drugset / Trial / NCT01202773
A Study in Participants With Rheumatoid Arthritis
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 in participants with an inadequate response to one or more tumor necrosis factor-alpha (TNF-α) inhibitors. 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
- 2013-03
- Completion
- 2014-01
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Tabalumab | Monoclonal antibody | 90 mg | Subcutaneous |
| Subject | Tabalumab | Monoclonal antibody | 120 mg | Subcutaneous |