Clinical Trials for Facioscapulohumeral Muscular Dystrophy

Find clinical trials for facioscapulohumeral muscular dystrophy. Discover research opportunities and treatment options in your area.

8 Active Trials Found

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A First-in-human Study of EPI-321 in Facioscapulohumeral Muscular Dystrophy

NCT ID: NCT06907875

This clinical trial is researching a new treatment called EPI-321 for adults with facioscapulohumeral muscular dystrophy (FSHD), a condition that affects muscle strength. The main goal of the study...

Recruiting

Phase: PHASE1 Type: interventional Locations: Atlanta, Georgia, United States, Auckland, , New Zealand

Personalized Training for People With Rare Neuromuscular Disorders

NCT ID: NCT06708468

This clinical trial is looking at how personalized exercise programs can help improve balance and physical function in adults with certain rare neuromuscular disorders, such as Charcot-Marie-Tooth ...

Recruiting

Phase: NA Type: interventional Locations: Bergen, , Norway, Tromsø, , Norway +10 more

Clinical Trial Readiness to Solve Barriers to Drug Development in FSHD

NCT ID: NCT03458832

This clinical trial is focused on improving drug development for a condition called facioscapulohumeral muscular dystrophy (FSHD), which affects muscle strength and movement. Researchers have recen...

Recruiting

Type: observational Locations: Kansas City, Kansas, United States, Seattle, Washington, United States +13 more

ADVANCED FSHD-COM: New Clinical Outcome Measures to Evaluate Non-ambulant FSHD Patients, a Pilot Study

NCT ID: NCT05453461

The ADVANCED FSHD-COM clinical trial is studying ways to measure how facioscapulohumeral muscular dystrophy (FSHD) affects patients who cannot walk. FSHD is a muscle disease that leads to weakness,...

Recruiting

Phase: NA Type: interventional Locations: Nice, Alpes Maritimes, France, Nice, Alpes Maritimes, France

Myotonic Dystrophy and Facioscapulohumeral Muscular Dystrophy Registry

NCT ID: NCT00082108

The Myotonic Dystrophy and Facioscapulohumeral Muscular Dystrophy Registry is a research project aimed at understanding two inherited muscle disorders: myotonic dystrophy (DM) and facioscapulohumer...

Recruiting

Type: observational Locations: Rochester, New York, United States

The United Kingdom Facioscapulohumeral Muscular Dystrophy Patient Registry

NCT ID: NCT04001582

The United Kingdom Facioscapulohumeral Muscular Dystrophy (FSHD) Patient Registry is a study aimed at better understanding FSHD, which is a type of muscle disease that affects how the muscles work....

Recruiting

Type: observational Locations: Newcastle Upon Tyne, , United Kingdom

Unraveling Metabolic Involvement in Facioscapulohumeral Dystrophy Through Metabolomics

NCT ID: NCT06086548

This clinical trial is studying facioscapulohumeral muscular dystrophy (FSHD), a common inherited muscle disease that affects how muscles function. Researchers want to understand more about the met...

Not yet recruiting

Type: observational

Biomarker Development for Muscular Dystrophies

NCT ID: NCT05019625

This clinical trial focuses on developing new ways to understand and measure muscular dystrophies, such as Myotonic Dystrophy and Duchenne Muscular Dystrophy, without needing painful muscle biopsie...

Recruiting

Type: observational Locations: Pittsburgh, Pennsylvania, United States, Boston, Massachusetts, United States +3 more

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