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Completed Not applicable Interventional

Intravitreous Pegaptanib Sodium Injection in Patients With Exudative Age-Related Macular Degeneration (AMD)

ClinicalTrials.gov ID: NCT00088192

Public ClinicalTrials.gov record NCT00088192. 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 Sep 3, 2026, 7:36 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

An Open Label, Non-Comparative Protocol for Use of Intravitreous Pegaptanib Sodium Injection Every 6 Weeks in Patients With Exudative Age-Related Macular Degeneration (AMD)

Brief summary

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

To provide Pegaptanib sodium injection to patients with subfoveal choroidal neovascularization (CNV) secondary to AMD, who are unable to participate in any of the Sponsor's other clinical studies with this drug for AMD, until such time as the patient's lesion is considered to have resolved or stabilized in the opinion of the treating ophthalmologist, or product becomes commercially available.

Study identification

NCT ID
NCT00088192
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
Eyetech Pharmaceuticals
Industry
Enrollment
Not listed

Conditions and interventions

Interventions

Drug

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
Jun 30, 2004
Primary completion
Not listed
Completion
Not listed
Last update posted
Aug 29, 2005

Started 2004

United States locations

U.S. sites
20
U.S. states
17
U.S. cities
19
Facility City State ZIP Site status
Doheny Eye Institute Los Angeles California 90033
Connecticut Retina Consultants, L.L.C. Bridgeport Connecticut 06606
New England Retina Associates Hamden Connecticut 06518
Retina Health Center Fort Myers Florida 33901
Retina Associates New Orleans Louisiana 70155
Cumberland Valley Retina Center Hagerstown Maryland 21740
New England Eye Center Boston Massachusetts 02111
Ophthalmic Consultants of Boston Boston Massachusetts 02114
Associated Retinal Consultants Royal Oak Michigan 48073
Eye Foundation of Kansas City Kansas City Missouri 64108
The Eye Center of Concord Concord New Hampshire 03301
Vitreo- Retinal Assoc. of NJ Belleville New Jersey 07109
Retina Associates of New Jersey, P.A. Teaneck New Jersey 07666
L.I. Vitreo-Retinal Consultants Great Neck New York 11021
Retina Associates of Cleveland Inc. Lakewood Ohio 44107
Dean A. McGee Eye Institute Oklahoma City Oklahoma 73104
The Casey Eye Institute Portland Oregon 97239
Palmetto Retina Center Columbia South Carolina 29204
Valley Retina Associates, P.A. McAllen Texas 78503
University of Vermont College of Medicine Burlington Vermont 05401

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 NCT00088192, 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 29, 2005 · Synced Sep 3, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00088192 live on ClinicalTrials.gov.

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