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Completed Phase 2 Interventional Results available

Safety, Tolerability, and Efficacy of Aflibercept in Patients With Neovascular Age-Related Macular Degeneration

ClinicalTrials.gov ID: NCT04126317

Public ClinicalTrials.gov record NCT04126317. 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 19, 2026, 9:37 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 Randomized, Single-Masked, Active-Controlled Phase 2 Study of the Safety, Tolerability, and Efficacy of Repeated Doses of High-Dose Aflibercept in Patients With Neovascular Age-Related Macular Degeneration

Brief summary

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

The primary objectives of the study are to determine the safety of high-dose aflibercept (hereafter referred to as HD) and to determine if HD provides greater intraocular pharmacodynamic (PD) effect and/or longer duration of action compared to intravitreal aflibercept injection (hereafter referred to as IAI).

Study identification

NCT ID
NCT04126317
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Regeneron Pharmaceuticals
Industry
Enrollment
106 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
Nov 4, 2019 (Actual)
Primary completion
May 14, 2021 (Actual)
Completion
Nov 30, 2021 (Actual)
Last update posted
Aug 14, 2023

2019 – 2021

United States locations

U.S. sites
45
U.S. states
24
U.S. cities
45
Facility City State ZIP Site status
Regeneron Study Site Phoenix Arizona 85020 —
Regeneron Study Site Sun City Arizona 85351 —
Regeneron Study Site Encino California 91436 —
Regeneron Study Site Fullerton California 92835 —
Regeneron Study Site Mountain View California 94040 —
Regeneron Study Site Palm Desert California 92211 —
Regeneron Study Site Sacramento California 95819 —
Regeneron Study Site Santa Ana California 92705 —
Regeneron Study Site Colorado Springs Colorado 80909 —
Regeneron Study Site Golden Colorado 80401 —
Regeneron Study Site Waterford Connecticut 06385 —
Regeneron Study Site Fort Lauderdale Florida 33309 —
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 Tallahassee Florida 32308 —
Regeneron Study Site Winter Haven Florida 33880 —
Regeneron Study Site Augusta Georgia 30909 —
Regeneron Study Site Marietta Georgia 30060 —
Regeneron Study Site Oak Forest Illinois 60452 —
Regeneron Study Site Hagerstown Maryland 21740 —
Regeneron Study Site Royal Oak Michigan 48073 —
Regeneron Study Site Bloomfield New Jersey 07003 —
Regeneron Study Site Teaneck New Jersey 07666 —
Regeneron Study Site Albuquerque New Mexico 87102 —
Regeneron Study Site Great Neck New York 11021 —
Regeneron Study Site Asheville North Carolina 28803 —
Regeneron Study Site Charlotte North Carolina 28210 —
Regeneron Study Site Columbus Ohio 43212 —
Regeneron Study Site Edmond Oklahoma 73013 —
Regeneron Study Site Portland Oregon 97221 —
Regeneron Study Site Kingston Pennsylvania 18704 —
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 Abilene Texas 79606 —
Regeneron Study Site Arlington Texas 76012 —
Regeneron Study Site Austin Texas 78705 —
Regeneron Study Site Houston Texas 77030 —
Regeneron Study Site The Woodlands Texas 77384 —
Regeneron Study Site Salt Lake City Utah 84107 —
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 1 non-U.S. site.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04126317, 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 Aug 14, 2023 · Synced Oct 19, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT04126317 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →