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Genetic Diseases, Inborn

Clinical trial condition

Genetic Diseases, Inborn

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

12,656 public trials 2,147 recruiting studies

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Genetic Diseases, Inborn trial results

Completed

ERG/5-HTP in Fragile X Syndrome (FXS)

NCT05030129

Conditions: Chromosome Disorders, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +10 more
Locations: Rush University Medical Center Chicago, Illinois, United States

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Completed

NGS Panel of Incomplete Forms of Ocular Albinism

NCT04495218

Conditions: Albinism, Albinism, Ocular, Amino Acid Metabolism, Inborn Errors, +12 more
Locations: Centre Hospitalier Universitaire de Bordeaux Bordeaux, France

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Completed

Health Outcomes of Parents With Cystic Fibrosis

NCT05829694

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Cystic Fibrosis, Digestive System Diseases, +6 more
Locations: National Jewish Health Denver, Colorado, United States

Johns Hopkins University Baltimore, Maryland, United States

Massachusetts General Hospital Boston, Massachusetts, United States

University of Minnesota Minneapolis, Minnesota, United States

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Completed

A Safety and Efficacy Study of STSP-0601 in Adult Patients With Hemophilia A or B With Inhibitor

NCT05027230

Conditions: Blood Coagulation Disorders, Blood Coagulation Disorders, Inherited, Coagulation Protein Disorders, +7 more
Locations: Hospital of Hematology, Chinese Academy of Medical Sciences Tianjin, Tianjin Municipality, China

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Completed

Single and Multiple Ascending Dose Study Assessing the Safety, Tolerability, PK and PD of AG10

NCT03294707

Conditions: Amyloid Cardiomyopathy, Transthyretin-Related, Amyloid Neuropathies, Amyloid Neuropathies, Familial, +13 more
Locations: Celerion Tempe, Arizona, United States

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Completed

Psychometric Validation of the Hemophilia Functional Ability Scoring Tool (Hemo-FAST)

NCT04731701

Conditions: Blood Coagulation Disorders, Blood Coagulation Disorders, Inherited, Coagulation Protein Disorders, +8 more
Locations: Swedish Orphan Biovitrum Clinical site Paris, Cochin, France

Swedish Orphan Biovitrum Clinical site Paris, Kremlin-Bicêtre, France

Swedish Orphan Biovitrum Clinical site Besançon, France

Swedish Orphan Biovitrum Clinical site Bordeaux, France

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Completed

Effect of Group-Task-Oriented Training on GMFM and ADL in Children With DS

NCT06459440

Conditions: Abnormalities, Multiple, Chromosome Disorders, Congenital Abnormalities, +8 more
Locations: Riphah International University Lahore, Punjab Province, Pakistan

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Completed

Impact on French Physician's Haemophilia Treatment Management Decision Based on Systematic Joint Examination

NCT04133883

Conditions: Blood Coagulation Disorders, Blood Coagulation Disorders, Inherited, Coagulation Protein Disorders, +6 more
Locations: Swedish Orphan Biovitrum Research site Angers, France

Swedish Orphan Biovitrum Research site Bordeaux, France

Swedish Orphan Biovitrum Research site Brest, France

Swedish Orphan Biovitrum Research site Caen, France

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Completed

The Risk of Falls Index for Patients With Neuromuscular Disorders

NCT05890833

Conditions: Autoimmune Diseases, Autoimmune Diseases of the Nervous System, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +26 more
Locations: Marko Mijic München, Bavaria, Germany

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Completed

Tourette Syndrome Deep Brain Stimulation

NCT02056873

Conditions: Basal Ganglia Diseases, Brain Diseases, Central Nervous System Diseases, +10 more
Locations: University of Florida Gainesville, Florida, United States

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Genetic Diseases, Inborn

Genetic Diseases, Inborn trial results

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