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Clinical Trial Summary

This study is to evaluate the therapeutic effect and safety of LPTAT in children with myopia.


Clinical Trial Description

The primary objective is to evaluate the superiority of LPTAT to placebo in slowing myopia progression through the change of SE(Spherical Equivalent), which is measured by cycloplegic autorefraction after 12-month treatment. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05529056
Study type Interventional
Source LitePharmTech Co., Ltd.
Contact GH KIM
Phone 82-70-8805-9682
Email ghkim@litepharm.com
Status Recruiting
Phase Phase 3
Start date May 25, 2022
Completion date December 31, 2023

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