Weight Loss

Survodutide

Also known as: BI 456906

Clinical Trials
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Key Facts: Survodutide

Category
Weight Loss
FDA Status
Not FDA Approved
Clinical Status
Phase 3 Clinical Trials - FDA Breakthrough Therapy Designation for MASH
Administration
Subcutaneous injection weekly
Typical Dose
Limited community data available
Frequency
See research protocols
Duration
Long-term use expected
Also Known As
BI 456906

Mechanism of Action

Survodutide activates both GLP-1 receptors (appetite suppression, glucose control) and glucagon receptors (increased energy expenditure, reduced liver fat). The glucagon component adds metabolic benefits beyond pure GLP-1 agonists.

Research Summary

Phase 2 showed 83% of patients had MASH resolution vs 18% placebo. Phase 3 SYNCHRONIZE trials for obesity expected to complete early 2026. LIVERAGE trials for MASH enrolling 3,000+ participants.

Trial Progress:Phase III
Pre
I
II
III
IV
FDA

Dosing Information

Human Trials·Human studies conducted, not FDA approved

Typical Dosing

Community experience

Common Dose

Limited community data available

Range

See research dosing

Frequency

See research protocols

Research Dosing

Scientific studies

Doses from clinical trials

Doses from Studies

Duration

Long-term use expected

Administration

Subcutaneous injection weekly

Timing & Administration

Best Time to Take

Before bed or morning (fasted)

Follow specific peptide protocol

Food Recommendation

Take on empty stomach

Why This Timing?

GH-related peptides work best on an empty stomach to maximize growth hormone release.

Possible Side Effects

Not everyone experiences these effects. Individual responses vary based on dosage, duration, and personal factors.

  • Nausea (55-75%)
  • Vomiting (41%)
  • Diarrhea (49%)
  • Constipation
  • GI effects during dose escalation
  • Currently in Phase 3 trials

References

Research This Peptide Further

Buy in shop

Survodutide from $272/kit

2 verified vendors, ≥99% purity, COAs included.

Compare prices

Frequently Asked Questions

What does Survodutide do?

A dual GLP-1/glucagon receptor agonist in development for obesity and MASH. Has FDA Breakthrough Therapy Designation for MASH with fibrosis.

How does Survodutide work?

Survodutide activates both GLP-1 receptors (appetite suppression, glucose control) and glucagon receptors (increased energy expenditure, reduced liver fat). The glucagon component adds metabolic benefits beyond pure GLP-1 agonists.

Is Survodutide FDA approved?

No, Survodutide is not currently FDA approved. Current status: Phase 3 Clinical Trials - FDA Breakthrough Therapy Designation for MASH

What are the side effects of Survodutide?

Reported side effects include: Nausea (55-75%), Vomiting (41%), Diarrhea (49%), Constipation, GI effects during dose escalation. Individual responses vary based on dosage, duration, and personal health factors.

What is the typical dose of Survodutide?

Community-reported common dose: Limited community data available (See research protocols). Range: See research dosing. Administration: Subcutaneous injection weekly. Community-reported doses. Not medical advice. Consult healthcare provider.

Related Peptides

Peptides commonly compared with Survodutide or used in similar applications.

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Cagrilintide

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Eloralintide

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A next-generation oral GLP-1 receptor agonist developed by Structure Therapeutics (now Ventyx Biosciences). Shows comparable weight loss to injectable GLP-1s with potentially fewer gastrointestinal side effects and a longer half-life, allowing flexible dosing.

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Semaglutide

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A GLP-1 receptor agonist with multiple FDA approvals including weight loss, T2D, CV risk reduction, and kidney protection. Wegovy pill approved Dec 2025 as first oral GLP-1 for weight loss.

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Tirzepatide

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Orforglipron

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