3 completed, 1 recruiting, 1 unknown. 1 Not applicable, 1 Phase 2.
| Phase | Trials | Status |
|---|---|---|
| Not applicable | 1 | Completed 1 |
| Phase 2 | 1 | Completed 1 |
Follow Hyperglycinemia, Nonketotic: new trials by email Literature Review of Hyperglycinemia, Nonketotic trials Research Report on Hyperglycinemia, Nonketotic
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 |
|---|---|---|---|---|---|---|
| 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 | Unknown | West Kazakhstan Medical University | 2250 | 2022-10-03 | 2023-06-18 | |
| 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 | |
| Neurobiology of a Mutation in Glycine Metabolism in Psychotic Disorders Glycine, placebo - Schizo-affective Disorder, Bipolar Disorder | Phase 2 | Completed | Mclean Hospital | 2 | 2012-12-10 | 2017-09-19 |
| Acute Glycine Pharmacodynamic Study Glycine administration - Schizophrenia, Psychotic Disorders | Not applicable | Completed | Mclean Hospital | 21 | 2010-07-01 | 2015-10-27 |
| Rare Disease Patient Registry & Natural History Study - Coordination of Rare Diseases at Sanford Rare Disorders, Undiagnosed Disorders | Recruiting | Sanford Health | 20000 | 2010-07-01 | 2026-10-28 |
Hyperargininemia (3) · 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency (2) · Acidemia, isovaleric (2) · Argininosuccinic Aciduria (2) · Ataxia with vitamin E deficiency (2) · Beta ketothiolase deficiency (2) · Biotinidase Deficiency (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) · Citrullinemia (2) · Cystinosis (2) · Glutaric Acidemia I (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) · Metabolic Diseases (5) · Nervous System Diseases (5) · Nutritional and Metabolic Diseases (5) · Metabolism, Inborn Errors (4) · Carbohydrate Metabolism, Inborn Errors (3) · Connective Tissue Diseases (3) · Genetic Diseases, X-Linked (3) · Mental Disorders (3)
Mclean Hospital (2) · Centre Hospitalier Universitaire de Liege (1) · Sanford Health (1) · West Kazakhstan Medical University (1)
United States (3) · Belgium (1) · Kazakhstan (1)
Deborah L Levy, PhD (1) · Gulmira M. Zharmakhanova, MD, PhD (1) · Laurent Servais (1) · Lyazzat M. Syrlybayeva, MD (1) · Marc J. Kaufman, Ph.D. (1) · Victoria I. Kononets, MD, MS (1)
R21MH097470 (1)