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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.

12,578 public trials 2,158 recruiting studies

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Genetic Diseases, Inborn trial results

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Feasibility and Tolerability Study of Smart Contact Lens With Healthy Subjects and Patients With Stargardt's Disease

NCT06989658

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Eye Diseases, Hereditary, +5 more
Locations: Centre Hospitalier National d'Ophtalmologie des Quinze-Vingts Paris, France

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Drug-Drug Interaction of JMKX003142 With Amiodarone and Febuxostat in Healthy Subjects

NCT07181265

Conditions: Abnormalities, Multiple, Autosomal Dominant Polycystic Kidney Disease (ADPKD), Ciliopathies, +12 more
Locations: Not specified

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Prevalence of Translocation Phenotyping in Children With Down Syndrome and Their Parents

NCT07175168

Conditions: Abnormalities, Multiple, Chromosomal Abnormalities, Chromosome Aberrations, +12 more
Locations: Not specified

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Phase I/II Clinical Study to Evaluate the Safety, Tolerability, and Efficacy of GC310 Injection in Patients With Wilson's Disease (WD)

NCT07173933

Conditions: Basal Ganglia Diseases, Brain Diseases, Brain Diseases, Metabolic, +16 more
Locations: Peking Union Medical College Beijing, China

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A Phase 3 Trial to Demonstrate the Superiority of 1% OPA-15406 Foam to the Vehicle in Adult Patients With Atopic Dermatitis

NCT07173478

Conditions: Atopic Dermatitis (AD), Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Dermatitis, +9 more
Locations: Mita Dermatology Clinic Tokyo, Japan

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Pediatric Arthropathy Beyond Inflammation: Clinical Spectrum and Diagnostic Approach at Assiut University Children Hospital

NCT07173010

Conditions: Arthropathy, progressive pseudorheumatoid, of childhood, Bone Diseases, Bone Diseases, Developmental, +36 more
Locations: Not specified

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Empagliflozin as a Potential Therapeutic Solution for Patients With Brugada Syndrome

NCT07146880

Conditions: Arrhythmias, Cardiac, Brugada Syndrome, Brugada Syndrome (BrS), +5 more
Locations: National Taiwan University Hospital Taipei, Taiwan

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Multicentre Longitudinal Study of Bone Mineralisation Characteristics in Marfan Syndrome and Ehlers-Danlos Syndrome

NCT07169669

Conditions: Abnormalities, Multiple, Bone Diseases, Bone Diseases, Developmental, +23 more
Locations: Not specified

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Transfusion Exchanges and Cognition in Sickle Cell Disease

NCT07168447

Conditions: Anemia, Anemia, Hemolytic, Anemia, Hemolytic, Congenital, +17 more
Locations: Assistance Publique - Hôpitaux de Paris Hôpital Avicenne Bobigny, Île-de-France Region, France

Hôpital Henri Mondor Créteil, Île-de-France Region, France

Hôpital Kremlin-Bicêtre Le Kremlin-Bicêtre, Île-de-France Region, France

GHU Paris Psychiatrie et Neurosciences - Hôpital Sainte-Anne Paris, Île-de-France Region, France

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Crisaborole 2% Versus Tacrolimus 0.1% in Children With Mild to Moderate Atopic Dermatitis

NCT07162896

Conditions: Atopic Dermatitis, Atopic Dermatitis (AD), Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +10 more
Locations: Shalamar Hospital Lahore Lahore, Punjab Province, Pakistan

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Genetic Diseases, Inborn

Genetic Diseases, Inborn trial results

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