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Clinical trial condition

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

Cascade Genetic Testing for Hereditary Breast/Ovarian Cancer and Lynch Syndrome in Switzerland

NCT03124212

Conditions
Adnexal Diseases, Breast Diseases, Breast Neoplasms, +34 more
Locations
  • HFR Fribourg - Hôpital Cantonal Fribourg, Canton of Fribourg, Switzerland
  • Hirslanden Clinic Des Grangettes Geneva, Canton of Geneva, Switzerland
  • Hôpital du Jura Service d'Oncologie Delémont, Canton of Jura, Switzerland
  • Katonsspital Winterthur Tumorzentrum Brustzentrum Winterthur, Canton of Zurich, Switzerland
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Recruiting

Study to Check the Safety of Fazirsiran and Learn if Fazirsiran Can Help People With Liver Disease and Scarring (Fibrosis) Due to an Abnormal Version of Alpha-1 Antitrypsin Protein

NCT05677971

Conditions
Alpha1-Antitrypsin Deficiency, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Digestive System Diseases, +9 more
Locations
  • University of Alabama at Birmingham Birmingham, Alabama, United States
  • St. Joseph's Hospital and Medical Center Phoenix, Arizona, United States
  • Mayo Clinic Phoenix, Arizona, United States
  • University of Arizona Thomas D. Boyer Liver Institute Tucson, Arizona, United States
View all 89 locations
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Recruiting

Dietary Treatment Strategies and Metabolic Control in Glycogen Storage Disease Type I

NCT06852612

Conditions
Carbohydrate Metabolism, Inborn Errors, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, +5 more
Locations
  • Department of Diabetes, Endocrinology, Nutritional Medicine and Metabolism, Inselspital, Bern University Hospital Bern, Switzerland
  • Department of Endocrinology, Diabetology and Clinical Nutrition, University Hospital Zurich Zurich, Switzerland
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Recruiting

Safety, Tolerability, Pharmacodynamic, Efficacy, and Pharmacokinetic Study of DYNE-101 in Participants With Myotonic Dystrophy Type 1

NCT05481879

Conditions
Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Heredodegenerative Disorders, Nervous System, +10 more
Locations
  • Stanford University Stanford, California, United States
  • University of Florida College of Medicine Gainesville, Florida, United States
  • Indiana University School of Medicine Indianapolis, Indiana, United States
  • University of Iowa Iowa City, Iowa, United States
View all 20 locations
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Recruiting

Drug Rediscovery for Rare Immune Mediated Inflammatory Diseases

NCT06285539

Conditions
Autoimmune Diseases, Behcet Syndrome, Behcet's Disease, +26 more
Locations
  • Amsterdam UMC Amsterdam, Netherlands
  • Zuyderland Medical Center Heerlen, Netherlands
  • Radboud university medical center Nijmegen, Netherlands
  • Erasmus MC Rotterdam, Netherlands
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