Photosensitization Study in Androgenetic Alopecia

Status Completed

Clinical Trial Summary

This study evaluates the potential for induction of photosensitization by P-3074 0.25% finasteride cutaneous solution compared to that of placebo vehicle cutaneous solution and a negative control (0.9% sodium chloride, NaCl)

Clinical Trial Description

Healthy male volunteers, drawn from the general population, will be treated with P-3074 solution, placebo vehicle control and 0.9% sodium chloride USP (negative control) by using 6 induction applications on the back area and Ultraviolet A (UVA)/Ultraviolet B (UVB) irradiations during the 3 week induction period, a 10 day rest period, and a challenge phase of a 24-hour patch application, UVA and UVB irradiation followed by evaluation of photosensitization over the subsequent 72 hours. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT02791243
Study type	Interventional
Source	Polichem S.A.
Contact
Status	Completed
Phase	Phase 1
Start date	May 9, 2016
Completion date	June 27, 2016

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