drugset / Trial / NCT03701399

Troriluzole in Adult Participants With Spinocerebellar Ataxia

NCT03701399

Phase 3 Active not recruiting 299 enrolled Biohaven Pharmaceuticals, Inc.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to compare the efficacy of Troriluzole (200 mg once daily) versus placebo after 48 weeks of treatment in subjects with spinocerebellar ataxia (SCA).

Timeline

Start
2019-03-08
Primary completion
2022-02-18
Completion
2026-08

Drugs

EvaluationDrugModalityDoseRoute
Subject Troriluzole Peptide 200 mg Oral