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

Outcome

Missed primary endpoint

paper The primary endpoint, change in corneal staining score from baseline to week 12, did not differ significantly among the control, HU00701, and HU007 groups PMID 33449860 ↗

Drugs

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

Indications