Phase 2 Ovarian 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 ovarian, fallopian tube, or peritoneal cancer that has come back or not gone away, and this was found within 6 months of finishing your most recent chemotherapy that contained platinum.
- Your cancer is one of these specific types: serous, endometrioid, mucinous, undifferentiated, clear cell, mixed epithelial, transitional cell, malignant Brenner's tumor, or adenocarcinoma (confirm with trial site if unsure of your type).
- You have had one prior chemotherapy treatment for your original diagnosis that included a platinum-based drug (such as carboplatin or cisplatin).
- You have had no more than two chemotherapy treatments in total for cancer that came back or did not go away.
- You may have had one additional non-chemotherapy treatment (such as hormones, monoclonal antibodies, or targeted therapy) for recurring or persistent disease.
- If you are able to become pregnant, you must have a negative pregnancy test before joining and must be using an effective form of contraception.
- Your bone marrow, kidneys, liver, and nervous system are all functioning well enough (as measured by blood tests — confirm with trial site).
- You have recovered from any recent surgery, radiation, or chemotherapy, with only mild or no lasting side effects.
- You do not currently have an active infection requiring antibiotics (a simple urinary tract infection is generally acceptable).
- Any hormone therapy aimed at your cancer must have been stopped at least one week before joining.
Who may not be able to join:
- Your cancer did not respond to platinum-based chemotherapy at all (known as platinum-refractory disease).
- You have been diagnosed with another cancer within the past 5 years (except for certain treated skin cancers).
- You are currently receiving chemotherapy or radiation therapy, or you have received any cancer-directed treatment — including biological or immune therapies — within the last three weeks.
- You have previously been treated with a type of drug called a kinase inhibitor (confirm with trial site if unsure).
- You have a history of certain serious gut problems, including fistula, significant bleeding, perforation, or peptic ulcer disease.
- You are currently pregnant or breastfeeding.
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: Michael McHale, University of California, San Diego
Phone: (858) 822-6275
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
Primary endpoints
To assess the safety and tolerability of VS-6063 plus paclitaxel and carboplatin chemotherapy (Measured Via Adverse Events); Objective response rate (ORR)
Can't join this trial?
Data last synced from ClinicalTrials.gov: 7 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.