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RECRUITING
NCT07373236
NA

The Effect of Endogenous GLP-1 on Glucagon Secretion in Type 1 Diabetes

Sponsor: Asger Lund, MD

View on ClinicalTrials.gov

Summary

Type 1 diabetes is a serious and burdensome disease that carries the risk of severe complications and premature death, partly due to low blood sugar, also called hypoglycaemia. This is a constant threat, as individuals with type 1 diabetes lack the body's natural safeguard against low blood sugar: the hormone glucagon, which is normally released from the pancreas. Recent research in mice suggests that this missing safeguard may be due to an imbalance in the hormones released from different cells in the pancreas. More specifically, glucagon-like peptide-1 (GLP-1) appears to play a role in the lack of glucagon secretion. By blocking this hormone using the substance exendin(9-39)NH₂, normalization of glucagon release during low blood sugar has been observed in mice with type 1 diabetes. The present study aims to investigate whether the same mechanism applies in humans with type 1 diabetes. If confirmed, this finding could form the basis for a novel adjunct treatment to insulin therapy and thereby potentially reduce the risk of hypoglycaemia in this patient group.

Official title: Examining the Effect of Endogenous Glucagon-like Peptide-1 on Glucagon Secretion in Type 1 Diabetes

Key Details

Gender

MALE

Age Range

18 Years - 70 Years

Study Type

INTERVENTIONAL

Enrollment

12

Start Date

2026-01-23

Completion Date

2026-03-31

Last Updated

2026-01-28

Healthy Volunteers

No

Conditions

Interventions

DRUG

exendin(9-39)amide

GLP-1 antagonist

DRUG

Saline (0.9% NaCl)

Placebo

Locations (1)

Gentofte Hospital

Hellerup, Denmark