Home
Conditions
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.

12,565 public trials 2,153 recruiting studies

Refine in advanced search Browse all conditions

Genetic Diseases, Inborn trial results

Recruiting

Extracellular Vesicles for HD

NCT06082713

Conditions: Basal Ganglia Diseases, Brain Diseases, Central Nervous System Diseases, +13 more
Locations: University of Central Florida Orlando, Florida, United States

View Trial Details

Recruiting

Walking Program in Fatty Liver Children With Phenylketonuria

NCT06718842

Conditions: Amino Acid Metabolism, Inborn Errors, Brain Diseases, Brain Diseases, Metabolic, +14 more
Locations: Cairo University Dokki, Giza Governorate, Egypt

View Trial Details

Recruiting

Low Energy Diet and Familial Partial Lipodystrophy

NCT03900286

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Diabetes, Diabetes Mellitus, +14 more
Locations: Cambridge University Hospital NHS Foundation Trust Cambridge, United Kingdom

View Trial Details

Recruiting

Video Capsule Examination in Patients With Lynch Syndrome

NCT06712095

Conditions: BMPR1A Gene Mutation, CDH1 Gene Mutation, CHEK2 Gene Mutation, +28 more
Locations: The Royal Marsden NHS Foundation Trust London, (Select), United Kingdom

View Trial Details

Recruiting

French Wilson Disease Registry

NCT05231876

Conditions: Basal Ganglia Diseases, Brain Diseases, Brain Diseases, Metabolic, +16 more
Locations: Hôpital Fondation Adolphe de Rothschild Paris, Île-de-France Region, France

View Trial Details

Recruiting

Osaka Cardiometabolic Epidemiological Study: Ohtori Study Part 2

NCT06694012

Conditions: Arterial Occlusive Diseases, Arteriosclerosis, Arthritis, +61 more
Locations: The Ohtori Health Promotion Center Sakai, Osaka, Japan

View Trial Details

Recruiting

Serotonin Control of Impulsivity in Tourette Disorder

NCT05942716

Conditions: Basal Ganglia Diseases, Behavior, Brain Diseases, +13 more
Locations: Service de neurologie C Hôpital neurologique Pierre Wertheimer/GHE Hospices Civils de Lyon Bron, France

Centre de Référence Syndrome Gilles de la Tourette Département de Neurologie Pôle des Maladies du Système Nerveux Hôpital de la Pitié-Salpêtrière Paris, France

View Trial Details

Recruiting

Orbital Radiotherapy in Grave's Ophthalmopathy 1 Week vs 2 Weeks (OraGO-1 Trial)

NCT06392906

Conditions: Autoimmune Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Endocrine System Diseases, +12 more
Locations: Faculty of Medicine Siriraj Hospital Mahidol University Bangkok Noi, Thailand

View Trial Details

Recruiting

Efficacy and Safety of GNT0003 Following Imlifidase Pre-treatment in Severe Crigler-Najjar Syndrome

NCT06518005

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Crigler-Najjar Syndrome, Genetic Diseases, Inborn, +4 more
Locations: Hopital Antoine BECLERE Clamart, France

View Trial Details

Recruiting

ADAPT Study: Long-term Safety Study of INZ-701 in Patients With ENPP1 Deficiency and ABCC6 Deficiency

NCT06462547

Conditions: Arterial Calcification, Arterial calcification of infancy, Autosomal Recessive Hypophosphatemic Rickets Type 2, +17 more
Locations: Mayo Clinic Rochester, Minnesota, United States

Clinilabs Drug Development Corporation Eatontown, New Jersey, United States

Necker-Enfants Malades Hospital Paris, France

Universitätsklinikum Hamburg-Eppendorf (UKE) Hamburg, Germany

View Trial Details

Genetic Diseases, Inborn

Genetic Diseases, Inborn trial results

Related conditions