Recruiting

[225Ac]Ac-PSMA-XT Injection for Metastatic Castration-resistant Prostate Cancer

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What is being tested

225Ac-PSMA-XT

Drug
Who is being recruted

Over 18 Years
See all eligibility criteria
How is the trial designed

Treatment Study

Phase 1
Interventional
Study Start: October 2024
See protocol details

Summary

Principal SponsorXiaorong Sun
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Study start date: October 14, 2024

Actual date on which the first participant was enrolled.

This study focuses on evaluating a new treatment called [225Ac]Ac-PSMA-XT Injection for patients suffering from metastatic castration-resistant prostate cancer (mCRPC). This type of cancer continues to grow despite treatments that lower testosterone levels. The study aims to assess how safe and effective this new treatment is, which could potentially provide a new option for patients with this aggressive form of prostate cancer. Participants in the study will receive the treatment through an injection. The study is designed to monitor how participants respond to the treatment and to check for any side effects to determine its safety and tolerability. Although specific primary outcomes are not listed, the study's primary focus is on understanding both the safety and potential benefits of this treatment in managing prostate cancer that has spread and is no longer responding to standard hormonal therapy.

Official TitleA Clinical Study to Evaluate the Safety, Tolerability and Preliminary Efficacy of [225Ac]Ac-PSMA-XT Injection in Patients With Metastatic Castration-resistant Prostate Cancer
NCT07135102
Principal SponsorXiaorong Sun
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

40 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Treatment Study

These studies test new ways to treat a disease, condition, or health issue. The goal is to see if a new drug, therapy, or approach works better or has fewer side effects than existing options.



Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Criteria

Male

Biological sex of participants that are eligible to enroll.

Over 18 Years

Range of ages for which participants are eligible to join.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Criteria

Inclusion Criteria: 1. have the ability to understand and sign an approved informed consent form (ICF). 2. \>= 18 years old. 3. Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1. 4. have a life expectancy \>6 months. 5. have histological, pathological, and/or cytological confirmation of prostate cancer. 6. PSMA Positron Emission Tomography (PET)/Computed Tomography (CT) scan positive 7. have a castrate level of serum/plasma testosterone (\<50 ng/dL or \<1.7 nmol/L). 8. have received at least one NAAD (such as enzalutamide and/or abiraterone); patients must have been previously treated undergone at least 1-2 prior taxane-based chemotherapy regimens or be unsuitable for taxane therapy (unsuitability includes contraindications, investigator-determined ineligibility, or patient refusal) in mCRPC stage. 9. progressive mCRPC. 10. have adequate organ function。 11. Subjects of childbearing potential voluntarily use an effective method of contraception, such as condoms, oral or injectable contraceptives, Intra-uterine device(IUD),etc., during treatment and within 6 months of the last use of the trial drug. Exclusion Criteria: 1. Previous treatment with any of the following within 6 months of enrollment: Strontium-89, Samarium-153, Rhenium-186, Rhenium-188, Radium-223, hemi-body irradiation. Previous PSMA-targeted radioligand therapy is not allowed. Known other malignancies. 2. Any systemic anti-cancer therapy (e.g. chemotherapy, immunotherapy or biological therapy within 28 days prior to day of enrollment. 3. Known hypersensitivity to the components of the study therapy or its analogs. 4. A superscan as seen in the baseline bone scan. 5. Patients with a history of Central Nervous System (CNS) metastases. 6. Uncontrolled, intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, cardiac arrhythmia, or other severe complications.

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Treatment Groups
Study Objectives

One single intervention group is designated in this study

This study does not include a placebo group 

Treatment Groups

Group I

Experimental

Study Objectives

Primary Objectives

Secondary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

Recruiting

Cancer Hospital of Shandong First Medical University

Jinan, ChinaOpen Cancer Hospital of Shandong First Medical University in Google Maps
Recruiting
One Study Center