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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

Registry of Fabry Disease - A Multicenter Observational Study

NCT00055016

Conditions: Brain Diseases, Brain Diseases, Metabolic, Brain Diseases, Metabolic, Inborn, +21 more
Locations: National Institutes of Health Clinical Center, 9000 Rockville Pike Bethesda, Maryland, United States

Transkaryotic Therapies, Inc. Cambridge, Massachusetts, United States

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Completed

Gene Therapy for Chronic Granulomatous Diseases - Long-term Follow-up

NCT00001476

Conditions: Chronic Disease, Chronic Granulomatous Disease, Communicable Disease, +15 more
Locations: National Institutes of Health Clinical Center, 9000 Rockville Pike Bethesda, Maryland, United States

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Completed

Unrelated Umbilical Cord Blood Transplantation Augmented With ALDHbr Umbilical Cord Blood Cells

NCT00692926

Conditions: Anemia, Anemia, Aplastic, Bone Marrow Diseases, +33 more
Locations: Duke University Medical Center Durham, North Carolina, United States

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Completed

Treatment of Rett Syndrome With rhIGF-1 (Mecasermin [rDNA]Injection)

NCT01253317

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Genetic Diseases, X-Linked, +7 more
Locations: Boston Children's Hospital Boston, Massachusetts, United States

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Completed

Examining Social, Emotional, and Cognitive Functioning in People With Fragile X and Down Syndromes

NCT00879515

Conditions: Abnormalities, Multiple, Anxiety Disorders, Child Developmental Disorders, Pervasive, +15 more
Locations: M.I.N.D. Institute, University of California, Davis Sacramento, California, United States

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Completed

Trial of Minocycline to Treat Children With Fragile X Syndrome

NCT01053156

Conditions: Chromosome Disorders, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +11 more
Locations: M.I.N.D. Institute at University of California at Davis Medical Center Sacramento, California, United States

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Completed

Safety and Efficacy of Benefix in Patients With Hemophilia B in Usual Care Settings in China

NCT02336178

Conditions: Blood Coagulation Disorders, Blood Coagulation Disorders, Inherited, Coagulation Protein Disorders, +7 more
Locations: Nanfang Hospital, Southern Medical University Guangzhou, Guangdong, China

The Affiliated Hospital of Guizhou Medical University Guiyang, Guizhou, China

Henan Provincial People's Hospital Zhengzhou, Henan, China

Tongji Hospital of Tongji Medical College of Huazhong University of Science and Technology Wuhan, Hubei, China

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Completed

Haploidentical Hematopoietic Stem Cell Transplantation Patients With Wiskott-Aldrich Syndrome

NCT00160355

Conditions: Blood Coagulation Disorders, Blood Coagulation Disorders, Inherited, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +13 more
Locations: St. Jude Children's Research Hospital Memphis, Tennessee, United States

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Completed

A Prospective Open-label Study of Aripiprazole in Fragile X Syndrome

NCT00420459

Conditions: Chromosome Disorders, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +10 more
Locations: Riley Child and Adolescent Psychiatry Clinic - Riley Hospital for Children Indianapolis, Indiana, United States

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Completed

Riluzole in Fragile X Syndrome

NCT00895752

Conditions: Chromosome Disorders, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +10 more
Locations: Riley Child and Adolescent Psychiatry Clinic - Riley Hospital for Children Indianapolis, Indiana, United States

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Genetic Diseases, X-Linked

Genetic Diseases, X-Linked trial results

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