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NCT05366036

A Study for Tecfidera (Dimethyl Fumarate) Capsules in Korean Participants With Relapsing-Remitting Multiple Sclerosis

Completed Last updated 9 May 2022
What this trial tests

trial testing No Intervention in Multiple Sclerosis, Relapsing-remitting in 172 participants. Completed in 14 January 2022.

Timeline
14 June 2017
Primary endpoint
14 January 2022
14 January 2022

Quick facts

Lead sponsorEisai Korea Inc.
StatusCompleted
Study typeOBSERVATIONAL
Enrollment172
Start date14 June 2017
Primary completion14 January 2022
Estimated completion14 January 2022
Sites20 locations across South Korea

Drugs / interventions tested

Conditions studied

Sponsor

Eisai Korea Inc. — full company profile →

Who can join

Adults 18 to 55, any sex, with Multiple Sclerosis, Relapsing-remitting. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other trials of No Intervention

Trials testing the same drug.

Other Eisai Korea Inc. trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05366036.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing