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Completed Phase 2 Interventional Results available

Dose-Finding Study Comparing the Safety and Efficacy of Latanoprost to a Novel Treatment for Glaucoma

ClinicalTrials.gov ID: NCT00441883

Public ClinicalTrials.gov record NCT00441883. 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 18, 2026, 7:39 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 2, 28 Day Parallel-Group, Double-Masked, Dose-Finding Study Comparing the Safety and Efficacy of PF-03187207 to Latanoprost

Brief summary

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

This study will evaluate the safety and efficacy of PF 03187207.

Study identification

NCT ID
NCT00441883
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Bausch & Lomb Incorporated
Industry
Enrollment
176 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
Mar 2007 (Type not available)
Primary completion
Feb 2008 (Actual)
Completion
Jul 2008 (Actual)
Last update posted
Sep 14, 2020

2007 – 2008

United States locations

U.S. sites
19
U.S. states
12
U.S. cities
18
Facility City State ZIP Site status
Pfizer Investigational Site Artesia California 90701 —
Pfizer Investigational Site Newport Beach California 92663 —
Pfizer Investigational Site Petaluma California 94954 —
Pfizer Investigational Site Poway California 92064 —
Pfizer Investigational Site Danbury Connecticut 06810-4004 —
Pfizer Investigational Site Jacksonville Florida 32204 —
Pfizer Investigational Site Ormond Beach Florida 32174 —
Pfizer Investigational Site Atlanta Georgia 30339 —
Pfizer Investigational Site Atlanta Georgia 30342 —
Pfizer Investigational Site Evansville Indiana 47710 —
Pfizer Investigational Site Louisville Kentucky 40217 —
Pfizer Investigational Site Rochester New York 14618 —
Pfizer Investigational Site Charlotte North Carolina 28210 —
Pfizer Investigational Site High Point North Carolina 27262 —
Pfizer Investigational Site Tulsa Oklahoma 74104 —
Pfizer Investigational Site Cranberry Township Pennsylvania 16066 —
Pfizer Investigational Site Pittsburgh Pennsylvania 15238 —
Pfizer Investigational Site Memphis Tennessee 38119 —
Pfizer Investigational Site Austin Texas 78705 —

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 NCT00441883, 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 Sep 14, 2020 · Synced Oct 18, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00441883 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →