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ILARIS®—Complete Response

Complete Response From Cryopyrin-Associated Periodic Syndromes (CAPS) Within the First Dosing Period (8 Weeks)*

  • 97% of CAPS patients treated with ILARIS® (canakinumab) achieved complete response within 8 weeks1,2

*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

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.
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Register for ILARIS Updates

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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