Viewing Study NCT00152425



Ignite Creation Date: 2024-05-05 @ 11:51 AM
Last Modification Date: 2024-10-26 @ 9:14 AM
Study NCT ID: NCT00152425
Status: COMPLETED
Last Update Posted: 2013-09-09
First Post: 2005-09-07

Brief Title: Study to Test the Effect of CDP870 in the Treatment of Crohns Disease Over 26 Weeks Comparing CDP870 to a Dummy Drug Placebo Following 3 Doses of Active Drug CDP870
Sponsor: UCB Pharma
Organization: UCB Pharma

Study Overview

Official Title: A Phase III Multi-national Multi-centre Double-blind Placebo-controlled Parallel Group 26 Week Study to Assess the Maintenance of Clinical Response to Humanised Anti-TNF PEG Conjugate CDP870 400 mg sc Dosed 4-weekly From Weeks 8 to 24 in the Treatment of Patients With Active Crohns Disease Who Have Responded to Open Induction Therapy Dosed at Weeks 0 2 and 4 With CDP870
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: A 26 week maintenance study of CDP870 in Crohns disease
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