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Review
. 2019 Dec 15;4(1):e000398.
doi: 10.1136/bmjophth-2019-000398. eCollection 2019.

Current and upcoming anti-VEGF therapies and dosing strategies for the treatment of neovascular AMD: a comparative review

Affiliations
Review

Current and upcoming anti-VEGF therapies and dosing strategies for the treatment of neovascular AMD: a comparative review

Saira Khanna et al. BMJ Open Ophthalmol. .

Abstract

Age-related macular degeneration is the leading cause of vision loss in the developed world, with the expected number of affected elderly individuals reaching 17.8 million. Antivascular endothelial growth factor (anti-VEGF) injection therapy has been instrumental in treating a disease process that was previously thought to be untreatable. Over the past two decades, landmark studies have demonstrated the efficacy of different anti-VEGF medications and investigated the optimal dosing regimen and delivery mechanism to increase overall vision and minimise patient burden. In this review, we outline landmark neovascular age-related macular degeneration clinical trials that have demonstrated level 1 evidence for its usage or have contributed to the understanding of how to dose these agents.

Keywords: Macula; Retina; Treatment Medical.

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Conflict of interest statement

Competing interests: SMH is a consultant or on speaker’s bureau for the following companies: Novartis/Alcon, Spark, Regeneron, Alimera Sciences, Clearside Biomedical, EyePoint Pharmaceuticals, OD-OS and Allergan. DAE is a speaker (S), consultant (C), investigator (I) or equity/stockholder (E) in the following companies: Genentech (C, I, S), Regeneron (C), Allergan (C, I, S), Clearside (C, I, E), Novartis (C, I, S), Alimera (C, I), Ophthotech (I), Opthea (I), US Retina (E), Hemera Biopharmaceuticals (E), Boston Image Reading Center (E), Notal Vision (C, S), Allegro (C), EyePoint (C), Mylan (I), Chengdu (I), Orbit Biomedical (C), Adverum (C) and Kodiak (C, I). TAC has an employment relationship with, and equity ownership in, Clearside Biomedical. This work was undertaken in his role as Volunteer Clinical Professor at the Indiana University School of Medicine.

Figures

Figure 1
Figure 1
The figure explores the relationship between the number of injections and the number of ETDRS letters gained. Even though the agents have different durability, there is a positive and clinically meaningful correlation. Only FDA registration and National Eye Institute trials were included in this analysis (bolded in table 1). Brolucizumab 3 mg dose is the triangle data point in the figure. BCVA, best corrected visual acuity; ETDRS, early treatment of diabetic retinopathy; FDA, Food and Drug Administration.

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