Phase 2 Ovarian Cancer Trial, Recruiting NCT06888921 Sponsor: Compugen Ltd Condition: Ovarian Cancer
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Phase 2 Ovarian Cancer Trial, Recruiting

NCT06888921
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:

  • People who have ovarian cancer, fallopian tube cancer, or primary peritoneal cancer that has come back and is still responding to platinum-based chemotherapy.
  • People who have completed at least 2 previous rounds of treatment that included a platinum-based chemotherapy drug.
  • People whose most recent chemotherapy course included at least 4 cycles of a platinum-based drug, and whose cancer showed a partial or complete response to that treatment.
  • People who have previously received maintenance therapy with bevacizumab or a PARP inhibitor (if they were eligible for it), or for whom a doctor has determined they are not a candidate for these therapies, or who have declined these therapies in writing.
  • People who have recovered from the side effects of their previous cancer treatments — generally to a mild level or better, except for hair loss, or nerve-related side effects which may be at a slightly higher level (confirm with trial site).

Who may not be able to join:

  • People who have had 4 or more separate rounds of chemotherapy drugs that directly kill cancer cells.
  • People who are currently taking high doses of steroids or other immune-suppressing medications within 2 weeks before the trial treatment would start.
  • People who have previously been treated with certain types of immune checkpoint therapy (including PD-1, PD-L1, anti-PVRIG, or TIGIT inhibitors, or similar drugs).
  • People who have cancer that has spread to the liver, confirmed by scan or biopsy, at the start or end of their most recent platinum-based chemotherapy.
  • People who needed fluid drained from the abdomen during the last 2 cycles of their most recent chemotherapy, or at any time after finishing that chemotherapy.
  • People who experienced a bowel blockage in the 6 weeks before entering the trial.
  • People who have active cancer spread to the brain or the lining of the brain or spinal cord.
  • People who have active hepatitis B, hepatitis C, or HIV infection.
  • People who have an active bacterial, fungal, or viral infection that is not under control or requires ongoing treatment with antibiotics, antifungals, or antiviral medications.
  • People who have received a live virus vaccine within 30 days before the planned start of trial treatment, or who would need one during the trial.
  • People who have had a severe allergic or hypersensitivity reaction to a monoclonal antibody medication, or who are allergic to any ingredient in the trial drugs.
  • People who have another serious or unstable medical condition happening at the same time.
  • People who have any other condition that, in the treating doctor's judgement, would make participation unsafe or affect the trial's results.
  • People who are currently in, or have recently been in, another clinical trial and received an experimental treatment or used an experimental device within 4 weeks before the first dose of this trial's treatment.
  • People who are pregnant, breastfeeding, or planning to become pregnant during the trial period.

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 12 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.

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Trial details

Status
Recruiting
Phase
Phase 2
Sponsor
Compugen Ltd
Registry
ClinicalTrials.gov
Start date
21 July 2025
Est. completion
1 March 2027

Where this trial is recruiting

🇫🇷 France 🇮🇱 Israel 🇺🇸 United States

Primary endpoints

To evaluate the effect of COM701 as a single agent on progression free survival when administered as a maintenance regimen in participants with relapsed PSOC

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: 12 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