Clinical trial
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 Crohn's Disease Who Have Responded to Open Induction Therapy (Dosed at Weeks 0, 2 and 4) With CDP870
NCT00152425 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 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 Crohn's Disease Who Have Responded to Open Induction Therapy (Dosed at Weeks 0, 2 and 4) With CDP870
- Lead sponsor
- UCB Pharma
- Phase
- Phase 3
- Overall status
- Completed
- Start date
- February 29, 2004
- Completion date
- May 31, 2005
- Enrollment
- 392
- Sites
- Not reported
Conditions
As the registry lists them; a condition with its own page is linked.
crohn's disease