drugset / Trial / NCT00443651
A Study of the Safety of Rituximab in Combination With Other Anti-Rheumatic Drugs in Subjects With Active Rheumatoid Arthritis
Non-randomizedParallel-groupOpen-labelTreatment
Summary
This is a Phase III, open-label study of a total of approximately 560 subjects with active rheumatoid arthritis (RA) who have had an inadequate response to one or more disease-modifying anti-rheumatic drugs (DMARDs). Enrollment in the study was conducted in two stages. In Stage I of the study, approximately 400 subjects receiving non-biological DMARDs (with the exception of methotrexate \[MTX\] monotherapy or MTX and leflunomide combination therapy) were enrolled. In Stage II of the study, approximately 160 subjects receiving a Federal Drug Administration-approved biological DMARD at the time of screening were enrolled.
Timeline
- Start
- 2007-01
- Primary completion
- 2011-05
- Completion
- 2013-02
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Rituximab | Monoclonal antibody | 500 mg | Intravenous |
| Subject | Rituximab | Monoclonal antibody | 1000 mg | Intravenous |
| Background | Methylprednisolone | Other / unclassified | 100 mg | Intravenous |
| Background | Prednisone | Other / unclassified | 10 mg | Oral |