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Efficacy and Safety Study of Oral Edaravone Administered in Subjects With ALS

ALS Clinical Trial

Official title:
A Phase 3b, Multicenter, Randomized, Double-Blind Study to Evaluate Efficacy and Safety of Oral Edaravone Administered for a Period of 48 Weeks in Subjects With Amyotrophic Lateral Sclerosis (ALS)

Clinical Trial Summary

To evaluate and compare the efficacy of two dosing regimens of oral edaravone in subjects with amyotrophic lateral sclerosis (ALS) based on the change in ALS Functional Rating Scale- Revised (ALSFRS-R) score from baseline up to Week 48:

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04569084
Study type Interventional
Source Mitsubishi Tanabe Pharma America Inc.
Contact
Status Terminated
Phase Phase 3
Start date November 13, 2020
Completion date September 29, 2023
View Details
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