Mucosal Healing Study in Crohn's Disease (CD)

PHASE3CompletedINTERVENTIONAL
Enrollment

89

Participants

Timeline

Start Date

February 28, 2006

Primary Completion Date

January 31, 2008

Study Completion Date

December 31, 2009

Conditions
Crohn's Disease
Interventions
BIOLOGICAL

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.

Trial Locations (19)

Unknown

Bonheiden

Brussels

Edegem

Leuven

Amiens

Besançon

Chambray-lès-Tours

Clichy

Grenoble

Lille

Marseille

Nice

Paris

Reims

Rouen

Strasbourg

Vandœuvre-lès-Nancy

Berlin

Bonn

Sponsors

Lead Sponsor

All Listed Sponsors
lead

UCB Pharma

INDUSTRY