Pegloticase
Pharmaceutical drug / From Wikipedia, the free encyclopedia
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Pegloticase (trade name Krystexxa) is a medication for the treatment of severe, treatment-refractory, chronic gout. It is a third line treatment in those in whom other treatments are not effective or are not tolerated.[2] The drug is administered by infusion intravenously. Since October 2023, Amgen Inc. has been the marketer of pegloticase in the U.S.
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Trade names | Krystexxa, Puricase |
AHFS/Drugs.com | Monograph |
MedlinePlus | a611015 |
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Routes of administration | Intravenous infusion |
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Bioavailability | N/A |
Elimination half-life | 10–12 days |
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Formula | C1549H2430N408O448S8 |
Molar mass | 34193.37 g·mol−1 |
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It was developed by Savient Pharmaceuticals.[3][4] It was approved in the United States in 2010, after two clinical trials found it 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 2013 for treatment of disabling tophaceous gout. In 2016 this authorization was ended at the request of Horizon Therapeutics PLC in Europe.[5]