Status:

COMPLETED

A Study to Evaluate the Efficacy and Safety of AD-208

Lead Sponsor:

Addpharma Inc.

Conditions:

Androgenetic Alopecia

Eligibility:

MALE

18-50 years

Phase:

PHASE3

Brief Summary

The purpose of this study is to evaluate the efficacy and safety of AD-208.

Detailed Description

The purpose of this study is to evaluate the efficacy and safety of AD-208 in male patients with androgenetic alopecia.

Eligibility Criteria

Inclusion

  • Male patients aged 18-50 years, inclusive
  • Patients who meet the appropriate criteria according to the classification of hair loss
  • Signed informed consent

Exclusion

  • Patients with hair loss disorders other than androgenetic alopecia
  • Other exclusions applied

Key Trial Info

Start Date :

June 9 2021

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

June 1 2023

Estimated Enrollment :

139 Patients enrolled

Trial Details

Trial ID

NCT04825561

Start Date

June 9 2021

End Date

June 1 2023

Last Update

July 21 2023

Active Locations (1)

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Page 1 of 1 (1 locations)

1

The Catholic University of Korea, Eunpyeong St. Mary's Hospital

Seoul, South Korea