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Phase 1b/2a Study of EYC-0305 in Patients With Neovascular Age-related Macular Degeneration

RecruitingPhase 1/2

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

Who can join

Ages 50 and older · All sexes

Full eligibility 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

About the study

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 is being tested

Sponsor: Eyconis INC. · Participants: 30 · Started: May 19, 2026

Contact the study team

Official record on ClinicalTrials.gov — NCT07587515

Locations in the U.S.

CaliforniaBeverly Hills, CA, Beverly Hills
North CarolinaWake Forest, NC, Wake Forest
PennsylvaniaErie, PA, Erie
TexasBellaire, TX, Bellaire
McAllen, TX, McAllen
The Woodlands, TX, The Woodlands

Conditions

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.