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Clinical trial condition

Hyperbilirubinemia, Hereditary

Explore clinical trials studying Hyperbilirubinemia, Hereditary. Study availability and eligibility vary by location and protocol.

11 public trials 4 recruiting studies

Hyperbilirubinemia, Hereditary trial results

Conditions
Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Crigler-Najjar Syndrome, Crigler-Najjar Syndrome Type I, +5 more
Locations
  • Alphaviva LLC Moscow, Russia
  • Federal State Budget Institution Research Center for Obstetrics, Gynecology and Perinatology Ministry of Healthcare Moscow, Russia
Conditions
Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Crigler-Najjar Syndrome, Genetic Diseases, Inborn, +4 more
Locations
  • Hopital Antoine BECLERE Clamart, France
  • ASST Papa Giovanni XXIII Bergamo, Italy
  • Azienda Ospedaliera Universitaria Federico II Naples, Italy
  • AMC Amsterdam, Netherlands
Conditions
3-Hydroxy 3-Methyl Glutaric Aciduria, 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency, 3-Hydroxy-3-Methylglutaryl-CoA Synthase 2 Deficiency, +368 more
Locations
  • CRMN, Hôpital La Citadelle Liège, Wallonia, Belgium
Conditions
Amino Acid Metabolism, Inborn Errors, Brain Diseases, Brain Diseases, Metabolic, +13 more
Locations
  • Saint Luc University Hospital Brussels, Belgium
  • Universitair Ziekenhuis (UZ) Antwerpen Edegem, Belgium
  • CHU Bicêtre Le Kremlin-Bicêtre, France
  • Hôpital Jeanne de Flandre, CHRU Lille Lille, France
Conditions
Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Crigler-Najjar Syndrome, Genetic Diseases, Inborn, +4 more
Locations
  • Children's Hospital at Montefiore The Bronx, New York, United States
  • Clinic for Special Children Strasburg, Pennsylvania, United States
  • Shaare Zedek Medical Center Jerusalem, Israel
  • King's College Hospital London, England, United Kingdom