Study detail
RecruitingPhase 2
An Eight-Week, Double-Masked, Randomized, Placebo-Controlled, Phase 2, Evaluation of the Safety and Efficacy of VSJ-110 Ophthalmic Solution in the Treatment of Dry Eye
Vanda Pharmaceuticals
Summary
The purpose of this study is to determine the safety and efficacy of VSJ-110 compared to placebo in the treatment of dry eye.
Eligibility
- Age range
- 18+ years
- Sex
- All
- Healthy volunteers
- No
Detailed criteria
Inclusion Criteria: * Be at least 18 years of age of either gender and any race. * Provide written informed consent and sign the HIPAA form. * Be willing and able to follow all instructions and attend all study visits. Exclusion Criteria: * Use of any of the disallowed medications during the washout and study period.
Interventions
- DrugVSJ-110
ophthalmic solution
- DrugPlacebo
ophthalmic solution
Locations (5)
- Vanda Investigational SiteNewport Beach, California
- Vanda Investigational SiteAndover, Massachusetts
- Vanda Investigational SiteShelby, North Carolina
- Vanda Investigational SiteMemphis, Tennessee
- Vanda Investigational SiteLynchburg, Virginia