drugset / Trial / NCT02055157

A Phase 2 Study of BMN 111 to Evaluate Safety, Tolerability, and Efficacy in Children With Achondroplasia

NCT02055157

Phase 2 Completed 35 enrolled BioMarin Pharmaceutical
Non-randomizedSequentialOpen-labelTreatment

Summary

This is a Phase 2, open-label, sequential cohort dose-escalation study of BMN 111 in children with achondroplasia. The primary objective is to assess the safety and tolerability of daily BMN 111 administered to children with achondroplasia.

Timeline

Start
2014-01-13
Primary completion
2017-10-02
Completion
2017-10-02

Drugs

EvaluationDrugModalityDoseRoute
Subject Vosoritide Peptide 2.5 ug/kg Subcutaneous
Subject Vosoritide Peptide 7.5 ug/kg Subcutaneous
Subject Vosoritide Peptide 15 ug/kg Subcutaneous
Subject Vosoritide Peptide 30 ug/kg Subcutaneous

Indications