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

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Androgenetic alopecia
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Brief Title

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

Official Title

A Multicenter, Randomized, Double-blind, Placebo-controlled, Parallel, Phase 3 Clinical Trial to Evaluate the Efficacy and Safety of AD-208 in Male Patients With Androgenetic Alopecia

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.

Study Phase

Phase 3

Study Type

Interventional

Primary Outcome

The amount of Change in the total number of hairs

Condition

Androgenetic Alopecia

Intervention

AD-208

Study Arms / Comparison Groups

 Active Comparator
Description:  AD-208 and Placebo of AD-2081

Publications

* Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.

Recruitment Information

Recruitment Status

Drug

Estimated Enrollment

130

Start Date

May 31, 2021

Completion Date

April 22, 2022

Primary Completion Date

October 1, 2021

Eligibility Criteria

        Inclusion Criteria:

          -  Male patients aged 18-50 years, inclusive

          -  Patients who meet the appropriate criteria according to the classification of hair
             loss

          -  Signed informed consent

        Exclusion Criteria:

          -  Patients with hair loss disorders other than androgenetic alopecia

          -  Other exclusions applied

Gender

Male

Ages

18 Years - 50 Years

Accepts Healthy Volunteers

No

Contacts

, +82-031-891-6916, [email protected]

Administrative Informations

NCT ID

NCT04825561

Organization ID

AD-208P3

Responsible Party

Sponsor

Study Sponsor

Addpharma Inc.

Study Sponsor

, ,

Verification Date

March 2021