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ABSTRACT: Objectives
The primary aim of this study was to assess the change in acne lesions and severity within all treatment groups over the course of a six-month study.Methods
This was a six-month, multisite, randomized, double-blind, controlled study in female subjects with mild-to-moderate acne to assess the clinical and psychological outcomes of treatment with biofilm disrupting acne cream 2x, biofilm disrupting acne cream 1x, biofilm disrupting acne cream without salicylic acid, 2.5% benzoyl peroxide (BPO) gel, and placebo. Subjects applied the assigned product to their face twice daily and were evaluated for clinical acne and quality of life outcomes at baseline and after six, 12, 18, and 24 weeks of treatment.Results
After 24 weeks of use, subjects treated with biofilm disrupting acne cream 2x had a significantly greater improvement in the Investigator Global Assessment (IGA), compared to those treated with 2.5% BPO gel. Based on dermatologic assessments, biofilm disrupting acne cream 2x, biofilm disrupting acne cream 1x, biofilm disrupting acne cream without salicylic acid, and placebo control were associated with less erythema and dryness, compared to 2.5% BPO gel.Limitations
Assessments within this study had the potential for subjective differences due to variability between evaluators.Conclucion
Biofilm disrupting acne cream 2x and biofilm disrupting acne cream 1x provided equivalent efficacy to 2.5% BPO gel with less of the adverse effects commonly associated with BPO, such as erythema and dryness. Both the biofilm disrupting acne cream without salicylic acid and the placebo control were associated with mild improvements to acne symptoms over the course of the 24-week study.Trial registry information
ClinicalTrials.gov, NCT03106766.
SUBMITTER: Marshall-Hudson A
PROVIDER: S-EPMC10110293 | biostudies-literature | 2023 Apr
REPOSITORIES: biostudies-literature

Marshall-Hudson Allyson A Tuley Michael M Damstra Maureen M Dosik Jonathan S JS Myntti Matthew F MF Porral Dianne D Palomo Janel J
The Journal of clinical and aesthetic dermatology 20230401 4
<h4>Objectives</h4>The primary aim of this study was to assess the change in acne lesions and severity within all treatment groups over the course of a six-month study.<h4>Methods</h4>This was a six-month, multisite, randomized, double-blind, controlled study in female subjects with mild-to-moderate acne to assess the clinical and psychological outcomes of treatment with biofilm disrupting acne cream 2x, biofilm disrupting acne cream 1x, biofilm disrupting acne cream without salicylic acid, 2.5% ...[more]