Therapeutic Use of Uricase
Uric acid can become insoluble after a long period of accumulation in human body and lead to crystallization in joints and serious gout; as for other creatures, who has uricase (urate oxidase) in their body, urate can be transformed to allantoin and easily be dissolved.
Therefore, exogenic uricase has the potential to be developed as an effective therapy for patients with hyperuricaemia and gout.
The FDA has approved the marketing of these two uricases, namely rasburicase and pegloticase. Rasburicase (Elitek), derived from Aspergillus flavus uricase, is produced in Saccharomyces cerevisiae, a yeast strain. As a non-PEGylated uricase, Rasburicase is FDA&EMA-approved for both paediatric and adult patients. It has a half-life of 16-22 hours and is administered intravenously (at a dose of 0.20 mg/kg) daily for up to 7 days.
Pegloticase (Krystexxa) is a PEGylated recombinant uricase with a longer half-life (6.4-13.8 days). Pegloticase, derived from mammalian pig and baboon liver uricase, is produced in Escherichia coli (E. coli) and covalently conjugated to monomethoxy-PEG (mPEG). In 2010, the FDA approved the use of pegloticase in gout patients refractory to conventional therapy. The recommended dose of pegloticase is 8 mg by intravenous infusion every two weeks.
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Uricase Pipelines
Generic name
|
Brand Name/Altermative name
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Expression System
|
Indications
|
Manufacturer
|
Latest stage
|
Pegloticase
|
Krystexxa, Puricase, PEG-uricase
|
E. coil
|
Refractory gout
|
Crealta Pharmaceuticals
|
Approval
|
Rasburicase
|
Elitek, Fasturtec, SR29142
|
Yeast (Saccharomyces cerevisiae)
|
Hyperuricaemia, Cancer
|
Sanofi-Aventis Groupe SA
|
Approval
|
Rasburicase biosimilar
|
Tuly
|
Yeast
|
Hyperuricaemia
|
Virchow Group
|
Approval
|
PEGylated Recombinant Uricase
|
1501
|
Pending Update
|
Hyperuricaemia
|
xiuzheng,
|
Phase II
|
ALLN-346
|
Engineered urate oxidase (UrOx)
|
Pending Update
|
Gout, Hyperuricaemia, Chronic kidney disease (CKD)
|
Allena Pharmaceuticals
|
Phase II
|
PEGylated Recombinant Uricase
|
JS103
|
Pending Update
|
Hyperuricaemia, gout
|
Junshi Biosciences
|
Phase I
|
Recombinant urate oxidase
|
Injectable recombinant urate oxidase
|
E. coil
|
Hyperuricaemia
|
Biodoor Biotechnology
|
Phase II
|
Pegylated recombinant uricase
|
HZBio1
|
E. coil
|
Gout
|
Chongqing Paijin Biotechnology;Hangzhou Longda Xinke Bio-pharmaceutical
|
Phase I/II
|
Pegadricase
|
Pegsitacase, URICASE-PEG 20
|
Yeast
|
Gout, tumor lysis yndrome (TLS)
|
EnzymeRx, 3sbio
|
Phase I
|
Pegylated recombinant uricase
|
PRX-115
|
Plant cell
|
Refractory gout
|
Protalix BioTherapeutics
|
Phase I
|
Pegylated recombinant uricase
|
Pending Update
|
Pending Update
|
Gout
|
China National Biotech Group Corporation (CNBG)
|
Phase I
|
Recombinant candida utilis uricase
|
Pending Update
|
Yeast
|
Hyperuricaemia
|
Beijing SL Pharmaceutical
|
Phase I
|
Reference:
[1] Schlesinger N, Pérez-Ruiz F, Lioté F. Mechanisms and rationale for uricase use in patients with gout. Nat Rev Rheumatol. 2023 Oct;19(10):640-649. doi: 10.1038/s41584-023-01006-3.