Phase 2 Prostate 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:
- The person must be male and aged 21 years or older.
- The person must be able to understand and sign a consent form, and be willing to follow the study's requirements.
- The person must have a confirmed diagnosis of prostate cancer that falls into one of these categories: high-risk prostate cancer (based on specific pathology scores, a PSA level of 20 or higher, or a certain tumour stage), or a specific type of intermediate-risk prostate cancer with certain unfavourable features (confirm with trial site for exact details).
- The person must agree to use an acceptable form of birth control and wear condoms for seven days after each PSMA injection, if sexually active.
- There must be no sign that the cancer has spread to other parts of the body, including nearby lymph nodes.
Who may not be able to join:
- People with clinical or technical factors that could interfere with the accuracy of the PET or MRI scans used in the study.
- People who have medical reasons that prevent them from safely receiving the PSMA injection used in the study.
- People who have medical reasons that prevent them from safely receiving a type of targeted radiation therapy to the prostate — this includes people who have previously had a certain prostate surgery (transurethral resection), have a prostate larger than 150cc, have a urinary symptom score above 20, or have had prior radiation to the prostate.
- People who, in the opinion of the research team, are considered unsuitable for the trial for any other reason.
- People who are currently taking, or planning to take, a medication called abiraterone.
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: Silvia Formenti, M.D., Weill Medical College of Cornell University
Phone: 646-962-3110
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
Clinical efficacy of prostate-specific membrane antigen (PSMA) Positron Emission Tomography (PET)/Magnetic Resonance(MR), MR-Linear Accelerator (LINAC) will be assessed by evaluating recurrence free survival
Can't join this trial?
Data last synced from ClinicalTrials.gov: 27 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.