Status:
COMPLETED
A 12-Week, Randomized, Double-Masked, Parallel Group Comparison Of Evening Dosing With Xalacom In Subjects With Glaucoma
Lead Sponsor:
Pfizer's Upjohn has merged with Mylan to form Viatris Inc.
Conditions:
Glaucoma, Open-Angle
Ocular Hypertension
Eligibility:
All Genders
18+ years
Phase:
PHASE3
Brief 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 P...
Eligibility Criteria
Inclusion
- Uni- or bilateral diagnosis of primary open angle glaucoma or ocular hypertension on beta-blocker monotherapy or dual therapy in which at least one medication is a beta-blocker for at least 4 weeks prior to screening
Exclusion
- Closed/ barely open anterior chamber angle or history of acute angle closure glaucoma.
- History of ALT (Argon Laser Trabeculoplasty) or SLT(selective Laser) within 3 months prior to screening
Key Trial Info
Start Date :
July 1 2005
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
June 1 2007
Estimated Enrollment :
500 Patients enrolled
Trial Details
Trial ID
NCT00159653
Start Date
July 1 2005
End Date
June 1 2007
Last Update
February 21 2021
Active Locations (55)
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1
Pfizer Investigational Site
Phoenix, Arizona, United States, 85032
2
Pfizer Investigational Site
Poway, California, United States, 92064
3
Pfizer Investigational Site
Redding, California, United States, 96002-2122
4
Pfizer Investigational Site
Redding, California, United States, 96002