drugset / Trial / NCT02961218

Study of Efficacy, Safety and Tolerability of ACZ885 (Canakinumab) in Pediatric and Young Adult Patients With Sickle Cell Anemia

NCT02961218

Phase 2 Completed 49 enrolled Novartis Pharmaceuticals
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The study assesses the efficacy, safety and tolerability of ACZ885 (canakinumab) in pediatric and young adult patients with sickle cell anemia (SCA).

Timeline

Start
2017-04-05
Primary completion
2019-06-27
Completion
2020-04-27

Drugs

EvaluationDrugModalityDoseRoute
Subject Canakinumab Monoclonal antibody 4 mg/kg Subcutaneous
Subject Canakinumab Monoclonal antibody 300 mg Subcutaneous

Indications