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Dasiglucagon

Dasiglucagon is a glucagon-receptor agonist developed as ZEGALOGUE for severe hypoglycemia. Historical approval and current US marketing status need to be distinguished.

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At a glance

Evidence stage
Approved use
Regulatory status
ZEGALOGUE was US-approved for severe hypoglycemia in diabetes from age 6; FDA application 214231 currently lists its products as discontinued.
Research context
Dasiglucagon is a glucagon-receptor agonist developed as ZEGALOGUE for severe hypoglycemia. Historical approval and current US marketing status need to be distinguished.

What this is

  • Dasiglucagon is a glucagon-receptor agonist developed as ZEGALOGUE for severe hypoglycemia. Historical approval and current US marketing status need to be distinguished.

What this isn't

  • A recommendation to use, prepare, combine, or administer a product
  • Evidence that a related molecule or a differently formulated product has the same effects

Key terms

Dasiglucagon is a glucagon-receptor agonist developed as ZEGALOGUE for severe hypoglycemia. Historical approval and current US marketing status need to be distinguished.

Dasiglucagon activates glucagon receptors in the liver, stimulating breakdown of stored glycogen and release of glucose into blood. It therefore depends on adequate liver glycogen reserves. It is a rescue medicine for low blood glucose, not a weight-management peptide or a replacement for insulin in diabetes. Product label.

Evidence limits

How to read the evidence

The FDA marketing record currently marks ZEGALOGUE presentations discontinued; this does not by itself establish a safety-related withdrawal. FDA application record. Its approval history should not be presented as proof of present supply, and investigational uses are separate from the rescue indication. Product-specific scope.

Sources appraised 2026-10-28. Educational information; not medical advice. Study findings apply to the populations, preparations and outcomes described.

External sources and citations

  1. Dasiglucagon — product label (DailyMed)
  2. Dasiglucagon phase 3 randomized trial
  3. FDA application NDA214231 — approval and marketing records

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