Clinical trial

A Study of the Safety and Effectiveness of Lyophilized Certolizumab Pegol in the…

NCT00175877 · UCB Pharma, Industry · Completed

Key facts

NCT number NCT00175877
Title A Study of the Safety and Effectiveness of Lyophilized Certolizumab Pegol in the Treatment of Signs and Symptoms of Rheumatoid Arthritis and in Prevention of Joint Damage in Patients With Active Rheumatoid Arthritis
Official 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…
Lead sponsor UCB Pharma, Industry
Status Completed
Phase Phase 3
Study type Interventional
Conditions Rheumatoid Arthritis
Intervention type Biological
Interventions Certolizumab Pegol
Enrollment 857
Start date Jun 1, 2005
Primary completion Feb 1, 2012
Completion Feb 1, 2012
First posted Sep 15, 2005
Last update posted Mar 26, 2020
Countries Argentina, Australia, Belgium, Bulgaria, Canada, Chile, Croatia, Czechia, Estonia, Finland, France, Hungary and 10 more

At a glance

  • 100–999 Study sites
  • Yes Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date:

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