2020
DOI: 10.1097/icu.0000000000000657
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Age-related macular degeneration therapy: a review

Abstract: Purpose of review The purpose of this review is to describe the current clinical landscape of potential future therapies for both nonexudative (dry) and exudative (wet) age-related macular degeneration (AMD). We highlight some of the more promising treatments that are furthest along in development. Recent findings Patients with dry AMD have long been hoping for a highly efficacious treatment that may slow disease progression or even help regain vision. … Show more

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Cited by 109 publications
(71 citation statements)
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“…Moreover, to date, no treatments exist to effectively protect RPE cells in patients with dry AMD. Hence, they are often inevitably destined to blindness [36]. Therefore, in order to improve the management of AMD, we investigated whether the RPE was structurally preserved by nanoceria particles' intravitreal injection in the acute light damage (LD) experimental model.…”
Section: Introductionmentioning
confidence: 99%
“…Moreover, to date, no treatments exist to effectively protect RPE cells in patients with dry AMD. Hence, they are often inevitably destined to blindness [36]. Therefore, in order to improve the management of AMD, we investigated whether the RPE was structurally preserved by nanoceria particles' intravitreal injection in the acute light damage (LD) experimental model.…”
Section: Introductionmentioning
confidence: 99%
“…Human pluripotent stem cells (hPSCs) comprise human embryonic stem cells (hESCs) and human-induced pluripotent stem cells (hiPSCs). There are two subtypes of cellbased treatments: stem cell therapies that involve delivering new retinal pigment epithelial (RPE) cells to the subretinal space, and non-stem cell therapies based on cell implantation, which generates protective factors [20].…”
Section: Cell-based Therapiesmentioning
confidence: 99%
“…The current treatments under investigation are delivered at monthly, bimonthly or 3 monthly intervals and have been shown to slow down GA lesion growth by up to 30% in 1 year, depending on the therapy and how often injections are delivered (table 1). 7 This would translate to lesions taking longer to affect central vision and patients therefore keeping useful central vision for a longer period.…”
Section: Strengths and Limitations Of This Studymentioning
confidence: 99%