drugset / Trial / NCT02961218
Study of Efficacy, Safety and Tolerability of ACZ885 (Canakinumab) in Pediatric and Young Adult Patients With Sickle Cell Anemia
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Canakinumab | Monoclonal antibody | 4 mg/kg | Subcutaneous |
| Subject | Canakinumab | Monoclonal antibody | 300 mg | Subcutaneous |