Formulation Comparison in Normal Volunteers

Status Completed

Clinical Trial Summary

This is a double-masked, single-center, crossover study in which normal volunteers will be randomized to receive one of two formulations of 0.5% AR-12286 Ophthalmic Solution for 8 days. Subjects will undergo a minimum 7-day washout, and then receive the alternate treatment for 8 days.

Clinical Trial Description

Not desired. ;

Study Design

Allocation: Randomized, Endpoint Classification: Safety Study, Intervention Model: Crossover Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment

Related Conditions & MeSH terms

Normal Volunteers

Clinical Trial Details

NCT number	NCT01250197
Study type	Interventional
Source	Aerie Pharmaceuticals
Contact
Status	Completed
Phase	Phase 1
Start date	November 2010
Completion date	December 2010

View Details

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