drugset / Trial / NCT00744042

Safety and Efficacy Study of Asfotase Alfa in Severely Affected Infants With Hypophosphatasia (HPP)

NCT00744042 ↗

Phase 1/2 Completed 11 enrolled Alexion Pharmaceuticals, Inc.
NaSingle-groupOpen-labelTreatment

Summary

This clinical trial studies the safety and efficacy of asfotase alfa in infants and young children with infantile onset HPP.

Timeline

Start
2008-09
Primary completion
2010-05
Completion
2010-05

Outcome

Met primary endpoint

registry MEDIAN Asfotase Alfa: 2.00 (0.00 to 2.33) Units on a scale NCT00744042 ↗

registry Asfotase Alfa; p = 0.0039; Wilcoxon signed-rank test NCT00744042 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject asfotase alfa Protein / enzyme biologic 1 mg/kg Subcutaneous
Subject asfotase alfa Protein / enzyme biologic 2 mg/kg Subcutaneous