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 been diagnosed (confirmed by lab testing of tissue) with high-grade serous ovarian cancer, primary peritoneal cancer, or fallopian tube cancer that has stopped responding to platinum-based chemotherapy.
- People who have been diagnosed (confirmed by lab testing of tissue) with a specific type of cancer called clear cell carcinoma, affecting the ovary, lining of the uterus (endometrium), vagina, vulva, or cervix.
- People whose cancer has come back or is still present, with evidence that it has grown or spread.
- People with platinum-resistant ovarian cancer who have received at least 1 but no more than 3 previous treatment courses for that cancer.
- People with clear cell cancer who have received at least 1 previous treatment course for that cancer.
- People with a known BRCA gene mutation (inherited or developed over time) where, if a PARP inhibitor drug was locally approved and available, that treatment was tried and either stopped working or was not tolerated.
- People who have at least one area of cancer that can be measured on a scan, according to standard measurement guidelines.
- People who have stored tumour tissue available from a previous biopsy or surgery, or who are willing to have a new biopsy taken.
- People who are in acceptable general health and have blood and organ test results within acceptable ranges.
- People who are able to become pregnant must agree to use highly effective contraception throughout the trial.
- People who are not currently pregnant, not planning to become pregnant, and not breastfeeding.
Who may not be able to join:
- People with a medical or mental health condition that would make it difficult to safely receive or follow the planned treatment and study procedures.
- People whose cancer never responded to their very first platinum-based chemotherapy, or whose cancer progressed within 3 months of finishing that first course of treatment.
- People who have previously been treated with certain immune-based therapies called checkpoint inhibitors (such as anti-PD-1, anti-PD-L1, or anti-CTLA-4 drugs) — though this restriction may not apply to people with clear cell endometrial or clear cell cervical cancer (confirm with trial site).
- People who currently have active cancer spread to the brain or the lining around the brain and spinal cord.
- People who have previously had a stem cell, tissue, or solid organ transplant.
- People who have had fluid drained from their abdomen within 4 weeks before starting the trial treatment.
- People who have had another cancer (blood cancer or solid tumour, stage 1 or higher) where surgery, radiation, or anti-cancer treatment was completed within the last 3 years — though people with certain low-risk skin cancers or very early-stage cancers that have been well controlled may still be considered eligible (confirm with trial site).
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: Pepi Pencheva, MacroGenics
Phone: 301-251-5172
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
Objective Response Rate (ORR) per Response Evaluation Criteria in Solid Tumors (RECIST) 1.1 criteria as determined by the investigator
Can't join this trial?
Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.