RecruitingPhase 4NCT06908694

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

GLP1-Receptor Agonists in Men With Prostate Cancer: Control of Cardiovascular Risk Factors and Prostate Biomarkers


Sponsor

Hamilton Health Sciences Corporation

Enrollment

20 participants

Start Date

Jul 2, 2025

Study Type

INTERVENTIONAL

Conditions

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

Sex: MALEMin Age: 18 Years

Inclusion Criteria5

  • 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
  • ≥30kg/m2 or
  • ≥27kg/m2 in the presence of at least one of hypertension, type 2 diabetes, obstructive sleep apnea or dyslipidemia

Exclusion Criteria6

  • 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

Interventions

DRUGSemaglutide Pen Injector

The semaglutide dose will be 0.25mg subcutaneously once weekly for weeks 1-4, then 0.5mg once weekly for weeks 5-8, then 1mg once weekly for weeks 9-12, then 1.7mg once weekly for weeks 13-16, and then 2.4mg for the remainder of the trial. Semaglutide dose may be decreased in the case of adverse events to the highest tolerated dose.


Locations(1)

Juravinski Cancer Centre

Hamilton, Ontario, Canada

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NCT06908694


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