drugset / Trial / NCT00533897

Phase IIIB Subcutaneous Missed Dose Study

NCT00533897

Phase 3 Completed 270 enrolled Bristol-Myers Squibb
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

EvaluationDrugModalityDoseRoute
Subject Abatacept Other / unclassified 125 mg Subcutaneous

Indications