drugset / Trial / NCT02406209

A Safety and Efficacy Study of NS2 in Patients With Anterior Uveitis

NCT02406209

Phase 2 Completed 45 enrolled Aldeyra Therapeutics, Inc.
RandomizedParallel-groupTriple-blindTreatment

Summary

This is a randomized, multi-center, investigator masked, comparator controlled study. The purpose of this study is to determine the efficacy and safety of NS2 in patients with non-infectious acute anterior uveitis. Subjects will be randomized 1:1:1 to receive multiple doses of NS2 0.5%, NS2 0.5% and Pred Forte® 1%, or Pred Forte® 1%. Free aldehydes are thought to be related to inflammatory diseases such as uveitis. NS2, a small molecule aldehyde trap, may decrease inflammation by lowering aldehyde levels.

Timeline

Start
2015-03
Primary completion
2016-04
Completion
2016-04

Drugs

EvaluationDrugModalityDoseRoute
Subject Prednisolone Other / unclassified 1 % Topical
Subject Reproxalap Other / unclassified 0.5 % Topical