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Bioalmanac

Survodutide

BI 456906

Clinical trials

Status reviewed 18 Aug 2026

A GLP-1 and glucagon dual agonist in phase 3, and one of the more advanced candidates for fatty liver disease rather than weight alone.

Storage

Freeze-dried powder
Refrigerated at 2–8 °C, protected from light.
After mixing
Refrigerated at 2–8 °C. Do not freeze once mixed.
Long-term, frozen
Unopened powder is stable at −20 °C or colder.

Reconstitution — 10 mg vial, 6000 mcg dose

On a 1 mL U-100 syringe. Check every figure against your own vial before drawing.

Water addedConcentrationVolume to drawUnitsDoses per vial
1 mL10 mg/mL0.6 mL60 units1.7
2 mL5 mg/mLExceeds a 1 mL barrel
3 mL3.333 mg/mLExceeds a 1 mL barrel
5 mL2 mg/mLExceeds a 1 mL barrel

Dose ranges reported in sources

Descriptions of what sources report, not recommendations.

GoalRangeFrequencySource
Phase 2 escalation1200–6000 mcgOnce weekly, escalating over several monthsClinical trial

When to stop

  • Severe, persistent abdominal pain, particularly radiating to the back.
  • Vomiting severe enough that you cannot keep fluids down.
  • A resting heart rate persistently higher than usual, or palpitations.
  • Yellowing of the skin or eyes, or pain in the upper right abdomen.
  • Any allergic response: rash, hives, facial swelling or difficulty breathing. Seek urgent care.

Not approved in any jurisdiction. In phase 3 development for obesity and for metabolic dysfunction-associated steatohepatitis. Anything sold as survodutide today is a research chemical.

Arithmetic on values you enter. Not medical advice. Not reviewed by a clinician. · bioalmanac.com/peptides/survodutide

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