drugset / Trial / NCT02960893

Trial in Adult Participants With Spinocerebellar Ataxia (SCA)

NCT02960893

Phase 2/3 Completed 141 enrolled Biohaven Pharmaceuticals, Inc.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The primary purpose of this study was to compare the efficacy of BHV-4157 (Troriluzole) 140 milligrams (mg) once daily versus placebo after 8 weeks of treatment in participants with spinocerebellar ataxia (SCA).

Timeline

Start
2016-12-15
Primary completion
2017-08-18
Completion
2024-09-20

Drugs

EvaluationDrugModalityDoseRoute
Subject Troriluzole Peptide 140 mg Oral