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A Phase 2 Study to Evaluate the Safety and Efficacy of CKD-498 in Female Patients With Androgenetic Alopecia

Androgenetic Alopecia Clinical Trial

Official title:
A Phase 2, Randomized, Double-blind, Multi-center, Parallel-group Trial to Evaluate the Efficacy and Safety of CKD-498 in Female Patients With Androgenetic Alopecia

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

Clinical Trial Details
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
View Details
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