drugset / Trial / NCT01373151
Phase IIB Rheumatoid Arthritis Dose Ranging Study for BMS-945429 in Subjects Who Are Not Responding to Methotrexate
RandomizedParallel-groupQuadruple-blindTreatment
Summary
The purpose of this study is to determine the effective dose of BMS-945429 in subjects with inadequate response to Methotrexate in the treatment of moderate to severe Rheumatoid Arthritis.
Timeline
- Start
- 2011-06
- Primary completion
- 2012-09
- Completion
- 2015-06
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Adalimumab | Monoclonal antibody | 40 mg | Subcutaneous |
| Subject | Clazakizumab | Monoclonal antibody | 25 mg | Subcutaneous |
| Subject | Clazakizumab | Monoclonal antibody | 100 mg | Subcutaneous |
| Subject | Clazakizumab | Monoclonal antibody | 200 mg | Subcutaneous |
| Subject | Methotrexate | Small molecule | 15 mg | Oral |