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Study identifier: NCT05795699 Synced from ClinicalTrials.gov · August 02, 2026
● Completed

A Study to Evaluate the Safety and Efficacy of K-321 Eye Drops After Descemetorhexis in Participants With Fuchs Endothelial Corneal Dystrophy (FECD)

Condition: Fuchs Endothelial Corneal Dystrophy  ·  Sponsor: Kowa Research Institute, Inc.

PhasePhase 3
Planned participants107
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

A study to assess the safety and efficacy of K-321 in participants with FECD after descemetorhexis.

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

Talk to the study team

No contact information is available for this study as per the public registry record.

Always discuss trial participation with your own doctor first.

Locations (50)

Keck Hospital of USCLos Angeles, California, United States
Macy Eye CenterLos Angeles, California, United States
Jules Stein Eye InstituteLos Angeles, California, United States
Byers Eye Institute at StanfordPalo Alto, California, United States
Sacramento Eye ConsultantsSacramento, California, United States
Gorovoy MD Eye SpecialistsFort Myers, Florida, United States
University of FloridaGainesville, Florida, United States
Bascom Palmer Eye InstituteMiami, Florida, United States
Bascom Palmer Eye Institute - NaplesNaples, Florida, United States
Eye Consultants of AtlantaAtlanta, Georgia, United States
Grene Vision GroupWichita, Kansas, United States
University of KentuckyLexington, Kentucky, United States

+ 38 more locations — full list on the registry record.

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