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β-SPECIFIC 4 Patients: Study of Pediatric EffiCacy and Safety wIth FIrst-line Use of Canakinumab An Open-label Canakinumab (ACZ885) Dose Reduction or Dose Interval Prolongation Efficacy and Safety Study in Patients With Systemic Juvenile Idiopathic Arthritis (SJIA)

Trial Profile

β-SPECIFIC 4 Patients: Study of Pediatric EffiCacy and Safety wIth FIrst-line Use of Canakinumab An Open-label Canakinumab (ACZ885) Dose Reduction or Dose Interval Prolongation Efficacy and Safety Study in Patients With Systemic Juvenile Idiopathic Arthritis (SJIA)

Status: Completed
Phase of Trial: Phase III/IV

Latest Information Update: 10 Jul 2019

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At a glance

  • Drugs Canakinumab (Primary) ; Corticosteroids; Methotrexate
  • Indications Juvenile rheumatoid arthritis
  • Focus Therapeutic Use
  • Acronyms Beta-SPECIFIC-4-Patients
  • Sponsors Novartis
  • Most Recent Events

    • 15 Jun 2019 Argentina, Hong Kong, Mexico and Peru were planned locations as per European Clinical Trials Database record.
    • 15 Jun 2019 Results (n=75) evaluating the efficacy and safety, presented at the 20th Annual Congress of the European League Against Rheumatism.
    • 24 Oct 2018 Results presented at the 82nd American College of Rheumatology and the 52nd Association of Rheumatology Health Professionals Annual Scientific Meeting
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