This is a phase 2, double masked, randomized, multi-center, parallel-group, 28-day study assessing the safety, tolerability and ocular hypotensive efficacy of AKB-9778 Ophthalmic Solution 4.0% administered once (AM) or twice (AM & PM) daily when used as an adjunctive therapy to latanoprost ophthalmic solution 0.005% once daily (PM) in subjects with elevated IOP due to OAG or OHT.
|Treatment||Placebo, Latanoprost ophthalmic solution, AKB-9778|
|Clinical Study Identifier||NCT04405245|
|Last Modified on||23 August 2020|
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