drugset / Trial / NCT05460507

Safety & Efficacy/Tolerability of Rhenium-186 NanoLiposomes (186RNL) for Patients Who Received a Prior 186RNL Treatment

NCT05460507 ↗

Phase 1 Recruiting 40 enrolled Plus Therapeutics
NaSingle-groupOpen-labelTreatment

Summary

This is an open-label, multicenter, Phase 1 study to establish the safety and efficacy/tolerability of a single dose of 186RNL by the intraventricular route (via intraventricular catheter) for recurrence glioma in patients who received a prior treatment of 186RNL.

Timeline

Start
2024-12-12
Primary completion
2028-03-01
Completion
2028-03-01

Drugs

EvaluationDrugModalityDoseRoute
Subject 186RNL Other / unclassified 8.8 ml Intravitreal
Subject 186RNL Other / unclassified 825.1 mbq Intravitreal

Indications