drugset / Trial / NCT01463059
Efficacy and Safety of Olokizumab With Rheumatoid Arthritis With Previously Failed to Anti-tumor Necrosis Factor (Anti-TNF) Therapy
RandomizedParallel-groupQuadruple-blindTreatment
Summary
The primary objective of this study is to evaluate the efficacy and safety of CDP6038 administered subcutaneous (sc) at various doses compared to placebo.
Timeline
- Start
- 2011-10
- Primary completion
- 2013-02
- Completion
- 2013-02
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Olokizumab | Monoclonal antibody | 60 mg | Subcutaneous |
| Subject | Olokizumab | Monoclonal antibody | 120 mg | Subcutaneous |
| Subject | Olokizumab | Monoclonal antibody | 240 mg | Subcutaneous |