Glucagon enhanced insulin absorption in Diabetes Mellitus type 1
EU CTIS ID: 2022-502455-57-01
What this study is testing
To investigate if micro-doses of glucagon at the same site as subcutaneous insulin delivery enhances the absorption of insulin and reduces postprandial glucose excursions in patients with diabetes mellitus type 1
- Therapeutic exploratory (Phase II)
A plain-language read of the study's public EU CTIS listing. The study team confirms the details.
Who can take part
You may be able to join if
- 1. DM1 for at least 1 year.
- 2. Age 18 – 70 years
- 3. Last known HbA1c <86 mmol/mol (< 10.0%)
- 4. Treated with continuous SC insulin infusion (CSII) by an insulin pump or with multiple daily insulin injections (MDII).
You likely can't join if
- 1. Pregnant women or women trying to conceive (women will not be screened by a pregnancy test).
- 2. Any chronic disease, including psychiatric illnesses, judged incompatible with participation in the study.
- 3. Unfit for participation for any reason as judged by the investigators
- 4. Known hypersensitivity to glucagon or any of the excipients of the drug formulation
- 5. Known phaeochromocytoma
The study team makes the final eligibility decision.
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 18-64 years, 65+ years. The study team makes the final eligibility decision.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from EU CTIS; the study team decides eligibility.