drugset / Trial / NCT03038399

Long-term Extension Study to Assess Vamorolone in Boys With Duchenne Muscular Dystrophy (DMD)

NCT03038399

Non-randomizedParallel-groupOpen-labelTreatment

Summary

This long-term extension study is an open-label, multiple-dose study to evaluate the long-term safety, tolerability, efficacy and PD of vamorolone administered once daily by liquid oral suspension over a Treatment Period of 24 months to young boys with DMD who participated in the VBP15-002 Phase IIa and VBP15-003 Phase IIa extension core studies.

Timeline

Start
2017-02-02
Primary completion
2020-04-30
Completion
2020-04-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Vamorolone Small molecule 0.25 mg/kg Oral
Subject Vamorolone Small molecule 0.75 mg/kg Oral
Subject Vamorolone Small molecule 2 mg/kg Oral
Subject Vamorolone Small molecule 6 mg/kg Oral