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:
- People who have given written consent to participate before any trial procedures begin
- People who have been confirmed through a tissue sample (biopsy) to have prostate adenocarcinoma (a specific type of prostate cancer), without small cell features
- People whose cancer stage, based on standard medical staging systems, falls within an early, localised range (no spread to lymph nodes or other parts of the body)
- People whose MRI scan confirms the cancer is at an early stage (T1, T2a, T2b, or T2c under AJCC staging)
- People whose biopsy Gleason score is 3+3 or 3+4 (also called Grade Group 1 or 2 — these are lower-risk categories)
- People whose PSA level is 15 ng/ml or below
- People with a general health performance status rated 0 or 1 on the WHO scale (meaning generally active and able to carry out daily activities)
- People whose urinary symptom score (International Prostate Symptom Score) is 10 or below (use of alpha blocker medications is permitted)
- People whose prostate gland, as measured by MRI, has a volume of 70 cc or less
- People who agree not to father a child during the trial treatment period and for 6 months after treatment ends
Who may not be able to join:
- People whose cancer has reached a more advanced local stage (T3a, T3b, or T4) based on clinical assessment or MRI
- People whose MRI shows significant tumour in the transitional zone (a specific inner region of the prostate) (confirm with trial site)
- People whose imaging shows cancer has spread to lymph nodes or other parts of the body
- People whose biopsy Gleason score is 4+3 or higher
- People currently using hormone therapy (androgen deprivation therapy) or other medications known to affect PSA levels
- People for whom it is not possible to have Calypso tracking beacons implanted (small devices used for precise radiation targeting during treatment)
- People with a history of blood cancer or another solid tumour cancer, unless they have been in remission for at least 3 years — with an exception for certain treated non-melanoma skin cancers
- People who have had radiotherapy to the pelvis in the past
- People who have previously had surgery for prostate cancer
- People who have had a transurethral resection of the prostate (TURP) procedure within the 12 weeks before joining the trial
- People who have a hip prosthesis (artificial hip replacement)
- People with serious or active other health conditions that may make the planned radiation treatment inadvisable
- People with significant medical, psychiatric, psychological, family, or geographical circumstances that, in the opinion of the trial investigator, could interfere with treatment, follow-up, or safety
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: Thomas Zilli, MD, University Hospital, Geneva
Phone: +41 79 55 32 563
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 performance; Progression free survival (PFS)
Can't join this trial?
Data last synced from ClinicalTrials.gov: 8 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.