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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

Recruiting

Neurophysiologic Biomarkers in Rett Syndrome

NCT05932589

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Genetic Diseases, X-Linked, +9 more
Locations: Children's Hospital of Los Angeles Los Angeles, California, United States

Children's Hospital Colorado Aurora, Colorado, United States

Boston Children's Hospital Brookline, Massachusetts, United States

Children's Hospital of Philadelphia Philadelphia, Pennsylvania, United States

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Recruiting

Magnetic Resonance Imaging and Biomarkers for Muscular Dystrophy

NCT01484678

Conditions: Becker Muscular Dystrophy, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Duchenne Muscular Dystrophy, +9 more
Locations: University of Florida Gainesville, Florida, United States

Oregon Health and Science University Portland, Oregon, United States

Children's Hospital of Philadelphia Philadelphia, Pennsylvania, United States

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Recruiting

Modeling Macrophages Activation Pattern in X-linked Adrenoleukodystrophy, Metachromatic Leukodystrophy and Adult Onset Leukoencephalopathy With Axonal Spheroids and Pigmented Glia

NCT04925349

Conditions: Adrenal Gland Diseases, Adrenal Insufficiency, Adrenoleukodystrophy, +37 more
Locations: AP-HP Hôpital Bicêtre Le Kremlin-Bicêtre, France

AP-HP Hôpital La Pitié Salpêtrière Paris, France

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Recruiting

A Study of Replagal in Children and Adults With Fabry Disease in India

NCT05067868

Conditions: Brain Diseases, Brain Diseases, Metabolic, Brain Diseases, Metabolic, Inborn, +19 more
Locations: Institute of Child Health Kolkata, India

All India Institute of Medical Sciences (AIIMS) New Delhi, India

Sir Gangaram Hospital New Delhi, India

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Recruiting

Combination of Ibuprofen, G-CSF and Plerixafor as Stem Cells Mobilization Regimen in Patients Affected by X-CGD

NCT03055247

Conditions: Chronic Disease, Chronic Granulomatous Disease X-linked (X-CGD), Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +12 more
Locations: Ospedale Pediatrico Bambino Gesù Rome, Lazio, Italy

Ospedale San Raffaele Milan, Lombardy, Italy

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Recruiting

The European Paediatric Network for Haemophilia Management ( PedNet Registry)

NCT02979119

Conditions: Blood Coagulation Disorders, Blood Coagulation Disorders, Inherited, Coagulation Protein Disorders, +10 more
Locations: Universitäts-Klinik für Kinder- und Jugendheilkunde Graz, Austria

Medical University of Vienna - Department of Paediatrics Vienna, Austria

Service of Pediatric Haematology University Hospital Leuven Leuven, Belgium

Division of Hematology/Oncology Hôpital St Justine Montreal, Canada

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IT and IV Lentiviral Gene Therapy for X-ALD

NCT03727555

Conditions: Adrenal Gland Diseases, Adrenal Insufficiency, Adrenoleukodystrophy, +22 more
Locations: Shenzhen Geno-immune Medical Institute Shenzhen, Guangdong, China

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UCB Transplant of Inherited Metabolic Diseases With Administration of Intrathecal UCB Derived Oligodendrocyte-Like Cells

NCT02254863

Conditions: Adrenal Gland Diseases, Adrenal Insufficiency, Adrenoleukodystrophy, +55 more
Locations: Duke University Medical Center Durham, North Carolina, United States

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Natural History and Structural Functional Relationships in Fabry Renal Disease Treatment Outcomes(Changes)in Fabry Renal Disease Study

NCT01581424

Conditions: Brain Diseases, Brain Diseases, Metabolic, Brain Diseases, Metabolic, Inborn, +19 more
Locations: University of Minnesota Minneapolis, Minnesota, United States

Universtity of Minnesota, Department of Pediatric Nephrology Minneapolis, Minnesota, United States

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Recruiting

Gene Editing as a Therapeutic Approach for Rett Syndrome

NCT05740761

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Genetic Diseases, X-Linked, +7 more
Locations: University of Siena Siena, Italy

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Genetic Diseases, X-Linked

Genetic Diseases, X-Linked trial results

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