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This multicenter study aimed to assess the short-term effectiveness and safety of faricimab in treatment-naïve patients with wet age-related macular degeneration (wAMD) in Japan. We retrospectively reviewed 63 eyes of 61 patients with wAMD, including types 1, 2, and 3 macular neovascularization as well as polypoidal choroidal vasculopathy (PCV). Patients received three consecutive monthly intravitreal injections of faricimab as loading therapy. Over these 3 months, visual acuity improved gradually compared to baseline. Moreover, the central foveal thickness decreased significantly at 1, 2, and 3 months compared to baseline (p < 0.0001). At 3 months after initiation of faricimab therapy, a dry macula (defined as absence of intraretinal or subretinal fluid) was achieved in 82% of the eyes. Complete regression of polypoidal lesions was observed in 52% of eyes with PCV. Subfoveal choroidal thickness also decreased significantly at 1, 2, and 3 months compared to baseline (p < 0.0001). Although retinal pigment epithelium tears developed in two eyes, there were no other ocular or systemic complications observed during the 3 months of loading therapy. In conclusion, loading therapy using faricimab resulted in improved visual acuity and retinal morphology in Japanese patients with wAMD without particular safety issues.
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http://dx.doi.org/10.1038/s41598-023-35759-4 | DOI Listing |
Clin Ophthalmol
August 2025
Department of Ophthalmology and Visual Science, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
Background: Diabetic macular edema (DME) is a leading cause of vision loss in working-age adults. Faricimab, a bispecific antibody targeting VEGF and Ang-2, has been shown to reduce treatment burden by enabling extended injection intervals. However, real-world, long-term data from Japanese populations are limited.
View Article and Find Full Text PDFCureus
July 2025
Department of Retina, Sarojini Devi Eye Hospital, Hyderabad, IND.
This case series explores the efficacy and safety of a monthly loading dose regimen of intravitreal faricimab in treatment-naïve patients with diabetic macular edema (DME) in an Indian clinical setting. In this retrospective analysis, five adult patients with treatment-naïve DME received faricimab (four intravitreal injections of 6 mg) on Day 0, Day 30, Day 60, and Day 90. Their best-corrected visual acuity (BCVA) and central macular thickness (CMT) were evaluated throughout the study.
View Article and Find Full Text PDFAm J Ophthalmol
August 2025
Department of Ophthalmology, Bascom Palmer Eye Institute, University of Miami, Miami, FL, 33136. Electronic address:
Topic: Faricimab in the treatment of treatment-resistant neovascular age-related macular degeneration (nAMD).
Clinical Relevance: While many studies on faricimab in treatment-resistant eyes have reported improvements in retinal thickness (RT), the impact on visual acuity (VA) remains inconsistent. Additionally, variability in dosing protocols-with some studies utilizing loading interval for the first three injections while others continuing at the prior injection interval-introduces further uncertainty regarding the optimal treatment strategy.
Int Ophthalmol
August 2025
Vitreoretinal Surgery Unit, Isola Tiberina Hospital - Gemelli Isola, Rome, Italy.
Purpose: To investigate the 12-month effectiveness and safety of intravitreal faricimab (IVF) in patients with neovascular age-related macular degeneration (nAMD) resistant to previous anti-VEGF treatment.
Methods: Prospective, monocentric study including consecutive patients with resistant/refractory nAMD switched to IVF between July 2023 and November 2024. Primary endpoints were safety, best corrected visual acuity (BCVA), central subfield thickness (CST), and subfoveal choroidal thickness.
Retina
July 2025
Ophthalmology Department, Catholic University "Sacro Cuore", Rome, Italy.
Purpose: To evaluate the morphometric changes in macular neovascularization (MNV) architecture after faricimab treatment in neovascular age-related macular degeneration (nAMD), comparing treatment-naïve and previously treated eyes.
Methods: Prospective study analyzing 45 eyes (18 treatment-naïve, 27 switched) with nAMD undergoing faricimab treatment. Optical coherence tomography angiography (OCTA) images were exported and the quantification of changes in MNV area, vessel area, vessel density, number of junctions, branching index, total vessel length, endpoints, and lacunarity was performed using AngioTool v0.