Novartis receives EC approval for Beovu, a next-generation anti-VEGF treatment for wet AMD, a leading cause of blindness worldwide

Novartis

17 February 2020 - Beovu (brolucizumab) is the only anti-VEGF treatment approved in Europe for wet AMD that offers the option to start eligible patients on three-month dosing intervals immediately after the loading phase.

Novartis today announced the European Commission (EC) has approved Beovu (brolucizumab) injection for the treatment of wet age-related macular degeneration (AMD). Beovu is the first EC-approved anti-VEGF treatment to demonstrate superior resolution of retinal fluid, a key marker of disease activity, versus aflibercept (secondary endpoints).

Beovu also offers the ability to start eligible wet AMD patients on a three-month dosing interval immediately after the loading phase. The EC decision is applicable to all 27 European Union member states as well as the UK, Iceland, Norway and Liechtenstein.

Read Novartis press release

Michael Wonder

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Michael Wonder

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Outcome , Medicine , Europe