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Completed Phase 2 Interventional Accepts healthy volunteers Results available

Study of the Safety and Efficacy of APX3330 in Diabetic Retinopathy

ClinicalTrials.gov ID: NCT04692688

Public ClinicalTrials.gov record NCT04692688. 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, 3:58 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

Randomized, Placebo-Controlled, Double-Masked Study of the Safety and Efficacy of Orally Administered APX3330 in Subjects With Moderately Severe to Severe Non-Proliferative Diabetic Retinopathy and Mild Proliferative Diabetic Retinopathy

Brief summary

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

The objective of this study is to evaluate the safety and efficacy of APX3330 to treat diabetic retinopathy (DR) and diabetic macular edema (DME).

Study identification

NCT ID
NCT04692688
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Opus Genetics, Inc
Industry
Enrollment
103 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Accepts healthy volunteers

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Apr 8, 2021 (Actual)
Primary completion
Jan 25, 2023 (Actual)
Completion
Jan 25, 2023 (Actual)
Last update posted
Jun 8, 2026

2021 – 2023

United States locations

U.S. sites
24
U.S. states
13
U.S. cities
23
Facility City State ZIP Site status
Clinical Site 9 Phoenix Arizona 85014 —
Clinical Site 8 Bakersfield California 93309 —
Clinical Site 5 Beverly Hills California 91607 —
Clinical Site 11 Palm Desert California 92260 —
Clinical Site 2 Sacramento California 95825 —
Clinical Site 24 Walnut Creek California 94598 —
Clinical Site 19 Miami Florida 33143 —
Clinical Site 7 Winter Haven Florida 33880 —
Clinical Site 6 Carmel Indiana 46290 —
Clinical Site 14 Hagerstown Maryland 21740 —
Clinical Site 22 Springfield Massachusetts 01107 —
Clinical Site 17 Grand Blanc Michigan 48439 —
Clinical Site 12 Albuquerque New Mexico 87113 —
Clinical Site 15 Shirley New York 11967 —
Clinical Site 20 Charlotte North Carolina 28210 —
Clinical Site 1 Rapid City South Dakota 57701 —
Clinical Site 18 Austin Texas 78705 —
Clinical Site 16 Bellaire Texas 77030 —
Clinical Site 10 Fort Worth Texas 76104 —
Clinical Site 4 McAllen Texas 78550 —
Clinical Site 3 San Antonio Texas 78240 —
Clinical Site 23 San Antonio Texas 78624 —
Clinical Site 13 Southlake Texas 76092 —
Clinical Site 21 Ogden Utah 84010 —

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 NCT04692688, 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 Jun 8, 2026 · 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 NCT04692688 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →