An Efficacy and Safety Study of Golimumab in Patients With Active Rheumatoid Arthritis Despite Methotrexate Therapy

Completed · Phase 3 · Has a placebo group

Conditions studied: Rheumatoid Arthritis

In brief

The purpose of this study is to evaluate the efficacy and safety of golimumab, alone or in combination with methotrexate (MTX), as compared to methotrexate alone in rheumatoid arthritis (RA) patients who have active rheumatoid arthritis despite treatment with MTX.

Key facts

Study ID

NCT00264550

Run by

Centocor, Inc.

People needed

444

Starts

2005-12-01

Expected to finish

2012-05-01

Last updated by the study team

2014-04-29

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Have a diagnosis of rheumatoid arthritis (RA) (according to the revised 1987 criteria of the ACR) for at least 3 months prior to screening
• Must have been treated with and tolerated methotrexate (MTX) at a dose of at least 15 mg/week for at least 3 months prior to screening, and have a MTX dose of >=15 mg/week and <=25 mg/week and stable for at least 4 weeks prior to screening
• Have active RA as defined by persistent disease activity with at least 4 swollen and 4 tender joints, at the time of screening and baseline, and at least 2 of the following 4 criteria: a)C-reactive protein (CRP) >=1.5 mg/dL at screening or erythrocyte sedimentation rate (ESR) by Westergren method of >= 28 mm in the first hour at screening or baseline, b)Morning stiffness of >= 30 minutes at screening and baseline, c)Bone erosion by x-ray and/or magnetic resonance imaging (MRI) prior to first administration of study agent, d)Anti-cyclic citrullinated peptide (anti-CCP) antibody-positive or rheumatoid factor (RF) positive at screening
• If using oral corticosteroids, must be on a stable dose equivalent to <= 10 mg of prednisone/day for at least 2 weeks prior to first administration of study agent
• Are considered eligible according to specified tuberculosis (TB) screening criteria

You may not qualify if…

• Have inflammatory diseases other than RA that might confound the evaluation of the benefit of golimumab therapy
• Have had treatment with disease-modifying anti-rheumatic drugs (DMARDs)/systemic immunosuppressives other than MTX, during the 4 weeks prior to the first administration of study agent
• Have had prior treatment with biologic anti-tumor necrosis factor (TNF) drugs (infliximab, etanercept, adalimumab)
• Have had history of, or ongoing, chronic or recurrent infectious disease.
• Have serious infection within 2 months prior to first administration of study agent
• Have a history of latent or active granulomatous infection, including TB, histoplasmosis, or coccidioidomycosis, prior to screening

Where it is running

• Study site — Mobile, Alabama, United States
• Study site — Palo Alto, California, United States
• Study site — Pasadena, California, United States
• Study site — Upland, California, United States
• Study site — Ormond Beach, Florida, United States
• Study site — Palm Harbor, Florida, United States
• Study site — Moline, Illinois, United States
• Study site — Kansas City, Missouri, United States
• Study site — St Louis, Missouri, United States
• Study site — Lincoln, Nebraska, United States
• Study site — Omaha, Nebraska, United States
• Study site — Duncansville, Pennsylvania, United States
• Study site — Richmond, Virginia, United States
• Study site — Buenos Aires, Argentina
• Study site — Córdoba, Argentina
• Study site — Rosario, Argentina
• Study site — S.M. de Tucuman, Argentina
• Study site — San Miguel de Tucumán, Argentina
• Study site — Clayton, Australia
• Study site — Maroochydore, Australia
• Study site — Melbourne, Australia
• Study site — Victoria, British Columbia, Canada
• Study site — St. John's, Newfoundland and Labrador, Canada
• Study site — Ottawa, Ontario, Canada
• Study site — Toronto, Ontario, Canada

Full record on ClinicalTrials.gov

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