Phase III Study of KX-826 With Adult Male Patients With AGA

Status Active, not recruiting

Clinical Trial Summary

This is a phase III, multi-center, randomized, double-blind, placebo-controlled clinical study to evaluate the efficacy and safety of KX-826 for topical use in Chinese adult male patients with androgenetic alopecia (AGA).

Clinical Trial Description

In this study, around 740 adult male subjects with AGA (rating IIIv, IV and V on Hamilton-Norwood scale) were to be enrolled. All subjects would be evaluated with 1:1 randomized to receive active drug or placebo in a double-blind fashion (370 subjects in each group), and would be treated for 24 weeks at the specified dose and frequency of each group. During the study, the subjects would undergo periodic efficacy and safety-related examinations and evaluation. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT06126965
Study type	Interventional
Source	Suzhou Kintor Pharmaceutical Inc,
Contact
Status	Active, not recruiting
Phase	Phase 3
Start date	December 29, 2021
Completion date	May 31, 2024

View Details

See also
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