Phase 2 Prostate Cancer Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- You have been diagnosed with prostate cancer that has been confirmed by a tissue sample as a specific type called adenocarcinoma (not rare types like small cell, neuroendocrine, or others)
- Doctors expect you to live for at least 3 months or more
- You are generally able to carry out daily activities with little or no restriction (as measured by a standard health scoring system called ECOG, rated 0 or 1)
- Your cancer can be measured or tracked using standard imaging methods
- You have already been treated with at least one hormone-blocking drug for prostate cancer, such as enzalutamide, darolutamide, apalutamide, or abiraterone acetate
- You have one or more cancer deposits (metastases) in the body that cannot be surgically removed
- You have had your testicles surgically removed and/or are on ongoing hormone-suppressing therapy, and your testosterone level is very low (below a specific threshold)
- Your prostate cancer has continued to grow or spread despite your most recent treatment
- Your kidneys, liver, and blood counts are functioning well enough to safely participate
- If you are sexually active with a partner who could become pregnant, you must use a condom (plus spermicide if available), avoid fathering a child, and not freeze or donate sperm during the trial; your partner is also recommended to use an additional contraceptive method
Additional requirements if joining Sub-study 1:
- You have only received one hormone-blocking drug (ARPI) so far
- A special type of scan (PSMA PET/CT scan) shows your cancer responds to a specific marker, with no areas that do not show up on this scan
- You are able to swallow and take tablets or capsules by yourself
Who may not be able to join:
- Your prostate cancer is a rare type other than adenocarcinoma (such as small cell, spindle cell, signet cell, neuroendocrine, or sarcomatous)
- You have a known blockage in your urinary tract that has not been treated
- Your cancer has spread to the brain
- You have cancer pressing on or threatening your spinal cord
- Your cancer has spread to the lining around the brain and spinal cord
- You have had, or currently have, a completely separate type of cancer in a different part of your body
- You have serious ongoing medical conditions at the same time (confirm with trial site)
- You have a history of scarring or inflammation of the lungs (not caused by infection)
- You have a history of, or signs suggesting, certain blood or bone marrow disorders (confirm with trial site)
- You still have significant side effects from a previous cancer treatment that have not resolved
- You are unable to swallow tablets or capsules, or have a digestive condition that would stop medication being absorbed properly
- You have an active infection, including tuberculosis, hepatitis B, or hepatitis C
- You have a known allergy or sensitivity to the study drug or any of its ingredients
Additional reasons you may not be able to join Sub-study 1:
- You have a history of seizures that are not well controlled, or you need more than two epilepsy medications
- You have had a severe brain injury or stroke in the past
- A bone scan shows a very widespread pattern of bone spread (called a "superscan")
- You have previously been treated with the specific drug AZD9574, or you have received more than one course of a type of drug called a PARP inhibitor
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Phone: 1-877-240-9479
Australian sites
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
1 site(s) in Australia. Confirm current status and contact details directly with the trial site.
Primary endpoints
Part A: Number of participants with treatment-emergent adverse events (TEAEs)including serious adverse events (SAEs), treatment-related AEs (TRAEs) and adverse events of special interests (AESIs); Part A: Number of participants with dose limiting toxicities (DLTs); Part B: Number of participants with TEAEs; Part B: Prostate Specific Antigen 50 (PSA50) response rate
Can't join this trial?
Data last synced from ClinicalTrials.gov: 27 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.