Overview

Evaluation of Efficacy of Ophthalmic Solution in Induced Allergic Conjunctivitis

Status:
Completed
Trial end date:
1969-12-31
Target enrollment:
Participant gender:
Summary
The purpose of this study is to establish the efficacy of R89674 0.25% ophthalmic solution compared with placebo in alleviating the signs and symptoms of conjunctival allergen challenge-induced allergic conjunctivitis
Phase:
Phase 3
Details
Lead Sponsor:
Vistakon Pharmaceuticals
Treatments:
Ophthalmic Solutions