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Clinical trial

A Phase III Multi-centre, Open-label, follow-on Study to CDP870-027, to Assess the Efficacy and Safety of Lyophilized CDP870 an Engineered Human Anti-TNF PEG Conjugate, as Additional Medication to Methotrexate, in the Treatment of Signs and Symptoms and Preventing Structural Damage in Patients With Active Rheumatoid Arthritis

NCT00175877 is registered in ClinicalTrials.gov with UCB Pharma as lead sponsor.

NCT NCT00175877
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Registry record

As filed in ClinicalTrials.gov.

Title
A Phase III Multi-centre, Open-label, follow-on Study to CDP870-027, to Assess the Efficacy and Safety of Lyophilized CDP870 an Engineered Human Anti-TNF PEG Conjugate, as Additional Medication to Methotrexate, in the Treatment of Signs and Symptoms and Preventing Structural Damage in Patients With Active Rheumatoid Arthritis
Lead sponsor
UCB Pharma
Phase
Phase 3
Overall status
Completed
Start date
June 30, 2005
Completion date
February 29, 2012
Enrollment
857 (actual)
Sites
121

Conditions

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

rheumatoid arthritis