drugset / Trial / NCT02296424

ß-SPECIFIC 4 Patients: Study of Pediatric EffiCacy and Safety wIth FIrst-line Use of Canakinumab

NCT02296424

Phase 3 Completed 182 enrolled Novartis Pharmaceuticals
Non-randomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study was to evaluate the efficacy observed with canakinumab dose reduction in a subgroup of patients in the extension study CACZ885G2301E1.

Timeline

Start
2014-11-17
Primary completion
2016-10-14
Completion
2017-09-25

Drugs

EvaluationDrugModalityDoseRoute
Subject Canakinumab Monoclonal antibody 1 mg/kg Subcutaneous
Subject Canakinumab Monoclonal antibody 2 mg/kg Subcutaneous
Subject Canakinumab Monoclonal antibody 4 mg/kg Subcutaneous