RecruitingNCT07598422
A Study to Assess the Effectiveness and Safety of Canakinumab in Clinical Use in Patients With Schnitzler's Syndrome
Specified Use-Results Study of ILARIS Solution for S.C. Injection (Schnitzler's Syndrome)
Sponsor
Novartis Pharmaceuticals
Enrollment
10 participants
Start Date
May 13, 2026
Study Type
OBSERVATIONAL
Conditions
Summary
The aim of this study is to assess the effectiveness and safety of Ilaris (canakinumab) in clinical use in patients with Schnitzler's syndrome.
Eligibility
Min Age: 0 Years
Inclusion Criteria2
- \. Patients diagnosed with Schnitzler's syndrome using canakinumab for the first time for the indication of Schnitzler's syndrome as described in the package insert.
- Patients starting treatment with canakinumab before conclusion of the contract for this study will also be included in the study so that all patients diagnosed with Schnitzler's syndrome who received canakinumab will be registered in this study.
Exclusion Criteria4
- Patients previously treated with canakinumab in Study IACT21071.
- All patients treated with canakinumab for the following indications:
- Indications: Cryopyrin-associated periodic syndromes (familial cold autoinflammatory syndrome, Muckle-Wells syndrome, neonatal onset multisystem inflammatory disease), hyper immunoglobulin D (IgD) syndrome (mevalonate kinase deficiency), tumor necrosis factor (TNF) receptor-associated periodic syndrome, familial mediterranean fever, systemic juvenile idiopathic arthritis, adult-onset Still's disease.
- Patients receiving canakinumab for off-label use under the Clinical Trials Act or GCP (e.g., patient-proposed healthcare services, investigator-initiated clinical trial).
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Locations(2)
View Full Details on ClinicalTrials.gov
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NCT07598422