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Neovascular (Wet) Age-Related Macular DegenerationVision and hearingBiologicalPhase 1, Phase 2

What this study is

This Phase 1b/2a study will primarily investigate the safety and tolerability of EYC-0305 delivered by intravitreal (IVT) injection every 24 weeks in patients with neovascular (wet) age-related macular degeneration (AMD). The pharmacokinetics (PK) and immunogenicity of EYC-0305, and the effect on disease activity and vision will also be evaluated.

What's being tested

  • EYC-0305

    Intervention · BIOLOGICAL

    Extended-delivery anti-VEGF

Study details

Official title
Open-Label, Multiple Ascending Dose Phase 1b/2a Study of the Safety and Tolerability of Intravitreal (IVT) EYC-0305 in Patients With Neovascular Age-Related Macular Degeneration
Sponsor
Eyconis INC.
Conditions
Neovascular (Wet) Age-Related Macular Degeneration
Enrolling
30 people
Starts
2026-05-19
Est. completion
2028-05
Design
Open-label, non-randomized, sequential groups, Phase 1, Phase 2
Record
View on ClinicalTrials.gov ↗