A Study on Rheumatoid Arthritis Patients Treated With Rituximab
- Registration Number
- NCT02622503
- Lead Sponsor
- Hoffmann-La Roche
- Brief Summary
The purpose of the study is to obtain an overall picture of rituximab treatments and treatment responses in RA patients.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 81
Inclusion Criteria
- Rheumatoid arthritis (RA) patients treated with rituximab in Finland
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Exclusion Criteria
- Not applicable
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Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Arm && Interventions
Group Intervention Description Patients with rheumatoid arthritis Rituximab Patients with rheumatoid arthritis receiving rituximab will be observed for treatment responses.
- Primary Outcome Measures
Name Time Method Information on previous RA treatments 3 months Information on rituximab treatment responses 3 months Information on concomitant medications 3 months
- Secondary Outcome Measures
Name Time Method