drugset / Trial / NCT02483884

PET/CT Imaging Study of the Safety and Diagnostic Performance of [68Ga]RM2 in Patients With Primary Prostate Cancer

NCT02483884

Phase 1/2 Terminated 30 enrolled Lantheus Biosciences Ltd.
Non-randomizedParallel-groupOpen-labelDiagnostic

Summary

The aim of this study is to investigate safety and diagnostic performance of the 68Ga labeled PET tracer \[68Ga\]RM2 for detection and localization of primary prostate cancer confirmed by histopathology of the prostate as a standard of truth. This is an open-label, multi center PET/CT (positron emission tomography/computed tomography) non-randomized study. The study comprises 2 parts with an interim analysis after Part 1. In Part 1 a total of 30 subjects with biopsy-proven primary prostate cancer will be enrolled. Three strata of patients for the first part will be enrolled based on their pretreatment recurrence risk assessment according to the NCCN guidelines: 10 patients with low, 10 patients with intermediate and 10 patients with high pretreatment risk of recurrence.

Timeline

Start
2015-05
Primary completion
2016-12
Completion
2016-12

Drugs

EvaluationDrugModalityDoseRoute
Subject 68Ga-RM2 Diagnostic / imaging agent 40 ug Intravenous
Subject 68Ga-RM2 Diagnostic / imaging agent 140 mbq Intravenous

Indications