OLUX-E® Foam Efficacy - Atopic Dermatitis
OLUX-E® Foam Effectively Clears Symptoms Overall With Proven Efficacy
Percent of Patients Clear or Almost Clear and Achieving Composite Endpoint of Treatment Success at Week 2*2,3
| Atopic Dermatitis Composite Endpoint (All 4 criteria had to be met) |
| - ISGA score of clear (0) or almost clear (1) |
| - Score of absent (0) or minimal (1) for erythema |
| - Score of absent (0) or minimal (1) for induration/papulation |
| - ≥2-grade improvement in ISGA score |
* Data derived from a phase 3, double-blind, randomized studies (at Week 2). An Investigator's Static Global Assessment (ISGA) score of clear (0) or almost clear (1) was utilized, reflecting the traditional definition of treatment success; success rates were 59% vs 16% for Vehicle Foam in atopic dermatitis patients (P<0.0001). The composite endpoints measuring treatment success required multiple criteria; success rates were 52% vs 14% for Vehicle Foam in atopic dermatitis patients (P<0.0001).
OLUX-E® Foam Effectively Treats Moderate to Severe Atopic Dermatitis.
Percent of Patients (n=251) Clear or Almost Clear of Atopic Dermatitis Symptoms at Week 2*2
*Results from a phase 3, double-blind, randomized study, which measured proportion of patients using OLUX-E® Foam vs Vehicle Foam who had a score of 0 or 1 for induration/papulation (56% vs 11%; P<0.0001), a score of 0 or 1 for erythema (53% vs 15%; P<0.0001), a score of 0 for pruritus (41% vs 8%; P<0.0001), and a score of 0 for lichenification (22% vs 4%; P <0.0001) at Week 2. Endpoints required a minimum 2-grade improvement.
Phase 3 Study

Baseline: Before OLUX-E® Foam.

After 2 weeks of OLUX-E® Foam BID treatment. Individual results may vary.
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Patient Information Brochure
Download this helpful patient information brochure to learn more about OLUX-E® Foam and dermatoses.