drugset / Trial / NCT01706263

U0289-402: An Open Label, 8 Week Study to Evaluate the Efficacy and Tolerability of MAXCLARITY II in Subjects With Acne

NCT01706263

Phase 4 Completed 28 enrolled Stiefel, a GSK Company GlaxoSmithKline · collab
NaSingle-groupOpen-labelTreatment

Summary

One of the main success factors in acne therapy is user compliance with treatment, product cost, availability and ease of use. Poor compliance may translate into decreased efficacy (either not improving symptoms well enough or not improving symptoms fast enough), tolerability issues or adverse effects (eg, erythema, dryness, or peeling of the skin), a lack of understanding of the instructions for use, or product cost/availability. Whatever the reason, poor compliance translates to decreased efficacy and increased frustration on the part of the user. The current study will evaluate the efficacy and tolerability of MAXCLARITY II, an over the counter, topical benzoyl peroxide (BPO) product line, in subjects with acne.

Timeline

Start
2009-08-01
Primary completion
2009-11-20
Completion
2009-11-20

Drugs

EvaluationDrugModalityDoseRoute
Subject Benzoyl Peroxide Other / unclassified 2.5 % Topical
Subject salicylic acid Small molecule 0.5 % Topical

Indications