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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.

12,656 public trials 2,147 recruiting studies
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Genetic Diseases, Inborn trial results

Completed

Cerebrotendinous Xanthomatosis (CTX) Prevalence Study

NCT02638220

Conditions
Cataract, Cerebrotendinous Xanthomatosis (CTX), Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +10 more
Locations
  • Travere Investigational Site Birmingham, Alabama, United States
  • Travere Investigational Site La Jolla, California, United States
  • Travere Investigational Site Los Angeles, California, United States
  • Travere Investigational Site Los Angeles, California, United States
View all 44 locations
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Completed

Study of DCR-PHXC-101 in Normal Healthy Volunteers and Patients With Primary Hyperoxaluria

NCT03392896

Conditions
Carbohydrate Metabolism, Inborn Errors, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Female Urogenital Diseases, +12 more
Locations
  • Boston Children's Hospital Boston, Massachusetts, United States
  • Centre d'Investigation Clinique - CIC 1407 - Hospices Civils de Lyon Bron, France
  • Universitätsklinikum Bonn-Institut für Klinische Chemie und Klinische Pharmakologie Bonn, Germany
  • University of Amsterdam Amsterdam, Netherlands
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