Last updated on October 2018

Perampanel for Sporadic Amyotrophic Lateral Sclerosis (ALS)


Brief description of study

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

Detailed Study 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)

Clinical Study Identifier: NCT03019419

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Makoto Urushitani, MD,PhD

Shiga University of Medical Science Hospital
Shiga, Japan

Recruitment Status: Closed


Brief Description Eligibility Contact Research Team


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