drugset / Trial / NCT03676335

Assess the Safety and Efficacy of CsA Ophthalmic Gel in Subjects With Dry Eye

NCT03676335

RandomizedParallel-groupSingle-blindTreatment

Summary

The purpose of this study is to explore the efficacy and safety of CsA ophthalmic gel in the treatment of moderate to severe tear deficiency dry eye with different dosage, frequency and concentration, and to preliminarily determine the optimal dosage, frequency and concentration, so as to provide a theoretical basis for the design of follow-up clinical studies.

Timeline

Start
2018-05-09
Primary completion
2019-06-30
Completion
2019-12-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Cyclosporine Peptide 0.15 mg Topical
Subject Cyclosporine Peptide 0.2 mg Topical
Subject Cyclosporine Peptide 0.3 mg Topical
Background Hypromellose Unknown 75 mg

Indications