drugset / Trial / NCT02309385

Safety and Efficacy Study of DSP-Visulex for the Treatment of Anterior Uveitis

NCT02309385

Phase 1/2 Completed 44 enrolled Aciont Inc National Eye Institute (NEI) · collab
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to determine the efficacy, safety, and tolerability of dexamethasone sodium phosphate Visulex (DSP-Visulex) after repeated-dose administration in patients with acute anterior uveitis.

Timeline

Start
2014-10
Primary completion
2017-03-03
Completion
2017-03-03

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Dexamethasone Small molecule 8 % Topical
Subject Dexamethasone Small molecule 15 % Topical
Comparator Prednisolone Other / unclassified 1 % Topical