The European Medicines Agency’s human medicines committee (CHMP) voted in favor of two new medicines and against two others this week, including a negative opinion for Apellis’ geographic atrophy treatment that has been approved in the US for almost a year.
Apellis anticipated the bad recommendation, announcing last month that it would file an appeal and seek re-examination. Its drug, Syfovre (pegcetacoplan), was approved in the US last February for the treatment of geographic atrophy following age-related macular degeneration, a condition that can lead to irreversible vision loss. However, its US launch was troubled by rare cases of an inflammatory eye condition called retinal vasculitis.
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