Start Date
January 31, 2013
Primary Completion Date
January 31, 2015
Study Completion Date
January 31, 2015
ACZ885
Canakinumab
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"
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
Lead Sponsor
PRINTO / PRCSG
UNKNOWN
Novartis Pharmaceuticals
INDUSTRY