drugset / Trial / NCT03088605
Safety and Efficacy of TOP1630 for Dry Eye Syndrome
RandomizedParallel-groupQuadruple-blindTreatment
Summary
In subjects with Dry Eye Syndrome: The primary objective of this study is to compare the safety and tolerability of TOP1630 Ophthalmic Solution to placebo. The secondary objectives are to compare the efficacy of TOP1630 Ophthalmic Solution to placebo for the treatment of the signs and symptoms of dry eye syndrome.
Timeline
- Start
- 2017-02-20
- Primary completion
- 2017-06-15
- Completion
- 2017-06-15
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | TOP1630 | Unknown | — | Other |