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Clinical Trial Summary

The purpose of this study is to evaluate the efficacy and safety of KH001 in patients with dentin hypersensitivity.


Clinical Trial Description

This study is multicenter, double-blind, placebo-controlled, randomized, parallel-designed, phase 2 study to evaluate the efficacy and safety of KH001. The total duration of the study will be approximately 7 to 11 weeks. Clinical safety evaluations will include physical examinations, vital signs, clinical laboratory results, and Adverse Event monitoring. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06264453
Study type Interventional
Source HysensBio Co., Ltd
Contact KeumHee Choi
Phone +82-2-502-6700
Email ckh113@hysensbio.com
Status Not yet recruiting
Phase Phase 2
Start date March 11, 2024
Completion date August 30, 2024

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