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Clinical trial condition

Metal Metabolism, Inborn Errors

Explore clinical trials studying Metal Metabolism, Inborn Errors. Study availability and eligibility vary by location and protocol.

206 public trials 36 recruiting studies
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Metal Metabolism, Inborn Errors trial results

Recruiting

Trientine Tetrahydrochloride Administered Once a Day for the First Line Treatment of Wilson's Disease Patients.

NCT07465718

Conditions
Basal Ganglia Diseases, Brain Diseases, Brain Diseases, Metabolic, +16 more
Locations
  • University of Colorado Anschutz School of Medicine Denver, Colorado, United States
  • Yale University School of Medicine New Haven, Connecticut, United States
  • University of Michigan Medical Centre Ann Arbor, Michigan, United States
  • Beijing YouAn Hospital, Capital Medical University Beijing, Beijing Municipality, China
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Recruiting

A First-in-human Study of KK8123 in Adults With X-linked Hypophosphatemia

NCT06525636

Conditions
Avitaminosis, Bone Diseases, Bone Diseases, Metabolic, +30 more
Locations
  • University of California - San Francisco San Francisco, California, United States
  • Yale Center for XLH/ Yale University School of Medicine New Haven, Connecticut, United States
  • Indiana University School of Medicine University Hospital Indianapolis, Indiana, United States
  • Mayo Clinic Rochester, Minnesota, United States
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Recruiting

Efficacy and Safety of Vamifeport in Adult Participants With Homeostatic Iron Regulator Gene (HFE)-Related Hereditary Hemochromatosis

NCT07332091

Conditions
Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Hemochromatosis, +7 more
Locations
  • Banner MD Anderson Gilbert, Arizona, United States
  • Infinity Clinical Trials San Diego, California, United States
  • Medical Oncology Associates of San Diego San Diego, California, United States
  • Green Leaf Clinical Trials Jacksonville, Florida, United States
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Recruiting

International Wilson's Disease Patient Registry (iWilson Registry)

NCT05239858

Conditions
Basal Ganglia Diseases, Brain Diseases, Brain Diseases, Metabolic, +16 more
Locations
  • University Hospital Leuven Leuven, Belgium
  • Hospices Civils de Lyon Bron, Auvergne-Rhône-Alpes, France
  • HF Adolphe de Rothschild Paris, Île-de-France Region, France
  • Charite-Univeritatsmedizin Berlin Hospital Berlin, Germany
View all 16 locations
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Recruiting

Prospective, Longitudinal, Observational Registry of Adult Patients With Hypophosphatasia (REG-HYPO)

NCT05596539

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
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Recruiting

A Study to Assess Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of ALE1 in Healthy Adults and Adults With Hypophosphatasia in Order to Identify Suitable Doses of ALE1

NCT07179640

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
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