drugset / Trial / NCT02936635

A Study for Patients Who Completed VITALITY-ALS (CY 4031)

NCT02936635

Phase 3 Completed 280 enrolled Cytokinetics
Non-randomizedSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to assess the long-term safety and tolerability of tirasemtiv in patients with ALS who had completed the double-blind placebo-controlled study of tirasemtiv in ALS (CY 4031).

Timeline

Start
2016-10-17
Primary completion
2018-10-26
Completion
2018-10-26

Drugs

EvaluationDrugModalityDoseRoute
Subject tirasemtiv Other / unclassified 250 mg Oral