drugset / Trial / NCT01435772

Extension Study for Patients Who Have Participated in a BMN 701 Study

NCT01435772 ↗

Phase 2 Terminated 21 enrolled BioMarin Pharmaceutical
Non-randomizedParallel-groupOpen-labelTreatment

Summary

This is a Phase 2 open-label, multiple dose study of BMN 701 administered by IV infusion every 2 weeks (qow) to patients with late-onset Pompe disease.

Timeline

Start
2011-08-15
Primary completion
2016-09-09
Completion
2016-09-09

Outcome

Outcome not reported

Stopped: “The study was terminated because BioMarin decided to end the overall development program based on competing corporate priorities.”

Drugs

EvaluationDrugModalityDoseRoute
Subject REVEGLUCOSIDASE ALFA Protein / enzyme biologic 5 mg/kg Intravenous
Subject REVEGLUCOSIDASE ALFA Protein / enzyme biologic 10 mg/kg Intravenous
Subject REVEGLUCOSIDASE ALFA Protein / enzyme biologic 20 mg/kg Intravenous