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Semaglutide for the Prevention Of Post-Transplant Diabetes Mellitus
Plain-language guide to NCT06913023: phase 2, phase 3 interventional trial of Semaglutide, 37 participants. Who took part, design and what was measured.
Key Facts
- Registry ID
- NCT06913023
- Phase
- phase 2, phase 3
- Status
- not yet recruiting
- Start
- 2026-09-05
- Completion (planned or actual)
- 2029-06-30
- Participants
- 37 (estimated)
- Design
- na, open label (everyone knows who gets what), treatment
- Conditions studied
- Kidney Transplant Recipient
- Results posted
- not yet
What This Study Did, in Plain Language
What Was Tested
In this phase 2, phase 3 trial, researchers set out to test Semaglutide.
It had 1 arm (groups): Semaglutide (experimental).
The registry classes the interventions as drug.
More on the Plan
A kidney transplant is the best treatment for people living with kidney failure as it allows people to live longer with a better quality of life.
However, one in four kidney transplant recipients will develop diabetes after transplant.
Kidney transplant recipients who get diabetes after transplant are up to three times more likely to have heart disease and die prematurely.
Semaglutide is a drug that is commonly used to treat diabetes and obesity.
Who Took Part
Enrollment: 37 planned participants were the target.
It was open to people of any sex aged from 18 years with no upper age limit.
Healthy volunteers were not accepted; participants needed the condition being studied.
Examples of who could join: Signed and dated written informed consent. Adult (≥18 years) recipients of a living or deceased donor kidney transplant. Between 4- and 12-weeks post kidney transplant. At risk for PTDM at the time of transplant based on the following criteria:. BMI ≥ 25 kg/m2, or.
The full record lists 9 inclusion and 12 exclusion criteria; among the exclusions: kidney-pancreas transplant recipient; acute coronary syndrome, transient ischemic attack or stroke within 30 days prior to screening; history of pancreatitis.
How the Study Was Run
It was run as a single-group and open-label study.
Everyone knew when Semaglutide was being given (open label), which is simpler to run but leaves more room for expectations to affect what is reported.
Everyone received the same intervention, so there was no separate comparison group inside the trial.
It started in 2026-09-05 with completion listed for 2029-06-30.
It ran at 2 sites in Canada (2).
Its stated primary purpose is treatment.
What Was Measured
Primary outcome: 2-hour OGTT (time frame: 24 weeks).
It also tracked 19 secondary outcomes, for example Incidence of Treatment-Emergent Adverse Events [Safety and Tolerability], Estimated GFR, Change in fasting blood glucose, GFR, Change in serum insulin and Change in HbA1c.
What This Means in Plain Language
Put simply, this is a phase 2, phase 3 trial of Semaglutide in 37 people.
Its size is small, so on its own it can only give an early look.
Its status is not yet recruiting; no results are posted to the registry yet, so nothing here describes outcomes.
More context: the Semaglutide compound page, all human trials.
Our Notes on the Compound
Semaglutide: The active ingredient in several prescription GLP-1 receptor agonist medicines (Ozempic, Wegovy, oral tablets).
Related Pages
Source: ClinicalTrials.gov record. This explanation is written by PeptideWhiz from the public record. For research and education only. Not medical advice; no dosing information is given.