drugset / Trial / NCT01275105

A Single-Center, Randomized, Double-Masked, Placebo and Active Controlled, Dose-Ranging Evaluation of the Duration of Action of Brimonidine Tartrate Ophthalmic Solution in the Control of Ocular Redness Induced by Conjunctival Allergen Challenge (CAC)

NCT01275105

Phase 2 Completed 68 enrolled Eye Therapies, LLC ORA, Inc. · collab
RandomizedParallel-groupDouble-blindPrevention

Summary

The purpose of this study is to evaluate the safety, efficacy, and dose response of brimonidine tartrate ophthalmic solution as compared to placebo in the prevention of allergen-induced conjunctival redness using a conjunctival allergen challenge (CAC) model. It is hypothesized that low-dose brimonidine tartrate ophthalmic solution will be more effective than vehicle in the prevention of conjunctival redness induced by conjunctival allergen challenge when instilled prior to the allergen challenge.

Timeline

Start
2011-01
Primary completion
2011-03
Completion
2011-03

Drugs

EvaluationDrugModalityDoseRoute
Comparator Brimonidine Small molecule 0.01 % Topical
Comparator Brimonidine Small molecule 0.025 % Topical
Comparator Oxymetazoline Other / unclassified 0.025 % Topical

Indications