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Clinical trial condition

Muscular Disorders, Atrophic

Explore clinical trials studying Muscular Disorders, Atrophic. Study availability and eligibility vary by location and protocol.

628 public trials 120 recruiting studies
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Muscular Disorders, Atrophic trial results

Recruiting

Trial Readiness and Endpoint Assessment in Pediatric Myotonic Dystrophy Extension

NCT06747884

Conditions
Childhood Myotonic Dystrophy, Congenital Myotonic Dystrophy, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +16 more
Locations
  • Virginia Commonwealth University Richmond, Virginia, United States
  • Arkansas Children's Hospital Little Rock, Arkansas, United States
  • University of Kansas Medical Center Kansas City, Kansas, United States
  • Hospital das Clínicas, University of São Paulo School of Medicine (HCFMUSP) Cerqueira César, São Paulo, Brazil
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Recruiting

Study of SRP-1001 in Adult and Adolescent Participants With Facioscapulohumeral Muscular Dystrophy Type 1

NCT06131983

Conditions
Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Muscular Diseases, +6 more
Locations
  • Liverpool Hospital Liverpool, New South Wales, Australia
  • Wesley Research Institute Auchenflower, Queensland, Australia
  • Sunshine Coast University Hospital Birtinya, Queensland, Australia
  • Alfred Health Melbourne, Victoria, Australia
View all 16 locations
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Recruiting

Study of SRP-1003 in Participants With Type 1 Myotonic Dystrophy

NCT06138743

Conditions
Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Heredodegenerative Disorders, Nervous System, +10 more
Locations
  • Liverpool Hospital Liverpool, New South Wales, Australia
  • Sunshine Coast University Hospital Birtinya, Queensland, Australia
  • Royal Brisbane And Women's Hospital Herston, Queensland, Australia
  • Alfred Health Melbourne, Victoria, Australia
View all 35 locations
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Recruiting

Modeling Mortality in Duchenne Muscular Dystrophy Cardiomyopathy: Identification of Surrogate Outcome Measures for DMD Drug Trials

NCT07674758

Conditions
Becker Muscular Dystrophy, Cardiomyopathies, Cardiomyopathy, +14 more
Locations
  • UC Davis Sacramento, California, United States
  • Children's National Washington D.C., District of Columbia, United States
  • Lurie Children's Chicago, Illinois, United States
  • Riley Children's Hospital Indianapolis, Indiana, United States
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Recruiting

A Study to Evaluate Del-brax (Also Referred to as AOC 1020) in Participants With FSHD

NCT07038200

Conditions
Congenital, Hereditary, and Neonatal Diseases and Abnormalities, FSH Muscular Dystrophy, FSHD, +25 more
Locations
  • University of California Irvine Orange, California, United States
  • Stanford University Palo Alto, California, United States
  • University of Colorado Denver, Colorado, United States
  • University of Florida Gainesville, Florida, United States
View all 46 locations
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Recruiting

Efficacy, Safety and Tolerability of Givinostat in Non-ambulant Patients With Duchenne Muscular Dystrophy

NCT05933057

Conditions
Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Duchenne Muscular Dystrophy, Genetic Diseases, Inborn, +8 more
Locations
  • Universitaire Ziekenhuizen Leuven Leuven, Belgium
  • British Columbia Children's Hospital Vancouver, British Columbia, Canada
  • The University of Western Ontario - Children's Health Research Institute London, Ontario, Canada
  • University of Ottawa - Children's Hospital of Eastern Ontario Ottawa, Ontario, Canada
View all 29 locations
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Recruiting

A Study of SGT-003 Gene Therapy in Duchenne Muscular Dystrophy (INSPIRE DUCHENNE)

NCT06138639

Conditions
Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Duchenne Muscular Dystrophy, Genetic Diseases, Inborn, +8 more
Locations
  • Arkansas Children's Hospital Little Rock, Arkansas, United States
  • University of California, Los Angeles Medical Center Los Angeles, California, United States
  • University of California, Davis Sacramento, California, United States
  • University of California San Diego, California, United States
View all 15 locations
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Recruiting

A Study Evaluating the Real-World Experience of Givinostat in Patients With Duchenne Muscular Dystrophy

NCT07127978

Conditions
Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Disease Attributes, Duchene Muscular Dystrophy, +12 more
Locations
  • Arkansas Children's Research Institute Little Rock, Arkansas, United States
  • Children's National Hospital Washington D.C., District of Columbia, United States
  • Ann and Robert H. Lurie Children's Hospital of Chicago Chicago, Illinois, United States
  • Boston Children's Hospital Boston, Massachusetts, United States
View Trial Details

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