ClinicalTrials.gov record
Recruiting Phase 2 Interventional

DT-168 in Keratoplasty Patients With Fuchs Endothelial Corneal Dystrophy

ClinicalTrials.gov ID: NCT07024693

Public ClinicalTrials.gov record NCT07024693. 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 May 19, 2026, 8:53 PM 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 Phase 2, Multicenter, Open-Label Study to Assess the Pharmacodynamics, Safety, and Tolerability of DT-168 Ophthalmic Solution in Patients With Fuchs Endothelial Corneal Dystrophy Undergoing Keratoplasty

Study identification

NCT ID
NCT07024693
Recruitment status
Recruiting
Study type
Interventional
Phase
Phase 2
Lead sponsor
Design Therapeutics, Inc.
Industry
Enrollment
28 participants

Conditions and interventions

Interventions

  • DT-168 Drug

Drug

Eligibility (public fields only)

Age range
30 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
Jul 29, 2025
Primary completion
Aug 31, 2026
Completion
Nov 30, 2026
Last update posted
Dec 28, 2025

2025 – 2026

United States locations

U.S. sites
2
U.S. states
2
U.S. cities
2
Facility City State ZIP Site status
DTX-168-201 Study Site Indianapolis Indiana 46260 Recruiting
DTX-168-201 Study Site Grand Rapids Michigan 49546 Recruiting

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT07024693, 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 Dec 28, 2025 · Synced May 19, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT07024693 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →