drugset / Trial / NCT01697319

Efficacy and Safety Study of BMN 110 for Morquio A Syndrome Patients Who Have Limited Ambulation

NCT01697319 ↗

Phase 2 Terminated 16 enrolled BioMarin Pharmaceutical
NaSingle-groupOpen-labelTreatment

Summary

The primary objective of this study is to evaluate the effect of 2.0 mg/kg/week BMN 110 in a patient population that has limited ambulation, in a period of up to 144 weeks.

Timeline

Start
2012-08
Primary completion
2014-10
Completion
2014-10

Drugs

EvaluationDrugModalityDoseRoute
Subject elosulfase alfa Protein / enzyme biologic 2 mg/kg Intravenous