drugset / Trial / NCT01371825
Safety, Tolerability, Efficacy, Pharmacokinetics, and Pharmacodynamics of Sebelipase Alfa in Children With Growth Failure Due to Lysosomal Acid Lipase Deficiency
NaSingle-groupOpen-labelTreatment
Summary
This was an open-label, repeat-dose, intra-participant dose-escalation study of SBC-102 (sebelipase alfa) in children with growth failure due to lysosomal acid lipase (LAL) Deficiency. Eligible participants received once-weekly (qw) infusions of sebelipase alfa for up to 5 years.
Timeline
- Start
- 2011-05-04
- Primary completion
- 2018-01-03
- Completion
- 2018-01-03
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | sebelipase alfa | Protein / enzyme biologic | 1 mg/kg | Intravenous |
| Subject | sebelipase alfa | Protein / enzyme biologic | 3 mg/kg | Intravenous |
| Subject | sebelipase alfa | Protein / enzyme biologic | 5 mg/kg | Intravenous |