This study will assess the safety, tolerability and efficacy of canakinumab treatment in Canadian patient diagnosed with cryopyrin-associated periodic syndrome over a period of 18 months.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
4
Alberta Children's Hospital, Department of Pediatrics
Calgary, Canada
Queen Elizabeth II Hospital
Halifax, Canada
Safety & tolerability of canakinumab by measuring the maintenance of response over time using the Investigators Clinical Assessment of Disease Activity scale and the evaluation of serum inflammation markers CRP (C-Reactive Protein), SAA (Serum Amyloid A.
Time frame: 18 months
Change in long term maintenance of Health-Related Quality of Life and productivity measured from baseline to end of study.
Time frame: Baseline, 18 months
Treatment adherence with canakinumab for the duration of the study.
Time frame: 18 months
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