Primary objective of the study was to evaluate the safety and efficacy of canakinumab on the clinical and inflammatory findings of Behced Disease patients with neurologic and vascular involvement.
Age range
18 Years – 60 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Number of Participants With Attacks
Timeframe: 30 days
Modified Expanded Disability Status Scale (EDSS)
Timeframe: 30 days
Neuro-Behçet's Disability Score (NBDS)
Timeframe: 30 days
Modified Ranking Score (mRS)
Timeframe: 30 days
Ataxia
Timeframe: 30 days
Physical Examination Scores Indicating Change in Muscle Strength
Timeframe: 30 days
C-reactive Protein (CRP) Values
Timeframe: 30 days
Erythrocyte Sedimentation Rate (ESR)
Timeframe: 30 days
SAA (Serum Amyloid A)
Timeframe: 30 days
Hemoptysis
Timeframe: 30 days
Visual Analogue Scores (VAS) for Headache
Timeframe: 30 days
Visual Analogue Scores (VAS) for Stomachache
Timeframe: 30 days
Visual Analogue Scores (VAS) for Extremity Assessments
Timeframe: 30 days
Visual Analogue Scores (VAS) for Patients' General Assessments
Timeframe: 30 days
Physician's Global Assessment
Timeframe: 30 days
Steroid Dose Regimen
Timeframe: 30 days
BDCAF (Behçet's Disease Current Activity Form)
Timeframe: 30 days
Extremity (Localized) Pain Assessment (VAS)
Timeframe: 30 days