NCT03150810
Who may be able to join
Who might be able to join this trial:
- You are 18 years of age or older and have an advanced or spreading (metastatic) solid tumour cancer
- You are relatively active and able to carry out daily activities with little or no limitation (confirm with trial site for exact fitness level required)
- Your cancer can be detected and measured or evaluated through scans or tests, except for prostate cancer patients who may not need measurable disease
- You are willing to provide a stored sample of tumour tissue
- For certain specific groups joining the expansion phase: you have ovarian cancer with a specific genetic mutation (HRD+ or BRCA) and have had at least one platinum-based chemotherapy treatment, without your cancer returning within 6 months of that treatment
- For certain specific groups: you have triple-negative breast cancer with a specific genetic mutation (HRD+ or BRCA) and have had up to 3 prior treatments for advanced disease
- For certain specific groups: you have prostate cancer with a specific genetic mutation (HRD+ or BRCA), with either no prior chemotherapy or up to two prior taxane-based chemotherapy treatments, and your prostate cancer has been documented as getting worse
- For certain specific groups: you have small cell lung cancer or gastric (stomach) cancer and have had no more than 2 prior treatments
- For certain specific groups: you have another type of solid tumour with a specific genetic mutation (HRD+) (confirm with trial site)
Who may not be able to join:
- You have previously been treated with a type of drug called a PARP inhibitor
- Your cancer has stopped responding to platinum-based chemotherapy (applies to the expansion phase of the trial)
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.
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
Dose Escalation: Number of Participants With Dose Limiting Toxicities (DLTs); Number of Participants Experiencing Adverse Events (AEs); Objective Response Rate (ORR)
Can't join this trial?
Data last synced from ClinicalTrials.gov: 30 June 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.