Study of 5% VVN001 Ophthalmic Solution in Dry Eye Disease
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.
Provided written informed consent prior to any study-related procedures. [+6]
Have a known hypersensitivity or contraindication to the IP or components of IP. [+2]