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Completed Phase 2 Interventional

Pegaptanib Sodium Compared to Sham Injection in Patients With Recent Vision Loss Due to Macular Edema Secondary to Central Retinal Vein Occlusion (CRVO)

ClinicalTrials.gov ID: NCT00088283

Public ClinicalTrials.gov record NCT00088283. 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, 7:07 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 Phase II Randomized, Dose-Ranging, Double-Masked, Multi-Center Trial, in Parallel Groups, Determining Safety, Efficacy and PK of Intravitreous Injections of Pegaptanib Sodium Compared to Sham Injection for 30 Weeks in Patients With Recent Vision Loss Due to Macular Edema Secondary to CRVO

Brief summary

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

Eyetech Pharmaceuticals Inc. and Pfizer, Inc. are studying an investigational drug, MacugenTM, for the possible treatment of CRVO. An investigational drug is one that has not been approved by the U.S. Food and Drug Administration (FDA). This investigational drug may slow the growth of abnormal blood vessels in the eye and may reduce tissue swelling in the eye. The purpose of this study is to compare the safety and efficacy of a Macugen™ injection to a "pretend" injection. In addition, the purpose of this study is to measure the action of the study drug in the body over a period of time and to check for the presence of the study drug in your blood (called pharmacokinetics or PK). This study will involve approximately 90 people. People who decide to participate will have an equal chance (1 in 3) to receive one of three study injections, two of which are Macugen™ and one of which is a "pretend" injection.

Study identification

NCT ID
NCT00088283
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Eyetech Pharmaceuticals
Industry
Enrollment
90 participants

Conditions and interventions

Interventions

Drug

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
May 2004 (Type not available)
Primary completion
Not listed
Completion
Not listed
Last update posted
Jan 19, 2007

Started 2004

United States locations

U.S. sites
35
U.S. states
21
U.S. cities
33
Facility City State ZIP Site status
Retina Centers, P.C., Northwest Location Tucson Arizona 85704 —
Retina Associates, SW Tucson Arizona 85710 —
Jules Stein Institute Los Angeles California 90095 —
Orange County Retina Associates Santa Ana California 92705 —
New England Retina Associates Hamden Connecticut 06518 —
Retina Group of Florida Fort Lauderdale Florida 33334 —
Bascom Palmer Eye Institute Miami Florida 33136 —
The University of Chicago Chicago Illinois 60637 —
Macula-Retina-Vitreous Service Indianapolis Indiana 46280 —
Vitreo-Retinal Consultants & Surgeons, P.A. Wichita Kansas 67214 —
Retina Associates New Orleans Louisiana 70155 —
Retina Group of Washington Chevy Chase Maryland 20815 —
Cumberland Valley Retina Center Hagerstown Maryland 21740 —
New England Eye Center Boston Massachusetts 02111 —
Massachusetts Eye & Ear Infirmary Boston Massachusetts 02114 —
Lahey Clinic, The Eye Institute Peabody Massachusetts 01960 —
Kresge Eye Institute Detroit Michigan 48201 —
Associated Retinal Consultants Royal Oak Michigan 48073 —
Eye Foundation of Kansas City Kansas City Missouri 64108 —
Charlotte Eye, Ear, Nose and Throat Associates, P.A. Charlotte North Carolina 28210 —
Duke University Eye Center Durham North Carolina 27710 —
The Cleveland Clinic Cleveland Ohio 44195 —
Retina Associates of Cleveland Inc. Lakewood Ohio 44107 —
Dean A. McGee Eye Institute Oklahoma City Oklahoma 73104 —
Casey Eye Institute Portland Oregon 97239 —
Wills Eye Institute Retina Research Philadelphia Pennsylvania 19107 —
Palmetto Retina Center Columbia South Carolina 29204 —
Southeastern Retina Associates Knoxville Tennessee 37909 —
Retina Research Institute of Texas, LLC Abilene Texas 79606 —
Austin Retina Associates Austin Texas 78705 —
Texas Retina Associates Dallas Texas 75231 —
VitreoRetinal Consultants Houston Texas 77030 —
Valley Retina Associates, P.A. McAllen Texas 78503 —
University of Wisconsin Madison Wisconsin 53705 —
The Eye Institute Milwaukee Wisconsin 53226 —

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 NCT00088283, 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 Jan 19, 2007 · 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 NCT00088283 live on ClinicalTrials.gov.

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