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A Study to Evaluate the Efficacy and Safety of KH001 in Patients With Dentin Hypersensitivity

Dentin Hypersensitivity Clinical Trial

Official title:
A Multicenter, Double-blind, Placebo-controlled, Randomized, Parallel-designed, Phase 2 Clinical Trial to Evaluate the Efficacy and Safety of KH001 in Patients With Dentin Hypersensitivity

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

Clinical Trial Details
NCT number NCT06264453
Study type Interventional
Source HysensBio Co., Ltd
Contact KeumHee Choi
Phone +82-2-502-6700
Email ckh113@hysensbio.com
Status Recruiting
Phase Phase 2
Start date March 19, 2024
Completion date August 30, 2024
View Details
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