Study of EO2002 for Corneal Edema

This study is testing a new treatment called EO2002 for people with corneal edema (swelling of the clear front part of your eye) caused by problems with the corneal endothelium (the inner layer of cells in your cornea). This condition can be due to Fuchs dystrophy or other causes. Researchers want to see if a single injection of EO2002, at one of two different doses, can improve your vision and is safe, compared to a placebo (an inactive injection). You may be able to join if you have symptomatic central corneal edema affecting your vision, and your vision is within a specific range. The study aims to enroll about 121 participants.

Study design
This study is an interventional trial that will randomly assign participants to receive one of two doses of EO2002 or a placebo. Approximately 121 participants are planned to be enrolled.
What's involved
Participants will receive a single injection and will be followed for 52 weeks to evaluate safety and efficacy.
Compensation
Not stated in the trial record.
Follow-up
Participants will be followed for 52 weeks after treatment.

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NCT07729137

Study of EO2002 in Subjects With Corneal Edema Secondary to Corneal Endothelial Dysfunction

Not Yet Recruiting
PHASE2Ages 21+InterventionalTreatment
Emmecell
~121 participants
Updated 2026-07-29 on ClinicalTrials.gov
What's tested:150K cells500K cellsPlacebo

At a glance

Recruiting sites
0 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
BCVA
Measured over 26 weeks
Corneal Edema
Fuchs
Fuchs Dystrophy
Fuchs' Endothelial Dystrophy
Endothelial Corneal Dystrophy
Corneal Endothelial Decompensation
Corneal Endothelial Cell Loss
Corneal Endothelial Disorder
Corneal Endothelial Dystrophy 1
Endothelial Cell Loss, Corneal
Pseudophakic Bullous Keratopathy
Pseudophakic Bullous Keratopathy (PBK)
1 sites across 1 states
California1
  • Noelia Kunzevitzky, PhD · STUDY_DIRECTOR · Emmecell

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  • BCVA26 weeks

    Proportion of study eyes achieving ≥ 15-letter best-corrected visual acuity (BCVA) improvement at 26 weeks post-treatment as compared to baseline.