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07 January 2025

Improved Fluid Resolution Rates With Faricimab For AMD Treatment

Promising outcomes observed following three loading injections of faricimab for neovascular age-related macular degeneration.

Neovascular age-related macular degeneration (AMD) remains one of the leading causes of blindness worldwide, compelling researchers to find innovative treatments to combat its effects. Recent studies have explored the effectiveness of faricimab, a novel bispecific antibody therapy targeting both vascular endothelial growth factor A (VEGF-A) and angiopoietin-2, which may hold promise for patients suffering from this condition.

A recent investigation conducted at Kim's Eye Hospital, Seoul, South Korea, examined the outcomes and predictive factors for fluid resolution following three loading injections of faricimab for treatment-naïve neovascular AMD. The study included 69 patients diagnosed with neovascular AMD who underwent three monthly injections of faricimab and evaluated changes across various parameters, including best-corrected visual acuity (BCVA) and central retinal thickness (CRT).

Results revealed significant improvements; BCVA improved from 0.64 ± 0.41 to 0.47 ± 0.39 (P < 0.001) over the three-month evaluation period. CRT also significantly reduced from 424.1 ± 155.5 μm at baseline to 266.3 ± 71.7 μm (P < 0.001), and the study found considerable resolution of subretinal fluid (SRF), intraretinal fluid (IRF), and serous pigment epithelial detachment (PED). By three months, only 15.9% of the patients exhibited SRF, down from 79.7% at the study's onset.

The authors emphasized the noteworthy relationship between the type of macular neovascularization (MNV) and fluid resolution rates. Notably, type 2 and type 3 MNV had the highest rates of complete fluid resolution, with 88.2% and 94.7% respectively. They concluded, "Three loading injections of faricimab resulted in significant functional and anatomical improvements...with a high rate of resolution of SRF, IRF, and serous PED." This indicates the potential for faricimab to establish itself as a first-line treatment option for this patient demographic.

This retrospective study not only highlights effective treatment outcomes for faricimab but also indicates the therapeutic value of early intervention with anti-VEGF therapies for patients with neovascular AMD. By effectively addressing the pathological fluid associated with the disease, the dual action of faricimab may lead to quicker and more sustained anatomical and functional improvements compared to existing treatment options.

With neovascular AMD being such a prevalent condition among older populations, the ability to significantly reduce retinal fluid and improve visual outcomes is of utmost importance. The findings from this study open the door to wider applications for faricimab as supplementary treatment within AMD management conversations. Future comparative studies and long-term evaluations will be necessary to fully ascertain the drug's efficacy and establish its place alongside other established therapies.

The findings from this study represent encouraging advancements for managing neovascular AMD, showcasing faricimab's potential to transform the treatment paradigm for patients who are newly diagnosed.