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Metabolic healthGlucagon analog

Dasiglucagon

Also known as: Zegalogue, ZP4207, ZP-GA-1

By the Peptide Dossier Editorial TeamUpdated How we source

Dasiglucagon is a glucagon analog formulated as a stable, ready-to-use liquid for severe hypoglycemia. Its June 2026 eligibility change uses a minimum weight rather than the original age cutoff.

Quick Facts

Class:Glucagon analog
Product status:Zegalogue is approved for severe hypoglycemia in people with diabetes weighing at least 20 kg.
Research context:FDA approved

A stable liquid rescue glucagon

Dasiglucagon, marketed as Zegalogue and developed as ZP4207/ZP-GA-1, modifies glucagon so it remains stable in aqueous solution. Traditional glucagon kits require powder/liquid mixing during an emergency; the analog can be supplied premixed as an autoinjector or prefilled syringe.

Rapid glucose release and recovery

It activates hepatic glucagon receptors to promote glycogenolysis and gluconeogenesis, releasing glucose into blood. The modifications primarily improve storage stability rather than changing the receptor’s fundamental action. In an adult type 1 diabetes Phase 3 study, median plasma-glucose recovery took 10 minutes versus 40 with placebo, with nearly all recovering by 15 minutes. A separate pediatric study supported use in children.

Supporting references: recovery.

Sources: [1]

From an age cutoff to a weight threshold

Dasiglucagon label evolution
DateFDA actionEligible population
2021Severe-hypoglycemia approval in diabetesOriginally ages 6 and older
June 2026Age cutoff replaced by weight boundaryAdults and children weighing at least 20 kg, about 44 pounds

Supporting references: Approved.

Sources: [2]

Caregiver rescue treatment

The ready-to-use medicine treats severe hypoglycemia in people with diabetes meeting the current weight requirement, often administered by a caregiver. As with glucagon, pheochromocytoma and insulinoma are contraindications.

Adverse effects and contraindication risks

Nausea/vomiting, headache, adult diarrhea and injection-site pain are common. Pheochromocytoma can lead to a pressure rise; insulinoma can lead to rebound low glucose. Serious allergy is also possible. Ready-to-use formulation does not remove these product-specific precautions.

References and further reading

This reference draws on Superpower’s Peptide Library and the research linked below. Peptide Dossier’s editorial team adapted and integrated the material on .

  1. 10.2337/dc20-2995Rapid glucose release and recoveryCited in: Rapid glucose release and recovery
  2. accessdata.fda.govFrom an age cutoff to a weight thresholdCited in: From an age cutoff to a weight threshold

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Disclaimer: This article is for informational and educational purposes only. It is not intended as medical advice. The information presented is based on published research and should not be used as a substitute for professional medical guidance. Always consult a qualified healthcare provider before starting any peptide protocol. Some peptides discussed may not be approved for human use by the FDA or equivalent regulatory bodies.