Real-World Safety Outcomes with Brolucizumab in Neovascular Age-Related Macular Degeneration: Findings from the IRIS® Registry

Marco A. Zarbin,Mathew W. MacCumber,Helene Karcher,Eser Adiguzel, Andrew Mayhook, Andrew LaPrise, Ver L. Bilano, Franklin Igwe,Michael S. Ip,Charles C. Wykoff

Ophthalmology and Therapy(2024)

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摘要
To assess real-world safety outcomes for adults with neovascular age-related macular degeneration (nAMD) treated with brolucizumab from the US-based IRIS® (Intelligent Research in Sight) Registry. In this retrospective study, 18,312 eyes (15,998 patients) treated with ≥ 1 intravitreal brolucizumab injections between 8 October 2019 (US launch date for brolucizumab) and 7 October 2021 were followed up for ≤ 2 years after first injection (index date). The study assessed the predefined incident ocular adverse events of intraocular inflammation (IOI), retinal vasculitis (RV), and retinal vascular occlusion (RO). Overall, 614/18,312 eyes (3.4
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关键词
Anti-vascular endothelial growth factor therapy,Brolucizumab,Intraocular inflammation,Neovascular age-related macular degeneration,Real-world evidence
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