RecruitingPhase 2NCT06594926

Working Out M0 Bipolar Androgen Therapy

Evaluating the Efficacy of Bipolar Androgen Therapy in Extending Metastasis-free Survival in Patients With M0 Castrate-resistant Prostate Cancer With PSA Progression But Not Radiological or Clinical Progression on Darolutamide


Sponsor

Australian and New Zealand Urogenital and Prostate Cancer Trials Group

Enrollment

69 participants

Start Date

Aug 14, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

The WOMBAT study will test if BAT can prolong the time it takes for nmCRPC prostate cancer to become detectable in other areas of the body (metastatic disease). Approximately 69 participants over the age of 18 with castrate resistant prostate cancer, no evidence of metastatic disease (M0) on conventional imaging (WBBS and CT scan at screening) and PSA only progression on darolutamide will be enrolled from approximately 8 sites within Australia. Participants will receive continuous androgen deprivation therapy with LHRH agonists/antagonists. The study intervention will be IM testosterone enthanate, injected on day 1 of each 56-day cycle. Concurrent darolutamide will be taken at a dose of 600mg BD on days 29-56 of each cycle. Both LHRH and agonist/antagonist and darolutamide are supplied through the PBS as standard of care medications. Administration of both testosterone and darolutamide will continue until disease progression, beyond disease progression, unacceptable toxicity, death, withdrawal of consent or study Sponsor termination of the study. Primary objective (endpoint) is to determine the metastasis-free survival (time from commencing BAT to evidence of metastases or death)


Eligibility

Sex: MALEMin Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study (WOMBAT) is testing bipolar androgen therapy — a treatment that alternates between very high and very low testosterone levels — in men with non-metastatic castration-resistant prostate cancer (cancer that is progressing despite hormone suppression, but hasn't visibly spread). **You may be eligible if...** - You have prostate cancer confirmed by biopsy - Your cancer is progressing (rising PSA on three separate occasions) despite castrate-level testosterone, while on darolutamide (a hormone-blocking drug) - No visible spread to other organs on standard scans (M0 status) - Your PSA is above 1.0 ng/mL - You are 18 or older with good general health (ECOG 0-1) - Your blood counts, liver, and kidney function are within acceptable ranges **You may NOT be eligible if...** - Your cancer has spread to other organs on standard imaging at any time in your disease history (except small pelvic lymph nodes) - You have neuroendocrine or small cell prostate cancer - Your life expectancy is less than 3 months - You have had previous testosterone therapy or certain other treatments Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGTestosterone Enanthate

Testosterone enanthate is a depot formulation used in Australia typically for androgen replacement in people with confirmed testosterone deficiency.


Locations(12)

The Canberra Hospital

Garran, Australian Capital Territory, Australia

The Border Cancer Hospital

Albury, New South Wales, Australia

St Vincents Hospital

Darlinghurst, New South Wales, Australia

GenesisCare North Shore

St Leonards, New South Wales, Australia

Sydney Adventist Hospital

Wahroonga, New South Wales, Australia

ICON Cancer Centre

Chermside, Queensland, Australia

Mater Misericordiae Ltd - QLD

South Brisbane, Queensland, Australia

Royal Adelaide Hospital

Adelaide, South Australia, Australia

Grampians Health

Ballarat, Victoria, Australia

Eastern Health - Box Hill

Box Hill, Victoria, Australia

Cabrini Health

Malvern, Victoria, Australia

Northeast Health Wangaratta

Wangaratta, Victoria, Australia

View Full Details on ClinicalTrials.gov

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NCT06594926


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