Viewing Study NCT00420303



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Last Modification Date: 2024-10-26 @ 9:30 AM
Study NCT ID: NCT00420303
Status: COMPLETED
Last Update Posted: 2010-07-20
First Post: 2007-01-08

Brief Title: Study Evaluating Etanercept for the Treatment of Refractory Heel Enthesitis in Spondylarthropathy
Sponsor: Wyeth is now a wholly owned subsidiary of Pfizer
Organization: Wyeth is now a wholly owned subsidiary of Pfizer

Study Overview

Official Title: A Multicentre Double-Blind Placebo-Controlled Randomized Study of Etanercept in the Treatment of Adults Patients With Refractory Heel Enthesitis in Spondylarthropathy
Status: COMPLETED
Status Verified Date: 2010-07
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: To assess the efficacy and safety of Etanercept in patients with spondylarthropathy and refractory heel enthesitis
Detailed Description: None

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