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Clinical Trial Summary

This is a multi-centers, randomized, double-blind, parallel-group, Phase 2 Trial to evaluate the efficacy and safety of CKD-498 in female patients with Androgenetic Alopecia


Clinical Trial Description

Participants were randomly assigned in a 1:1:1:1 ratio to the following group: 3 dose of CKD-498 and Placebo. The patients are prescribed oral administration of the appropriate IP daily (3 tablets: actual medication and placebo) for 24 weeks. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05677438
Study type Interventional
Source Chong Kun Dang Pharmaceutical
Contact Jiwon Lee, Project Leader
Phone +82-2-2194-0470
Email jwl@ckdpharm.com
Status Recruiting
Phase Phase 2
Start date December 20, 2022
Completion date April 30, 2024

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