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Study identifier: NCT07729137 Synced from ClinicalTrials.gov · July 27, 2026
● Not Yet Recruiting

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

Condition: Corneal Edema · Fuchs · Fuchs Dystrophy  ·  Sponsor: Emmecell

PhasePhase 2
Planned participants121
Who can joinAll sexes, 21 Years to no upper limit
Healthy volunteersNo

About this study

This study will evaluate the safety and effectiveness of a single injection of EO2002 at one of two dose levels (150,000 or 500,000 magnetic human corneal endothelial cells \[mHCECs\]), compared with a placebo injection, in participants with corneal edema caused by corneal endothelial dysfunction.

This description comes directly from the study's public registry record.

Talk to the study team

Clinical Operations - Emmecell  ·  650-769-4232  ·  clinicaltrials@emmecell.com

Always discuss trial participation with your own doctor first.

Locations (1)

Clinical Site 1Menlo Park, California, United States

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Source record: clinicaltrials.gov/study/NCT07729137