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Completed Phase 2 Interventional Results available

Safety and Efficacy of PF-04217329 in Patients With Glaucoma or Elevated Eye Pressure.

ClinicalTrials.gov ID: NCT00572455

Public ClinicalTrials.gov record NCT00572455. 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 28, 2026, 2:38 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 2-STAGE, PHASE 2, DOUBLE-MASKED, RANDOMIZED, VEHICLE CONTROLLED, DOSE RESPONSE TRIAL OF PF-04217329 AND THE MARKETED FORMULATION OF LATANOPROST IN PATIENTS WITH PRIMARY OPEN ANGLE GLAUCOMA OR OCULAR HYPERTENSION

Brief summary

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

To evaluate the safety and efficacy of PF-04217329.

Study identification

NCT ID
NCT00572455
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Pfizer
Industry
Enrollment
318 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
Dec 11, 2007 (Actual)
Primary completion
Jun 26, 2009 (Actual)
Completion
Jun 26, 2009 (Actual)
Last update posted
Apr 30, 2021

2007 – 2009

United States locations

U.S. sites
23
U.S. states
12
U.S. cities
20
Facility City State ZIP Site status
Sall Research Medical Center Artesia California 90701 —
Eye Research Foundation Newport Beach California 92663 —
North Bay Eye Associates, Inc. Petaluma California 94954 —
Centre For Health Care Poway California 92064 —
Atlantic Institute of Clinical Research Daytona Beach Florida 32114 —
Florida Health Care Plans Daytona Beach Florida 32114 —
Eye Associates of Fort Myers Fort Myers Florida 33901 —
International Eye Associates, PA Ormond Beach Florida 32174 —
Coastal Research Associates,LLC Atlanta Georgia 30339 —
Omni Eye Services of Atlanta Atlanta Georgia 30342 —
Eye Care Centers Management, Inc. Morrow Georgia 30260 —
The Eye Group of Southern Indiana Evansville Indiana 47710 —
Taustine Eye Center Louisville Kentucky 40217 —
Rochester Ophthalmological Group, PC Rochester New York 14618 —
Charlotte Eye Ear Nose and Throat Associates, PA Charlotte North Carolina 28210 —
Cornerstone Eye Care High Point North Carolina 27262 —
Mark J. Weiss, MD. Inc. Tulsa Oklahoma 74104 —
Glaucoma Care Center at Century Eye Care Bristol Pennsylvania 19007 —
Wills Eye Institute Philadelphia Pennsylvania 19107 —
Bluestein Custom Vision Charleston South Carolina 29414-5893 —
Total Eye Care, PA Memphis Tennessee 38119 —
Texan Eye Care, PA Austin Texas 78746 —
Eye Physicians of Austin Austin Texas 78756 —

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 NCT00572455, 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 Apr 30, 2021 · Synced Oct 28, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00572455 live on ClinicalTrials.gov.

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