Independent directory Public ClinicalTrials.gov records United States
ClinicalTrials.gov record
Completed Phase 2 Interventional Results available

Study to Investigate the Safety and Efficacy of K-321 in Patients With Fuchs Endothelial Corneal Dystrophy (FECD) Following Descemetorhexis

ClinicalTrials.gov ID: NCT04250207

Public ClinicalTrials.gov record NCT04250207. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 22, 2026, 1:44 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Double-Masked, Randomised, Placebo-Controlled, Parallel-Group, 12 Week, Phase 2 Study to Investigate the Safety and Efficacy of K-321 Eye Drops After Descemetorhexis in Patients With Fuchs Endothelial Corneal Dystrophy

Study identification

NCT ID
NCT04250207
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Kowa Research Institute, Inc.
Industry
Enrollment
65 participants

Conditions and interventions

Interventions

  • K-321 Solution Drug
  • Placebo Solution Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jun 22, 2020
Primary completion
Sep 21, 2021
Completion
Jun 26, 2022
Last update posted
Nov 4, 2024

2020 – 2022

United States locations

U.S. sites
19
U.S. states
12
U.S. cities
17
Facility City State ZIP Site status
Jules Stein Eye Institute Los Angeles California 90095
Byers Eye Institute at Stanford Palo Alto California 94304
UC Davis Eye Center Sacramento California 95817
Sacramento Eye Consultants Sacramento California 98515
Gorovoy MD Eye Specialists Fort Myers Florida 33907
UF Health Eye Center Gainesville Florida 32605
Chicago Cornea Consultants Ltd Hoffman Estates Illinois 60169
Arbor Centers For Eyecare Orland Park Illinois 60467
Price Vision Group Indianapolis Indiana 46260
Massachusetts Eye and Ear Infirmary Boston Massachusetts 02114
W Kellogg Eye Center Ann Arbor Michigan 48105
Minnesota Eye Consultants Bloomington Minnesota 55431
Eye Associates of New Mexico Albuquerque New Mexico 87109
NY Langone Health New York New York 10017
Cincinnati Eye Institute Cincinnati Ohio 45242
Devers Eye Institute Portland Oregon 97210
Casey Eye Institute - OHSU Portland Oregon 97239
Vantage EyeCare, LLC Bala-Cynwyd Pennsylvania 19004
UPMC Eye Center Pittsburgh Pennsylvania 15213

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 10 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04250207, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Nov 4, 2024 · Synced Jul 22, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT04250207 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →