An Open-label, Multi-arm, Non-comparative Safety and Tolerability Study of Canakinumab (ACZ885) in Patients With Active Systemic Juvenile Idiopathic Arthritis (SJIA)

PHASE3WithdrawnINTERVENTIONAL
0
Timeline

Start Date

January 31, 2013

Primary Completion Date

January 31, 2015

Study Completion Date

January 31, 2015

Conditions
Systemic Juvenile Idiopathic Arthritis
Interventions
DRUG

ACZ885

DRUG

Canakinumab

DRUG

Canakinumab

"Patients rolling over into this study from CACZ885G2301E1 (Cohort 1) will continue on their established canakinumab dose of either 4 mg/kg SC given every 4 weeks or 2mg/kg SC given every 4 weeks, until eligible for dose reduction.~Canakinumab-naïve patients"

DRUG

Canakinumab

Patients rolling over into this study from CACZ885G2301E1(Cohort 2) will receive a standard canakinumab dose of 4mg/kg SC given every 4 weeks, until eligible for dose reduction

Sponsors
All Listed Sponsors
collaborator

PRINTO / PRCSG

UNKNOWN

lead

Novartis Pharmaceuticals

INDUSTRY