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Clinical trial

A Phase III Multi-national, Multi-centre, Open Label, Safety Study to Assess the Safety of Chronic Therapy With the Humanised Anti-TNF PEG Conjugate CDP870 400 mg sc, (Dosed 4-weekly), in the Treatment of Patients With Active Crohn's Disease Who Have Previously Completed Studies CDP870-031 or CDP870-032

NCT00160524 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 Chronic Therapy With the Humanised Anti-TNF PEG Conjugate CDP870 400 mg sc, (Dosed 4-weekly), in the Treatment of Patients With Active Crohn's Disease Who Have Previously Completed Studies CDP870-031 or CDP870-032
Lead sponsor
UCB Pharma SA
Phase
Phase 3
Overall status
Completed
Start date
July 31, 2004
Completion date
August 31, 2012
Enrollment
596 (actual)
Sites
206

Conditions

As the registry lists them; a condition with its own page is linked.

crohn's disease