Clinical Trials Directory

Trials / Completed

CompletedNCT00856622

A Study Demonstrating The Effect Of Latanoprost In Combination With Timolol, Latanoprost Alone And Timolol Alone On Eye Pressure In Open Angle Glaucoma Or Ocular Hypertension In Patients

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.

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

Summary

The purpose of this study is to demonstrate that fixed combination of latanoprost and timolol (PhXA41) has better IOP lowering effect than the individual monotherapies.

Conditions

Interventions

TypeNameDescription
DRUGi. Fixed combination of latanoprost 0.005% and timolol 0.5%one drop in the morning and placebo in the evening
DRUGtimolol 0.5% ophthalmic solutionone drop in the morning and evening
DRUGlatanoprost 0.005% ophthalmic solutionplacebo in the morning and latanoprost .005% in the evening

Timeline

Start date
1997-08-01
Primary completion
1999-06-01
Completion
1999-06-01
First posted
2009-03-06
Last updated
2021-02-21

Locations

37 sites across 1 country: Germany

Source: ClinicalTrials.gov record NCT00856622. Inclusion in this directory is not an endorsement.