Clinical Trials Directory

Trials / Recruiting

RecruitingNCT06246123

A Study of Jyseleca Tablet (Filgotinib Maleate) in Korean Participants

Post Marketing Surveillance of Jyseleca Tab. (Filgotinib Maleate) in Korean Subjects

Status
Recruiting
Phase
Study type
Observational
Enrollment
2,040 (estimated)
Sponsor
Eisai Korea Inc. · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to collect and evaluate the following information in relation to the safety and the efficacy of Jyseleca tablet (Filgotinib Maleate) 100 milligram (mg) and 200 mg in this post marketing setting: (1) Serious adverse events and adverse drug reactions (2) Unexpected adverse events and adverse drug reactions not reflected in precautions for use (3) Known adverse drug reactions (4) Non-serious adverse events and adverse drug reactions (5) Other safety and effectiveness related information will be evaluated in accordance with the permitted articles under the actual conditions of use in Korea.

Conditions

Interventions

TypeNameDescription
OTHERNon-interventionalNo intervention will be administered.

Timeline

Start date
2024-02-27
Primary completion
2027-07-30
Completion
2027-07-30
First posted
2024-02-07
Last updated
2026-04-07

Locations

64 sites across 1 country: South Korea

Source: ClinicalTrials.gov record NCT06246123. Inclusion in this directory is not an endorsement.