Trials / Completed
CompletedNCT01736527
Tear Fluid Levels of Loteprednol Etabonate Ophthalmic Gel 0.5% Following a Single Instillation
Tear Fluid Levels of Loteprednol Etabonate Ophthalmic Gel 0.5% at 6, 9, 12, and 24 Hours Following a Single Instillation in Healthy Volunteers
- Status
- Completed
- Phase
- Phase 1
- Study type
- Interventional
- Enrollment
- 12 (actual)
- Sponsor
- Bausch & Lomb Incorporated · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Accepted
Summary
To assess the levels of loteprednol etabonate (LE) in tear fluid following a single topical instillation of LE ophthalmic gel 0.5% formulation to healthy volunteers.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | LE Gel | Single drop of LE Gel 0.5% administered to the study eye on visit 2 |
Timeline
- Start date
- 2013-01-01
- Primary completion
- 2013-01-01
- Completion
- 2013-04-01
- First posted
- 2012-11-29
- Last updated
- 2013-11-08
- Results posted
- 2013-11-08
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT01736527. Inclusion in this directory is not an endorsement.