drugset / Trial / NCT01895985

Efficacy of Latanoprostene Bunod in Lowering Intraocular Pressure in Japanese Healthy Male Volunteers

NCT01895985

Phase 1 Completed 24 enrolled Bausch & Lomb Incorporated
NaSingle-groupOpen-labelTreatment

Summary

The objective of this study is to evaluate the effect of latanoprostene bunod dosed once daily (QD) in reducing intraocular pressure (IOP) measured over a 24-hour period in healthy subjects.

Timeline

Start
2013-07
Primary completion
2013-08
Completion
2013-10

Drugs

EvaluationDrugModalityDoseRoute
Subject Latanoprostene bunod Small molecule 0.024 % Topical

Indications

No indication recorded.