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Completed Phase 1Phase 2 Interventional Results available

A Phase 1/2 Study of AURN001 in Subjects With Corneal Edema Secondary to Corneal Endothelial Dysfunction (ABA-1)

ClinicalTrials.gov ID: NCT06041256

Public ClinicalTrials.gov record NCT06041256. 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 Oct 23, 2026, 10:35 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

CLARA: A Phase 1/2 Multi-center, Randomized, Double-Masked, Prospective, Parallel-Arm Study of AURN001 in Subjects With Corneal Edema Secondary to Corneal Endothelial Dysfunction (ABA-1)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The goal of this clinical trial is to compare different doses of AURN001 in patients with corneal edema secondary to corneal endothelial dysfunction. The main questions the clinical trial aims to answer are whether AURN001 effective and safe. Participants will receive a single injection of AURN001. A comparison between low, medium, and high doses of AURN001 against the contribution of each element, cells alone and Y27632 alone, will be conducted to determine the effects on corneal edema.

Study identification

NCT ID
NCT06041256
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1, Phase 2
Lead sponsor
Aurion Biotech
Industry
Enrollment
97 participants

Conditions and interventions

Interventions

Combination Product · Biological · Drug

Eligibility (public fields only)

Age range
18 Years to 99 Years
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
Oct 18, 2023 (Actual)
Primary completion
Oct 25, 2024 (Actual)
Completion
Apr 15, 2025 (Actual)
Last update posted
Dec 17, 2025

2023 – 2025

United States locations

U.S. sites
17
U.S. states
15
U.S. cities
16
Facility City State ZIP Site status
Aurion Biotech site Little Rock Arkansas 72205 —
Aurion Biotech site Los Angeles California 90067 —
Aurion Biotech site San Francisco California 94158 —
Aurion Biotech site Atlanta Georgia 30339 —
Aurion Biotech site Indianapolis Indiana 46260 —
Aurion Biotech site Wichita Kansas 67206 —
Aurion Biotech site Minnetonka Minnesota 55305 —
Aurion Biotech site Garden City New York 11576 —
Aurion Biotech site Winston-Salem North Carolina 27157 —
Aurion Biotech site Cincinnati Ohio 45242 —
Aurion Biotech site Oklahoma City Oklahoma 73104 —
Aurion Biotech site Bala-Cynwyd Pennsylvania 19004 —
Aurion Biotech site Sioux Falls South Dakota 57108 —
Aurion Biotech site Houston Texas 77027 —
Aurion Biotech site Houston Texas 77055 —
Aurion Biotech site Norfolk Virginia 23502 —
Aurion Biotech site Seattle Washington 98125 —

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 3 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06041256, 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 17, 2025 · Synced Oct 23, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT06041256 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →