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 been diagnosed (confirmed by a lab test of tissue or cells) with a specific type of high-grade ovarian, fallopian tube, or primary peritoneal cancer.
- Your cancer has stopped responding to platinum-based chemotherapy (a common cancer treatment), meaning it either kept growing during treatment or came back within about 6 months of your last platinum treatment — or you have progressed after a second course of platinum-based treatment.
- You have received no more than 2 additional treatment regimens beyond platinum-based chemotherapy (note: maintenance therapies like PARP inhibitors or bevacizumab do not count as separate regimens).
- You are 18 years of age or older at the time of signing the consent form.
- Your cancer can be measured on a scan (according to a standard medical measurement system called RECIST 1.1).
- You are willing and able to give written consent to participate.
- You are generally able to carry out daily activities with little or no limitation (confirm with trial site).
- Your liver, kidneys, blood, lungs, and blood-clotting functions are all working well enough (confirm with trial site).
Who may not be able to join:
- You have received chemotherapy, a biologic treatment, an experimental treatment, or radiation therapy within the last 3 weeks before starting the trial drug.
- You are currently taking any other cancer treatment or experimental drug.
- You have another serious or significant ongoing illness or medical condition (confirm with trial site).
- You currently have an active HIV infection.
- You currently have an active hepatitis B or hepatitis C infection.
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 Needle, MD, Cybrexa Therapeutics
Phone: 860-717-2731
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
Percentage of Subjects With Complete Response (CR) or Partial Response (PR) [Objective Response Rate (ORR)]
Can't join this trial?
Data last synced from ClinicalTrials.gov: 22 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.