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
| Phase | Phase 3 |
|---|---|
| Study type | Interventional |
| Ages | 18 Years to 50 Years |
| Sex | Men only |
| Enrollment | 288 (estimated) |
| Sponsor | Chong Kun Dang Pharmaceutical Industry-sponsored |
| Locations | 1 site (Seoul) |
| Status | Recruiting |
| Started | April 8, 2025 |
| Main results expected | September 30, 2027 |
| Study ends | June 30, 2028 |
| Registry record updated | September 3, 2026 |
| Trial ID | NCT06916793 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
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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
Other studies for the same condition or treatment. Recruiting studies are listed first.
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PP405 0.05% topically applied gel for adult men with pattern hair loss
A topical gel called PP405 is being tested in adult men with androgenetic alopecia to see if it can help with hair growth and is safe over a year.
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EPI-001 for androgenetic alopecia in adults
This early-phase study tests autologous dermal papilla cell therapy (EPI-001) to see if it is safe and can help hair grow in people with androgenetic alopecia.
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JAK2 levels in balding and non-balding scalp before and after topical minoxidil
This will test whether three months of topical minoxidil changes JAK2 protein levels in the scalps of adults (18–50) with mild to moderate androgenetic alopecia.
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Secretome versus PRP injections to improve hair density in androgenetic alopecia
This will try secretome injections versus platelet-rich plasma (PRP) injections to see which more effectively increases hair density and the terminal-to-vellus hair ratio in adults with androgenetic alopecia.
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Fractional laser plus exosome vs. laser plus placebo for androgenetic alopecia
This study tests whether adding a human umbilical cord mesenchymal stem cell exosome solution to fractional laser therapy helps men with androgenetic alopecia grow more hair than laser therapy with a placebo.
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Once-daily 5% minoxidil foam for female pattern hair loss
This will try once-daily 5% minoxidil foam to see if it increases hair count in adult women with androgenetic alopecia compared with a placebo.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.