drugset / Trial / NCT04085991

Two TraCer PositROn EmiSSion Tomography ComBination for Efficacy EstimatiOn of Prostate Specific Membrane Antigen Radioligand Therapy in Patients With Metastatic Prostate Cancer

NCT04085991

Phase 2 Terminated 11 enrolled Sir Mortimer B. Davis - Jewish General Hospital
NaSingle-groupOpen-labelTreatment

Summary

Single-arm, open-label, phase II trial in 200 competent adult male patients with Eastern Cooperative Oncology Group performance status (ECOG PS) of 0-3 and progressive metastatic prostate cancer, failing, failed, refused, not eligible for or no access to further approved lines of therapy. Patients will undergo sequential FDG positron emission tomography (PET) and 18F-DCFPyL PET to assess FDG/DCFPyL concordance fraction. Patients with DCFPyL/FDG concordance of 50% or greater will be treated with 131I-PSMA-1095 radioligand therapy (RLT). Best post-treatment serum prostate specific antigen response will be compared to concordance fraction.

Timeline

Start
2020-07-31
Primary completion
2023-01-15
Completion
2023-01-15

Drugs

EvaluationDrugModalityDoseRoute
Subject 131I-PSMA-1095 Other / unclassified 3700 mbq Intravenous