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Study identifier: NCT04569084 Synced from ClinicalTrials.gov · August 05, 2026
● Terminated

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

Condition: ALS  ·  Sponsor: Shionogi

PhasePhase 3
Planned participants384
Who can joinAll sexes, 18 Years to 75 Years
Healthy volunteersNo

About this study

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:

This description comes directly from the study's public registry record.

Talk to the study team

No contact information is available for this study as per the public registry record.

Always discuss trial participation with your own doctor first.

Locations (95)

St. Joseph's Hospital and Medical Center (SJHMC)Phoenix, Arizona, United States
HonorHealth NeurologyScottsdale, Arizona, United States
Woodland Research NorthwestRogers, Arkansas, United States
UCSD Medical CenterLa Jolla, California, United States
Loma Linda University Health Care - Department of NeurologyLoma Linda, California, United States
University California Los Angeles Medical Center (UCLA)Los Angeles, California, United States
University of California Irvine (UCI) Health - Women's Healthcare CenterOrange, California, United States
University of Colorado Anschutz Medical CampusAurora, Colorado, United States
UF Health Cancer CenterGainesville, Florida, United States
Mayo ClinicJacksonville, Florida, United States
University of South Florida (USF) - Carol and Frank Morsani Center for Advanced Health Care (CAHC)Tampa, Florida, United States
Emory University - School of MedicineAtlanta, Georgia, United States

+ 83 more locations — full list on the registry record.

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