drugset / Trial / NCT01626378

Safety and Efficacy Study Evaluating TRx0237 in Subjects With Behavioral Variant Frontotemporal Dementia (bvFTD)

NCT01626378 ↗

Phase 3 Completed 220 enrolled TauRx Therapeutics Ltd
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to demonstrate the safety and efficacy of TRx0237 in the treatment of patients with behavioral variant frontotemporal dementia (bvFTD).

Timeline

Start
2013-05
Primary completion
2016-02
Completion
2016-02

Drugs

EvaluationDrugModalityDoseRoute
Subject HYDROMETHYLTHIONINE Small molecule 100 mg —