Carglumic acid
Carglumic acid is an orphan drug, marketed by Orphan Europe under the trade name Carbaglu. Carglumic acid is used for the treatment of hyperammonaemia in patients with N-acetylglutamate synthase deficiency.[1][2] The initial daily dose ranges from 100 to 250 mg/kg, adjusted thereafter to maintain normal plasma levels of ammonia.
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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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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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ECHA InfoCard | 100.116.323 |
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Formula | C6H10N2O5 |
Molar mass | 190.155 g·mol−1 |
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The US FDA approved it for treatment of hyperammonaemia on March 18, 2010. Orphan Drug exclusivity expired on March 18, 2017.[3]
Adverse effects
The most common adverse effects include vomiting, abdominal pain, fever, and tonsillitis.[4]
References
- Caldovic L, Morizono H, Daikhin Y, Nissim I, McCarter RJ, Yudkoff M, Tuchman M (2004). "Restoration of ureagenesis in N-acetylglutamate synthase deficiency by N-carbamylglutamate". J Pediatr. 145 (4): 552–4. doi:10.1016/j.jpeds.2004.06.047. PMID 15480384.
- Elpeleg O, Shaag A, Ben-Shalom E, Schmid T, Bachmann C (2002). "N-acetylglutamate synthase deficiency and the treatment of hyperammonemic encephalopathy". Ann Neurol. 52 (6): 845–9. doi:10.1002/ana.10406. PMID 12447942. S2CID 24604774.
- "Patent and Exclusivity Search Results".
- Drugs.com: Professional Drug Facts for Carglumic Acid.
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