- Pegloticase
-
Pegloticase Clinical data AHFS/Drugs.com monograph MedlinePlus a611015 Pregnancy cat. ? Legal status ? Routes intravenous Pharmacokinetic data Bioavailability N/A Half-life 10–12 days Identifiers CAS number 885051-90-1 ATC code M04AX02 UNII R581OT55EA KEGG D09316 ChEMBL CHEMBL1237025 Chemical data Formula ? Mol. mass 497 kDa (polymer-modified tetramer) (what is this?) (verify) Pegloticase (trade name Krystexxa, formerly Puricase)[1] is a drug for the treatment of severe, treatment-refractory, chronic gout, developed by Savient Pharmaceuticals.[2][3] In September 2010, the FDA approved pegloticase for marketing in the United States after two clinical trials demonstrated that the drug lowered uric acid levels and reduced deposits of uric acid crystals in joints and soft tissue.
Mechanism of action
Pegloticase is a recombinant porcine-like uricase. Similarly to rasburicase, both enzymes metabolise 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.[4]
References
- ^ Savient to Present Multiple Abstracts At the European League Against Rheumatism (EULAR) 2009 Annual Congress
- ^ Statement on a nonproprietary name adopted by the USAN Council
- ^ Savient Pharmaceuticals: Uricase
- ^ Biggers, K; Scheinfeldt, N (2008). Current Opin. Investig. Drugs 9 (4): 422–429.
External links
- Krystexxa (pegloticase) Injection, for intravenous infusion: Full prescribing information
Antigout preparations (M04) Uricosurics primary: Probenecid • Sulfinpyrazone • Benzbromarone • Isobromindione
secondary: Amlodipine • Atorvastatin • Fenofibrate • Guaifenesin • LosartanXanthine oxidase inhibitors purine analogues: Allopurinol# • Oxypurinol • Tisopurine
other: Febuxostat • Inositols (Phytic acid, Myo-inositol)Mitotic inhibitors Other M: JNT
anat(h/c, u, t, l)/phys
noco(arth/defr/back/soft)/cong, sysi/epon, injr
proc, drug(M01C, M4)
This drug article relating to the musculoskeletal system is a stub. You can help Wikipedia by expanding it.