Prostate Cancer Trial, Recruiting NCT07089550 Sponsor: IRCCS Azienda Ospedaliero-Universitaria di Bologna Condition: Prostate Cancer
Back to Prostate Cancer

Prostate Cancer Trial, Recruiting

NCT07089550
Recruiting Not Applicable

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 with advanced prostate cancer (a specific type that is not neuroendocrine carcinoma, which is a rarer form)
  • You are scheduled to have a PSMA PET scan to check how far your cancer has spread before starting treatment
  • You are being considered for one or more of the following treatments: abiraterone, enzalutamide, apalutamide, darolutamide, docetaxel, cabazitaxel, olaparib, radiotherapy, lutetium-177-PSMA, or actinium-225-PSMA
  • You are willing and able to sign a consent form agreeing to take part in the study and allow your data to be used

Who may not be able to join:

  • You are unable to lie flat and stay still for the length of time needed to complete the PET/CT scan
  • Your prostate cancer is known to have a significant neuroendocrine component (a specific rarer feature of some prostate cancers — confirm with trial site if unsure)
  • You currently have another active cancer, unless it is a common type of non-melanoma skin cancer

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.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 27 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Principal Investigator: Andrea Farolfi, IRCCS Azienda Ospedaliero-Universitaria di Bologna

Phone: +390512143959

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

Status
Recruiting
Phase
Not Applicable
Sponsor
IRCCS Azienda Ospedaliero-Universitaria di Bologna
Registry
ClinicalTrials.gov
Start date
2 April 2025
Est. completion
26 April 2034

Where this trial is recruiting

🇮🇹 Italy

Primary endpoints

number of PSMA-avid lesions (count); metabolic tumor volume (MTV in cm 3); maximum standardized uptake value (SUVmax, dimensionless); mean standardized uptake value (SUVmean, dimensionless)

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

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.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov