Clinical trial Recruiting at 1 site Phase 3 Interventional Ages 18 to 50 Men only

CKD-843 for male pattern baldness: a new treatment in Phase 3

Official title: A Randomized, Double-blind, Multi-center, Placebo-controlled, Parallel-group Phase 3 Trial to Evaluate the Efficacy and Safety of CKD-843 in Male Patients With Androgenetic Alopecia

Run by Chong Kun Dang Pharmaceutical · NCT06916793 · Data updated 2026-11-12

We’re testing CKD-843 in men aged 18–50 with androgenetic alopecia to see if it helps hair loss over 12 months.

Quick facts

PhasePhase 3
Study typeInterventional
Ages18 Years to 50 Years
SexMen only
Enrollment288 (estimated)
SponsorChong Kun Dang Pharmaceutical
Industry-sponsored
Locations1 site (Seoul)
StatusRecruiting
StartedApril 8, 2025
Main results expectedSeptember 30, 2027
Study endsJune 30, 2028
Registry record updatedSeptember 3, 2026
Trial IDNCT06916793 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are men aged 18–50 with a clinical diagnosis of androgenetic alopecia and who consent to contraception during and for 24 weeks after the study.

Probably not a fit

Patients with other types of hair loss, significant scalp disease, major organ or mental health issues, or who do not agree to contraception requirements may not benefit.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This is a multicenter, randomized, double-blind study that compares two doses of CKD-843 to placebo and to dutasteride in men with androgenetic alopecia. Participants are assigned to one of four groups and followed for 12 months to measure hair growth and safety. The trial uses parallel groups and blinding to reduce bias. The lead sponsor is Chong Kun Dang Pharmaceutical, with the trial conducted at Seoul National University Hospital in Seoul, Korea.

Why it matters

Potential benefit: If successful, CKD-843 could offer an effective new option to improve hair growth in men with androgenetic alopecia.

How similar studies have gone: Previous trials in similar hair-growth approaches have shown mixed results; this study tests a novel approach in a rigorous Phase 3 design.

Who can join: the full rules

Show full inclusion / exclusion criteria
Key Inclusion Criteria:

* Male of age 18-50 years
* Clinical Diagnosis of Androgenetic Alopecia
* Written informed consent

Key Exclusion Criteria:

* Other types of Alopecia or other diseases that can cause hair loss
* Clinically significant scalp disease such as seborrheic dermatitis or psoriasis
* Clinically significant hepatic disease, thyroid disease, or mental illness, as determined by the Investigator
* Participants who do not agree to use contraception during the trial and for 24 weeks after the last dose, and plan to provide sperm or conceive within 24 weeks after the last dose

Where it's running

  • Seoul National University Hospital
    Seoul, South Korea
    Recruiting

Study contacts

  • Principal investigator: OhSang Kwon, MD, PhD — Seoul National University Hospital
  • Study coordinator: OhSang Kwon, MD, PhD
  • Email: oskwon@snu.ac.kr
  • Phone: +2-2072-2417

Similar studies

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.