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Genetic Diseases, X-Linked

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Genetic Diseases, X-Linked

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

1,243 public trials 227 recruiting studies

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Genetic Diseases, X-Linked trial results

Completed

Study of Reduced Toxicity Myeloablative Conditioning Regimen for Wiskott-Aldrich Syndrome (WAS)

NCT00885833

Conditions: Blood Coagulation Disorders, Blood Coagulation Disorders, Inherited, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +13 more
Locations: Seoul National University Hospital Seoul, Chongno-gu, South Korea

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Completed

Impact of Conservative Treatment by Custom-made Orthoses in Patients With Haemophilic Ankle Arthropathy

NCT00638001

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

A Study Evaluating Glycosphingolipid Clearance in Patients Treated With Agalsidase Alfa Who Switch to Agalsidase Beta

NCT01650779

Conditions: Brain Diseases, Brain Diseases, Metabolic, Brain Diseases, Metabolic, Inborn, +19 more
Locations: Coral Springs, Florida, United States

Decatur, Georgia, United States

Baltimore, Maryland, United States

Grand Rapids, Michigan, United States

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Completed

Safety and Efficacy of Hunterase

NCT01645189

Conditions: Carbohydrate Metabolism, Inborn Errors, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Connective Tissue Diseases, +17 more
Locations: Samsug Medical Center Seoul, South Korea

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Completed

A Phase 1 Study To Evaluate the Safety of Migalastat Hydrochloride Given Intravenously to Healthy Volunteers

NCT02082327

Conditions: Brain Diseases, Brain Diseases, Metabolic, Brain Diseases, Metabolic, Inborn, +19 more
Locations: PRA International Groningen, Netherlands

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Completed

Pulmonary Involvement in Patients With Fabry Disease

NCT01632111

Conditions: Brain Diseases, Brain Diseases, Metabolic, Brain Diseases, Metabolic, Inborn, +19 more
Locations: University Hospital Zurich, Division of Internal Medicine Zurich, Switzerland

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Completed

Paricalcitol in Fabry Disease

NCT02090608

Conditions: Brain Diseases, Brain Diseases, Metabolic, Brain Diseases, Metabolic, Inborn, +29 more
Locations: federico II university, department of nephrology Naples, Italy

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Completed

KUL0401: An Open-label Pilot Study of Oxatomide in Steroid-Naive Duchenne Muscular Dystrophy

NCT00033813

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

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Completed

Evaluation of Limb-Girdle Muscular Dystrophy

NCT00893334

Conditions: Becker Muscular Dystrophy, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, +13 more
Locations: Children's National Medical Center Washington D.C., District of Columbia, United States

Carolinas Medical Center Charlotte, North Carolina, United States

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Completed

Safety Study of Flavocoxid in Duchenne Muscular Dystrophy

NCT01335295

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Duchenne Muscular Dystrophy, Genetic Diseases, Inborn, +8 more
Locations: Department of Neuroscience, Psychiatry and Anestesiology, Policlinico of Messina Messina, ME, Italy

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Genetic Diseases, X-Linked

Genetic Diseases, X-Linked trial results

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