Safety and Efficacy Study of Cyclosporine Ophthalmic Emulsion in Post-LASIK Patients

• Status: Completed
• Trial end date: 2009-06-01
• Target enrollment: 0
• Participant gender: All

Summary

This study will evaluate the safety and efficacy of cyclosporine ophthalmic emulsion administered twice daily following LASIK surgery

• Phase: Phase 2
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Allergan
• Treatments: Cyclosporine; Cyclosporins; Lubricant Eye Drops

Criteria

Inclusion Criteria:

• Patient is scheduled for bilateral LASIK surgery

• Patient is in good general health

• Eye glasses prescription of -1 to -8

Exclusion Criteria:

• Significant Dry Eye

• Presence of eye disease

• Uncontrolled systemic disease