Scroll over the words in bold for brief definitions.

ILARIS®—Sustained Response

Sustained, Long-Lasting Response From Cryopyrin-Associated Periodic Syndromes (CAPS)*

  • Sustained, complete clinical improvement was demonstrated in patients receiving ILARIS® (canakinumab) versus placebo over the 24-week, double-blind withdrawal period of the clinical trial (3 doses)1,2
  • A disease flare was defined as a CRP and/or SAA values >30 mg/L and either a score of mild or worse for disease activity or a score of minimal or worse for disease activity and skin disease1,2
Images of urticaria, conjunctivitis & arthralgia

Sustained Improvement in Inflammation Markers

  • Serum amyloid A (SAA) and C-reactive protein (CRP) levels in patients receiving ILARIS® were normalized and sustained1,2
Images of urticaria, conjunctivitis & arthralgia

*The pivotal study included an 8-week, open-label period (Part 1) and a 24-week, randomized, double-blind, placebo-controlled withdrawal period (Part 2).1,2
Using last observation carried forward (LOCF) in intent-to-treat (ITT) population.

ILARIS® Patient Support Program

The ILARIS® Patient Support Program provides patients with information and tools to assist in managing their treatment with ILARIS® and helps to identify resources that can assist with payment for their medication.
Learn More

Register for ILARIS Updates

Sign up here for ILARIS® Direct and stay current with news about ILARIS®.

References:

  • 1. Lachmann HJ, Kone-Paut I, Kuemmerle-Deschner JB, et al; for the Canakinumab in CAPS Study Group. Use of canakinumab in the cryopyrin-associated periodic syndrome. N Engl J Med. 2009;360:2416-2425.
  • 2. Ilaris [prescribing information]. East Hanover, NJ: Novartis Pharmaceuticals Corporation; 2009.



isi-Professional www.fda.gov/medwatch full prescribing information