drugset / Trial / NCT02296424
ß-SPECIFIC 4 Patients: Study of Pediatric EffiCacy and Safety wIth FIrst-line Use of Canakinumab
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Canakinumab | Monoclonal antibody | 1 mg/kg | Subcutaneous |
| Subject | Canakinumab | Monoclonal antibody | 2 mg/kg | Subcutaneous |
| Subject | Canakinumab | Monoclonal antibody | 4 mg/kg | Subcutaneous |