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US 9,377,454 B2Granted
Methods and kits for predicting infusion reaction risk and antibody-mediated loss of response by monitoring serum uric acid during pegylated uricase therapy
AssigneeCrealta Pharmaceuticals LLC
InventorsTheresa Rosario-Jansen, David Erick Wright
Life of this patent
Estimating the term…
Abstract
Methods and kits for predicting infusion reaction risk and antibody-mediated loss of response during intravenous PEGylated uricase therapy in gout patients is provided. Routine SUA monitoring can be used to identify patients receiving PEGylated uricase who may no longer benefit from treatment and who are at greater risk for infusion reactions.
Claims6
A method of treating a patient suffering from gout having a serum uric acid (SUA) level of 6 mg/dl or less, and reducing the incidence of infusion reaction in said patient, the method comprising:
- administering to said patient, a PEGylated uricase at a dosage of 8 mg every two weeks;
- after a first period of time, determining the SUA level of said patient, and
- if said SUA level of the patient is maintained below 6 mg/dl, continuing said administration of PEGylated uricase at a dosage of 8 mg every two weeks, whereas if said SUA level of the patient is above 6 mg/dl, discontinuing said administration thereby reducing the incidence of infusion reaction in said patient, wherein said patient previously received ineffective allopurinol therapy or has a medical history in which allopurinol therapy is contraindicated.
Dependencies are inferred from the claim text.