Roche (RHHBY) announced that the European Medicines Agency has approved Vabysmo or faricimab, 6.0 mg single-dose prefilled syringe for use in the treatment of neovascular or 'wet' age-related macular degeneration, diabetic macular edema and macular edema following retinal vein occlusion. Vabysmo PFS delivers the same medicine as the currently available 6.0 mg Vabysmo vials in a ready-to-use format. The company noted that Vabysmo PFS provides ophthalmologists with the first and only CE-labelled needle for intravitreal injection.
Levi Garraway, Roche's Chief Medical Officer and Head of Global Product Development, said: "This simplified administration may thereby help reduce the treatment burden for patients and retina specialists."
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