A Study on the Use of Canakinumab Among Familial Mediterranean Fever and Still's Disease Patients

Sponsor
Novartis Pharmaceuticals
Study ID
NCT07517250
Status
Recruiting
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Conditions

Eligibility Criteria

Sex
ALL
Age
1 Year - N/A
Healthy Volunteers
Not accepted

Study Details

This study aims to assess and characterize the treatment patterns, and long-term clinical outcomes and demographic characteristics of patients diagnosed with Familial Mediterranean fever (FMF) and Still's disease (including systemic juvenile idiopathic arthritis \[SJIA\] and adult-onset Still's disease \[AOSD\]) that received canakinumab for at least 6 months.

Key Dates

Start date
Mar 15, 2026
Status verified
Jun 2026
Primary completion
Dec 3, 2026
Completion
Dec 3, 2026

Study Design

Enrollment
160 participants (estimated)

Arms

  • Arm: FMF Cohort
    Patients diagnosed with FMF that received canakinumab for at least 6 months.
  • Arm: SJIA Cohort
    Patients diagnosed with SJIA that received canakinumab for at least 6 months.
  • Arm: AOSD Cohort
    Patients diagnosed with AOSD that received canakinumab for at least 6 months.

Primary Outcome Measure

Percentage of Patients With Clinically Inactive Disease Under Treatment With Canakinumab Received in First or Second or More Lines of Treatment With Biologic Agents [ Time Frame: Up to 3 years ]

Central Contacts