drugset / Trial / NCT02832063

Clinical Trial in Subjects With Mild to Moderate Acne Vulgaris

NCT02832063 ↗

Phase 2/3 Completed 372 enrolled AOBiome LLC
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to demonstrate the safety, tolerability and efficacy of B244 administered over 12 weeks to participants with mild to moderate acne vulgaris relative to placebo.

Timeline

Start
2016-08
Primary completion
2017-07-19
Completion
2017-07-19

Drugs

EvaluationDrugModalityDoseRoute
Comparator B244 Other / unclassified — Topical

Indications