drugset / Trial / NCT06713135

A Study on Safety and Effectiveness of Long-term Treatment With Vamorolone in Boys With Duchenne Muscular Dystrophy

NCT06713135

Phase 4 Active not recruiting 80 enrolled Santhera Pharmaceuticals
NaSingle-groupOpen-labelTreatment

Summary

This study aims to assess safety and effectivness of long-term treatment with vamorolone in boys with Duchenne Muscular Dystrophy (DMD) who have completed prior studies with vamorolone.

Timeline

Start
2024-11-10
Primary completion
2028-09
Completion
2028-09

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Vamorolone Small molecule 2 mg/kg Oral
Subject Vamorolone Small molecule 6 mg/kg Oral
Subject Vamorolone Small molecule 80 mg Oral
Subject Vamorolone Small molecule 240 mg Oral