drugset / Trial / NCT06360133

Study of 5% VVN001 Ophthalmic Solution in Dry Eye Disease

NCT06360133 ↗

Phase 3 Recruiting 700 enrolled VivaVision Biotech, Inc
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This is a Phase 3, randomized, double-Masked, vehicle-controlled, multi-center study designed to evaluate the safety and efficacy of 5% VVN001 Ophthalmic Solution versus vehicle in Chinese subjects with dry eye disease.

Timeline

Start
2024-04-01
Primary completion
2026-03-31
Completion
2026-03-31

Drugs

EvaluationDrugModalityDoseRoute
Subject VVN001 Small molecule 5 % —

Indications