drugset / Trial / NCT00426218

Safety, Efficacy and Pharmacokinetics of Subcutaneous ACZ885 in Patients With Systemic Juvenile Idiopathic Arthritis (SJIA)

NCT00426218

Phase 1/2 Completed 26 enrolled Novartis
Non-randomizedParallel-groupOpen-labelTreatment

Summary

This study is a multi-center, open label, repeated dose, range finding study to evaluate the safety, tolerability, immunogenicity, pharmacokinetics and efficacy of ACZ885, a fully human anti-interleukin-1B (anti-IL-1B) monoclonal antibody, given subcutaneously in pediatric subjects with active SJIA.

Timeline

Start
2006-12
Primary completion
2010-03
Completion

Drugs

EvaluationDrugModalityDoseRoute
Subject Canakinumab Monoclonal antibody Subcutaneous