A Study to Assess the Safety and Efficacy of Adalimumab When Added to Inadequate Standard Anti-Rheumatic Therapy in Patients With Active Rheumatoid Arthritis
- Sponsor
- Abbott
- Study ID
- NCT00448383
- Phase
- PHASE3
- Status
- Completed
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- adalimumab — BIOLOGICAL40mg every other week
Study Details
This is an open-label, multi-center study in which adalimumab (D2E7) is administered subcutaneously 40 mg every other week in addition to current anti-rheumatic therapies. Patients must have active disease despite standard anti-rheumatic therapy.
Key Dates
- Start date
- Sep 30, 2002
- Status verified
- Jul 2008
- Primary completion
- Nov 30, 2004
Study Design
- Enrollment
- 6,610 participants (actual)
- Allocation
- NON_RANDOMIZED
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: 1Open-label adalimumab
Primary Outcome Measure
Change of disease activity score (DAS28) compared with study entry [ Time Frame: Week 12 ]
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