drugset / Trial / NCT00443651

A Study of the Safety of Rituximab in Combination With Other Anti-Rheumatic Drugs in Subjects With Active Rheumatoid Arthritis

NCT00443651 ↗

Phase 3 Completed 578 enrolled Genentech, Inc. Biogen · collab
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

EvaluationDrugModalityDoseRoute
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

Indications