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Completed Phase 2 Interventional Results available

Safety and Efficacy of Repeated Intravitreal Administration of Vascular Endothelial Growth Factor (VEGF) Trap in Patients With Wet Age-Related Macular Degeneration (AMD)

ClinicalTrials.gov ID: NCT00320788

Public ClinicalTrials.gov record NCT00320788. 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 Jun 26, 2026, 11:49 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, Controlled Study of the Safety, Tolerability and Biological Effect of Repeated Intravitreal Administration of VEGF Trap in Patients With Neovascular Age-Related Macular Degeneration

Study identification

NCT ID
NCT00320788
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Regeneron Pharmaceuticals
Industry
Enrollment
159 participants

Conditions and interventions

Interventions

  • aflibercept injection (VEGF Trap-Eye, BAY86-5321) Biological

Biological

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
Mar 31, 2006
Primary completion
May 31, 2008
Completion
Jul 31, 2008
Last update posted
Feb 29, 2012

2006 – 2008

United States locations

U.S. sites
18
U.S. states
14
U.S. cities
18
Facility City State ZIP Site status
Associated Retina Consultants Phoenix Arizona 85020
Retina Centers, PC Tucson Arizona 85704
Retina Vitreous Associates Medical Group Beverly Hills California 90211
Loma Linda University Health Care Loma Linda California 92354
Southeast Retina Center Augusta Georgia 30909
University of Chicago Chicago Illinois 60637
Midwest Eye Institute Indianapolis Indiana 46280
Johns Hopkins Hospital School of Medicine Baltimore Maryland 21287
Ophthalmic Consultants of Boston Boston Massachusetts 02114
New England Retina Consultants PC West Springfield Massachusetts 10189
Charlotte Eye, Ear, Nose & Throat Asssociates Charlotte North Carolina 28210
Dean A. McGee Eye Institute Oklahoma City Oklahoma 73104
Retina Northwest PC Portland Oregon 97210
Retina Diagnostic and Treatment Assoc., LLC Philadelphia Pennsylvania 19107
Black Hills Regional Eye Institute Rapid City South Dakota 57701
Retina-Vitreous Associates, P.C. Nashville Tennessee 37203
Vitreoretinal Consultants Scurlock Tower Texas Medical Center Houston Texas 77030
Medical Center Ophthamology San Antonio Texas 78240

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 NCT00320788, 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 Feb 29, 2012 · Synced Jun 26, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00320788 live on ClinicalTrials.gov.

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