Clinical Pharmacology Study of Oral Edaravone in Patients With Amyotrophic Lateral Sclerosis
NCT04176224 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 9
Last updated 2026-05-22
Summary
To evaluate the pharmacokinetics of single doses of edaravone oral suspension in Patients with Amyotrophic Lateral Sclerosis
Conditions
- Japanese Patients With ALS
Interventions
- DRUG
-
MT-1186
Suspension
Sponsors & Collaborators
-
Tanabe Pharma Corporation
lead INDUSTRY
Principal Investigators
-
General Manager · Tanabe Pharma Corporation
Study Design
- Allocation
- NA
- Purpose
- OTHER
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 20 Years
- Max Age
- 75 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2019-04-17
- Primary Completion
- 2019-09-04
- Completion
- 2019-09-04
Countries
- Japan
Study Locations
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