Viewing Study NCT00134368


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Study NCT ID: NCT00134368
Status: COMPLETED
Last Update Posted: 2008-08-07
First Post: 2005-08-22
Is NOT Gene Therapy: False
Has Adverse Events: False

Brief Title: Study of the Efficacy and Safety of Etanercept in Adults With Vitiligo
Sponsor: University of Medicine and Dentistry of New Jersey
Organization:

Study Overview

Official Title: Pilot, Investigator-Initiated, Proof-of-Concept, Study of the Efficacy and Safety of Etanercept (Enbrel) in Adults With Vitiligo
Status: COMPLETED
Status Verified Date: 2008-08
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: No
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The purpose of this study is to investigate the efficacy and safety of etanercept in adults with vitiligo.
Detailed Description: Subjects will self-administer etanercept 50 mg SQ twice weekly for 6 months. Lesion repigmentation will be evaluated at monthly visits.

Study Oversight

Has Oversight DMC:
Is a FDA Regulated Drug?:
Is a FDA Regulated Device?:
Is an Unapproved Device?:
Is a PPSD?:
Is a US Export?:
Is an FDA AA801 Violation?: