CompletedPhase 2NCT05677438
A Phase 2 Study to Evaluate the Safety and Efficacy of CKD-498 in Female Patients With Androgenetic Alopecia
Studying Alopecia
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Chong Kun Dang Pharmaceutical
- Principal Investigator
- ChangHun Huh, MD, PhD.Seoul National University Bundang Hospital
- Intervention
- CKD-498 dose#1(drug)
- Enrollment
- 121 enrolled
- Eligibility
- 19-54 years · FEMALE
- Timeline
- 2022 – 2023
Study locations (1)
- Seoul National University Bundang Hospital, Gyeonggi-do, South Korea
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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