drugset / Trial / NCT01722526

Tolerability and Safety Study of Recombinant Human Acid Sphingomyelinase in Acid Sphingomyelinase Deficiency Patients

NCT01722526 ↗

Phase 1 Completed 5 enrolled Genzyme, a Sanofi Company
NaSingle-groupOpen-labelTreatment

Summary

To evaluate the safety, tolerability, pharmacokinetic, and pharmacodynamic profile of rhASM in adult patients with Acid Sphingomyelinase Deficiency (ASMD) following repeated-dose administration.

Timeline

Start
2013-03
Primary completion
2014-01
Completion
2014-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Olipudase alfa Protein / enzyme biologic 3 mg/kg Intravenous