drugset / Trial / NCT01895972

Long-Term Safety of Latanoprostene Bunod Ophthalmic Solution 0.024% in Japanese Subjects With OAG or OHT

NCT01895972

Phase 3 Completed 130 enrolled Bausch & Lomb Incorporated
NaSingle-groupOpen-labelTreatment

Summary

The objective of this study is to demonstrate the clinical safety of latanoprostene bunod 0.024% once daily (QD) over a 1-year treatment period.

Timeline

Start
2013-07-05
Primary completion
2015-04-02
Completion
2015-04-14

Drugs

EvaluationDrugModalityDoseRoute
Subject Latanoprostene bunod Small molecule 0.024 % Topical