← Human Trials & Peer-Reviewed Studies
Investigation of GLP1-Receptor Agonists in Men With Prostate Cancer Taking Androgen Deprivation Therapy
Plain-language guide to NCT06908694: phase 4 interventional trial of Semaglutide, 20 participants. Who took part, design and what was measured.
Key Facts
- Registry ID
- NCT06908694
- Phase
- phase 4
- Status
- active, not recruiting
- Start
- 2025-07-02
- Completion (planned or actual)
- 2027-10-31
- Participants
- 20 (estimated)
- Design
- na, open label (everyone knows who gets what), treatment
- Conditions studied
- Prostate Cancer
- Results posted
- not yet
What This Study Did, in Plain Language
What Was Tested
The trial (phase 4) is built around Semaglutide.
GAIN PC CONTROL is a study investigating Glucagon-Like Peptide-1 Receptor Agonists in men with prostate cancer who are being treated with androgen deprivation therapy.
It had 1 arm (groups): Semaglutide (experimental).
The registry classes the interventions as drug.
More on the Plan
Patients who meet eligibility criteria and who provide informed consent will be enrolled to receive semaglutide.
Following enrollment, all participants will undergo a baseline visit, a 1-month telephone follow-up visit, 3-month visit, 6-month and a 12-month (Close-out) visit.
Who Took Part
Enrollment: 20 planned participants were the target.
It was open to men only 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: Have a physician diagnosis of PC. Must be receiving or planned to receive ADT (gonadotropin releasing hormone agonist or antagonist ± androgen receptor pathway inhibitor). ≥27kg/m2 in the presence of at least one of hypertension, type 2 diabetes, obstructive sleep apnea or dyslipidemia.
The full record lists 5 inclusion and 6 exclusion criteria; among the exclusions: type 1 diabetes; taking a glp-1 ra; \<18 years of age.
How the Study Was Run
Design: single-group and open-label.
Being open-label, the Semaglutide study did not mask who received what.
Everyone received the same intervention, so there was no separate comparison group inside the trial.
It started in 2025-07-02 with completion listed for 2027-10-31.
It ran at 1 site in Canada.
Its stated primary purpose is treatment.
What Was Measured
Primary outcome: Number of Serious Adverse Events (time frame: 12 months). Number of Adverse Events leading to Drug Discontinuation (time frame: 6 months). Measure of Weight (time frame: 12 months).
What This Means in Plain Language
Put simply, this is a phase 4 trial of Semaglutide in 20 people.
Its size is small, so on its own it can only give an early look.
Its status is active not 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.