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Genetic Diseases, X-Linked

Clinical trial condition

Genetic Diseases, X-Linked

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

1,244 public trials 227 recruiting studies

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Genetic Diseases, X-Linked trial results

Completed

Acamprosate in Youth With Fragile X Syndrome

NCT01300923

Conditions: Autism Spectrum Disorder, Autism Spectrum Disorders, Child Development Disorders, Pervasive, +15 more
Locations: Riley Child and Adolescent Psychiatry Clinic - Riley Hospital for Children Indianapolis, Indiana, United States

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Completed

Total-Body Irradiation Followed By Cyclosporine and Mycophenolate Mofetil in Treating Patients With Severe Combined Immunodeficiency Undergoing Donor Bone Marrow Transplant

NCT00008450

Conditions: Adenosine Deaminase Deficiency, Autosomal Recessive Disorder, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +17 more
Locations: Fred Hutch/University of Washington Cancer Consortium Seattle, Washington, United States

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Completed

Choroideremia Gene Therapy Clinical Trial

NCT02553135

Conditions: Choroid Diseases, Choroideremia, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +5 more
Locations: Bascom Palmer Eye Institute, University of Miami Miami, Florida, United States

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Completed

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

NCT02760277

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

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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

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Completed

Pharmacological Treatment of Rett Syndrome With Statins

NCT02563860

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Genetic Diseases, X-Linked, +7 more
Locations: Montefiore Medical center The Bronx, New York, United States

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Completed

HSCT for High Risk Inherited Inborn Errors

NCT00383448

Conditions: Adrenal Gland Diseases, Adrenal Insufficiency, Adrenoleukodystrophy, +55 more
Locations: Masonic Cancer Center, University of Minnesota Minneapolis, Minnesota, United States

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Completed

Gait Evaluation in Haemophiliac Patients

NCT00824798

Conditions: Blood Coagulation Disorders, Blood Coagulation Disorders, Inherited, Coagulation Protein Disorders, +10 more
Locations: Cliniques universitaires Saint-Luc Brussels, Belgium

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Completed

Assessment of Cardiopulmonary Function in Duchenne Muscular Dystrophy

NCT02195999

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Genetic Diseases, X-Linked, +7 more
Locations: Clinical and Translational Research Building Gainesville, Florida, United States

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Completed

2D Strain Evaluation: Children With Duchenne Muscular Dystrophy Versus Healthy Children

NCT02418338

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Duchenne Muscular Dystrophy, Genetic Diseases, Inborn, +8 more
Locations: Pediatric and Congenital Cardiology and Pulmonology Department, Arnaud De Villeneuve University Hospital Montpellier, France

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Genetic Diseases, X-Linked

Genetic Diseases, X-Linked trial results

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