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Completed Phase 3 Interventional

A Study of Glaucoma or Ocular Hypertension in Patients Within the United States

ClinicalTrials.gov ID: NCT00800267

Public ClinicalTrials.gov record NCT00800267. 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 Nov 6, 2026, 2:44 PM EST

All trial information on this site comes from the official ClinicalTrials.gov public API (clinicaltrials.gov/api/v2), run by the U.S. National Library of Medicine. We only display that public information; we do not add opinions, endorsements, or any other intent. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A 6-month, Randomized, Double-masked Comparison of Fixed Combination of Latanoprost and Timolol With the Individual Components, Continuing Into a 6-month Open Label Safety Study of Fixed Combination in Patients With Glaucoma or Ocular Hypertension. A Multicenter Study in the United States

Brief summary

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

Safety and efficacy study comparing between fixed combination latanoprost-timolol and its component parts.

Study identification

NCT ID
NCT00800267
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Enrollment
418 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
Jul 1997 (Type not available)
Primary completion
Jun 1999 (Actual)
Completion
Jun 1999 (Actual)
Last update posted
Feb 18, 2021

1997 – 1999

United States locations

U.S. sites
53
U.S. states
23
U.S. cities
42
Facility City State ZIP Site status
Pfizer Investigational Site Anaheim California 92801 —
Pfizer Investigational Site Anaheim California 92807 —
Pfizer Investigational Site Sacramento California 95819 —
Pfizer Investigational Site Sacramento California 95823 —
Pfizer Investigational Site San Francisco California 94115 —
Pfizer Investigational Site Boulder Colorado 80304-3573 —
Pfizer Investigational Site Denver Colorado 80210 —
Pfizer Investigational Site Largo Florida 34640 —
Pfizer Investigational Site Tampa Florida 33613 —
Pfizer Investigational Site Atlanta Georgia 30322 —
Pfizer Investigational Site Atlanta Georgia 30342 —
Pfizer Investigational Site Atlanta Georgia 30349 —
Pfizer Investigational Site East Point Georgia 30223 —
Pfizer Investigational Site Griffin Georgia 30223 —
Pfizer Investigational Site Morrow Georgia 30260 —
Pfizer Investigational Site Chicago Illinois 60612 —
Pfizer Investigational Site Wheaton Illinois 60187 —
Pfizer Investigational Site Elkhart Indiana 46515 —
Pfizer Investigational Site Mishawaka Indiana 46545 —
Pfizer Investigational Site South Bend Indiana 46601 —
Pfizer Investigational Site South Bend Indiana 46617 —
Pfizer Investigational Site Iowa City Iowa 52245 —
Pfizer Investigational Site Louisville Kentucky 40207 —
Pfizer Investigational Site Baltimore Maryland 21201 —
Pfizer Investigational Site Owings Mills Maryland 21117 —
Pfizer Investigational Site Boston Massachusetts 02111 —
Pfizer Investigational Site Golden Valley Minnesota 55422 —
Pfizer Investigational Site Minneapolis Minnesota 55421 —
Pfizer Investigational Site Kansas City Missouri 64111 —
Pfizer Investigational Site Kansas City Missouri 64114 —
Pfizer Investigational Site Warrensburg Missouri 64093 —
Pfizer Investigational Site Concord New Hampshire 03301 —
Pfizer Investigational Site South Plainfield New Jersey 07080 —
Pfizer Investigational Site Charlotte North Carolina 28204 —
Pfizer Investigational Site Charlotte North Carolina 28210 —
Pfizer Investigational Site Charlotte North Carolina 28260 —
Pfizer Investigational Site Matthews North Carolina 28105 —
Pfizer Investigational Site Monroe North Carolina 28112 —
Pfizer Investigational Site Portland Oregon 97201 —
Pfizer Investigational Site Portland Oregon 97210 —
Pfizer Investigational Site Wyomissing Pennsylvania 19610 —
Pfizer Investigational Site Charleston South Carolina 29412 —
Pfizer Investigational Site Mt. Pleasant South Carolina 29464-3245 —
Pfizer Investigational Site Memphis Tennessee 38119 —
Pfizer Investigational Site Austin Texas 78731-4941 —
Pfizer Investigational Site Galveston Texas 77555-1141 —
Pfizer Investigational Site Houston Texas 77030 —
Pfizer Investigational Site Charlottesville Virginia — —
Pfizer Investigational Site Richmond Virginia 23219 —
Pfizer Investigational Site Richmond Virginia 23235 —
Pfizer Investigational Site Tacoma Washington 98431 —
Pfizer Investigational Site Madison Wisconsin 53705 —
Pfizer Investigational Site Madison Wisconsin 53715 —

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 NCT00800267, 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 18, 2021 · Synced Nov 6, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00800267 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →