sugar control. The glucagon action increases energy expenditure and promotes fat burning in the liver, which is why it shows particular promise for fatty liver disease.

Common uses

Side effects

Key research

Safety notes

  • Not yet FDA-approved. Phase 3 trials ongoing with approval likely no earlier than 2027
  • Phase 2 had a 24.6% discontinuation rate due to GI side effects, mostly from rapid dose escalation
  • Phase 3 trials use slower, more gradual dose titration to reduce GI issues
  • FDA granted Breakthrough Therapy designation for MASH in adults

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