drugset / Trial / NCT04839367

Positron Emission Tomography (PET) Imaging of Participants With Confirmed Prostate Cancer Using 64Cu-SAR-bisPSMA (PROPELLER)

NCT04839367 ↗

Phase 1 Completed 30 enrolled Clarity Pharmaceuticals Ltd
Non-randomizedSequentialOpen-labelDiagnostic

Summary

The aim of this study is to determine the safety and tolerability of 64Cu-SARbisPSMA in participants with untreated, confirmed Prostate Cancer.

Timeline

Start
2021-07-13
Primary completion
2022-10-19
Completion
2022-10-19

Drugs

EvaluationDrugModalityDoseRoute
Subject 64Cu-SAR-bisPSMA Diagnostic / imaging agent 100 mbq Intravenous
Subject 64Cu-SAR-bisPSMA Diagnostic / imaging agent 150 mbq Intravenous
Subject 64Cu-SAR-bisPSMA Diagnostic / imaging agent 200 mbq Intravenous

Indications