Pipeline (Phase 3)

Survodutide (survodutide (BI 456906))

Dual agonist showing strong weight loss + liver benefits in NASH trials.

Avg weight loss
~19%
Cost
Not
Dosing
Once weekly
FDA Status
Pipeline

Survodutide (BI 456906) is a dual GLP-1 / glucagon receptor agonist developed by Boehringer Ingelheim and Zealand Pharma. Phase 2 trials showed ~19% weight loss over 46 weeks; Phase 3 trials in obesity and MASH/NASH are ongoing.

Overview

Survodutide is currently in Phase 3 development for obesity, type 2 diabetes, and MASH (metabolic dysfunction-associated steatohepatitis). Unlike tirzepatide (GLP-1 + GIP), survodutide combines GLP-1 with glucagon agonism — different from retatrutide because no GIP component.

How Survodutide Works

GLP-1 reduces appetite and slows gastric emptying. Glucagon receptor agonism increases energy expenditure and may directly target liver fat — making survodutide particularly promising for MASH/NASH.

Dosing & Schedule

Phase 2 weekly doses 0.6-4.8 mg. Phase 3 doses still being finalized.

Effectiveness — Trial Data

Phase 2: 19% weight loss at top dose. MASH trial showed strong reduction in liver fat.

Side Effects

Similar GI profile to other GLP-1s. Glucagon agonism could theoretically raise blood sugar, monitored in trials.

Cost — How Much Survodutide Costs in 2026

Not yet on market. Expected approval 2026-2027.

Who Is Survodutide For?

Investigational. Once approved, likely indicated for obesity, type 2 diabetes, and MASH/NASH.

Survodutide Alternatives

Available now: tirzepatide, semaglutide.

Frequently Asked Questions

Is survodutide a GLP-1?
Yes — survodutide is a dual GLP-1 / glucagon receptor agonist.
When will survodutide be approved?
Expected 2026-2027 depending on Phase 3 trial timelines.

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