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Clinical trial condition

Muscular Dystrophy, Duchenne

Explore clinical trials studying Muscular Dystrophy, Duchenne. Study availability and eligibility vary by location and protocol.

36 public trials 4 recruiting studies
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Muscular Dystrophy, Duchenne trial results

Completed

Rimeporide in Patients With Duchenne Muscular Dystrophy

NCT02710591

Conditions
Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Genetic Diseases, X-Linked, +7 more
Locations
  • I-Motion - Hôpital Armand Trousseau Paris, Île-de-France Region, France
  • San Raffaele Hospital Milan, Italy
  • Santa Creu i Sant Pau Hospital Barcelona, Spain
  • UCL Institute of Child Health and Great Ormond Street Hospital London, United Kingdom
View Trial Details
Completed

Phase III Study of Idebenone in Duchenne Muscular Dystrophy (DMD)

NCT01027884

Conditions
Ambulatory Care, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, +13 more
Locations
  • University of California Davis Medical Center Sacramento, California, United States
  • Children's Hospital Colorado Aurora, Colorado, United States
  • University of Florida Gainesville, Florida, United States
  • Carolinas Medical Center, Neurosciences and Spine Institute Charlotte, North Carolina, United States
View all 23 locations
View Trial Details
Completed

Modified Diet Trial: A Study of SMT C1100 in Paediatric Patients With DMD Who Follow a Balanced Diet

NCT02383511

Conditions
Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Genetic Diseases, X-Linked, +7 more
Locations
  • Heart of England NHS Foundation Trust - Heart Lands Hospital Birmingham, United Kingdom
  • Alder Hey Children's NHS Foundation Trust Liverpool, United Kingdom
  • Great Ormond Street Hospital for Children NHS Foundation Trust London, United Kingdom
  • Central Manchester University Hospitals NHS Foundation Trust- Royal Manchester Children's Hospital Manchester, United Kingdom
View Trial Details
Completed

Study of Daily Pentoxifylline as a Rescue Treatment in Duchenne Muscular Dystrophy

NCT00243789

Conditions
Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Genetic Diseases, X-Linked, +7 more
Locations
  • Children's National Medical Center Washington D.C., District of Columbia, United States
  • Mayo Clinic Rochester, Minnesota, United States
  • Washington University, St. Louis St Louis, Missouri, United States
  • Children's Hospital of Pittsburgh Pittsburgh, Pennsylvania, United States
View Trial Details

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