drugset / Trial / NCT01609062

Safety and Exercise Study of Two Doses of BMN 110 for Morquio A Syndrome

NCT01609062 ↗

Phase 2 Terminated 25 enrolled BioMarin Pharmaceutical
RandomizedParallel-groupTriple-blindTreatment

Summary

The primary objective of this study was to evaluate the safety of a 2.0 mg/kg/week and a 4.0 mg/kg/week of BMN 110 in patients with Morquio A syndrome for up to 196 weeks. Secondary objectives were to investigate the effect of the two doses on exercise capacity for up to 196 weeks. In addition, the pharmacokinetic (PK) parameters of both doses of BMN 110 was assessed.

Timeline

Start
2012-04
Primary completion
2014-11
Completion
2014-11

Drugs

EvaluationDrugModalityDoseRoute
Subject elosulfase alfa Protein / enzyme biologic 2 mg/kg Intravenous
Subject elosulfase alfa Protein / enzyme biologic 4 mg/kg Intravenous