Carglumic acid
| Clinical data | |
|---|---|
| Trade names | Carbaglu, Ucedane | 
| Other names | (S)-2-ureidopentanedioic acid | 
| AHFS/Drugs.com | Monograph | 
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| Routes of administration  | By mouth | 
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| Pharmacokinetic data | |
| Bioavailability | 30% | 
| Protein binding | Undetermined | 
| Metabolism | Partial | 
| Elimination half-life | 4.3 to 9.5 hours | 
| Excretion | Fecal (60%) and kidney (9%, unchanged) | 
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| CompTox Dashboard (EPA) | |
| ECHA InfoCard | 100.116.323 | 
| Chemical and physical data | |
| Formula | C6H10N2O5 | 
| Molar mass | 190.155 g·mol−1 | 
| 3D model (JSmol) | |
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Carglumic acid, sold under the brand name Carbaglu among others, is used for the treatment of hyperammonaemia. Carglumic acid is a carbamoyl phosphate synthetase 1 (CPS 1) activator.
The most common adverse effects include vomiting, abdominal pain, pyrexia (fever), and tonsillitis, anemia, diarrhea, ear infection, other infections, nasopharyngitis, decreased hemoglobin levels, and headache.
It was approved for medical use in the United States in March 2010. Carglumic acid is an orphan drug. It is available as a generic medication.