Clinical trial
A Phase III Multi-national, Multi-centre, Double-blind Placebo-controlled Parallel Group, 26 Week Study to Assess the Safety and Efficacy of the Humanised Anti-TNF PEG Conjugate, CDP870 400 mg sc, (Dosed at Weeks 0, 2, 4 Then 4-weekly to Week 24), in the Treatment of Patients With Active Crohn's Disease
NCT00152490 is registered in ClinicalTrials.gov with UCB Pharma as lead sponsor.
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Registry record
As filed in ClinicalTrials.gov.
- Title
- A Phase III Multi-national, Multi-centre, Double-blind Placebo-controlled Parallel Group, 26 Week Study to Assess the Safety and Efficacy of the Humanised Anti-TNF PEG Conjugate, CDP870 400 mg sc, (Dosed at Weeks 0, 2, 4 Then 4-weekly to Week 24), in the Treatment of Patients With Active Crohn's Disease
- Lead sponsor
- UCB Pharma
- Phase
- Phase 3
- Overall status
- Completed
- Start date
- December 31, 2003
- Completion date
- May 31, 2005
- Enrollment
- 604
- Sites
- Not reported
Conditions
As the registry lists them; a condition with its own page is linked.
crohn's disease