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Biotinidase Deficiency

Clinical trial condition

Biotinidase Deficiency

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

4 public trials 1 recruiting study

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Biotinidase Deficiency trial results

Recruiting

Neonatal Screening of Biotinidase Deficiency: Genotype-phenotype Correlation and Clinical Follow-up

NCT06723925

Conditions: Amino Acid Metabolism, Inborn Errors, Biotinidase Deficiency, Carbohydrate Metabolism, Inborn Errors, +6 more
Locations: IRCCS Azienda Ospedaliero-Universitaria di Bologna Bologna, Italy

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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

Study of ORL-1B in Patients With Biotinidase Deficiency

NCT03269045

Conditions: Amino Acid Metabolism, Inborn Errors, Biotinidase Deficiency, Carbohydrate Metabolism, Inborn Errors, +6 more
Locations: Not specified

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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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