Phase 1 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:
- People who are generally well enough to carry out daily activities with little to no limitation (this is measured using a standard scale called ECOG, where a score of 0 or 1 is required)
- People who have been diagnosed with prostate cancer that has spread to other parts of the body, of a specific type (adenocarcinoma) that does not have small-cell or neuroendocrine features
- People who have previously been treated with a newer type of hormone therapy that targets the androgen receptor, such as abiraterone, enzalutamide, apalutamide, or darolutamide
- People who have previously been treated with a chemotherapy drug called a taxane, or who a doctor has determined are not suitable for taxane treatment, or who have chosen not to have taxane treatment
- People with a known BRCA1 or BRCA2 gene mutation who have previously been treated with a type of drug called a PARP inhibitor, or who a doctor has determined are not suitable for PARP inhibitor treatment (this applies where such treatment is approved and available)
Who may not be able to join:
- People who have received approved cancer treatment within the past 14 to 28 days before the trial starts (the exact timeframe depends on the specific drug used — confirm with trial site)
- People who have taken part in another clinical trial and received an experimental treatment within the past 28 days before the trial starts
- People who have previously been treated with a type of drug called an AR protein degrader
- People who have cancer that has spread to the brain or the lining around the brain or spinal cord that has not yet been treated
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
Principal Investigator: Clinical Trials, Genentech, Inc.
Phone: 888-662-6728 (U.S. Only)
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
4 site(s) in Australia. Confirm current status and contact details directly with the trial site.
Primary endpoints
Percentage of Participants with Adverse Events; Percentage of Participants Who Experience Dose-limiting Toxicities (DLTs)
Can't join this trial?
Data last synced from ClinicalTrials.gov: 23 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.