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Survodutide

Also known as: BI 456906, GLP-1/glucagon dual agonist

limited human dataNot FDA approvedResearch only
Mechanism of Action

Survodutide is a catalog-expanded glp1 entry in ProtoComp's source-backed compound corpus. It is included for search, calculator math, stack awareness, and future research curation based on expand compound catalog, explicit_target_list, local_seed, project_target. Published dosing, cycle length, and clinical-use claims are intentionally left null until compound-specific evidence is reviewed.

Recorded Dose Range
Low0.6 mg/week
Typical2.4-3.6 mg/week
High6 mg/week

Phase 2 obesity trial used dose-escalation up to 6 mg/week over 46 weeks. Phase 3 program ongoing for obesity and MASH.

Recorded Cycle Range

No cycle range recorded.

Administration
Routessubcutaneous
FrequencyOnce weekly
Preferred timingSame day each week
Recorded Cautions

Contraindications

  • Personal or family history of medullary thyroid carcinoma (class label)

Common side effects

  • Nausea
  • Vomiting
  • Diarrhea
  • Decreased appetite
  • Headache

Serious risks

  • Pancreatitis risk (class effect)
  • Glucagon-mediated transient hyperglycemia in non-diabetic users (mechanism-related)

Drug interactions

  • Insulin
  • Sulfonylureas

Requires monitoring

  • Blood glucose
  • Heart rate

Pregnancy / breastfeeding

Avoid — limited human data

Common Misconceptions
  • Glucagon agonism increases energy expenditure but can transiently raise blood glucose — distinct mechanism vs pure GLP-1 agonists
  • Not yet approved — investigational only
Next Steps

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ProtoComp provides reference information and summarizes your logged data. It is not medical advice. Confirm protocol changes with your clinician.