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Completed Phase 3 Interventional Results available

Study of the Efficacy and Safety of Intravitreal (IVT) Aflibercept for the Improvement of Moderately Severe to Severe Nonproliferative Diabetic Retinopathy (NPDR)

ClinicalTrials.gov ID: NCT02718326

Public ClinicalTrials.gov record NCT02718326. 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 21, 2026, 12:47 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 3, Double-Masked, Randomized Study of the Efficacy and Safety of Intravitreal Aflibercept Injection in Patients With Moderately Severe to Severe Nonproliferative Diabetic Retinopathy

Brief summary

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

The primary objective of the study is to assess the efficacy of intravitreal (IVT) aflibercept compared to sham treatment in the improvement of moderately severe to severe nonproliferative diabetic retinopathy (NPDR). The secondary objectives of the study are: * To characterize the safety of IVT aflibercept in patients with moderately severe to severe NPDR * To determine if IVT aflibercept will prevent the worsening of diabetic retinopathy and reduce the incidence of DME * To determine the anatomic effects of IVT aflibercept in patients with moderately severe to severe NPDR

Study identification

NCT ID
NCT02718326
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Regeneron Pharmaceuticals
Industry
Enrollment
402 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
Mar 29, 2016 (Actual)
Primary completion
Aug 6, 2018 (Actual)
Completion
Jul 16, 2019 (Actual)
Last update posted
Jul 30, 2020

2016 – 2019

United States locations

U.S. sites
71
U.S. states
28
U.S. cities
66
Facility City State ZIP Site status
Regeneron Study Site Phoenix Arizona 85020 —
Regeneron Study Site Tucson Arizona 85704 —
Regeneron Study Site Arcadia California 91007 —
Regeneron Study Site Beverly Hills California 90211 —
Regeneron Study Site Encino California 91436 —
Regeneron Study Site Fullerton California 92835 —
Regeneron Study Site La Jolla California 92093 —
Regeneron Study Site Mountain View California 94040 —
Regeneron Study Site Oakland California 94609 —
Regeneron Study Site Oceanside California 92056 —
Regeneron Study Site Sacramento California 95841 —
Regeneron Study Site Colorado Springs Colorado 80909 —
Regeneron Study Site Golden Colorado 80401 —
Regeneron Study Site New London Connecticut 06320 —
Regeneron Study Site Altamonte Springs Florida 32701 —
Regeneron Study Site Deerfield Beach Florida 33064 —
Regeneron Study Site Fort Myers Florida 33912 —
Regeneron Study Site Lakeland Florida 33805 —
Regeneron Study Site Largo Florida 33770 —
Regeneron Study Site Melbourne Florida 32901 —
Regeneron Study Site Miami Florida 33126 —
Regeneron Study Site Miami Florida 33143 —
Regeneron Study Site Orlando Florida 32806 —
Regeneron Study Site Plantation Florida 33324 —
Regeneron Study Site Tallahassee Florida 32308 —
Regeneron Study Site Tampa Florida 33612 —
Regeneron Study Site Winter Haven Florida 33880 —
Regeneron Study Ssites Marietta Georgia 30060 —
Regeneron study Site Tucker Georgia 30084 —
Regeneron Study Site Chicago Illinois 60612 —
Regeneron Study Site Oak Forest Illinois 60452 —
Regeneron Study Site Indianapolis Indiana 46290 —
Regeneron Study Site New Albany Indiana 47150 —
Regeneron Study Site Lexington Kentucky 40509 —
Regeneron Study Site Baltimore Maryland 21204 —
Regeneron Study Siste Baltimore Maryland 21209 —
Regeneron Study Site Baltimore Maryland 21287 —
Regeneron Study Site Hagerstown Maryland 21740 —
Regeneron Study Site Boston Massachusetts 02114 —
Regeneron Study Site Henderson Nevada 89052 —
Regeneron Study Site Bloomfield New Jersey 07003 —
Regeneron Study Site Albuquerque New Mexico 87109 —
Regeneron Study Site Asheville North Carolina 28803 —
Regeneron Study Site Charlotte North Carolina 28210 —
Regeneron Study Site Columbus Ohio 43212 —
Regeneron Study Site Oklahoma City Oklahoma 73104 —
Regeneron Study Site Medford Oregon 97504 —
Regeneron Study Site Kingston Pennsylvania 18704 —
Regeneron Study Site Philadelphia Pennsylvania 19107 —
Regeneron Study Site Florence South Carolina 29501 —
Regeneron Study Site Ladson South Carolina 29456 —
Regeneron Study Site West Columbia South Carolina 29169 —
Regeneron Study Site Rapid City South Dakota 57701 —
Regeneron Study Site Chattanooga Tennessee 37421 —
Regeneron Study Site Germantown Tennessee 38138 —
Regeneron Study Site Nashville Tennessee 37203 —
Regeneron Study Site Nashville Tennessee 37232 —
Regeneron Study Site Abilene Texas 79606 —
Regeneron Study Site 1 Austin Texas 78705 —
Regeneron Study Site 2 Austin Texas 78705 —
Regeneron Study Site Dallas Texas 75231 —
Regeneron Study Site Harlingen Texas 78559 —
Regeneron Study Site Houston Texas 77030 —
Regeneron Study Site San Antonio Texas 78240 —
Regeneron Study Site The Woodlands Texas 77384 —
Regeneron Study Site Willow Park Texas 76087 —
Regeneron Study Site Salt Lake City Utah 84132 —
Regeneron Study Site Burlington Vermont 05401 —
Regeneron Study Site Fairfax Virginia 22031 —
Regeneron Study Site Spokane Washington 99204 —
Regeneron Study Site Morgantown West Virginia 26506 —

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 18 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02718326, 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 30, 2020 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02718326 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →