NCT02964377
- Conditions
- Cardiomyopathies, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +11 more
- Locations
-
- UC Davis Medical Center Sacramento, California, United States
Clinical trial condition
Muscular Dystrophies
Explore clinical trials studying Muscular Dystrophies. Study availability and eligibility vary by location and protocol.
453 public trials
90 recruiting studies
Muscular Dystrophies trial results
NCT04018820
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Heredodegenerative Disorders, Nervous System, +10 more
- Locations
-
- Groupe de recherche interdisciplinaire sur les maladies neuromusculaires Saguenay, Quebec, Canada
NCT03218995
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Duchenne Muscular Dystrophy, Genetic Diseases, Inborn, +8 more
- Locations
-
- Universitair ziekenhuis Gent Ghent, Belgium
- Armand-Trousseau Hospital Paris, France
- Site Fondazione Policlinico Universitario Agostino Gemelli Roma, Italy
- UCL Great Ormond Street Institute of Child Health London, United Kingdom
Completed
Safety and Dose Finding Study of NS-065/NCNP-01 in Boys With Duchenne Muscular Dystrophy (DMD)
NCT02740972
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Duchenne Muscular Dystrophy, Genetic Diseases, Inborn, +8 more
- Locations
-
- UC Davis Sacramento, California, United States
- University of Florida Health Gainesville, Florida, United States
- Lurie Children's Hospital Chicago, Illinois, United States
- Washington University St Louis, Missouri, United States
NCT03236662
- Conditions
- Becker Muscular Dystrophy, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, +8 more
- Locations
-
- UC Davis Medical Center Sacramento, California, United States
NCT04173234
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Duchenne Muscular Dystrophy, Genetic Diseases, Inborn, +8 more
- Locations
-
- Hacettepe University, Faculty of Physical Therapy and Rehabilitation Ankara, Altındağ, Turkey (Türkiye)
NCT02239224
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Facioscapulohumeral Muscular Dystrophy (FSHD), Genetic Diseases, Inborn, +7 more
- Locations
-
- aTyr Pharma Investigative Site Rochester, New York, United States
- aTyr Pharma Investigative Site Columbus, Ohio, United States
- aTyr Pharma Investigative Site Marseille, France
- aTyr Pharma Investigative Site Rome, Italy
NCT01506518
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Genetic Diseases, X-Linked, +7 more
- Locations
-
- The University of North Carolina at Chapel Hill Hospitals Chapel Hill, North Carolina, United States
NCT01183767
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Duchenne Muscular Dystrophy, Genetic Diseases, Inborn, +8 more
- Locations
-
- Charité University Berlin Berlin, Germany
- DRK Kliniken Berlin, Westend, Pädiatrie Berlin, Germany
- Diakonisches Werk Oldenburg SPZ Oldenburg, Germany
Completed
Safety, Tolerability and Pharmacokinetics of ERX-963 in Adults With Myotonic Dystrophy Type 1
NCT03959189
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Disorders of Excessive Somnolence, Dyssomnias, +15 more
- Locations
-
- Stanford Neurosciences Health Center Palo Alto, California, United States
- Sleep Medicine Specialists of South Florida Miami, Florida, United States
- University of Iowa Iowa City, Iowa, United States
- The Center for Sleep & Wake Disorders Chevy Chase, Maryland, United States