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公开(公告)号:US12188927B2
公开(公告)日:2025-01-07
申请号:US18630584
申请日:2024-04-09
Applicant: Horizon Therapeutics USA, Inc.
Inventor: Theresa Rosario-Jansen , David Erick Wright
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.
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公开(公告)号:US11639927B2
公开(公告)日:2023-05-02
申请号:US17036110
申请日:2020-09-29
Applicant: Horizon Therapeutics USA, Inc.
Inventor: Theresa Rosario-Jansen , David Erick Wright
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.
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公开(公告)号:US11982670B2
公开(公告)日:2024-05-14
申请号:US18104578
申请日:2023-02-01
Applicant: Horizon Therapeutics USA, Inc.
Inventor: Theresa Rosario-Jansen , David Erick Wright
CPC classification number: G01N33/5308 , A61K9/0019 , A61K38/44 , A61K47/60 , A61P19/02 , C12Y107/03003 , G01N33/6893 , G01N2333/90694 , G01N2800/107 , G01N2800/52 , G01N2800/56
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.
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公开(公告)号:US11598767B2
公开(公告)日:2023-03-07
申请号:US17934119
申请日:2022-09-21
Applicant: Horizon Therapeutics USA, Inc.
Inventor: Theresa Rosario-Jansen , David Erick Wright
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.
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公开(公告)号:US20230028134A1
公开(公告)日:2023-01-26
申请号:US17934119
申请日:2022-09-21
Applicant: Horizon Therapeutics USA, Inc.
Inventor: Theresa Rosario-Jansen , David Erick Wright
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.
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