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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.

1,243 public trials 227 recruiting studies

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Genetic Diseases, X-Linked trial results

Completed

A Double-blind, Escalating Dose, Randomized, Placebo-controlled Study Assessing PK, Safety, Tolerability in Non-ambulant DMD Subjects

NCT01128855

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Genetic Diseases, X-Linked, +7 more
Locations: GSK Investigational Site Columbus, Ohio, United States

GSK Investigational Site Paris, France

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Completed

Use of Busulfan as Conditioning Agent for a Second Stem Cell Transplant

NCT00092937

Conditions: Bronchial Diseases, Bronchiolitis, Bronchiolitis Obliterans, +23 more
Locations: National Institutes of Health Clinical Center, 9000 Rockville Pike Bethesda, Maryland, United States

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Completed

Stem Cell Gene Therapy to Treat X-Linked Severe Combined Immunodeficiency (XSCID)

NCT00028236

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, DNA Repair-Deficiency Disorders, Genetic Diseases, Inborn, +9 more
Locations: National Institutes of Health Clinical Center, 9000 Rockville Pike Bethesda, Maryland, United States

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Completed

Analysis of the Nervous System in Patients With Fabry's Disease

NCT00001491

Conditions: Brain Diseases, Brain Diseases, Metabolic, Brain Diseases, Metabolic, Inborn, +20 more
Locations: National Institutes of Health Clinical Center, 9000 Rockville Pike Bethesda, Maryland, United States

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Completed

Posaconazole to Treat Invasive Fungal Infections

NCT00033982

Conditions: Bacterial Infections and Mycoses, Chronic Disease, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +18 more
Locations: Schering-Plough Research Institute Kenilworth, New Jersey, United States

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Completed

Influences on Female Adolescents' Decisions Regarding Testing for Carrier Status of XSCID

NCT00006335

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, DNA Repair-Deficiency Disorders, Genetic Diseases, Inborn, +9 more
Locations: National Institutes of Health Clinical Center, 9000 Rockville Pike Bethesda, Maryland, United States

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Completed

Study to Collect Data on Fabry Disease Patients With Enhanceable Alpha-Galactosidase A Activity

NCT00106912

Conditions: Brain Diseases, Brain Diseases, Metabolic, Brain Diseases, Metabolic, Inborn, +20 more
Locations: National Institutes of Health Clinical Center, 9000 Rockville Pike Bethesda, Maryland, United States

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Completed

Study of Megakaryocytes From Patients With Abnormal Platelet Vesicles

NCT00086476

Conditions: Albinism, Albinism, Oculocutaneous, Amino Acid Metabolism, Inborn Errors, +36 more
Locations: National Institutes of Health Clinical Center, 9000 Rockville Pike Bethesda, Maryland, United States

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Completed

Genetic Analysis of Oculocerebrorenal Syndrome of Lowe

NCT00359515

Conditions: Abnormalities, Multiple, Amino Acid Transport Disorders, Inborn, Brain Diseases, +23 more
Locations: National Institutes of Health Clinical Center, 9000 Rockville Pike Bethesda, Maryland, United States

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Completed

Developing Newborn Screening for Infants With Primary Immunodeficiency

NCT00113464

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, DNA Repair-Deficiency Disorders, Genetic Diseases, Inborn, +9 more
Locations: Yale University New Haven, Connecticut, United States

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Genetic Diseases, X-Linked

Genetic Diseases, X-Linked trial results

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