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Recruiting Phase 2

A Phase II Trial of Bicalutamide in Patients Receiving Intravesical BCG for Non-muscle Invasive Bladder Cancer

NCT05327647 · tracked via the Priya Life Science Canada tracker
Phase
Phase 2
Started
2022-06-23
Last updated
2026-10-26

Condition(s) studied

Non-Muscle Invasive Bladder Cancer

Investigational drug(s) / intervention(s)

Bicalutamide →Control Arm

Bicalutamide: Induction intravesical BCG with bicalutamide 150 mg for 90 days

Control Arm: Induction BCG

Study summary

This is a phase II randomized controlled clinical trial comparing standard induction BCG versus bicalutamide and standard induction BCG among patients with non-muscle invasive bladder cancer.

Eligibility

Sex
MALE
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: 1. Males, age 18 or greater. 2. Patients with histologically confirmed non-muscle invasive urothelial carcinoma. 3. Patients have been recommended for a course of intravesical BCG induction treatment by their urologist 4. Patients who received gemcitabine, epirubicin or mitomycin C instillations immediately post-operatively will be eligible for enrollment. 5. Patients with partners of child-bearing potential must agree to 2 acceptable forms of birth control and be continued for at least 3 months after study drug is discontinued. Exclusion Criteria: 1. Patients who have received induction BCG therapy within the last 5 years will be ineligible for enrolment. 2. Patients with a history of myocardial infarction or hospital admission for heart failure within the previous 12 months or who have unstable cardiovascular status will be ineligible for enrolment. 3. Patients who have uncontrolled hypertension (for our purposes, defined as those having a systolic blood pressure \> 160 documented on 2 occasions despite appropriate medical therapy) will similarly be ineligible. 4. Patients with a history of liver disease whose hepatic enzymes, alkaline phosphatase or bilirubin are greater than twice the upper limit of normal will be ineligible. 5. Patients with clinical hypogonadism, those on androgen replacement therapy, or those with prostate cancer or other diseases treated with systemic hormonal therapy will be ineligible for study enrolment. Patients receiving 5ARIs will not be excluded. 6. Patients who have cancer treatment ongoing or planned in the near future which can be anticipated to decrease their 2-year survival or BCa treatment plan will be ineligible. 7. Patients taking an investigational drug within 2 weeks of enrolment into this study will be ineligible. 8. Patients receiving or planning to receive coumadin therapy will be ineligible.

Primary outcome measure(s)

  • Rate of bladder tumour recurrence — 3 years
    To time to bladder tumor recurrence compared to the standard of care induction BCG

Trial sites (7)

FacilityCityRegionStatus
London Health Sciences Centre London Ontario Recruiting
University Health Network, Princess Margaret Cancer Centre Toronto Ontario Recruiting
Centre intégré de santé et services sociaux de Chaudière Appalaches Lévis Quebec Recruiting
Centre Hospitalier de l'Université De Montréal_CHUM Montreal Quebec Recruiting
McGill University Health Centre_CUSM Montreal Quebec Recruiting
CHU de Québec-Université Laval Québec Quebec Recruiting
CIUSSS de l'Estrie - CHUS Sherbrooke Quebec Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05327647 on ClinicalTrials.gov ↗ ← All trials in Canada