Status:

COMPLETED

A Safety and Efficacy Trial of TTHX1114 in People With CED

Lead Sponsor:

Trefoil Therapeutics, Inc.

Conditions:

Corneal Endothelial Dystrophy

Eligibility:

All Genders

18+ years

Phase:

PHASE2

Brief Summary

Expanded access, open label study at a single dose level in patients with CED that in the opinion of the investigators might benefit from TTHX1114

Eligibility Criteria

Inclusion

  • Male or female, 18 years of age or older
  • Subjects who are women of childbearing potential (WOCBP) must be using an acceptable method of birth control (See Section 6.4.3)
  • Proposed Study Eye that has been diagnosed with an ocular condition that, in the opinion of the Investigator, could possibly benefit from TTHX1114 administration, and has a measurable efficacy endpoint
  • Fellow Eye with 20/100 BCVA or better
  • No concurrent ocular or medical condition that would impair the assessment of safety and efficacy

Exclusion

  • Prior exposure to TTHX1114
  • Intolerance, hypersensitivity, or significant allergy to any drug compound, food, or other substance (Note: This includes all components and excipients of the study drug)
  • Current or recent (e.g., the 28 days prior to Study Day 0) participation in any other, interventional clinical research study
  • History of:
  • Ocular cancer (including melanoma)
  • Herpetic keratitis
  • Documented and repeated elevated IOP in either eye
  • Posterior Polymorphous Corneal Dystrophy (PPCD; aka Schlichting dystrophy)
  • Uveitis
  • Use of any concomitant medications that may interfere with the assessment of safety and efficacy
  • Any other reason (e.g., serious systemic disease or uncontrolled medical condition) that, in the opinion of the Investigator could increase the subject's risk, interfere with the interpretation of the study results, or affect the subject's ability to provide informed consent or comply with the study

Key Trial Info

Start Date :

November 30 2021

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

October 31 2023

Estimated Enrollment :

41 Patients enrolled

Trial Details

Trial ID

NCT04812067

Start Date

November 30 2021

End Date

October 31 2023

Last Update

November 7 2023

Active Locations (2)

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Page 1 of 1 (2 locations)

1

Trefoil Study Site

Atlanta, Georgia, United States, 30342

2

Trefoil Study Site

Washington, Missouri, United States, 30090