Following people with Familial Mediterranean Fever or Still's Disease who take canakinumab
Observes how people with these conditions fare after at least 6 months on canakinumab.
Plain-language title generated from the registry record
Registry title: A Study on the Use of Canakinumab Among Familial Mediterranean Fever and Still's Disease Patients
Key facts
- Where
- Basel, SwitzerlandSee the site
Where in Switzerland
- NovartisBasel, SwitzerlandTaking people
Questions to ask the study team
- How often do I need to come in, and for how long each time?
- Are travel costs paid?
- Can I keep my own doctor?
- What happens if I want to stop?
Trial details
- Who runs it
- Novartis Pharmaceuticals
- Trial code
- NCT07517250
- Record updated
- 9 June 2026
- Original description
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.Read full original descriptionShow less
Non-interventional Study on the Use of ILARIS® (Canakinumab) Among Familial Mediterranean Fever and Still's Disease Patients Across Europe and Israel
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.
Inclusion: Pediatric or adult patients who were prescribed canakinumab before October 2021 and received canakinumab for at least 6 months for the treatment of FMF or Still's disease (including SJIA or AOSD); Have data on clinical characteristics and treatments available for at least 3 years following the initiation of canakinumab treatment.
Exclusion: Patients Aged <2 Years (24 Months) at Index Date.