drugset / Trial / NCT02461719

Efficacy and Safety Study of TJCS for Treatment of Moderate to Severe Dry Eye Syndromes

NCT02461719

Phase 3 Completed 158 enrolled Taejoon Pharmaceutical Co., Ltd.
RandomizedParallel-groupTriple-blindTreatment

Summary

The purpose of this clinical Study is TJCS Eye Drops 0.05%(Cyclosporine ophthalmic nano-emulsion) group and Restasis Eye Drops 0.05%(Cyclosporine ophthalmic suspension) group 12 weeks after treatment, each treatment group comparisons for evaluation of efficacy and safety in Moderate to Severe Dry Eye Disease.

Timeline

Start
2014-01
Primary completion
2014-09
Completion
2014-10

Drugs

EvaluationDrugModalityDoseRoute
Comparator Cyclosporine Peptide 0.05 % Other

Indications