A Study for Tecfidera (Dimethyl Fumarate) Capsules in Korean Participants With Relapsing-Remitting Multiple Sclerosis
NCT05366036 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 172
Last updated 2022-05-09
Summary
The primary purpose of this study is to evaluate the overall safety and efficacy of Tecfidera (Dimethyl Fumarate) as an oral treatment for Korean participants with relapsing-remitting multiple sclerosis (MS) under routine clinical practice.
Conditions
- Multiple Sclerosis, Relapsing-remitting
Interventions
- OTHER
-
No Intervention
This is a non-interventional study.
Sponsors & Collaborators
-
Eisai Korea Inc.
lead INDUSTRY
Eligibility
- Min Age
- 18 Years
- Max Age
- 55 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2017-06-14
- Primary Completion
- 2022-01-14
- Completion
- 2022-01-14
Countries
- South Korea
Study Locations
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