A Study of the Safety and Efficacy of Golimumab in Subjects With Rheumatoid Arthritis That Are Methotrexate-naive

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, as compared to methotrexate alone in rheumatoid arthritis subjects who have not been previously treated with methotrexate.

Key facts

Study ID

NCT00264537

Run by

Centocor, Inc.

People needed

637

Starts

2005-12-01

Expected to finish

2012-06-01

Last updated by the study team

2014-09-05

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 first administration of study agent
• Are methotrexate (MTX)-naïve (ie, have not received more than 3 weekly doses of MTX for RA at any time)
• 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 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.

You may not qualify if…

• Can not have inflammatory diseases other than RA that might confound the evaluation of the benefit of golimumab therapy
• No treatment with disease-modifying anti-rheumatic drugs (DMARDs)/systemic immunosuppressives during the 4 weeks prior to the first administration of study agent
• No prior treatment with biologic anti-TNF drugs (infliximab, etanercept, adalimumab)
• No history of, or ongoing, chronic or recurrent infectious disease
• No serious infection within 2 months prior to first administration of study agent.

Where it is running

• Study site — Mobile, Alabama, United States
• Study site — Upland, California, United States
• Study site — Jacksonville, Florida, United States
• Study site — Miami, Florida, United States
• Study site — Coeur d'Alene, Idaho, United States
• Study site — Moline, Illinois, United States
• Study site — Springfield, Illinois, United States
• Study site — Kansas City, Kansas, United States
• Study site — Witchita, Kansas, United States
• Study site — Saint Paul, Minnesota, United States
• Study site — Kansas City, Missouri, United States
• Study site — Lincoln, Nebraska, United States
• Study site — Charlotte, North Carolina, United States
• Study site — Duncansville, Pennsylvania, United States
• Study site — Dallas, Texas, United States
• Study site — Fort Worth, Texas, United States
• Study site — Lubbock, Texas, 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 — Maroochydore, Australia
• Study site — Melbourne, Australia
• Study site — Birmingham, Alabama, United States

Full record on ClinicalTrials.gov

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