Survodutide
Also known as: BI 456906
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Survodutide from $272/kit
2 verified vendors, ≥99% purity, COAs included.
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
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.
Dosing Information
Typical Dosingⓘ
Community experience
Limited community data available
See research dosing
See research protocols
Research Dosingⓘ
Scientific studies
Doses from clinical trials
Doses from Studies
Titrated up to 4.8mg weekly
Various dose levels studied
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
- https://pubmed.ncbi.nlm.nih.gov/38330987/
- https://pubmed.ncbi.nlm.nih.gov/37330144/
- https://clinicaltrials.gov/ct2/show/NCT05486871
Research This Peptide Further
Buy in shop
Survodutide from $272/kit
2 verified vendors, ≥99% purity, COAs included.
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.
Retatrutide
Clinical TrialsA triple agonist targeting GLP-1, GIP, and glucagon receptors. Phase 3 trials show up to 28.7% weight loss (71 lbs average), the highest of any obesity drug. Expected FDA approval late 2026 to early 2027.
Weight LossCagrilintide
Clinical TrialsA long-acting amylin analog developed by Novo Nordisk for obesity treatment. Works through a different mechanism than GLP-1 agonists, targeting amylin receptors in the brain to reduce appetite and slow gastric emptying. Shows enhanced weight loss when combined with semaglutide (CagriSema).
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Clinical TrialsA 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.
Weight LossSemaglutide
FDAA 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.
Weight LossTirzepatide
FDAA dual GIP/GLP-1 receptor agonist representing the next generation of incretin-based therapies. Shows superior weight loss compared to semaglutide in head-to-head trials. First medication approved for obstructive sleep apnea.
Weight LossOrforglipron
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