Skip to main content
OpenTrials

Clinical trial condition

Hypophosphatasia

Explore clinical trials studying Hypophosphatasia. Study availability and eligibility vary by location and protocol.

35 public trials 6 recruiting studies

Hypophosphatasia trial results

Conditions
Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Enthesopathy, Genetic Diseases, Inborn, +10 more
Locations
  • CHU de Bordeaux- Hôpital Pellegrin Place Amélia Raba Léon - 12è étage - Rhumatologie - Bordeaux, France
  • CHU Lille Lille, France
  • Hospices Civils de Lyon Lyon, France
  • CHU Nice Nice, France
Conditions
Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Hypophosphatasia, +5 more
Locations
  • New Zealand Clinical Research Grafton, Auckland, New Zealand
  • Fortrea Clinical Research Unit Leeds, United Kingdom
  • Universitätsklinikum Würzburg Würzburg, Germany
Conditions
Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Hypophosphatasia, +4 more
Locations
  • Clinical Trial Site Hartford, Connecticut, United States
  • Clinical Trial Site Chicago, Illinois, United States
  • Clinical Trial Site Boston, Massachusetts, United States
  • Clinical Trial Site Kansas City, Missouri, United States
Conditions
Bone Diseases, Bone Diseases, Metabolic, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +11 more
Locations
  • Clinic of Internal Medicine III, Department of Oncology, Haematology, Rheumatology and Clinical Immunology, University Hospital Bonn Bonn, North Rhine-Westphali, Germany

NCT02306720

Conditions
Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Hypophosphatasia, +5 more
Locations
  • Research Site Centennial, Colorado, United States
  • Research Site Hartford, Connecticut, United States
  • Research Site Tampa, Florida, United States
  • Research Site Decatur, Georgia, United States
View all 64 locations

NCT03655223

Conditions
17 Alpha-Hydroxylase Deficiency, 3-Hydroxy-3-Methylglutaric Aciduria, 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency, +456 more
Locations
  • RTI International Research Triangle Park, North Carolina, United States
Conditions
Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Hypophosphatasia, +4 more
Locations
  • Research Site Indianapolis, Indiana, United States
  • Research Site Garden City, New York, United States
  • Research Site Durham, North Carolina, United States
  • Research Site Columbus, Ohio, United States
View all 65 locations