Researchers build tools to speed up search for FSHD treatments
NCT ID NCT04038138
Summary
This study aims to create better tools for future clinical trials in facioscapulohumeral muscular dystrophy (FSHD). Researchers will follow 100 adults with FSHD for two years to test new ways of measuring muscle function and disease progression. The goal is to provide researchers with reliable methods to test whether new drugs are working in future treatment trials.
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Contacts and locations
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Locations
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CHRU de Lille
Lille, Hauts-de-France, 59000, France
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CHU de Nice
Nice, Provence-Alpes-Côte d'Azur Region, 06000, France
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Myology institute Association
Paris, Île-de-France Region, 75013, France
Conditions
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