ALS Clinical Trial - Perampanel for 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

See also
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Terminated	`NCT03373981` - Non-invasive Brain Stimulation for the Treatment of Depression Symptoms in ALS	N/A

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

Perampanel for Sporadic Amyotrophic Lateral Sclerosis (ALS)

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms