Viewing Study NCT02984020


Ignite Creation Date: 2025-12-25 @ 4:19 AM
Ignite Modification Date: 2026-03-06 @ 2:40 AM
Study NCT ID: NCT02984020
Status: COMPLETED
Last Update Posted: 2024-08-27
First Post: 2016-11-03
Is NOT Gene Therapy: True
Has Adverse Events: True

Brief Title: Korean Post-marketing Surveillance for Xeljanz
Sponsor: Pfizer
Organization:

Study Overview

Official Title: Korean Post-marketing Surveillance for Xeljanz(Registered) in Rheumatoid Arthritis and Psoriatic Arthritis Patients
Status: COMPLETED
Status Verified Date: 2024-08
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The objective of this study is to identify any problems and questions with respect to the safety and efficacy of Xeljanz during the post-marketing period as required by the regulation of MFDS.
Detailed Description: None

Study Oversight

Has Oversight DMC: False
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: