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Dasiglucagon

Also known as: Zegalogue, ZP4207

Stable glucagon analog in a ready-to-use injection, FDA-approved in 2021 as Zegalogue for severe hypoglycemia in diabetes. Prescription medication.

Last updated

Mechanism of Action

Dasiglucagon is a glucagon analog with seven amino acid substitutions that make it stable and soluble in an aqueous solution, so it does not need to be mixed before injection or form fibrils like native glucagon. It activates the glucagon receptor on liver cells, triggering glycogen breakdown and glucose release into the blood. This raises blood glucose within minutes during severe hypoglycemia.

Half-life
~30 minutes
Administration Routes
Subcutaneous
Research Status
Clinical

Reported Benefits

  • Rapid treatment of severe hypoglycemia in adults and children with diabetes
  • Ready-to-use autoinjector or prefilled syringe with no reconstitution
  • Studied for preventing hypoglycemia in congenital hyperinsulinism

Potential Side Effects

  • Nausea and vomiting
  • Headache
  • Injection-site pain
  • Hypertensive crisis risk in pheochromocytoma (warning)

Common Dosing

Labeled use is a single 0.6 mg subcutaneous rescue dose for severe hypoglycemia, which a caregiver can give; a second dose may be given if there is no response, and emergency help should be sought. Prescribing and training are supervised by the prescribing clinician.

The dosing information above is aggregated from research literature and anecdotal community reports for educational purposes only. It is not a recommendation, prescription, or medical advice. Peptides are sold as research chemicals only and are not intended for human use.

Contraindications

  • Pheochromocytoma
  • Insulinoma

No documented stacking partners for Dasiglucagon yet.

  • Dasiglucagon-A Next-Generation Glucagon Analog for Rapid and Effective Treatment of Severe Hypoglycemia: Results of Phase 3 Randomized Double-Blind Clinical Trial

    2021

    View
  • Dasiglucagon, a next-generation ready-to-use glucagon analog, for treatment of severe hypoglycemia in children and adolescents with type 1 diabetes: Results of a phase 3, randomized controlled trial

    2021

    View
  • Dasiglucagon for the Treatment of Congenital Hyperinsulinism: A Randomized Phase 3 Trial in Infants and Children

    2024

    View

Yes, as Zegalogue in March 2021 for severe hypoglycemia in adults and children with diabetes. An application for congenital hyperinsulinism received complete response letters in 2023 and 2024 over a third-party manufacturing site, and approval for that use is not confirmed as of 2026.

Native glucagon is unstable in solution and traditionally had to be mixed from powder in an emergency. Dasiglucagon's modified sequence keeps it stable as a liquid, so it comes ready to inject.

PeptideChat is for educational and research purposes only. Nothing on this site constitutes medical advice. Peptides are sold as research chemicals only and are not intended for human use. These statements have not been evaluated by the FDA and are not intended to diagnose, treat, cure, or prevent any disease. PeptideChat is an independent educational resource — not a pharmacy, compounding, or 503A/503B outsourcing facility — and does not sell products or provide medical advice.