Viewing Study NCT07058051


Ignite Creation Date: 2025-12-24 @ 11:55 PM
Ignite Modification Date: 2026-01-05 @ 6:07 PM
Study NCT ID: NCT07058051
Status: COMPLETED
Last Update Posted: 2025-11-19
First Post: 2025-07-01
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: Cross-sectional Study to Characterize Real World Burden of Disease in Patients With Vitiligo in China
Sponsor: AbbVie
Organization:

Study Overview

Official Title: Cross-sectional Study to Characterize Real World Burden of Disease in Patients With Vitiligo in China
Status: COMPLETED
Status Verified Date: 2025-11
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 purpose of this study is to evaluate the patterns of treatment, healthcare resources utilized and the burdens associated with non-segmental vitiligo (NSV) amongst participants in China

This study is a cross-sectional, multicenter, observational study of vitiligo patients in China. The cross-sectional design is sufficient to characterize the overall current burden of NSV.
Detailed Description: Cross-Sectional

Study Oversight

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