Sozinibercept Combination Therapy for Neovascular Age-related Macular Degeneration : Phase 2b Study Subgroup Analysis by Lesion Type
BACKGROUND AND OBJECTIVE: The purpose of this study was to evaluate the angiographic predictors of response to the anti-vascular endothelial growth factor-C/-D agent, sozinibercept
Veröffentlicht in: | Ophthalmic surgery, lasers & imaging retina. - 2013. - (2025) vom: 01. Feb., Seite 1-10 |
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1. Verfasser: | |
Weitere Verfasser: | , , , , |
Format: | Online-Aufsatz |
Sprache: | English |
Veröffentlicht: |
2025
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Zugriff auf das übergeordnete Werk: | Ophthalmic surgery, lasers & imaging retina |
Schlagworte: | Journal Article |
Zusammenfassung: | BACKGROUND AND OBJECTIVE: The purpose of this study was to evaluate the angiographic predictors of response to the anti-vascular endothelial growth factor-C/-D agent, sozinibercept PATIENTS AND METHODS: Prespecified and post hoc subgroup analyses of a phase 2b, randomized, double-masked, sham-controlled trial of 240 participants with treatment-naïve neovascular age-related macular degeneration, comparing monthly intravitreal sozinibercept 0.5 mg or 2 mg, plus ranibizumab 0.5 mg, versus monthly ranibizumab monotherapy RESULTS: Visual acuity benefits at week 24 were greatest in participants with occult lesions receiving 2 mg sozinibercept combination therapy (+15.65 [n = 53] letters versus +9.62 [n = 51] with ranibizumab monotherapy; least squares mean difference +6.03; P = 0.0009). A composite analysis of occult and minimally classic lesions excluding retinal angiomatous proliferation (n = 175/240) also favored sozinibercept over control (+16.08 versus +10.34 letters; +5.74; P = 0.0002). Structural outcomes mirrored sozinibercept visual acuity benefits, with less leakage and smaller lesions on multimodal imaging CONCLUSION: Angiographic lesion characteristics were found to predict the response to sozinibercept combination therapy. [Ophthalmic Surg Lasers Imaging Retina 2025;56:XX-XX.] |
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Beschreibung: | Date Revised 25.02.2025 published: Print-Electronic Citation Status Publisher |
ISSN: | 2325-8179 |
DOI: | 10.3928/23258160-20250108-04 |