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Can a diabetes drug stop diabetes before it starts in transplant patients?
NCT ID NCT06913023
First seen Sep 16, 2026 · Last updated Sep 17, 2026 · Updated 1 time
Summary
Researchers are testing whether semaglutide, a drug used for diabetes and weight loss, can prevent post-transplant diabetes in kidney transplant recipients. The trial enrolls 37 adults who are 4 to 12 weeks past transplant and at risk for diabetes. Participants receive weekly semaglutide injections for 24 weeks, and researchers measure blood sugar after a glucose drink to see if the drug improves sugar handling. They also track side effects to assess safety.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- semaglutide, a GLP-1 receptor agonist drug given as a weekly injection
- What this could lead to
- If it works, semaglutide could become a way to prevent diabetes in kidney transplant recipients, a group at high risk for the condition.
- What could go wrong
- This is a small, early-phase trial of 37 people, so results may not hold in larger groups. Semaglutide can cause gastrointestinal side effects, and its safety in transplant patients on multiple medications is still being studied.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 2/3
Runs two stages together: whether the treatment works, then large-scale confirmation.
- Participants
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About 37 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Sep 2026
An estimate. Start dates often move.
- Expected to finish
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Dec 2029
An estimate. End dates often move.
- Lead sponsor
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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
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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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: 1. Signed and dated written informed consent. 2. Adult (≥18 years) recipients of a living or deceased donor kidney transplant 3. Between 4- and 12-weeks post kidney transplant 4. Stable kidney function defined as an eGFR \> 30 ml/min/1.73m2 (CKD-EPI) 5. At risk for PTDM at the time of transplant based on the following criteria: 1. BMI ≥ 25 kg/m2, or 2. Fasting plasma glucose 6.1-6.9 mmol/L (impaired fasting glucose), or 3. 2hr OGTT plasma glucose 7.8-11.0 (impaired glucose tolerance), or 4. HbA1C 5.5-6.4% (at risk for DM or prediabetes). Exclusion Criteria: 1. Established diagnosis of type 1 or type 2 DM as per Diabetes Canada (including the need for glucose-lowering therapy for hyperglycemia at the time of screening) 2. Kidney-Pancreas transplant recipient 3. Acute coronary syndrome, transient ischemic attack or stroke within 30 days prior to screening 4. History of pancreatitis 5. Personal or family history of medullary thyroid cancer or MEN2B 6. Women who are pregnant, nursing or plan on becoming pregnant whilst in the trial 7. Use of GLP1RA in the 30 days prior to screening 8. Contraindication to MRI (applicable only to those undergoing the optional MRI assessments) 9. With known or suspected hypersensitivity to semaglutide or related products 10. Patient not able to understand and comply with study requirements, based on Investigator's judgment. 11. Any other clinical condition that, based on Investigator's judgement, would jeopardize patient safety during trial participation or would affect the study outcom 12. History of glucose-galactose malabsorption syndrome
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
2 sites. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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St. Paul's Hospital
Vancouver, British Columbia, V6Z 1Y6, Canada
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Toronto General Hospital
Toronto, Ontario, M5G 2N2, Canada
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