EYC-0305 in Neovascular (Wet) AMD: First-in-Patients Safety and Tolerability Study
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
Run by Eyconis INC. · NCT07587515 · Data updated 2026-11-12
This study tests whether EYC-0305 given as an eye injection every 24 weeks is safe and tolerable in people 50 and older with wet AMD.
Quick facts
| Phase | Phase1; Phase2 |
|---|---|
| Study type | Interventional |
| Ages | 50 Years and up |
| Sex | All |
| Enrollment | 30 (estimated) |
| Sponsor | Eyconis INC. Academic / other |
| Locations | 7 sites (Beverly Hills, California and 6 other locations) |
| Status | Recruiting |
| Started | May 19, 2026 |
| Main results expected | May 2028 |
| Study ends | May 2028 |
| Registry record updated | October 9, 2026 |
| Trial ID | NCT07587515 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are adults 50+ with active neovascular AMD who are willing to undergo regular eye visits and imaging.
✕Probably not a fit
Patients with uncontrolled systemic conditions or ocular factors that preclude imaging or participation may not benefit.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This Phase 1b/2a trial evaluates the safety, tolerability, pharmacokinetics, and immunogenicity of intravitreal EYC-0305 administered every 24 weeks in adults with neovascular AMD. It also examines how the drug affects disease activity and vision over time. The study collects PK data and safety information to guide future development. Participants will undergo regular eye exams and imaging to monitor response and adverse events. Primary goals focus on safety in early-dose cohorts, with exploratory signals of efficacy.
Why it matters
Potential benefit: If successful, EYC-0305 could offer a longer-interval treatment option for wet AMD.
How similar studies have gone: Other similar anti-VEGF–like approaches have shown safety in early-phase trials, but this exact regimen is novel.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Men or women 50 years and older with neovascular (wet) AMD meeting all study-specified eligibility criteria * Willing and able to comply with clinic visits and study-related procedures * Provide signed informed consent Exclusion Criteria: * Known hypersensitivity or known allergy that would preclude study drug administration * Inability to obtain ophthalmic imaging, eg, due to media opacity, inadequate pupillary dilation, allergy to fluorescein dye or lack of venous access * Uncontrolled diabetes mellitus * History of cerebrovascular accident (CVA) or myocardial infarction within 180 days of the Day 1 visit * Renal failure, dialysis, or history of renal transplant * Concurrent psychiatric or medical condition that in the opinion of the Investigator will interfere with study participation or completion * Pregnant or breastfeeding women
Where it's running
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Beverly Hills, CA
Beverly Hills, California, United States Recruiting -
Modesto, CA
Modesto, California, United States Recruiting -
Wake Forest, NC
Wake Forest, North Carolina, United States Recruiting -
Erie, PA
Erie, Pennsylvania, United States Recruiting -
Bellaire, TX
Bellaire, Texas, United States Recruiting -
McAllen, TX
McAllen, Texas, United States Recruiting
Show 1 more location
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The Woodlands, TX
The Woodlands, Texas, United States Recruiting
Study contacts
- Study coordinator: Kim Reed, OD, FAAO
- Email: info@eyconis.com
- Phone: 1-866-392-6647
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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AIV007 Periocular Shot for Wet AMD
This trial tests whether a periocular injection of AIV007 can improve vision and safety in people with wet age-related macular degeneration, compared with the standard Eylea injections.
-
Long-term follow-up for patients with wet age-related macular degeneration receiving SKG0106
This study is testing how well and safely the treatment SKG0106 works for people with wet age-related macular degeneration over a long period after their last injection.
-
Treatment for wet age-related macular degeneration using 4D-150
This study is testing a new gene therapy called 4D-150 to see if it can improve vision in adults with wet age-related macular degeneration who are already receiving other treatments.
-
JWK001 subretinal therapy for neovascular AMD
This study tests a single subretinal dose of JWK001 at different levels in people with wet age-related macular degeneration who have previously responded to anti-VEGF treatment.
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Ixo-vec Contralateral Dosing in Bilateral Wet AMD
Researchers are testing whether giving Ixo-vec to the second eye of adults with bilateral wet AMD is safe and helps vision over time.
-
Using OCT Angiography to Diagnose and Evaluate Wet AMD
This study is testing if a special imaging technique can help doctors find new blood vessels in older adults with wet age-related macular degeneration and see how blood flow might affect the condition.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.