Abstract Objective: The purpose of this study was to evaluate the efficacy and safety of low- to medium-dose (160 mg/W or 80 mg/W) telitacicept in adults at high risk of progression to IgA nephropathy. Methods: This was a single-center retrospective study. The study included adults at high risk for progression of IgA nephropathy who were treated with telitacicept between November 2022 and April 2024 and followed for at least 24 weeks. Results: In this study of 11 patients, telitacicept significantly reduced proteinuria by 64.38% (p Conclusion: In this real-world study, low- to medium-dose of telitacicept combined with conventional therapy showed rapid onset efficacy and safety for treating high-risk progressive IgA patients.
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Juan Pei
Xiuhua Xu
Ruihong Huang
First Affiliated Hospital of Xiamen University
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Pei et al. (Fri,) studied this question.
www.synapsesocial.com/papers/68f43eeb854d1061a58ab9d0 — DOI: https://doi.org/10.21203/rs.3.rs-7621514/v1