← Back to Clinical Trials
Recruiting Phase 4 NCT06908694

NCT06908694 Investigation of GLP1-Receptor Agonists in Men With Prostate Cancer Taking Androgen Deprivation Therapy

◆ AI Clinical Summary
Plain-language summary for patients
Clinical Trial Summary
NCT ID NCT06908694
Status Recruiting
Phase Phase 4
Sponsor Hamilton Health Sciences Corporation
Condition Prostate Cancer
Study Type INTERVENTIONAL
Enrollment 20 participants
Start Date 2025-07-02
Primary Completion 2026-07-31

Eligibility & Interventions

Sex Male only
Min Age 18 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
Semaglutide Pen Injector

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

Phase 4 studies follow an already-approved treatment in real-world conditions to monitor long-term safety and effectiveness.

This trial targets 20 participants in total. It began in 2025-07-02 with a primary completion date of 2026-07-31.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

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.

Eligibility Criteria

Inclusion Criteria: * Have a physician diagnosis of PC * Must be receiving or planned to receive ADT (gonadotropin releasing hormone agonist or antagonist ± androgen receptor pathway inhibitor) * Elevated BMI 1. ≥30kg/m2 or 2. ≥27kg/m2 in the presence of at least one of hypertension, type 2 diabetes, obstructive sleep apnea or dyslipidemia Exclusion Criteria: * Type 1 diabetes * Taking a GLP-1 RA * \<18 years of age * History of pancreatitis * Personal or family history of medullary cancer of the thyroid * Multiple endocrine neoplasia type 2

Contact & Investigator

Central Contact

Sarah Karampatos, BASc, MSc

✉ sarah.karampatos@phri.ca

📞 905-296-5795

Principal Investigator

Darryl Leong, MBBs,MPH,PhD,FRACP,FESC

PRINCIPAL INVESTIGATOR

Population Health Research Institute and McMaster University

Frequently Asked Questions

Who can join the NCT06908694 clinical trial?

This trial is open to male participants only, aged 18 Years or older, studying Prostate Cancer. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

What phase is the NCT06908694 trial and what does that mean for participants?

Phase 4 studies are conducted after a treatment has been approved. They monitor long-term safety and real-world effectiveness in a broader patient population.

Is NCT06908694 currently recruiting?

Yes, NCT06908694 is actively recruiting participants. Contact the research team at sarah.karampatos@phri.ca for enrollment information.

Where is the NCT06908694 trial being conducted?

This trial is being conducted at Hamilton, Canada.

Who is sponsoring the NCT06908694 clinical trial?

NCT06908694 is sponsored by Hamilton Health Sciences Corporation. The principal investigator is Darryl Leong, MBBs,MPH,PhD,FRACP,FESC at Population Health Research Institute and McMaster University. The trial plans to enroll 20 participants.

Related Trials

Related Intelligence Guides

In-depth guides covering this condition's trials, eligibility, and what to expect.

ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology