EYC-0305 for Age-Related Macular Degeneration
(OVERTURE Trial)
What You Need to Know Before You Apply
What is the purpose of this trial?
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.
Are You a Good Fit for This Trial?
This trial is for men and women aged 50 or older who have neovascular (wet) age-related macular degeneration. Participants must be able to attend clinic visits, follow study procedures, and give informed consent.Inclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Treatment
Participants receive intravitreal (IVT) injections of EYC-0305 every 24 weeks to assess safety, tolerability, pharmacokinetics, and immunogenicity.
Follow-up
Participants are monitored for safety and effectiveness after treatment, including effects on disease activity and vision.
What Are the Treatments Tested in This Trial?
Interventions
- EYC-0305
Trial Overview
The study is testing the safety of EYC-0305, given as an injection into the eye every 24 weeks, in people with wet AMD. Researchers will also look at how the drug moves through the body and its effects on vision.
How Is the Trial Designed?
4
Treatment groups
Experimental Treatment
Find a Clinic Near You
Who Is Running the Clinical Trial?
Eyconis INC.
Lead Sponsor
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