The purpose of this study is to evaluate the efficacy and safety of APSMNF in the treatment of male androgenetic alopecia.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
336
Clinica Geral Investiga Ltda
Campinas, São Paulo, Brazil
Variation in hair density assessed by phototrichogram.
Time frame: Change from baseline after 24 weeks of treatment.
Adverse events incidence and classification
Time frame: Through study completion, up to 24 weeks
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