drugset / Trial / NCT00533897
Phase IIIB Subcutaneous Missed Dose Study
RandomizedParallel-groupDouble-blindTreatment
Summary
The purpose of the study is to determine whether subcutaneous abatacept administered to patients with rheumatoid arthritis is associated with increased immunogenicity or increased safety events upon withdrawal and reintroduction.
Timeline
- Start
- 2007-11
- Primary completion
- 2008-12
- Completion
- 2014-02
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Abatacept | Other / unclassified | 125 mg | Subcutaneous |