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Completed Phase 2 Interventional

A Study of the Efficacy and Safety of KUS121 in Participants With Acute Non-Arteritic Central Retinal Artery Occlusion (CRAO)

ClinicalTrials.gov ID: NCT06178055

Public ClinicalTrials.gov record NCT06178055. 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 26, 2026, 7:01 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

A Phase 2, Double-masked, Randomized, Sham-controlled, Multiple-dose Study of the Efficacy and Safety of Intravitreal KUS121 in the Treatment of Non-Arteritic Central Retinal Artery Occlusion (CRAO)

Brief summary

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

Central retinal artery occlusion (CRAO) is an ophthalmologic emergency which leads to severe and permanent vision loss. There is no evidence-based therapy for CRAO. The objective of this GION study is to evaluate the efficacy and safety of KUS121 intravitreal (IVT) injection in participants with acute non-arteritic CRAO.

Study identification

NCT ID
NCT06178055
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Enrollment
17 participants

Conditions and interventions

Eligibility (public fields only)

Age range
20 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
Apr 16, 2024 (Actual)
Primary completion
Mar 3, 2025 (Actual)
Completion
Nov 30, 2025 (Actual)
Last update posted
Feb 18, 2026

2024 – 2025

United States locations

U.S. sites
11
U.S. states
7
U.S. cities
11
Facility City State ZIP Site status
The Retina Partners Encino California 91436 —
Salehi Retina Institute, Inc Huntington Beach California 92647 —
Kaiser Permanente Oakland Med Ctr. Oakland California 94611 —
Florida Retina Institute Jacksonville Florida 32216 —
Cumberland Valley Retina Consultants Hagerstown Maryland 21740 —
Kresge Eye Institute/Wayne State University Detroit Michigan 48201 —
NYEE Infirmary of Mount Sinai New York New York 10003 —
UH Eye Institute Cleveland Ohio 44106 —
Austin Retina Associates Austin Texas 78705 —
Retina Consultants of Texas San Antonio Texas 78240 —
Retina Consultants of Texas The Woodlands Texas 77384 —

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 NCT06178055, 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 Feb 18, 2026 · Synced Oct 26, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT06178055 live on ClinicalTrials.gov.

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