EC Approves Broader Use of Novartis’ Lucentis
The European Commission has approved eye drug Lucentis to treat patients with visual impairment due to macular edema secondary to retinal vein occlusion.
Novartis has received approval for broader use of its eye drug Lucentis (ranibizumab). The European Commission has approved the drug to treat patients with visual impairment due to macular edema secondary to retinal vein occlusion (branch RVO and central RVO). RVO is a sudden-onset disease that makes it difficult for patients to cope with daily activities such as reading, cooking and driving.
Lucentis is already approved in more than 85 countries for the treatment of wet age-related macular degeneration (AMD) and in more than 30 countries for the treatment of visual impairment due to diabetic macular edema (DME).
Novartis says Lucentis is the first anti-VEGF therapy licensed for the treatment of both bra
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