Resources for HCPs to give to patients

Indications1

Periodic fever syndromes
ILARIS® (canakinumab) is indicated for the treatment of the following autoinflammatory periodic fever syndromes in adults, adolescents and children aged 2 years and older:

  • Cryopyrin-associated periodic syndromes (CAPS), including:

    • Muckle-Wells syndrome (MWS)

    • Neonatal-onset multisystem inflammatory disease (NOMID)/chronic infantile neurological, cutaneous, articular syndrome (CINCA)

    • Severe forms of familial cold autoinflammatory syndrome (FCAS)/familial cold urticaria (FCU) presenting with signs and symptoms beyond cold-induced urticarial skin rash

  • Tumour necrosis factor receptor associated periodic syndrome (TRAPS)

  • Hyperimmunoglobulin D syndrome (HIDS)/mevalonate kinase deficiency (MKD)

  • Familial Mediterranean Fever (FMF)

    • ILARIS should be given in combination with colchicine, if appropriate

Still’s disease
ILARIS is indicated in patients who have responded inadequately to previous therapy with non-steroidal anti-inflammatory drugs (NSAIDs) and systemic corticosteroids, for the treatment of active Still’s disease, including:

  • Adult-onset Still’s disease (AOSD) 

  • Systemic juvenile idiopathic arthritis (SJIA) in patients aged 2 years and older 

  • ILARIS can be given as monotherapy or in combination with methotrexate 

Gouty arthritis
ILARIS is indicated for the symptomatic treatment of adult patients with frequent gouty arthritis attacks (at least 3 attacks in the previous 12 months) in whom NSAIDs and colchicine are contraindicated, are not tolerated, or do not provide an adequate response, and in whom repeated courses of corticosteroids are not appropriate.


Resources for HCPs to share with patients who have been prescribed ILARIS to treat their periodic fever syndrome or Still’s disease.

Please do not show this webpage to patients, or direct them to this webpage. Instead, please direct patients to the patient portal.


Patient guide to ILARIS treatment

A booklet about what ILARIS is, how it works, and things to know before starting treatment.

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Image preview. ILARIS® (canakinumab) patient guide - English.

Patient guide – English

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Image preview. ILARIS® (canakinumab) patient guide - Arabic.

Patient guide – Arabic

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Image preview. ILARIS® (canakinumab) patient guide - Turkish.

Patient guide – Turkish

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Image preview. ILARIS® (canakinumab) patient guide to using the ILARIS Sensoready® pen.

Patient guide to using the ILARIS Sensoready® pen

A booklet containing important information to know before starting treatment with the Ilaris Sensoready® pen, as well as step-by-step instructions for using the device correctly.


AOSD, adult-onset Still's disease; CAPS, cryopyrin-associated periodic syndromes; CINCA, chronic infantile neurological, cutaneous, articular syndrome; FCAS,  familial cold autoinflammatory syndrome; FCU, familial cold urticaria;  FMF, familial Mediterranean fever; HCP, healthcare professional; HIDS, hyperimmunoglobulin D syndrome; MKD, mevalonate kinase deficiency; MWS,  Muckle-Wells syndrome; NOMID, neonatal-onset multisystem inflammatory disease; NSAID, non-steroidal anti-inflammatory drug; SJIA, systemic juvenile idiopathic arthritis; TRAPS, tumour necrosis factor receptor-associated periodic syndrome.

Reference

  1. ILARIS® (canakinumab) Summary of Product Characteristics.

UK |  September 2025 | FA-11307389-1

Adverse events should be reported. Reporting forms and information can be found at www.mhra.gov.uk/yellowcard. Adverse events should also be reported to Novartis online through the pharmacovigilance intake (PVI) tool at www.novartis.com/report, or alternatively email [email protected] or call 01276 698370.