Prospective Observational Study to Evaluate Secukinumab Treatment Effectiveness in Pediatric Patients With Active Juvenile Enthesitis-related or Psoriatic Arthritis
- Sponsor
- Novartis Pharmaceuticals
- Study ID
- NCT06431750
- Status
- Not Yet Recruiting
Notify me when recruiting opens
Save your spot on the interest list for this study. We'll keep your details with this study so our team can follow up when recruiting opens.
Add your contact details and location so we can keep your interest tied to this study.
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 6 Years - 18 Years
- Healthy Volunteers
- Not accepted
Interventions
- Secukinumab — OTHERThis is an observational study, there is no treatment allocation.
Study Details
This is a multicenter, non-interventional, cohort study in pediatric patients with active juvenile enthesitis-related or psoriatic arthritis
Key Dates
- Start date
- Apr 30, 2025
- Status verified
- Jan 2025
- Primary completion
- Aug 30, 2028
- Completion
- Aug 30, 2028
Study Design
- Enrollment
- 150 participants (estimated)
Arms
- Arm: Secukinumabpediatric patients with active ERA/jPsA for whom routine treatment with secukinumab according to the approved national label is initiated during 4 to 8 weeks prior to enrollment
Primary Outcome Measure
Drug survival rate [ Time Frame: 24 months ]
Central Contacts
- Novartis Pharmaceuticals+41613241111
- Novartis Pharmaceuticals
Related Studies
- Development of a Therapeutic Endpoint in Pediatric Rheumatologic ConditionsRecruiting · Children's National Research Institute · Washington D.C., District of Columbia
- Study of Oral Upadacitinib and Subcutaneous/Intravenous Tocilizumab to Evaluate Change in Disease Activity, Adverse Events and How Drug Moves Through the Body of Pediatric and Adolescent Participants With Active Systemic Juvenile Idiopathic Arthritis.PHASE3 · Recruiting · AbbVie · Phoenix, Arizona
- Pain in Juvenile ArthritisRecruiting · Washington University School of Medicine · St Louis, Missouri