Clinical trial
A Phase III Multi-national, Multi-centre, Open Label, Safety Study to Assess the Safety of Re-exposure After a Variable Interval and Subsequent Chronic Therapy With the Humanised Anti-TNF PEG Conjugate CDP870 400 mg sc, (Dosed at Weeks 0, 2 and 4 Then Every 4 Weeks), in the Treatment of Patients With Active Crohn's Disease Who Have Previously Been Withdrawn From Studies CDP870-031 or CDP870-032 Due to an Exacerbation of Crohn's Disease.
NCT00160706 is registered in ClinicalTrials.gov with UCB Pharma SA as lead sponsor.
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Registry record
As filed in ClinicalTrials.gov.
- Title
- A Phase III Multi-national, Multi-centre, Open Label, Safety Study to Assess the Safety of Re-exposure After a Variable Interval and Subsequent Chronic Therapy With the Humanised Anti-TNF PEG Conjugate CDP870 400 mg sc, (Dosed at Weeks 0, 2 and 4 Then Every 4 Weeks), in the Treatment of Patients With Active Crohn's Disease Who Have Previously Been Withdrawn From Studies CDP870-031 or CDP870-032 Due to an Exacerbation of Crohn's Disease.
- Lead sponsor
- UCB Pharma SA
- Phase
- Phase 3
- Overall status
- Completed
- Start date
- February 29, 2004
- Completion date
- May 31, 2012
- Enrollment
- 310 (actual)
- Sites
- 141
Conditions
As the registry lists them; a condition with its own page is linked.
crohn's disease