Safety and Efficacy Study of DE-110 Ophthalmic Suspension for the Treatment of Dry Eye Disease
| Status: | Completed |
|---|---|
| Conditions: | Ocular |
| Therapuetic Areas: | Ophthalmology |
| Healthy: | No |
| Age Range: | 18 - Any |
| Updated: | 10/14/2017 |
| Start Date: | November 2010 |
| End Date: | October 2011 |
A Phase II, Prospective, Randomized, Observer-masked, Parallel-group, Multi-center Study Assessing the Safety and Efficacy of Two Concentrations Compared to Placebo for the Treatment of Dry Eye Disease
Investigate the Safety and Efficacy of Two Concentrations of DE-110 Compared to Placebo for
the Treatment of Dry Eye Disease
the Treatment of Dry Eye Disease
Inclusion Criteria:
- Confirmed diagnosis of dry eye
- Not wear contact lenses during study
- 18 years or older
- Understand and provide written consent
- Negative pregnancy test and use acceptable method of contraception
Exclusion Criteria:
- Use of any topical ocular medication
- Any type of ocular surgery
- Diagnosis of on-going ocular infection and/or allergic conjunctivitis
- Uncontrolled systemic conditions/lid abnormalities
- Corneal transplants
- Females who are pregnant, nursing or planning a pregnancy
- Participation in another drug trial concurrently or within 30 days prior to study
We found this trial at
14
sites
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