drugset / Trial / NCT01050998
A Study to Evaluate the Efficacy and Safety of CAM-3001 (Drug) in Subjects With Rheumatoid Arthritis
RandomizedParallel-groupDouble-blindTreatment
Summary
The primary objectives of this study is to assess the safety, tolerability and efficacy of multiple doses of the mavrilimumab (CAM-3001) administered subcutaneously in subjects with moderately active Rheumatoid Arthritis (RA).
Timeline
- Start
- 2010-01-05
- Primary completion
- 2011-06-09
- Completion
- 2012-07-27
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Mavrilimumab | Monoclonal antibody | 10 mg | Subcutaneous |
| Subject | Mavrilimumab | Monoclonal antibody | 30 mg | Subcutaneous |
| Subject | Mavrilimumab | Monoclonal antibody | 50 mg | Subcutaneous |
| Subject | Mavrilimumab | Monoclonal antibody | 100 mg | Subcutaneous |