drugset / Trial / NCT01202760
A Rheumatoid Arthritis Study in Participants
RandomizedParallel-groupTriple-blindTreatment
Summary
The primary purpose of this study is to help answer if LY2127399 is safe and effective in the treatment of rheumatoid arthritis with or without background disease-modifying anti-rheumatic drug (DMARD) therapy. This study is comprised of 2 periods: Period 1 - 24-week blinded treatment Period 2 - 48-week post-treatment follow-up
Timeline
- Start
- 2011-01
- Primary completion
- 2012-12
- Completion
- 2013-07
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Tabalumab | Monoclonal antibody | 90 mg | Subcutaneous |
| Subject | Tabalumab | Monoclonal antibody | 120 mg | Subcutaneous |