89
Participants
Start Date
February 28, 2006
Primary Completion Date
January 31, 2008
Study Completion Date
December 31, 2009
Certolizumab pegol
Certolizumab pegol (CDP870) 400 mg administered subcutaneously (sc) at Weeks 0, 2 and 4 (induction doses), then every 4 weeks (Q4W) until Week 52. Investigators can escalate dosage to CDP870 400 mg 2-weekly (Q2W) at any time after Week 10 for lack of response/remission. After Week 52 patients can continue to receive treatment until study drug end, either Q4W or Q2W, according to their administration frequency at Week 52.
Bonheiden
Brussels
Edegem
Leuven
Amiens
Besançon
Chambray-lès-Tours
Clichy
Grenoble
Lille
Marseille
Nice
Paris
Reims
Rouen
Strasbourg
Vandœuvre-lès-Nancy
Berlin
Bonn
Lead Sponsor
UCB Pharma
INDUSTRY