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Completed Phase 3 Interventional Results available

A 3-month Study to Assess the Safety of ONS-5010 in Subjects With Visual Impairment Due to Retinal Disorders

ClinicalTrials.gov ID: NCT04516278

Public ClinicalTrials.gov record NCT04516278. 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 24, 2026, 5:19 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 3-month Study to Assess the Safety of ONS-5010 in Subjects With Visual Impairment Due to Retinal Disorders, NORSE THREE

Brief summary

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

The study will evaluate the safety of ophthalmic bevacizumab in subjects diagnosed with a retinal condition that would benefit from treatment with intravitreal injection of bevacizumab, including: exudative age-related macular degeneration, diabetic macular edema, or branch retinal vein occlusion.

Study identification

NCT ID
NCT04516278
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Outlook Therapeutics, Inc.
Industry
Enrollment
197 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 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
Oct 1, 2020 (Actual)
Primary completion
Feb 10, 2021 (Actual)
Completion
Feb 10, 2021 (Actual)
Last update posted
Jul 17, 2026

2020 – 2021

United States locations

U.S. sites
20
U.S. states
10
U.S. cities
20
Facility City State ZIP Site status
Clinical Site Tucson Arizona 85710 —
Clinical Site Beverly Hills California 90211 —
Clinical Site Glendale California 91203 —
Clinical Site Long Beach California 90807 —
Clinical Site Palm Desert California 92260 —
Clinical Site Poway California 92064 —
Clinical Site Clearwater Florida 33761 —
Clinical Site Winter Haven Florida 33880 —
Clinical Site Oak Forest Illinois 60452 —
Clinical Site Springfield Illinois 62704 —
Clinical Site Hagerstown Maryland 21740 —
Clinical Site Albuquerque New Mexico 87109 —
Clinical Site Chambersburg Pennsylvania 17201 —
Clinical Site Rapid City South Dakota 57701 —
Clinical Site Germantown Tennessee 38138 —
Clinical Site Abilene Texas 79606 —
Clinical Site Arlington Texas 76012 —
Clinical Site McAllen Texas 78503 —
Clinical Site San Antonio Texas 78251 —
Clinical Site Willow Park Texas 76087 —

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 NCT04516278, 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 17, 2026 · Synced Oct 24, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT04516278 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →