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Efficacy and Safety of PRO-118 Ophthalmic Solution in Allergic Conjunctivitis — PRO-118  

Conjunctivitis, Allergic Clinical Trial

Official title:
STUDY TO EVALUATE THE EFFICACY AND SAFETY OF PRO-118 OPHTHALMIC SOLUTION IN ALLERGIC CONJUNCTIVITIS

Clinical Trial Summary

The purpose of this study is to evaluate the efficacy and safety of four doses of PRO-118 ophthalmic solution ophthalmic solution compared with placebo, for the treatment of seasonal (SAC) and perennial (PAC) allergic conjunctivitis.

Clinical Trial Description

A phase II, double-masked, randomized, placebo-controlled, parallel-group and multicenter clinical trial, to evaluate and compared the clinical efficacy and safety of four doses of PRO-118 ophthalmic solution ( PRO-118 0.015% qd, PRO-118 0.015% twice daily , PRO-118 0.020% qd, PRO-118 0.020% twice daily) for the treatment of seasonal (SAC) and perennial (PAC) allergic conjunctivitis. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01541904
Study type Interventional
Source Laboratorios Sophia S.A de C.V.
Contact
Status Withdrawn
Phase Phase 2
Start date March 2011
Completion date February 2012
View Details
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