Could blocking GLP-1 restore the Body's natural defense against low blood sugar?
NCT ID NCT07373236
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This completed study looked at why people with type 1 diabetes lose their natural defense against low blood sugar—the hormone glucagon. Researchers tested whether blocking a hormone called GLP-1 with a drug (exendin(9-39)amide) could restore glucagon release during low blood sugar. Twelve adults with type 1 diabetes took part, receiving either the blocker or a placebo. The goal was to see if this mechanism works in humans, which could lead to new treatments to reduce hypoglycemia risk.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- exendin(9-39)amide (a GLP-1 blocker)
- What this could lead to
- If successful, this could point toward a new add-on treatment to insulin therapy that lowers the risk of dangerously low blood sugar in type 1 diabetes.
- What could go wrong
- This is a very small, early-stage study (12 people) testing a mechanism, not a treatment. Results may not lead to a usable therapy, and the blocker itself may have side effects.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
-
12 people
The number who actually took part.
- Started
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Jan 2026
- Finished
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Apr 2026
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
18 to 70 years
- Sex
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Male participants only
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Caucasian ethnicity * Age between 18 and 70 years * T1D (diagnosed according to the criteria of the World Health Organization) with HbA1c \<69 mmol/mol (\<8.5%) * Body mass index between 19 and 30 kg/m2 * T1D duration of 2-30 years * C-peptide negative (5 gram arginine-stimulated C-peptide ≤100 pmol/l) * Treatment with a stable basal-bolus or insulin pump regimen for ≥3 months Exclusion Criteria: * Anaemia (haemoglobin below normal range) * Late microvascular complications except mild non-proliferative retinopathy * Liver disease (Evaluated by alanine aminotransferase (ALAT) and/or aspartate aminotransferase (ASAT) \>2 times normal values) or a history of hepatobiliary disorder * Kidney disease (serum creatinine above normal range) * Treatment with any glucose-lowering drugs beside insulin * Active or recent (within 5 years) malignant disease * Regular tobacco smoking or use of other nicotine-containing products * Any condition considered incompatible with participation by the investigators.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Gentofte Hospital
Hellerup, 2100, Denmark
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Other studies related to the condition(s) this trial covers.
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