An Effectiveness and Safety Study of CNTO 1275 in Patients With Active Psoriatic Arthritis

PHASE2CompletedINTERVENTIONAL
Enrollment

146

Participants

Timeline

Start Date

December 31, 2005

Primary Completion Date

March 31, 2007

Study Completion Date

September 30, 2007

Conditions
Psoriatic Arthritis
Interventions
DRUG

CNTO 1275 63 mg

The patients will receive 90 mg (or 63 mg after filtration) subcutaneous injection on Weeks 0, 1, 2, and 3; Placebo subcutaneous injection on Weeks 12 and 16.

DRUG

Placebo

The patients will receive placebo subcutaneous injection on Weeks 0, 1, 2, and 3; At weeks 12 and 16 the patients will receive CNTo1275 90 mg (or 63 mg after filtration) subcutaneous injection

Trial Locations (25)

Unknown

Macon

Boise

Normal

Indianapolis

Covington

Boston

Ann Arbor

Las Vegas

New Brunswick

New York

Wilmington

Salt Lake City

Calgary

Edmonton

Surrey

Barrie

Hamilton

Toronto

Windsor

Aarhus C

Hellerup

København NV

Hus

Tampere

Geneva

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Centocor, Inc.

INDUSTRY

NCT00267956 - An Effectiveness and Safety Study of CNTO 1275 in Patients With Active Psoriatic Arthritis | Biotech Hunter | Biotech Hunter