drugset / Trial / NCT01844518

Pharmacokinetics, Efficacy and Safety of Abatacept Administered Subcutaneously (SC) in Children and Adolescents With Active Polyarticular Juvenile Idiopathic Arthritis (pJIA) and Inadequate Response (IR) to Biologic or Non Biologic Disease Modifying Anti-rheumatic Drugs (DMARDs)

NCT01844518

Phase 3 Completed 219 enrolled Bristol-Myers Squibb
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to estimate Abatacept steady-state trough concentration (Cmin) at Day 113 in children and adolescents with pJIA

Timeline

Start
2013-08-30
Primary completion
2015-03-12
Completion
2023-02-01

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Abatacept Other / unclassified 50 mg Subcutaneous
Subject Abatacept Other / unclassified 87.5 mg Subcutaneous
Subject Abatacept Other / unclassified 125 mg Subcutaneous