Viewing Study NCT00134368



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Last Modification Date: 2024-10-26 @ 9:13 AM
Study NCT ID: NCT00134368
Status: COMPLETED
Last Update Posted: 2008-08-07
First Post: 2005-08-22

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

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: None
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?: None