The Catholic University of Korea, Eunpyeong St. Mary's Hospital
Seoul, South Korea
NCT Number: NCT04825561
The purpose of this study is to evaluate the efficacy and safety of AD-208.
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Notify Me18 year–50 year
Male
Interventional
Phase 3
Seoul, South Korea
The purpose of this study is to evaluate the efficacy and safety of AD-208 in male patients with androgenetic alopecia.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
PO, Once daily(QD), 24weeks
PO, Once daily(QD), 24weeks
PO, Once daily(QD), 24weeks
PO, Once daily(QD), 24weeks
Time frame: Baseline, Week 24
The amount of change in the total number of hairs in the unit area
Addpharma Inc.
Industry
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
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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