drugset / Trial / NCT02917512

Efficacy and Safety Study of HU00701/HU007 Eye Drops in Patients With Dry Eye Syndrome

NCT02917512

Phase 2 Completed 114 enrolled Huons Co., Ltd.
RandomizedParallel-groupDouble-blindTreatment

Summary

A multicenter, Placebo controlled, Restasis® referenced, Randomized, Double blind, Phase II Study to Evaluate the Efficacy and Safety of HU00701/HU007 Eye Drops in Adult Patients with Dry Eye Syndrome

Timeline

Start
2016-03
Primary completion
2016-12
Completion
2016-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Cyclosporine Peptide 0.01 % Other
Subject Cyclosporine Peptide 0.02 % Other
Subject Cyclosporine Peptide 0.05 % Other

Indications