Phase 2 Ovarian Cancer Trial, Recruiting NCT03287271 Sponsor: Michael McHale Condition: Ovarian Cancer
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Phase 2 Ovarian Cancer Trial, Recruiting

NCT03287271
Recruiting Phase 2

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.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 7 July 2026
Phase 2: approximately ~30% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

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

Status
Recruiting
Phase
Phase 2
Sponsor
Michael McHale
Registry
ClinicalTrials.gov
Start date
6 February 2018
Est. completion
1 April 2025

Where this trial is recruiting

🇺🇸 United States

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?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

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.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov