173
Participants
Start Date
June 24, 2016
Primary Completion Date
July 13, 2018
Study Completion Date
July 13, 2018
Brinzolamide 1%/brimonidine tartrate 0.2% ophthalmic suspension
Brinzolamide/brimonidine vehicle
Inactive ingredients used as placebo comparator
Travoprost 0.004%/timolol 0.5% solution
1 drop instilled in the affected eye(s) daily in the morning (at 9:00) or in the evening (at 21:00) for up to 10 days during the Screening/Eligibility Phase and 42 days during the Treatment Phase
Contact Alcon for Locations (Europe, Asia, and Latin America), Fort Worth
Lead Sponsor
Alcon Research
INDUSTRY