CHMP recommends EU approval of Roche's Susvimo for neovascular age-related macular degeneration

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โดย Roche·Read original
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The European Medicines Agency's Committee for Medicinal Products for Human Use has recommended approval of Roche's Susvimo for the treatment of neovascular age-related macular degeneration. Susvimo is the first continuous delivery treatment that offers an alternative to standard-of-care eye injections, using the Contivue refillable implant to deliver a customized formulation of ranibizumab with as few as two treatments per year. The positive recommendation is based on data from the LADDER, Archway, and Portal studies showing Susvimo maintained vision equivalent to monthly intravitreal ranibizumab injections, with longer-term data supporting maintenance of vision up to seven years. A final decision from the European Commission is expected in the near future. Neovascular age-related macular degeneration affects 1.7 million people in the European Union and is a leading cause of blindness in people over 60.

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CHMP positive opinion for Susvimo EU approval for nAMD

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