• Gout

Krystexxa Generic Name & Formulations

General Description

Pegloticase 8mg/mL (as uricase protein) in phosphate buffered saline; for IV infusion after dilution.

Pharmacological Class

PEGylated uric acid specific enzyme.

How Supplied

Single-use vial—1


Generic Availability


Krystexxa Indications


Chronic gout in adult patients refractory to conventional therapy.

Limitations of Use

Not for treating asymptomatic hyperuricemia.

Krystexxa Dosage and Administration


Discontinue oral urate-lowering agents before starting; do not institute while on pegloticase therapy. Premedicate with antihistamines and corticosteroids. Give by IV infusion over at least 2 hours via gravity feed, syringe-type pump, or infusion pump. ≥18yrs: 8mg once every 2 weeks, co-administered with weekly oral methotrexate 15mg and folic/folinic acid supplementation. May give pegloticase as monotherapy if methotrexate is contraindicated or not clinically appropriate. If co-administering with methotrexate, start weekly methotrexate and folic/folinic acid supplementation at least 4wks prior to initiation, and during treatment. Slow rate, or stop and restart at lower rate, if infusion reaction occurs; observe at least 1 hour post-infusion.


<18yrs: not established.

Krystexxa Contraindications


G6PD deficiency.

Krystexxa Boxed Warnings

Boxed Warning

Anaphylaxis and infusion reactions. G6PD deficiency associated hemolysis. Methemoglobinemia.

Krystexxa Warnings/Precautions


Administer in healthcare setting by clinicians prepared to manage anaphylaxis and infusion reactions. Monitor closely for anaphylaxis/infusion reactions for an appropriate period of time after administration and esp. in those receiving retreatment after a drug-free interval >4 weeks. Monitor serum uric acid levels before each infusion; discontinue if levels increase to >6mg/dL, particularly with 2 consecutive levels >6mg/dL (increased risk of anaphylaxis and infusion reactions). Screen patients at risk for G6PD deficiency prior to initiation (eg, African, Mediterranean, or Southern Asian ancestry). Give gout flare prophylaxis for at least the first 6 months of pegloticase therapy. CHF. Pregnancy. Nursing mothers: not recommended.

Krystexxa Pharmacokinetics

See Literature

Krystexxa Interactions


May be potentiated by methotrexate. May potentially bind with other PEGylated products.

Krystexxa Adverse Reactions

Adverse Reactions

Co-administered with methotrexate: gout flares, arthralgia, COVID-19, nausea, fatigue. As monotherapy: gout flares, infusion reactions, nausea, contusion, ecchymosis, nasopharyngitis, constipation, chest pain, anaphylaxis, vomiting.

Krystexxa Clinical Trials

See Literature

Krystexxa Note

Not Applicable

Krystexxa Patient Counseling

See Literature