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Clinical Trial Summary

This study will assess the safety, tolerability, and efficacy of SM04554 at concentrations of 0.15% and 0.25%. Improved knowledge of the changes in hair counts and immunohistochemical analysis associated with androgenetic alopecia (AGA) before and after treatment with SM04554 and compared to placebo may lead to a greater understanding of the underlying mechanisms of action of SM04554.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02503137
Study type Interventional
Source Samumed LLC
Contact
Status Completed
Phase Phase 2
Start date August 2015
Completion date April 2016

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