NCT07284511RecruitingPhase 2/3
A Clinical Trial Using Tirzepatide to Help Adults With Type 1 Diabetes Automatically Control Their Blood Sugar
Fully Closed-Loop Glucose Control in Adults With Type 1 Diabetes Using Tirzepatide: a Randomized, Multi-center, Open-label, Non-inferiority, Parallel Trial
Source: ClinicalTrials.gov · Last updated 27 May 2026
Brief summary (registry, in English)
This research study is testing whether a weekly medication called tirzepatide can help adults with type 1 diabetes use their insulin pump more easily, specifically by reducing or eliminating the need to count carbohydrates at meals. People with type 1 diabetes must take insulin for life, and even with advanced insulin pumps and continuous glucose monitors, many still struggle to keep blood sugar within the target range. One of the biggest challenges is carbohydrate counting, which requires estimating the amount of carbohydrates in every meal to give the correct insulin dose. Tirzepatide is a medication currently approved for type 2 diabetes and weight management. Early research suggests it may also help people with type 1 diabetes by lowering appetite, slowing digestion, reducing insulin needs, and smoothing after-meal blood sugar rises. This study will include 105 adults with type 1 diabetes at centers in Canada and Switzerland. Everyone will use the Tandem Control-IQ insulin pump with a Dexcom G7 continuous glucose monitor. Participants are randomly assigned to one of two groups: Tirzepatide group: Participants receive weekly tirzepatide injections. After the dose is gradually increased over 12 weeks, they will eventually try using their insulin pump without entering carbohydrate amounts at meals. Control group: Participants continue their usual therapy and keep counting carbohydrates for their mealtime insulin doses. The main goal of the study is to learn whether people taking tirzepatide can safely maintain good blood sugar control without counting carbs, compared with standard care. All participants will attend several clinic visits and share their glucose, insulin, and health data throughout the 32-week trial. Some centers will also conduct heart/fitness, or body-composition tests. As with any medication, tirzepatide may cause side effects such as nausea, vomiting, diarrhea, or decreased appetite. Rare but serious risks like gallbladder disease or pancreatitis are also monitored. Pregnancy must be avoided during the trial. Overall, this study aims to understand whether adding tirzepatide to automated insulin delivery can simplify diabetes management, reduce burden, and maintain safe and effective glucose control for adults living with type 1 diabetes.
- Status (registry)
- Recruiting
- Phase (registry)
- Phase 2/3
- Study type
- Interventional
- Enrollment
- 105 (estimated)
- First submitted
- 19 Nov 2025
- Start date
- 19 May 2026
- Primary completion date
- Jan 2028
- Lead sponsor
- McGill University Health Centre/Research Institute of the McGill University Health Centre
- Diseases
- Obesity, Type 1 diabetes
- NCT number
- NCT07284511
What you commit to
- Study type: Interventional · Phase 2/3
- Planned participants: 105
- From 19 May 2026 to the primary completion date, Jan 2028
- 4 sites in 2 countries
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Other illness
- History of acute or chronic pancreatitis.
- Personal or family history of medullary thyroid cancer or multiple endocrine neoplasia type 2.
- History of bariatric surgery within the last 6 months.
- Medical or psychiatric illness likely to interfere with participation (e.g. cirrhosis, active cancer, decompensated schizophrenia), per investigator judgment.
- Inability or unwillingness to comply with safe diabetes management practices, in the view of the investigator.
Lab values
- Severe renal impairment with eGFR \<30 mL/min/1.73 m2 (CKD-EPI), measured within the last four months.
Other
- Use of GLP1-RAs within the last four weeks.
- Use of antihyperglycemic agents other than insulin or metformin within the last 2 weeks.
- Planned or ongoing pregnancy.
- Breastfeeding.
- Severe hypoglycemia requiring hospitalization in the past 2 months. Severe hypoglycemia is defined as requiring the assistance of another person, due to altered consciousness, to administer carbohydrates, glucagon, or other resuscitative actions.
- Diabetic ketoacidosis within the last 2 months.
- Clinically significant proliferative diabetic retinopathy or gastroparesis, as per the judgment of the investigator.
- Current or ≤ 1 month use of supraphysiological doses of oral or intravenous glucocorticoids.
- Any safety concern that, in the investigator's judgment, precludes participation.
Who the study is looking for
- Age ≥ 18 years.
- Clinical diagnosis of type 1 diabetes for ≥ 1 year, per investigator judgment (confirmatory C-peptide and autoantibodies not required).
- A BMI ≥ 27 kg/m2.
- HbA1c \> 6.5%, and \< 12%.
- Current therapy: multiple daily injections or insulin pump.
- Willingness to use Tandem Control IQ insulin pump system with the use of rapid or ultra rapid-acting insulins compatible with Tandem Control-IQ pump (e.g. Fiasp is not compatible)
- Active carbohydrate counting for prandial insulin dosing.
- Individuals of childbearing potential must be using or agree to use an effective birth-control method. Childbearing potential refers to participants of the female sex post-menarche who have not reached menopause and who do not have a medical condition causing sterility (e.g., hysterectomy). Post-menopausal state refers to the absence of menses for 12 months without any alternative cause.
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (4)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| McGill University Health Centre Coordinator of this site? Confirm its status | Montreal | Canada | Not yet recruiting |
| Institut de Recherches Cliniques de Montreal Coordinator of this site? Confirm its status | Montreal | Canada | Not yet recruiting |
| Hygea Medical Clinic Coordinator of this site? Confirm its status | Montreal | Canada | Recruiting |
| Insel Hospital, University Hospital Bern Coordinator of this site? Confirm its status | Bern | Switzerland | Not yet recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.