RecruitingPhase 1NCT07135102
A Clinical Study to Evaluate the Safety, Tolerability and Preliminary Efficacy of [225Ac]Ac-PSMA-XT Injection in Patients With Metastatic Castration-resistant Prostate Cancer
Sponsor
Xiaorong Sun
Enrollment
40 participants
Start Date
Oct 14, 2024
Study Type
INTERVENTIONAL
Conditions
Summary
The purpose of this study is to determine the safety and efficacy of 225Ac -labeled PSMA ligand(PSMA-XT) in the treatment of mCRPC
Eligibility
Sex: MALEMin Age: 18 Years
Plain Language Summary
Simplified for easier understanding
This study is testing a new investigational drug in men with prostate cancer that has spread and is no longer responding to hormone therapy (castration-resistant prostate cancer). The cancer must be detectable by a specialized scan called a PSMA PET/CT scan.
**You may be eligible if...**
- You are 18 or older and have confirmed prostate cancer
- Your cancer has spread and is castration-resistant (testosterone is at very low levels but cancer continues to grow)
- Your cancer shows up on a PSMA PET/CT scan
- You have already received at least one hormone-based treatment (like enzalutamide or abiraterone)
- You have also received at least one prior taxane chemotherapy (like docetaxel), or are not a good candidate for chemotherapy
- You are in reasonably good health (ECOG 0-1) and have a life expectancy of more than 6 months
**You may NOT be eligible if...**
- Your testosterone is not adequately suppressed
- You have not had appropriate prior treatments
- Your organ function is not adequate for this experimental therapy
Talk to your doctor to see if this trial is right for you.
This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.
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Interventions
DRUG225Ac-PSMA-XT
Patients will receive 225Ac-PSMA-XT administration at an interval of 6 weeks between each dose.
Locations(1)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT07135102