An Observational Study on Patients With Rheumatoid Arthritis Treated With MabThera (Rituximab)
- Sponsor
- Hoffmann-La Roche
- Study ID
- NCT01075477
- Status
- Completed
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- rituximab [Mabthera/Rituxan] — DRUGAs prescribed by physician
Study Details
This observational study will assess the execution, efficacy and safety of treatment with MabThera in patients with rheumatoid arthritis. Data from patients receiving MabThera according to local treatment guidelines will be collected for 29 months. Target sample size is 100-200 patients.
Key Dates
- Start date
- Sep 30, 2009
- Status verified
- Nov 2016
- Primary completion
- Dec 31, 2011
- Completion
- Dec 31, 2011
Study Design
- Enrollment
- 151 participants (actual)
Arms
- Arm: Cohort
Primary Outcome Measure
Efficacy: DAS28 [ Time Frame: 29 months ]
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