Phase 1b/2a Study of EYC-0305 in Patients With Neovascular Age-related Macular Degeneration
Sponsor: Eyconis INC. • ClinicalTrials.gov ID: NCT07587515
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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.
Interventions
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EYC-0305
(Biological)
Extended-delivery anti-VEGF
Eligibility criteria
Conditions
Locations
- Beverly Hills, CA — Beverly Hills, California, United States
- Modesto, CA — Modesto, California, United States
- Wake Forest, NC — Wake Forest, North Carolina, United States
- Erie, PA — Erie, Pennsylvania, United States
- Bellaire, TX — Bellaire, Texas, United States
- McAllen, TX — McAllen, Texas, United States
- The Woodlands, TX — The Woodlands, Texas, United States
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Learn MoreOfficial Source
Data sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
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