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CHMP Approves Eydenzelt Biosimilar

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Published:16th Dec 2024
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The Committee for Medicinal Products for Human Use (CHMP) adopted a positive opinion, recommending the granting of a marketing authorisation for the medicinal product Eydenzelt, intended for the treatment of neovascular (wet) age-related macular degeneration (AMD), visual impairment due to macular oedema secondary to retinal vein occlusion (branch RVO or central RVO), visual impairment due to diabetic macular oedema (DME) and visual impairment due to myopic choroidal neovascularisation (myopic CNV)

The applicant for this medicinal product is Celltrion Healthcare Hungary Kft.

Eydenzelt will be available as 40 mg/ml solution for injection in pre-filled syringe and vial. The active substance of Eydenzelt is aflibercept, an antineovascularisation agent (ATC code: S01LA05). Aflibercept is a recombinant fusion protein consisting of the extracellular domains of human VEGF receptor 1 and 2 fused to the Fc portion of human IgG1. By acting as a soluble decoy for the natural VEGF receptors, aflibercept inhibits their activation, thereby reducing angiogenesis.

Condition: AMD/CVO/DME/myopic CNV
Type: drug

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