NCT01689480
- Conditions
- Behavior, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, +8 more
- Locations
-
- CHU de Grenbole Grenoble, France
- CHU de Saint-Etienne Saint-Etienne, France
Clinical trial condition
Muscular Dystrophy, Facioscapulohumeral
Explore clinical trials studying Muscular Dystrophy, Facioscapulohumeral. Study availability and eligibility vary by location and protocol.
14 public trials
5 recruiting studies
Muscular Dystrophy, Facioscapulohumeral trial results
NCT01116570
- Conditions
- Behavior, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, +8 more
- Locations
-
- CHU de Grenoble Grenoble, France
- CHU de Saint-Etienne Saint-Etienne, France
NCT00004685
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Disease Attributes, Genetic Diseases, Inborn, +13 more
- Locations
-
Not specified
Active, Not Recruiting
Phase 2 Open-label Extension Study of AOC 1020 in Participants With Facioscapulohumeral Muscular Dystrophy (FSHD)
NCT06547216
- Conditions
- Atrophies, Facioscapulohumeral, Atrophy, Facioscapulohumeral, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +33 more
- Locations
-
- University of California Los Angeles Los Angeles, California, United States
- Stanford University Palo Alto, California, United States
- University of California San Diego San Diego, California, United States
- University of Colorado Denver, Colorado, United States