Genentech, a member of the Roche, announced the FDA has approved the Vabysmo 6.0 mg single-dose prefilled syringe, or PFS, for use in the treatment of wet, or neovascular, age-related macular degeneration, or AMD, diabetic macular edema, or DME, and macular edema following retinal vein occlusion, or RVO. Together, these three conditions affect close to three million people in the U.S. The Vabysmo PFS will become available to U.S. retina specialists and their patients in the coming months.
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