Viewing Study NCT00291668



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Last Modification Date: 2024-10-26 @ 9:23 AM
Study NCT ID: NCT00291668
Status: COMPLETED
Last Update Posted: 2020-08-03
First Post: 2006-02-10

Brief Title: Clinical Study of CDP870Certolizumab Pegol in Patients With Active Crohns Disease
Sponsor: UCB Pharma
Organization: UCB Pharma

Study Overview

Official Title: A Phase II Multi-center Double-blind Placebo-controlled Parallel-group Dose-response Study to Assess the Safety and Efficacy of CDP870Certolizumab Pegol Dosed Subcutaneously in Patients With Active Crohns Disease
Status: COMPLETED
Status Verified Date: 2020-07
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: This is a multi-centre randomized double-blind dose response clinical study of CDP870 in patients with 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
Secondary IDs
Secondary ID Type Domain Link
2014-004399-42 EUDRACT_NUMBER None None