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Clinical Trial Summary

This is a multicenter open-label, prospective study in subjects with dark skin from one of the 3 ethnic/race backgrounds: Asian, Latin American and Black/African-American and with moderate to severe acne vulgaris on the face.

All eligible subjects will receive Adapalene 0.3% - BPO 2.5% gel (Epiduo Forte/TactuPump Forte) once daily on whole face.

The purpose of this trial is to evaluate subject reported outcomes with the combination of Adapalene 0.3% - BPO 2.5%, Epiduo Forte / TactuPump Forte gel, after 16 weeks of treatment of moderate to severe acne in dark skin phototypes (IV to VI).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02932267
Study type Interventional
Source Galderma
Contact
Status Completed
Phase Phase 3
Start date February 2, 2017
Completion date January 10, 2018

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