3 completed, 1 active not recruiting, 1 unknown. 1 Not applicable, 1 Phase 2.
| Phase | Trials | Status |
|---|---|---|
| Not applicable | 1 | Completed 1 |
| Phase 2 | 1 | Completed 1 |
Follow Tyrosinemia, Type I: new trials by email Literature Review of Tyrosinemia, Type I trials Research Report on Tyrosinemia, Type I
Tick up to 5 trials to compare them side by side (eligibility, arms, endpoints, adverse events) in a Literature Matrix.
| Trial | Phase | Status | Sponsor | Enrollment | Start | Updated |
|---|---|---|---|---|---|---|
| Acceptability/Tolerance of Protein Substitutes in Tablet Form for the Dietary Management of Rare Aminoacidopathies Zero minis (range of protein substitutes in tablet form) - Tyrosinemia, Type I, Tyrosinemia, Type II | Unknown | metaX Institut fuer Diatetik GmbH | 15 | 2024-04-01 | 2024-03-07 | |
| Baby Detect : Genomic Newborn Screening Congenital Adrenal Hyperplasia, Familial Hyperinsulinemic Hypoglycemia 1 | Completed | Centre Hospitalier Universitaire de Liege | 6824 | 2022-09-01 | 2025-08-12 | |
| Evaluation of TYR Sphere TYR sphere - Tyrosinemias, Alkaptonuria | Not applicable | Completed | Vitaflo International, Ltd | 18 | 2019-10-01 | 2024-02-16 |
| Early Check: Expanded Screening in Newborns Confirmatory Testing - Spinal Muscular Atrophy, Fragile X Syndrome | Active not recruiting | RTI International | 30000 | 2018-10-15 | 2026-07-01 | |
| Phase II Study of the Enzyme Inhibitor NTBC for Tyrosinemia Type I NTBC - Tyrosinemia, Type I | Phase 2 | Completed | National Center for Research Resources (NCRR) | 1994-11-01 | 2005-06-24 |
Tyrosinemias (5) · 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency (2) · Acidemia, isovaleric (2) · Alkaptonuria (2) · Anemia, Sickle Cell (2) · Argininosuccinic Aciduria (2) · Ataxia with vitamin E deficiency (2) · Basal ganglia disease, biotin-responsive (2) · Beta ketothiolase deficiency (2) · Biotinidase Deficiency (2) · Brown-Vialetto-Van Laere syndrome (2) · Carbamoyl-Phosphate Synthase I Deficiency Disease (2) · Carnitine palmitoyl transferase 1A deficiency (2) · Carnitine palmitoyl transferase 2 deficiency (2) · Carnitine-Acylcarnitine Translocase Deficiency (2)
Amino Acid Metabolism, Inborn Errors (5) · Brain Diseases (5) · Brain Diseases, Metabolic (5) · Brain Diseases, Metabolic, Inborn (5) · Central Nervous System Diseases (5) · Congenital, Hereditary, and Neonatal Diseases and Abnormalities (5) · Genetic Diseases, Inborn (5) · Nervous System Diseases (5) · Nutritional and Metabolic Diseases (5) · Metabolic Diseases (4) · Metabolism, Inborn Errors (4) · Disease Attributes (3) · Pathologic Processes (3) · Pathological Conditions, Signs and Symptoms (3) · Abnormalities, Multiple (2)
Centre Hospitalier Universitaire de Liege (1) · National Center for Research Resources (NCRR) (1) · RTI International (1) · Vitaflo International, Ltd (1) · metaX Institut fuer Diatetik GmbH (1)
Belgium (1) · United Kingdom (1) · United States (1)
Anita MacDonald (1) · Anita MacDonald, Professor (1) · Curt Scharfe, MD, PhD (1) · Jess G. Thoene (1) · Laurent Servais (1)