drugset / Trial / NCT01757184

Acid Lipase Replacement Investigating Safety and Efficacy (ARISE) in Participants With Lysosomal Acid Lipase Deficiency

NCT01757184 ↗

Phase 3 Completed 66 enrolled Alexion Pharmaceuticals, Inc.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This Phase 3 study evaluated the efficacy and safety of 1 milligram/kilogram (mg/kg) intravenous (IV) infusions of SBC-102 (sebelipase alfa) administered every other week (qow) in participants with late onset lysosomal acid lipase deficiency (LAL-D) (cholesteryl ester storage disease \[CESD\]). Late-onset LAL-D is an underappreciated cause of cirrhosis, liver failure and dyslipidemia. There is currently no standard treatment for LAL-D other than supportive care. Enzyme replacement therapy may be a potential new treatment option for LAL-D participants.

Timeline

Start
2013-01-22
Primary completion
2014-05-30
Completion
2018-12-11

Outcome

Met primary endpoint

registry NUMBER Double-blind Sebelipase Alfa: 31 percentage of participants NUMBER Double-blind Placebo: 7 percentage of participants NCT01757184 ↗

registry analysis (superiority test); Double-blind Sebelipase Alfa vs Double-blind Placebo; p = 0.0271; Fisher Exact NCT01757184 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject sebelipase alfa Protein / enzyme biologic 1 mg/kg Intravenous