drugset / Trial / NCT03088605

Safety and Efficacy of TOP1630 for Dry Eye Syndrome

NCT03088605 ↗

Phase 2 Completed 69 enrolled ORA, Inc. Topivert Pharma Ltd · collab
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

EvaluationDrugModalityDoseRoute
Subject TOP1630 Unknown — Other

Indications