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Clinical trial condition

Genetic Diseases, Inborn

Explore clinical trials studying Genetic Diseases, Inborn. Study availability and eligibility vary by location and protocol.

12,537 public trials 2,139 recruiting studies
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Genetic Diseases, Inborn trial results

Recruiting

A Prospective Sub-Study of the Global Hypophosphatasia Registry

NCT05234567

Conditions
Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Hypophosphatasia, +4 more
Locations
  • Clinical Trial Site Hartford, Connecticut, United States
  • Clinical Trial Site Chicago, Illinois, United States
  • Clinical Trial Site Boston, Massachusetts, United States
  • Clinical Trial Site Kansas City, Missouri, United States
View Trial Details
Recruiting

The Efficacy and Safety of Once Daily Mexiletine PR in Patients With Myotonic Dystrophy Type 1 and Type 2

NCT06523400

Conditions
Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Heredodegenerative Disorders, Nervous System, +9 more
Locations
  • Laboratory for Muscle Diseases and Neuropathies Leuven, Belgium
  • Aarhus University Hospital Aarhus, Denmark
  • Ludug-Maximilians University München, Germany
  • Azienda Ospedaliera Universitaria Policlinico Tor Vergata Rome, Italy
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Recruiting

Study of ARO-DUX4 in Adult and Adolescent Patients With Facioscapulohumeral Muscular Dystrophy Type 1

NCT06131983

Conditions
Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Facio-Scapulo-Humeral Dystrophy, Genetic Diseases, Inborn, +7 more
Locations
  • Research Site 2 Liverpool, New South Wales, Australia
  • Research Site 3 Auchenflower, Queensland, Australia
  • Research Site 1 Birtinya, Queensland, Australia
  • Research Site 4 Melbourne, Victoria, Australia
View all 17 locations
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Recruiting

PALLAS Laser for Skin Diseases

NCT07250997

Conditions
Alopecia, Alopecia Areata, Atopic Dermatitis, +19 more
Locations
  • University of Szeged, Albert Szent-Györgyi Clinical Centre, Department of Dermatology and Allergology Szeged, Csongrád-Csanád Vármegye, Hungary
View Trial Details
Recruiting

A Retrospective Study to Characterize Participants With Propionic Acidemia

NCT05769621

Conditions
Amino Acid Metabolism, Inborn Errors, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, +4 more
Locations
  • University of Stanford Medical Center Stanford, California, United States
  • Johns Hopkins University Baltimore, Maryland, United States
  • University of Michigan Hospital Ann Arbor, Michigan, United States
  • Children's Hospital of Philadelphia Philadelphia, Pennsylvania, United States
View all 29 locations
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Recruiting

The Spanish National Registry for Myotonic Dystrophy Type 1

NCT07385443

Conditions
Congenital, Hereditary, and Neonatal Diseases and Abnormalities, DM1, Genetic Diseases, Inborn, +14 more
Locations
  • Hospitals within the DM1 network Multiple Locations, Andalusia, Spain
  • Hospitals within the DM1 network Multiple Locations, Basque Country, Spain
  • Hospitals within the DM1 network Multiple Locations, Canary Islands, Spain
  • Hospitals within the DM1 network Multiple Locations, Cantabria, Spain
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Recruiting

North American Mitochondrial Disease Consortium Patient Registry and Biorepository (NAMDC)

NCT01694940

Conditions
Abnormalities, Multiple, Acid-Base Imbalance, Acidosis, +86 more
Locations
  • University of California San Diego San Diego, California, United States
  • Lucile Packard Children's Hospital Stanford, California, United States
  • Children's Hospital of Colorado Aurora, Colorado, United States
  • Children's National Medical Center Washington D.C., District of Columbia, United States
View all 17 locations
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