EyePoint Shares Crash After Duravyu Phase 3 Stumble in Wet AMD, But Treatment Burden Reduction Shines

EyePoint Pharmaceuticals' (EYPT) shares plunged roughly 67–71% on August 17, 2026, after Duravyu missed the primary endpoint in the LUGANO Phase 3 trial for wet AMD, failing to show non‑inferiority to aflibercept (Eylea) in best‑corrected visual acuity (BCVA) in the full population.

The company attributed the miss to vision loss in 9 of 211 Duravyu patients unrelated to wet AMD; in an unplanned (ad hoc) analysis excluding these patients, Duravyu did meet non‑inferiority (p=0.0096).

Despite the primary endpoint failure, Duravyu reduced treatment burden by ~42% versus aflibercept through Week 56 and showed a favorable safety profile and high supplement‑free rates, positions that some analysts say still support further development pending the second Phase 3 (LUCIA) readout in late 2026.

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