Efficacy and Safety of 5% Minoxidil Foam in Female Androgenetic Alopecia

Exclusion Criteria

• •Trial participants with known hypersensitivity to minoxidil or any excipient of the investigational product.
• •Trial participants with known hair loss disorders other than androgenetic alopecia (AGA)
• •Trial participants with any scalp disorder at screening that may interfere with efficacy evaluation, as determined by the investigator.
• •Lactating women
• •Trial participants with history of hypotension or uncontrolled hypertension
• •Trial participants with clinically significant abnormal laboratory findings at screening that may compromise efficacy and safety assessments, as determined by the investigator.
• •Trial participants with clinically significant ECG abnormalities at screening
• •Trial participants with history of malignancy prior to screening.
• •Trial participants known to have conditions or disorders that may affect hair growth or compromise study results.
• •Trial participants with history of using systemically administered therapeutic drugs prior to screening that may interfere with efficacy evaluation, etc.
• •Trial participants with history of topical minoxidil application to alopecia-affected areas prior to screening.
• •Trial participants with no response to prior minoxidil treatment for alopecia
• •Trial participants with history of 5α-reductase inhibitor use prior to screening.
• •Trial participants with history of spironolactone or cyproterone treatment prior to screening.
• •Trial participants with history of autologous platelet-rich plasma (PRP) administration prior to screening.
• •Trial participants with history of chemotherapy, cytotoxic agents, scalp radiation, and/or low-level laser therapy (LLLT) or surgical scalp procedures for FAGA prior to screening.
• •Trial participants with history of using medical shampoos or solutions containing ingredients or other components that may interfere with efficacy evaluation prior to screening.
• •Trial participants planning hair transplantation during the study period, or using hair weaving, non-breathable wigs, or hair bonding during treatment.
• •Trial participants in other interventional clinical trials within 3 months before screening (excluding non-interventional studies and screen failures) , or planned concurrent clinical trial enrollment.
• •Trial participants with history of major surgery within 3 months before screening or planning major surgery during the study period.
• •Trial participants deemed by the investigator to have other conditions that may compromise compliance or render them unsuitable for the study.