Efficacy, Safety and Durability of Faricimab▼ in Neovascular Age-Related Macular Degeneration: Week 48 Results From the Phase 3 TENAYA and LUCERNE Trials

This presentation reports the week 48 primary results from the phase 3 TENAYA and LUCERNE trials of faricimab▼, a bispecific antibody that independently binds and neutralizes Ang-2 and VEGF-A, in patients with neovascular age-related macular degeneration. TENAYA and LUCERNE investigated the efficacy, safety, and durability of faricimab▼, administered at individualized treatment intervals of up to every 16 weeks, compared with aflibercept administered every 8 weeks.

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