Amino Acid Metabolism, Inborn Errors
Information
- Disease name
- Amino Acid Metabolism, Inborn Errors
- Disease ID
- Description
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
Genes | Mutation | Description | Source | Links |
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NCT ID | Status | Phase | Summary | Start date | Completion date |
---|---|---|---|---|---|
NCT00004767 | Completed | Phase 2 | Phase II Study of Sodium Phenylbutyrate, Sodium Benzoate, Sodium Phenylacetate, and Dietary Intervention for Urea Cycle Disorders | January 1985 | |
NCT00345605 | Completed | Phase 2 | Arginine and Buphenyl in Patients With Argininosuccinic Aciduria (ASA), a Urea Cycle Disorder | February 2008 | November 2012 |
NCT06337864 | Not yet recruiting | N/A | Evaluating the Efficacy and Safety of Large Neutral Amino Acids in the Treatment of Classical Phenylketonuria | May 2024 | December 2027 |
NCT00237315 | Recruiting | Longitudinal Study of Urea Cycle Disorders | February 2006 | July 2026 | |
NCT01141075 | Terminated | Phase 2 | Ataluren for Nonsense Mutation Methylmalonic Acidemia | July 19, 2010 | November 3, 2011 |
NCT00004307 | Unknown status | Phase 1 | Study of Treatment and Metabolism in Patients With Urea Cycle Disorders | December 1999 |
- MeSH unique ID (MeSH (Medical Subject Headings))
- D000592