Tyrosinemia: Clinical Trials

3 trials for Tyrosinemia, newest first

ClinicalTrials Daily  ·  Areas  ·  Conditions  ·  Drugs  ·  Sponsors  ·  

1 completed, 1 recruiting, 1 unknown. 2 Not applicable.

By phase and status

PhaseTrialsStatus
Not applicable2Completed 1, Recruiting 1

Follow Tyrosinemia: new trials by email Literature Review of Tyrosinemia trials Research Report on Tyrosinemia

Trials newest first · largest first

Tick up to 5 trials to compare them side by side (eligibility, arms, endpoints, adverse events) in a Literature Matrix.

TrialPhaseStatusSponsorEnrollmentStartUpdated
GMP Powdered Substitutes in PKU and TYR
GMP Intervention Product - Phenylketonuria, Tyrosinemia
Not applicableRecruitingNutricia UK Ltd402025-05-202025-12-19
Selective Screening of Children for Hereditary Metabolic Diseases by Tandem Mass Spectrometry in Kazakhstan
Obtaining Dry Blood Spots From Healthy Newborns (Aged 1-7 Days), Obtaining Dry Blood Spots From Healthy Children Aged 8 Days - 7 Years, Obtaining Dry Blood Spots From Healthy Children Aged 8-18 Years - Propionic/Methylmalonic Acidemias, Maple Syrup Urine Disease
UnknownWest Kazakhstan Medical University22502022-10-032023-06-18
Evaluation of TYR Sphere in France
Tyr sphere - Tyrosinemia, AKU
Not applicableCompletedVitaflo International, Ltd142021-12-012025-11-28

Narrower conditions

Tyrosinemias (3)  ·  2-Methylbutyryl-CoA Dehydrogenase Deficiency (1)  ·  3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency (1)  ·  3-Methylglutaconic Aciduria, Type I (1)  ·  3-methylcrotonyl CoA carboxylase 1 deficiency (1)  ·  Acidemia, isovaleric (1)  ·  Alkaptonuria (1)  ·  Argininosuccinic Aciduria (1)  ·  Beta ketothiolase deficiency (1)  ·  Biotinidase Deficiency (1)  ·  Carbamoyl-Phosphate Synthase I Deficiency Disease (1)  ·  Carnitine palmitoyl transferase 1A deficiency (1)  ·  Carnitine palmitoyl transferase 2 deficiency (1)  ·  Carnitine-Acylcarnitine Translocase Deficiency (1)  ·  Citrullinemia (1)

Broader conditions

Amino Acid Metabolism, Inborn Errors (3)  ·  Brain Diseases (3)  ·  Brain Diseases, Metabolic (3)  ·  Brain Diseases, Metabolic, Inborn (3)  ·  Central Nervous System Diseases (3)  ·  Congenital, Hereditary, and Neonatal Diseases and Abnormalities (3)  ·  Genetic Diseases, Inborn (3)  ·  Metabolic Diseases (3)  ·  Nervous System Diseases (3)  ·  Nutritional and Metabolic Diseases (3)  ·  Metabolism, Inborn Errors (2)  ·  Carbohydrate Metabolism, Inborn Errors (1)  ·  Connective Tissue Diseases (1)  ·  Genetic Diseases, X-Linked (1)  ·  Hyperhomocysteinemia (1)

Interventions

Aging (1)

Sponsors

Nutricia UK Ltd (1)  ·  Vitaflo International, Ltd (1)  ·  West Kazakhstan Medical University (1)

Countries

France (1)  ·  Kazakhstan (1)  ·  United Kingdom (1)

Top investigators

Gary Hubbard, Dr (1)  ·  Gulmira M. Zharmakhanova, MD, PhD (1)  ·  Jean-Baptiste Arnoux (1)  ·  Lyazzat M. Syrlybayeva, MD (1)  ·  Victoria I. Kononets, MD, MS (1)

Results publications

PMID 38283151