1,286
Participants
Start Date
April 30, 2005
Primary Completion Date
August 31, 2009
Study Completion Date
August 31, 2009
Abatacept
IV solution, IV infusion, between 500mg and 1gram based on body weight, monthly, 6 months.
Non-biologic Disease Modifying Anti-Rheumatic Drug (DMARD)
During the study, subjects continued to receive 1 or more background non-biologic DMARDs (e.g. methotrexate, leflunomide) at the dose level(s) and regimen(s) administered at the time of abatacept treatment onset (Day 1).
Anti-Tumor Necrosing Factor (TNF) Therapy
Any of the anti-TNF therapies (Infliximab, Adalimumab, Etanercept, etc.)administered at the approved label dose for at least 3 months
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Lead Sponsor
Bristol-Myers Squibb
INDUSTRY