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Completed Phase 2 Interventional

Study to Evaluate Suprachoroidally Administered CLS-AX in the Treatment of Neovascular Age-Related Macular Degeneration

ClinicalTrials.gov ID: NCT05891548

Public ClinicalTrials.gov record NCT05891548. 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 Sep 2, 2026, 5:27 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

ODYSSEY: A Phase 2b Study of Suprachoroidally Administered CLS-AX in Participants With Neovascular Age-Related Macular Degeneration

Brief summary

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

Phase 2b, randomized, double-masked, parallel-group, active-controlled, multicenter, 36-week study designed to assess the safety and efficacy of suprachoroidally administered CLS-AX 1.0 mg with a flexible dosing regimen in participants with neovascular age-related macular degeneration previously treated with intravitreal anti-vascular endothelial growth factor (VEGF) standard of care therapy. Only one eye will be chosen as the study eye.

Study identification

NCT ID
NCT05891548
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Clearside Biomedical, Inc.
Industry
Enrollment
60 participants

Conditions and interventions

Eligibility (public fields only)

Age range
50 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
May 30, 2023
Primary completion
Aug 19, 2024
Completion
Aug 19, 2024
Last update posted
Jul 24, 2025

2023 – 2024

United States locations

U.S. sites
32
U.S. states
15
U.S. cities
31
Facility City State ZIP Site status
Associated Retina Consultants Phoenix Arizona 85020
Retinal Research Institute, LLC Phoenix Arizona 85053
California Retina Consultants Bakersfield California 93309
Retina Consultants of Orange County Fullerton California 92835
Northern California Retina Vitreous Associates Medical Group, Inc Mountain View California 94040
Retina Consultants San Diego Poway California 92064
Retinal Consultants of Southern California Redlands California 92374
Retinal Consultants Medical Group, Inc. Sacramento California 95825
Retina Group of Florida Fort Lauderdale Florida 33308
Florida Retina Consultants Lakeland Florida 33805
Retina Specialty Institute Pensacola Florida 32503
Retina Associates of Florida Tampa Florida 33609
Southeast Retina Center Augusta Georgia 30909
Georgia Retina, PC Marietta Georgia 30060
Illinois Retina Associates Oak Park Illinois 60304
Wolfe Eye Clinic Des Moines Iowa 50266
Cumberland Valley Retina Consultants Hagerstown Maryland 21740
Vitreo-Retinal Associates, PC Worcester Massachusetts 01605
Sierra Eye Associates Reno Nevada 89431
Envision Ocular LLC Bloomfield New Jersey 07003
Western Carolina Retinal Associates P.A. Asheville North Carolina 28803
Tennessee Retina PC Nashville Tennessee 37203
Retina Research Institute of Texas Abilene Texas 79606
Texas Retina Associates - Arlington Arlington Texas 76012
Austin Retina Austin Texas 78705
Retina Consultants of Texas-Bellairre Bellaire Texas 77401
Texas Retina Associates - Dallas Dallas Texas 75231
Retina Consultants of Texas - Katy Katy Texas 77494
Texas Retina Associates-Plano Plano Texas 75075
Retina Consultants of Texas-San Antonio San Antonio Texas 78240
Retina Group of Washington Fairfax Virginia 22031
Spokane Eye Clinical Research Spokane Washington 99204

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 NCT05891548, 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 Jul 24, 2025 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT05891548 live on ClinicalTrials.gov.

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