Corticosteroid Sparing Effect of Certolizumab in Crohn's Disease

PHASE3TerminatedINTERVENTIONAL
Enrollment

174

Participants

Timeline

Start Date

November 30, 2006

Primary Completion Date

July 31, 2009

Study Completion Date

July 31, 2009

Conditions
Crohn's Disease
Interventions
BIOLOGICAL

certolizumab pegol 400 mg

Certolizumab pegol 400 mg provided in solution for subcutaneous injection (2 x 200 mg/mL) in single-use vials for administration at Weeks 0, 2, 4 and then every 4 weeks until Week 36. Two vials will be required for each dosing.

OTHER

Placebo

Placebo (commercially available sodium chloride 0.9% (preservative free)) provided for subcutaneous injection in single-use vials for administration at Weeks 0, 2, 4 and then every 4 weeks until Week 36. Two vials will be required for each dosing.

Trial Locations (68)

Unknown

Birmingham

Montgomery

Tucson

La Jolla

Oceanside

Orange

Palo Alto

Roseville

Golden

Clearwater

Gainesville

Hialeah

Jacksonville

North Miami Beach

Sarasota

Winter Park

Marietta

Savannah

Chicago

Bloomington

Topeka

Bowling Green

Louisville

Metairie

Annapolis

Newton

Chesterfield

Dearborn

Troy

Rochester

Ocean Springs

Kansas City

Mexico

New York

Syracuse

Chapel Hill

Charlotte

Raleigh

Cincinnati

Cleveland

Dayton

Tulsa

Columbia

Germantown

Austin

Irving

Salt Lake City

Burlington

Chesapeake

Richmond

Seattle

Madison

Milwaukee

Monroe

Calgary

Edmonton

Abbotsford

Vancouver

Winnipeg

Halifax

London

Toronto

Saskatoon

Frankfurt

Heidleberg

Jena

Magdeburg

Ulm

Sponsors

Lead Sponsor

All Listed Sponsors
lead

UCB Pharma

INDUSTRY

NCT00349752 - Corticosteroid Sparing Effect of Certolizumab in Crohn's Disease | Biotech Hunter | Biotech Hunter