Facioscapulohumeral Muscular Dystrophy research hub
3 indexed studies · 2 currently recruiting
- active not recruiting
Clinical Trial Readiness to Solve Barriers to Drug Development in FSHD
This study aims to improve how we test new treatments for Facioscapulohumeral Muscular Dystrophy (FSHD). Researchers are developing new ways to measure the disease and planning how to choose the right people for future drug trials, helping get effective medicines to patients sooner.
United States · France · Germany - recruitingPHASE3
A Study to Evaluate Del-brax (Also Referred to as AOC 1020) in Participants With FSHD
This study is testing a new medicine called del-brax for people with Facioscapulohumeral Muscular Dystrophy (FSHD). Researchers want to see if it's safe and effective in improving or slowing down the condition. It involves receiving treatment every six weeks for over a year.
United States · Canada · Denmark - recruiting
The United Kingdom Facioscapulohumeral Muscular Dystrophy Patient Registry
This study is gathering information about people in the UK who have Facioscapulohumeral Muscular Dystrophy (FSHD). It helps researchers understand the condition better and find people who might want to join future medical trials for new treatments.
United Kingdom