Apellis submits marketing authorisation application to the EMA for pegcetacoplan for geographic atrophy

Apellis Pharmaceuticals

16 December 2022 - Apellis Pharmaceuticals today announced that the company has submitted a marketing authorisation application to the European Medicines Agency for intravitreal pegcetacoplan, an investigational, targeted C3 therapy, for the treatment of geographic atrophy secondary to age-related macular degeneration.

The submission is based on results from the Phase 3 DERBY and OAKS trials at 24 months.

Read Apellis Pharmaceuticals press release

Michael Wonder

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Michael Wonder

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Medicine , Europe , Dossier