drugset / Trial / NCT05166109

A Study to Assess Vamorolone in Becker Muscular Dystrophy (BMD)

NCT05166109

RandomizedParallel-groupQuadruple-blindTreatment

Summary

This Phase II pilot study is a randomized, double-blind, placebo-controlled study to evaluate the safety, tolerability, PK, PD, and exploratory clinical efficacy of vamorolone 500mg (250mg for body weight \<50 kg) daily administered orally compared to placebo over a treatment period of 24 weeks in males with BMD. Funding Source - FDA OOPD

Timeline

Start
2022-07-07
Primary completion
2025-08-18
Completion
2025-08-18

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Vamorolone Small molecule 250 mg Oral
Subject Vamorolone Small molecule 500 mg Oral