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Recruiting NCT07517250

NCT07517250 A Study on the Use of Canakinumab Among Familial Mediterranean Fever and Still's Disease Patients

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Clinical Trial Summary
NCT ID NCT07517250
Status Recruiting
Phase
Sponsor Novartis Pharmaceuticals
Condition Familial Mediterranean Fever
Study Type OBSERVATIONAL
Enrollment 160 participants
Start Date 2026-03-15
Primary Completion 2026-12-03

Eligibility & Interventions

Sex All sexes
Min Age 1 Year
Max Age N/A
Study Type OBSERVATIONAL

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 160 participants in total. It began in 2026-03-15 with a primary completion date of 2026-12-03.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

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.

Eligibility Criteria

Inclusion criteria: * 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 criteria: • Patients Aged \<2 Years (24 Months) at Index Date.

Contact & Investigator

Central Contact

Novartis Pharmaceuticals

✉ novartis.email@novartis.com

📞 +41613241111

Principal Investigator

Novartis Pharmaceuticals

STUDY DIRECTOR

Novartis Pharmaceuticals

Frequently Asked Questions

Who can join the NCT07517250 clinical trial?

This trial is open to participants of all sexes, aged 1 Year or older, studying Familial Mediterranean Fever. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07517250 currently recruiting?

Yes, NCT07517250 is actively recruiting participants. Contact the research team at novartis.email@novartis.com for enrollment information.

Where is the NCT07517250 trial being conducted?

This trial is being conducted at Basel, Switzerland.

Who is sponsoring the NCT07517250 clinical trial?

NCT07517250 is sponsored by Novartis Pharmaceuticals. The principal investigator is Novartis Pharmaceuticals at Novartis Pharmaceuticals. The trial plans to enroll 160 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology