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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.

357 public trials 57 recruiting studies
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Muscular Dystrophy, Duchenne trial results

Completed

A Clinical Study to Assess the Efficacy and Safety of GSK2402968 in Subjects With Duchenne Muscular Dystrophy

NCT01254019

Conditions
Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Genetic Diseases, X-Linked, +7 more
Locations
  • GSK Investigational Site Buenos Aries, Buenos Aires, Argentina
  • GSK Investigational Site Leuven, Belgium
  • GSK Investigational Site Curitiba, Paraná, Brazil
  • GSK Investigational Site Porto Alegre, Rio Grande do Sul, Brazil
View all 47 locations
View Trial Details
Completed

A Study to Assess Vamorolone in Boys With Duchenne Muscular Dystrophy (DMD)

NCT02760264

Conditions
Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Duchenne Muscular Dystrophy, Genetic Diseases, Inborn, +8 more
Locations
  • University of California Davis Davis, California, United States
  • University of Florida Gainesville, Florida, United States
  • Nemours Children's Hospital Orlando, Florida, United States
  • Ann & Robert H. Lurie Children's Hospital Chicago, Illinois, United States
View Trial Details
Completed

Historically Controlled Trial of Corticosteroids in Young Boys With Duchenne Muscular Dystrophy

NCT02167217

Conditions
Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Duchenne Muscular Dystrophy, Genetic Diseases, Inborn, +8 more
Locations
  • University of California Davis Sacramento, California, United States
  • Nemours Hospital Orlando, Florida, United States
  • Laurie Children's Hospital Of Chicago Chicago, Illinois, United States
  • Washington University in Saint Louis St Louis, Missouri, United States
View Trial Details
Completed

Phase I/II Study of PRO044 in Duchenne Muscular Dystrophy (DMD)

NCT01037309

Conditions
Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Duchenne Muscular Dystrophy, Genetic Diseases, Inborn, +8 more
Locations
  • UZ Leuven Leuven, Belgium
  • S.Anna Hospital Ferrara, Italy
  • Leiden University Medical Center Leiden, Netherlands
  • The Queen Silvia Children's Hospital Gothenburg, Sweden
View Trial Details
Completed

Sodium Nitrate to Improve Blood Flow

NCT02847975

Conditions
Becker Muscular Dystrophy, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, +8 more
Locations
  • Cedars-Sinai Heart Institute Los Angeles, California, United States
  • Cedars-Sinai Medical Center Los Angeles, California, United States
View Trial Details
Completed

Clinical Trial of Coenzyme Q10 and Lisinopril in Muscular Dystrophies

NCT01126697

Conditions
Becker Muscular Dystrophy, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Duchenne Muscular Dystrophy, +11 more
Locations
  • Children's National Medical Center Washington D.C., District of Columbia, United States
  • Lurie Children's Hospital Chicago, Illinois, United States
  • Carolinas Medical Center Charlotte, North Carolina, United States
  • University of Pittsburgh Pittsburgh, Pennsylvania, United States
View Trial Details

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