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:
- 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.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
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?
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.