drugset / Trial / NCT01654484

A Study Assessing the Safety and Efficacy of DE-117 Ophthalmic Solution in Patients With POAG or OHT

NCT01654484

Phase 1/2 Completed 60 enrolled Santen Inc.
RandomizedParallel-groupSingle-blindTreatment

Summary

The purpose of this study is to investigate the safety and efficacy of up to three concentrations of DE-117 ophthalmic solution (Low Dose, Medium Dose, and High Dose) as monotherapy and as adjunctive therapy (DE-117 ophthalmic solution with 0.0015% tafluprost) in subjects with primary open-angle glaucoma or ocular hypertension.

Timeline

Start
2012-07
Primary completion
2012-11
Completion
2012-11

Drugs

EvaluationDrugModalityDoseRoute
Comparator Tafluprost Other / unclassified 0.0015 % Other
Subject omidenepag isopropyl Small molecule Other

Indications