Clinical Trials Directory

Trials / Completed

CompletedNCT00140049

A 12week, Randomized, Evaluator-Masked, Parallel Group Comparing Evening Dosing Of Xalacom Vs Cosopt In Subj W/ Glaucoma

A 12-Week Randomized, Evaluator-Masked, Parallel-Group, Multinational, Multi-Center Study Comparing The Efficacy And Safety Of The Fixed Combination Of Latanoprost And Timolol (Xalacom) With The Fixed Combination Of Dorzolamide And Timolol (Cosopt) In Patients With Open-Angle Glaucoma Or Ocular Hypertension.

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
238 (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 the statistical non inferiority of the combination of latanoprost and timolol given in the evening time once a day vs the combination of dorzamalide and timolol twice a day based on intraocular pressure measurements at 8 AM, 12 noon \& 4 PM during a 12 week treatment.

Conditions

Interventions

TypeNameDescription
DRUGXalacom
DRUGCosopt

Timeline

Start date
2005-07-01
Completion
2006-07-01
First posted
2005-08-31
Last updated
2021-02-18

Locations

25 sites across 5 countries: France, Germany, Greece, Italy, Sweden

Source: ClinicalTrials.gov record NCT00140049. Inclusion in this directory is not an endorsement.