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Phase IV study to evaluate the efficacy of a vegf trap-eye in subjects with neovascular age-related macular degeneration (wamd), without optimal response to repeated monthly intravitreal injections of anti vegf-a therapy

Despite the success of anti-VEGF A drugs, some patients do not respond optimally even at monthly doses with little gain or even loss of visual acuity, as well as persistent or increasing fluid in the retina.

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Aflibercept (VEGF Trap-Eye), a VEGF receptor fusion protein, has been recently approved by the FDA for wAMD. VEGF Trap-Eye has a higher binding affinity and a different mode of action which not only blocks VEGF-A like the current treatment, but also blocks PIGF and VEGF-B, thus blocking both VEGFR-1 and VEGFR-2 angiogenic effects. VEGF Trap-Eye given every 8 weeks after 3 monthly loading doses, has been shown to be non inferior in terms of VA results to monthly ranibizu-mab during the first year of treatment, but it offers a much lower cli-nical burden for patients, caregivers and physicians. Due to its different mode of action, its longer duration of activity and its higher affinity for ligands, VEGF Trap-Eye offers a a good opportunity to explore an alternative therapy to investigate in those patients who do not fully respond to current anti VEGF therapy.

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