Phase 1 Prostate Cancer Trial, Recruiting NCT07621692 Sponsor: National Taiwan University Hospital Condition: Prostate Cancer
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Phase 1 Prostate Cancer Trial, Recruiting

NCT07621692
Recruiting Phase 1

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 aged 20 years or older who are able to understand and agree to the study requirements, including blood tests and scans
  • People who have been diagnosed with prostate cancer (a specific type called adenocarcinoma) that has spread to other parts of the body and is no longer responding to hormone-lowering treatments (known as metastatic castration-resistant prostate cancer)
  • People who have had their testicles surgically removed, or who are receiving ongoing hormone-suppressing injections or implants, with testosterone levels confirmed to be very low (below 50 ng/dL)
  • People who have previously received at least one course of taxane-based chemotherapy and at least one hormone-blocking medication (such as abiraterone, enzalutamide, apalutamide, or darolutamide), unless a doctor determined these were not medically suitable
  • People who have previously received a type of targeted radiation treatment called lutetium-177 PSMA therapy, unless a doctor determined it was not suitable or the person declined it
  • People whose cancer is confirmed to be getting worse, shown by rising PSA blood test results on at least two separate occasions at least one week apart, or by new or growing areas of cancer seen on scans
  • People whose cancer shows strong uptake on a specialised PSMA PET/CT scan (a type of imaging that detects a protein on prostate cancer cells) performed within the past 12 weeks
  • People with a life expectancy of at least 6 months and who are reasonably able to carry out daily activities (as assessed by a standard medical scale)
  • People with blood counts and organ function results within acceptable ranges, including healthy enough levels of red blood cells, white blood cells, platelets, kidney function, and liver function
  • People who are willing to use appropriate barrier contraception during the study if sexually active

Who may not be able to join:

  • People who have had a previous allergic reaction to PSMA-targeted treatments or to radioactive metal compounds used in similar therapies
  • People who have received radioligand therapy (either radium-223 or lutetium-177 PSMA) within the past 6 months
  • People who have had surgery or radiation treatment within the past 4 weeks
  • People who have received any systemic prostate cancer treatment within the past 4 weeks, including hormone-blocking drugs, chemotherapy, or PARP inhibitor medications
  • People whose cancer scans show a pattern where the cancer is active on one type of scan (FDG PET) but shows very little uptake on the PSMA scan, suggesting the cancer may not respond well to PSMA-targeted treatment (confirm with trial site)
  • People with a blockage in the urinary tract causing kidney swelling (hydronephrosis) that has not already been treated
  • People with brain metastases or cancer affecting the lining around the brain or spinal cord that are causing symptoms, or with spinal cord compression, unless these have already been appropriately treated
  • People who have another active cancer that currently requires systemic treatment
  • People with serious heart conditions, such as a recent heart attack or unstable chest pain
  • People with another severe or uncontrolled illness, including uncontrolled infections, that could put them at risk during the study

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 6 July 2026
Phase 1: approximately ~10% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Principal Investigator: Ching-Chu Lu, National Taiwan University Hospital

Phone: +886-2-2322-0322

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
Phase 1
Registry
ClinicalTrials.gov
Start date
1 January 2026
Est. completion
31 December 2030

Where this trial is recruiting

🇹🇼 Taiwan

Primary endpoints

Treatment-emergent adverse events

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: 6 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