Cancer Hospital of Shandong First Medical University
Jinan, Shandong, 100023, China
Location status: Recruiting
NCT Number: NCT07135102
The purpose of this study is to determine the safety and efficacy of 225Ac -labeled PSMA ligand(PSMA-XT) in the treatment of mCRPC
Interested in participating?
Request Info18 year and older
Male
Interventional
Phase 1
Jinan, Shandong, 100023, China
Location status: Recruiting
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Known other malignancies.
Patients will receive 225Ac-PSMA-XT administration at an interval of 6 weeks between each dose.
Time frame: Through study completion, assessed up to 2 years
To evaluate the safety and tolerability of [177Lu]Lu-PSMA-XT Injection assessed from the number and incidence of patients with adverse events using CTCAE v5.0 and physical examination, electrocardiogram and laboratory abnormality, etc.
Time frame: Through study completion, assessed up to 2 years
Incidence and severity of dose-limiting toxicities.
Time frame: Through study completion, assessed up to 2 years.
PSA50 response was defined as the proportion of participants who had a >= 50% decrease in PSA from baseline confirmed by a PSA measurement >= 4 weeks later.
Time frame: Through study completion, assessed up to 2 years.
Radiographic progression-free survival (rPFS) was defined as the time (in months) from the date of enrollment to the date of radiographic disease progression per the Prostate Cancer Clinical Trials Working Group 3 (PCWG3) criteria or death due to any cause.
Time frame: Through study completion, assessed up to 2 years.
Overall Response Rate (ORR) was defined as the proportion of participants with Best Overall Response (BOR) of Complete Response (CR) or Partial Response (PR). ORR was based on RECIST 1.1 response for patients with measurable disease at baseline.
Time frame: Through study completion, assessed up to 2 years.
Duration of Response (DOR) was defined as the duration between the date of first documented Best Overall Response (BOR) of Complete Response (CR) or Partial Response (PR) and the date of first documented radiographic progression or death due to any cause .
Time frame: Through study completion, assessed up to 2 years.
Disease control rate (DCR) was defined as the proportion of participants with Best Overall Response (BOR) of Complete Response (CR) or Partial Response (PR) or Stable Disease (SD) according to RECIST v1.1.
Xiaorong Sun
Other
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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