The purpose of this study is to compare the intraocular pressure (IOP)-lowering efficacy and safety of two combination products in patients with open-angle glaucoma or ocular hypertension.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
319
One drop in the study eye(s) once daily, 9 PM, for 6 weeks
One drop in the study eye(s) twice daily for 6 weeks
One drop in the study eye(s) once daily for 6 weeks
Mean Intra-Ocular Pressure (IOP)
Time frame: 6 weeks
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