drugset / Trial / NCT01371825

Safety, Tolerability, Efficacy, Pharmacokinetics, and Pharmacodynamics of Sebelipase Alfa in Children With Growth Failure Due to Lysosomal Acid Lipase Deficiency

NCT01371825 ↗

Phase 2/3 Completed 9 enrolled Alexion Pharmaceuticals, Inc.
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

EvaluationDrugModalityDoseRoute
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

Indications