Pegloticase
| Clinical data | |
|---|---|
| Trade names | Krystexxa |
| AHFS/Drugs.com | Monograph |
| MedlinePlus | a611015 |
| License data |
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| Routes of administration | Intravenous |
| ATC code | |
| Legal status | |
| Legal status | |
| Pharmacokinetic data | |
| Bioavailability | N/A |
| Elimination half-life | 10–12 days |
| Identifiers | |
| CAS Number | |
| IUPHAR/BPS | |
| ChemSpider |
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| UNII | |
| KEGG | |
| ChEMBL | |
| Chemical and physical data | |
| Formula | C1549H2430N408O448S8 (peptide monomer) |
| Molar mass | 497 kg/mol (polymer-modified tetramer) g·mol−1 |
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Pegloticase (trade name Krystexxa, formerly Puricase)[2] is a drug for the treatment of severe, treatment-refractory, chronic gout, developed by Savient Pharmaceuticals.[3][4]
In September 2010, the FDA approved pegloticase for marketing in the United States after two clinical trials demonstrated the drug lowered uric acid levels and reduced deposits of uric acid crystals in joints and soft tissue. The European Medicines Agency (EMA) granted marketing authorization in January 2013 for treatment of disabling tophaceous gout. Pegloticase is the first drug approved for this indication. Krystexxa is currently marketed in the U.S. by Crealta Pharmaceuticals LLC.
The drug is administered by infusion intravenously under the direction of a rheumatologist.
Medical uses
It is an option for the 3% of people who are intolerant to other medications.[5] Pegloticase is given as an intravenous infusion every two weeks,[5] and has been found to reduce uric acid levels in this population.[6] It is likely useful for tophi but has a high rate of side effects.[7]
Side effects
Pegloticase may show immunogenicity.[8]
Mechanism of action
Pegloticase is a recombinant porcine-like uricase. Similarly to rasburicase, it metabolises uric acid to allantoin. This reduces the risk of precipitates, since allantoin is five to ten times more soluble than uric acid.
In contrast to rasburicase, pegloticase is pegylated to increase its elimination half-life from about eight hours to ten or twelve days, and to decrease the immunogenicity of the foreign uricase protein. This modification allows for an application just once every two to four weeks, making this drug suitable for long-term treatment.[9]
Chemistry
Pegloticase is a tetrameric protein composed of four identical chains of about 300 amino acids each. Approximately nine of the 30 lysine residues in each chain are PEGylated. These PEG chains consist of about 225 ethylene glycol units each (10 kg/mol PEG).[3]
See also
References
- ^ "FDA-sourced list of all drugs with black box warnings (Use Download Full Results and View Query links.)". nctr-crs.fda.gov. FDA. Retrieved 22 Oct 2023.
- ^ Savient to Present Multiple Abstracts At the European League Against Rheumatism (EULAR) 2009 Annual Congress
- ^ a b Statement on a nonproprietary name adopted by the USAN Council
- ^ Savient Pharmaceuticals: Uricase
- ^ a b "FDA approves new drug for gout". FDA. September 14, 2010.
- ^ Sundy, JS (Aug 17, 2011). "Efficacy and tolerability of pegloticase for the treatment of chronic gout in patients refractory to conventional treatment: two randomized controlled trials". JAMA: the Journal of the American Medical Association. 306 (7): 711–20. doi:10.1001/jama.2011.1169. PMID 21846852.
{{cite journal}}: Unknown parameter|coauthors=ignored (|author=suggested) (help) - ^ Sriranganathan, MK; Vinik, O; Bombardier, C; Edwards, CJ (Oct 20, 2014). "Interventions for tophi in gout". The Cochrane database of systematic reviews. 10: CD010069. doi:10.1002/14651858.CD010069.pub2. PMID 25330136.
- ^ Abraham J. Domb, Neeraj Kumar (2 August 2011). Biodegradable Polymers in Clinical Use and Clinical Development. John Wiley & Sons.
- ^ Biggers, K; Scheinfeldt, N (2008). Current Opinion in Investigational Drugs. 9 (4): 422–429.
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External links
- Krystexxa (pegloticase) Injection, for intravenous infusion: Full prescribing information
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