Clinical Trials Directory

Trials / Completed

CompletedNCT00277498

A 12-week, Randomized, Double-masked, Parallel Group Comparison of Evening Dosing With Xalacom in Subjects With Glaucoma

A 12-Week, Randomized, Double-Masked, Parallel Group Comparison Of Xalacom Given In The Evening, Xalatan Given In The Evening, And Timolol Given In The Morning In Patients With Open Angle Glaucoma Or Ocular Hypertension In The United States.

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
528 (planned)
Sponsor
Pfizer's Upjohn has merged with Mylan to form Viatris Inc. · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

To demonstrate statistical superiority of the combination of latanoprost and timolol to the individual therapy of latanoprost and timolol based on intraocular pressure measurements at 8 AM, 10 AM, 4 PM at weeks 2, 6 and 12.

Conditions

Interventions

TypeNameDescription
DRUGXalacom
DRUGXalatan
DRUGTimolol

Timeline

Start date
2005-12-01
Completion
2007-06-01
First posted
2006-01-16
Last updated
2021-02-18

Locations

64 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT00277498. Inclusion in this directory is not an endorsement.