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Comparing Efficacy and Safety of TJO-083 in Dry Eye Diseases Patients

Dry Eye Clinical Trial

Official title:
A Multi-center, Randomized, Double-blinded, Active Control, Parallel, Phase 3 Trial to Evaluate the Efficacy and Safety of TJO-083 in Dry Eye Diseases Patients

Clinical Trial Summary

In patients with dry eye syndrome, the test drug(TJO-083) or the control drug is administered for 12 weeks, and the corneal staining of each group would be evaluated. The purpose of this clinical Study is to demonstrate that the test drug is not clinically inferior to the control drug.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06427031
Study type Interventional
Source Taejoon Pharmaceutical Co., Ltd.
Contact Sukyoung Kwon, MPH., PhD
Phone +82-799-0175
Email skkwon@taejoon.co.kr
Status Recruiting
Phase Phase 3
Start date July 14, 2023
Completion date March 1, 2025
View Details
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