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Description

7.3 Ferroptosis and retinitis pigmentosa (RP) Retinitis pigmentosa (RP) is a hereditary eye disease, mainly with autosomal recessive inheritance, accompanied by dystrophic degenerative changes (112)

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Pissios P, et al

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The company does communicate expected timelines through the patient portal

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It has been shown to inhibit inflammatory pathways, reducing the phosphorylation of NF-B p65, a key mediator of inflammation

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Response: We appreciate the commenter's support for allowing ASM to overlap with other Innovation Center models

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VitaleGde HerderWWvan KoetsveldPMWaaijersMSchoordijkWCrozeEet al

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