HomeTrialNCT07024693
🔬NCT07024693Phase 2RECRUITING

DT-168 in Keratoplasty Patients With Fuchs Endothelial Corneal Dystrophy

Study Summary

The purpose of this study is to evaluate the pharmacodynamics, safety, and tolerability of DT-168 Ophthalmic Solution in pre-keratoplasty patients with Fuchs endothelial corneal dystrophy.

Interventions / Drugs
View on ClinicalTrials.gov ↗
Study Details
Enrollment28 participants
Primary Completion
Lead SponsorDesign Therapeutics, Inc.
Data Retrieved2026-04-11 04:12:02.533386+00:00
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