Clinical trial

A 12week, Randomized, Evaluator-Masked, Parallel Group Comparing Evening Dosing…

NCT00140049 · Pfizer's Upjohn has merged with Mylan to form Viatris Inc., Industry · Completed

Key facts

NCT number NCT00140049
Title A 12week, Randomized, Evaluator-Masked, Parallel Group Comparing Evening Dosing Of Xalacom Vs Cosopt In Subj W/ Glaucoma
Official title 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…
Lead sponsor Pfizer's Upjohn has merged with Mylan to form Viatris Inc., Industry
Status Completed
Phase Phase 4
Study type Interventional
Conditions Glaucoma, Open Angle, Ocular Hypertension
Intervention type Drug
Interventions Xalacom, Cosopt
Enrollment 238
Start date Jul 1, 2005
Completion Jul 1, 2006
First posted Aug 31, 2005
Last update posted Feb 18, 2021
Countries France, Germany, Greece, Italy, Sweden

At a glance

  • 10–99 Study sites
  • No Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date:

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