A Clinical Study Evaluating the Safety and Efficacy of SI-614 Ophthalmic Solution in Patients With Dry Eye.

• Status: Completed
• Trial end date: 1969-12-31
• Target enrollment: 0
• Participant gender: All

Summary

The purpose of this study is to assess the safety and effectiveness of SI-614 solution compared with placebo solution in treating patients with dry eye.

• Phase: Phase 2/Phase 3
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Seikagaku Corporation
• Treatments: Ophthalmic Solutions

Criteria

Inclusion Criteria:

• Be at least 18 years of age

• Have provided written informed consent

• Have dry eye in both eyes

Exclusion Criteria:

• Use of contact lenses

• Have an uncontrolled systemic disease

• Have an uncontrolled psychiatric condition, or substance or alcohol abuse

• Women who is pregnant, nursing or planning a pregnancy