drugset / Trial / NCT03936426

Peptide Receptor Radionuclide Therapy Administered to Participants With Meningioma With 67Cu-SARTATE™

NCT03936426 ↗

Phase 1/2 Completed 5 enrolled Clarity Pharmaceuticals Ltd
NaSingle-groupOpen-labelTreatment

Summary

The primary purpose of this study is to investigate the safety and tolerability of a single dose of Cu-64 SARTATE and multiple doses of Cu-67 SARTATE administered to participants with meningioma. All participants in this study will be injected with a single dose of Cu-64 SARTATE to demonstrate how it is absorbed in the body. Then participants will receive individualised doses of Cu-67 SARTATE for up to 4 cycles.

Timeline

Start
2018-07-09
Primary completion
2019-09-19
Completion
2019-09-19

Drugs

EvaluationDrugModalityDoseRoute
Subject 64Cu-SARTATE Diagnostic / imaging agent 200 mbq Intravenous
Subject 67Cu-SARTATE Unknown 5100 mbq Intravenous

Indications