drugset / Trial / NCT00705367

Phase I Study in China - Tolerability of a Single Dose of Abatacept 30 mg/kg

NCT00705367

Phase 1 Completed 13 enrolled Bristol-Myers Squibb
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of this study is to determine whether abatacept at a dose 30 mg/kg via intravenous infusion is safe and well tolerated in the treatment of lupus nephritis in mainland Chinese subjects with systemic lupus erythematosus (SLE)

Timeline

Start
2008-08
Primary completion
2009-01
Completion
2011-07

Drugs

EvaluationDrugModalityDoseRoute
Subject Abatacept Other / unclassified 10 mg/kg Intravenous
Subject Abatacept Other / unclassified 30 mg/kg Intravenous

Indications