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

Last updated:
2026-07-18
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View trial details

Overview

Official protocol title:

A DOUBLE-MASKED, RANDOMIZED, PLACEBO-CONTROLLED, PARALLEL-GROUP, 12-WEEK ADMINISTRATION WITH TWO-WEEK GRADUAL DOSE TAPER PHASE AND 38-WEEK FOLLOW-UP PHASE, PHASE 3 STUDY TO INVESTIGATE THE SAFETY AND EFFICACY OF RIPASUDIL (K-321) EYE DROPS AFTER SIMULTANEOUS CATARACT SURGERY AND DESCEMETORHEXIS IN SUBJECTS WITH FUCHS ENDOTHELIAL CORNEAL DYSTROPHY

Intervention/treatment:
RIPASUDIL
Medical condition:
FUCHS ENDOTHELIAL CORNEAL DYSTROPHY
Protocol code:
K-321-303
Control number:
274908
Status:
Closed
Approved:
May 29, 2023
Trial phase:
Phase 3
For more information:
ClinicalTrials.gov - NCT05826353
This is an external link. The information is not authorized by the Government of Canada.

Eligibility

Sex: ALL
Age
18 Years and older
Accepts healthy volunteers: No

Contacts and locations

Contact
Sponsor
KOWA RESEARCH INSTITUTE, INC

Locations

British Columbia

Dr. Greg Moloney
Vancouver, British Columbia, 2000

Ontario

Precision Cornea Centre
Ottawa, Ontario, K1G 5L1
Prism Eye Institute - Mississauga-Oakville
Oakville, Ontario, L5L 1W8
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