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Genetic Diseases, Inborn

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Genetic Diseases, Inborn

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

12,537 public trials 2,139 recruiting studies

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Genetic Diseases, Inborn trial results

Recruiting

Optimizing Parameters of Low-Intensity Focused Ultrasound for Pallidal Modulation in Huntington's Disease

NCT07513844

Conditions: Basal Ganglia Diseases, Brain Diseases, Central Nervous System Diseases, +13 more
Locations: Department of Rehabilitation Medicine, The First Affiliated Hospital of Fujian Medical University Fuzhou, Fujian, China

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Recruiting

SAFE Study: Safety of aPCC Following Emicizumab Prophylaxis

NCT04563520

Conditions: Blood Coagulation Disorders, Blood Coagulation Disorders, Inherited, Coagulation Protein Disorders, +8 more
Locations: Children's Healthcare of Atlanta Atlanta, Georgia, United States

Emory University Hospital Atlanta, Georgia, United States

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the Effects of Febuxostat Dose Tapering in Gout Patients Optimally Controlled for 5 Years or More

NCT06622603

Conditions: Arthritis, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Crystal Arthropathies, +10 more
Locations: Seoul National University Bundang Hospital Seongnam-si, Gyeonggi-do, South Korea

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MAGNIFY - Pulmonary Magnetic Resonance Imaging for Cystic Fibrosis

NCT07192679

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Cystic Fibrosis, Cystic Fibrosis (CF), +6 more
Locations: University of Sheffield MRI Unit Sheffield, United Kingdom

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Tofacitinib for Glucocorticoid-Resistant Moderate-to-Severe Thyroid Eye Disease

NCT07547930

Conditions: Autoimmune Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Endocrine System Diseases, +13 more
Locations: The First Affiliated Hospital of Xiamen University Xiamen, Fujian, China

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Efficacy of Omaveloxolone Treatment for Dysphagia in French Patients With Friedreich's Ataxia

NCT07013292

Conditions: Brain Diseases, Central Nervous System Diseases, Cerebellar Diseases, +11 more
Locations: CHU NICE Nice, Alpes Maritimes, France

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Prodromal Parkinsonian Features in GBA1 Mutation Carriers

NCT05253560

Conditions: Brain Diseases, Brain Diseases, Metabolic, Brain Diseases, Metabolic, Inborn, +16 more
Locations: Michal Becker- Cohen Jerusalem, Please Select..., Israel

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Effects of Bisphosphonates on OI-Related Hearing Loss

NCT04152551

Conditions: Bone Diseases, Bone Diseases, Developmental, Brittle Bone Disorder, +25 more
Locations: Hospital for Special Surgery New York, United States

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Natural History Study of Patients With EYS-Associated RP

NCT07228793

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Eye Diseases, Hereditary, +5 more
Locations: Oftalmic Clinical Research Center Moscow, Russia

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A Clinical Study of PGN-EDODM1 in People With Myotonic Dystrophy Type 1

NCT06667453

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Heredodegenerative Disorders, Nervous System, +10 more
Locations: University of Calgary Calgary, Alberta, Canada

Ottawa Hospital Research Institute (OHRI) Ottawa, Ontario, Canada

CIUSSS du Saguenay-Lac-Saint-Jean Chicoutimi, Quebec, Canada

Montreal Neurological Institute Montreal, Quebec, Canada

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Genetic Diseases, Inborn

Genetic Diseases, Inborn trial results

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