Viewing Study NCT00138840



Ignite Creation Date: 2024-05-05 @ 11:48 AM
Last Modification Date: 2024-10-26 @ 9:14 AM
Study NCT ID: NCT00138840
Status: COMPLETED
Last Update Posted: 2008-12-04
First Post: 2005-08-26

Brief Title: Study of STA-5326 Mesylate in Patients With Moderate to Severe Crohns Disease
Sponsor: Synta Pharmaceuticals Corp
Organization: Synta Pharmaceuticals Corp

Study Overview

Official Title: A Randomized Double-Blind Placebo-Controlled Clinical Study of the Oral IL-1223 Inhibitor STA-5326 Mesylate for the Induction of Clinical Response in Patients With Crohns Disease
Status: COMPLETED
Status Verified Date: 2008-12
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: STA-5326 is an experimental drug that has been shown to block the release of interleukin-12 from peripheral blood mononuclear cells Given this activity on the immune system STA-5326 mesylate is a potential treatment for various autoimmune diseases such as Crohns disease that are mediated by the inappropriate expression of Th1 cytokines

This study is evaluating the use of STA-5326 mesylate in patients with moderate to severe active Crohns disease Study visits include a screening visit 9 treatment period visits over 6 months and a follow-up visit that will occur 30 days following the end of treatment Study drug treatment will continue for up to 6 months
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