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Clinical trial condition

Tyrosinemia, Type I

Explore clinical trials studying Tyrosinemia, Type I. Study availability and eligibility vary by location and protocol.

4 public trials 0 recruiting studies
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Tyrosinemia, Type I trial results

Completed

Baby Detect : Genomic Newborn Screening

NCT05687474

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
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Completed

Evaluation of TYR Sphere

NCT04196959

Conditions
Alkaptonuria, Amino Acid Metabolism, Inborn Errors, Brain Diseases, +13 more
Locations
  • National Alkaptonuria Centre, Royal Liverpool University Hospital Liverpool, Merseyside, United Kingdom
  • Birmingham Children's Hospital Birmingham, West Midlands, United Kingdom
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Active, Not Recruiting

Early Check: Expanded Screening in Newborns

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
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