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Clinical Trial Summary

To investigate the safety and the efficacy of perampanel in patients with sporadic amyotrophic lateral sclerosis


Clinical Trial Description

To evaluate the effect of peramanel for 48 weeks on progression of disease in subjects with ALS, as measured by ALS Functional Rating Scale-Revised (ALSFRS-R) ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03019419
Study type Interventional
Source Tokyo Medical University
Contact
Status Completed
Phase Phase 2
Start date April 24, 2017
Completion date December 23, 2020

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