Marked Improvement in Skin Lesions

Zedman® (Tapinarof Cream) Demonstrated Skin Lesion Improvement and Good Safety in an 8-Week Phase III Randomized Controlled Study

Evaluated in a multicenter Phase III study in China enrolling 271 patients aged ≥2 years with atopic dermatitis.
35 centers; 1% tapinarof cream n=183, placebo n=88; twice daily for 8 weeks.
Marked Improvement in Skin Lesions
In the Pediatric Subgroup (Aged 2–17)
At Week 8, 69.2% of patients achieved EASI75
(Placebo 31.0%)
In the Overall Study Population
Zedman® 54.4% vs Placebo 25.5% (P<0.001)
In the Pediatric Subgroup (Aged 2–17)
At Week 8, 61.5% of patients achieved IGA 0/1 (Clear or Almost Clear)
(Placebo 31.0%)
In the Overall Study Population
Zedman® 46.2% vs Placebo 21.4% (P<0.001)
The most common adverse reactions in patients with atopic dermatitis treated with Zedman® Cream include application site reactions, folliculitis, and contact dermatitis. EASI75: ≥75% improvement in Eczema Area and Severity Index; vIGA-AD: Validated Investigator's Global Assessment for Atopic Dermatitis; IGA-AD efficacy defined as IGA-AD score of 0 (Clear) or 1 (Almost Clear).
Week 8 EASI75: Zedman® vs Placebo
Important Safety Information
Indication: Zedman® (Tapinarof Cream, concentration/strength per package insert)is a drug with an aryl hydrocarbon receptor (AhR)-related mechanism of action. It is indicated for the topical treatment of patients aged 2 years and older.
*Observed adverse events (% placebo-adjusted): application site reactions (7.6%), folliculitis (3.2%), contact dermatitis (0.4%), headache (1.6%).