drugset / Trial / NCT02028312

A Phase IV, Randomized, Parallel Group, Investigator-Masked Evaluation of the Effect of Loteprednol Etabonate Ophthalmic Gel 0.5% on the Initiation of Dry Eye Treatment With Restasis®

NCT02028312

Phase 4 Withdrawn Edward Holland, MD
RandomizedParallel-groupSingle-blindTreatment

Summary

A pilot study to evaluate the impact of Lotemax® Gel (loteprednol etabonate ophthalmic gel 0.5%) on the initiation of Restasis® (cyclosporine ophthalmic emulsion 0.05%) therapy in subjects with dry eye.

Timeline

Start
2014-01
Primary completion
2016-02
Completion
2016-06

Drugs

EvaluationDrugModalityDoseRoute
Comparator Loteprednol Etabonate Other / unclassified 0.5 % Other
Comparator Cyclosporine Peptide 0.05 % Other

Indications