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Clinical Trial Summary

The purpose of this study is to evaluate the safety of oral edaravone at a dose of 105 mg administered once daily for 10 days out of a 14-day period, followed by a 14-day drug-free period. This study will be continued until the earlier date when oral edaravone is commercially available at each site in Japan or August 2023.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05568615
Study type Interventional
Source Mitsubishi Tanabe Pharma Corporation
Contact
Status Completed
Phase Phase 3
Start date October 26, 2022
Completion date June 27, 2023

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