Study to Investigate the Safety and Efficacy of K-321 in Patients With Fuchs Endothelial Corneal Dystrophy (FECD) Following Descemetorhexis
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The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details. |
ClinicalTrials.gov Identifier: NCT04250207 |
Recruitment Status :
Recruiting
First Posted : January 31, 2020
Last Update Posted : January 22, 2021
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Sponsor:
Kowa Research Institute, Inc.
Information provided by (Responsible Party):
Kowa Research Institute, Inc.
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No Study Results Posted on ClinicalTrials.gov for this Study
Recruitment Status : | Recruiting |
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Estimated Primary Completion Date : | March 2021 |
Estimated Study Completion Date : | October 2021 |