drugset / Trial / NCT02163824

Safety and Efficacy of KPI-121 in Subjects With Postsurgical Inflammation

NCT02163824

Phase 3 Completed 380 enrolled Kala Pharmaceuticals, Inc.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The primary purpose of this study is to determine the efficacy and safety of KPI-121 ophthalmic suspension compared to placebo in subjects who have undergone cataract surgery. The efficacy and safety of two different concentrations and two different dosing regimens of KPI-121 are also being assessed.

Timeline

Start
2014-05
Primary completion
2014-12
Completion
2014-12

Drugs

EvaluationDrugModalityDoseRoute
Comparator Loteprednol Etabonate Other / unclassified 0.25 % Topical
Comparator Loteprednol Etabonate Other / unclassified 1 % Topical

Indications

No indication recorded.