Powerful skin clearance

VTAMA cream demonstrated a favorable safety profile and was well tolerated in patients with atopic dermatitis down to 2 years of age1

Studied in a diverse patient population of
more than 800 patients with atopic dermatitis (AD) down to 2 years of age

813 patients with moderate to severe atopic dermatitis were studied in ADORING 1 and ADORING 2, the pivotal, phase 3 studies of VTAMA. Patients were aged 2 years and older, with a vIGA-ADTM score ≥3, EASI score ≥6, and BSA 5%-35% and were randomized 2:1 to receive VTAMA or vehicle daily for 8 weeks. The primary endpoint was vIGA-AD success.1,*

of patients were
2-17 years old1

Mean
BSA

of patients had
skin of color1,†

BSA, body surface area; EASI, Eczema Area and Severity Index; vIGA-AD, Validated Investigator Global Assessment for Atopic Dermatitis. vIGA-AD is a trademark of Eli Lilly and Co.

*vIGA-AD success, defined as vIGA-AD score of 0 (clear) or 1 (almost clear) and ≥2-grade improvement from baseline at Week 8.

Based on self-reported race and Fitzpatrick skin type.1

Powerful skin clearance1

Up to 46% of patients down to 2 years of age achieved clear or almost clear skin

45.4% and 46.4% of patients on VTAMA achieved vIGA-AD success vs 13.9% and 18.0% of patients on vehicle at Week 8 in the pivotal studies, ADORING 1 (P<0.0001) and ADORING 2 (P<0.0001), respectively.1

Up to 59% of patients down to 2 years of age achieved EASI75

55.8% and 59.1% of patients on VTAMA achieved EASI75 vs 22.9% and 21.2% of patients on vehicle at Week 8 in the pivotal studies, ADORING 1 (P<0.0001) and ADORING 2 (P<0.0001), respectively.1

The most common adverse reactions (incidence ≥1%) in patients with atopic dermatitis treated with VTAMA cream were upper respiratory tract infection, folliculitis, lower respiratory tract infection, headache, asthma, vomiting, ear infection, pain in extremity, and abdominal pain.

EASI75, ≥75% improvement in Eczema Area and Severity Index; vIGA-AD, Validated Investigator Global Assessment for Atopic Dermatitis. vIGA-AD is a trademark of Eli Lilly and Co.

*vIGA-AD success defined as vIGA-AD=0 (clear) or 1 (almost clear) and ≥2-grade improvement from baseline at Week 8.

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§vIGA-AD success, defined as vIGA-AD score of 0 (clear) or 1 (almost clear) and a ≥2-grade improvement from baseline at Week 8.
P<0.0001.

View Study Design

Visible results

Primary Endpoint Success2,**
Age: 7
Gender: Male
Fitzpatrick Skin Type: VI
Patient: 2016-013
Baseline
Week 2
Week 4
Week 8
Physician
Rated
vIGA-AD=3
EASI=8.2
Patient/Caregiver Rated
POEM=20
PP-NRS††=7
Physician
Rated
vIGA-AD=3
EASI=4.8
Patient/Caregiver Rated
POEM=7
PP-NRS††=2.3
Physician
Rated
vIGA-AD=2
EASI=2.4
Patient/Caregiver Rated
POEM=4
PP-NRS††=2.3
Physician
Rated
vIGA-AD=1
EASI=1.1
Patient/Caregiver Rated

Please note that the scores reflect a global assessment of the patient’s atopic dermatitis, whereas the images are only representative of one lesion or body area. Individual results may vary.

EASI, Eczema Area and Severity Index. Measure of disease severity that incorporates body surface and lesion intensity into a composite score from 0 to 72, with higher scores indicating more severe disease.
POEM, Patient-Oriented Eczema Measure. 7-item questionnaire to measure eczema severity focusing on the disease as experienced by the patient. Scores range from 0 to 28, with higher score indicating more severe disease.
PP-NRS, Peak Pruritus-Numeric Rating Scale. Patients were asked to rate their pruritus severity over a 24-hour period on a scale of 0 (no itch) to 10 (worst itch imaginable).
vIGA-AD, Validated Investigator Global Assessment for Atopic Dermatitis. Measure of AD severity with scores ranging from 0 (clear) to 4 (severe). vIGA-AD is a trademark of Eli Lilly and Co.

**Primary endpoint success defined as vIGA-AD score of 0 (clear) or 1 (almost clear) and a ≥2-grade improvement from baseline at Week 8.
††Week 2, 4, and 8 are averages.

Itch Relief

See how VTAMA may provide itch relief

INDICATION: VTAMA® (tapinarof) cream, 1% is an aryl hydrocarbon receptor (AhR) agonist indicated for the topical treatment of atopic dermatitis in adults and pediatric patients 2 years of age and older.

SELECTED SAFETY INFORMATION

Adverse Events: In atopic dermatitis, the most common adverse reactions (incidence ≥1%) were: upper respiratory tract infection, folliculitis, lower respiratory tract infection, headache, asthma, vomiting, ear infection, pain in extremity, and abdominal pain.

INDICATION: VTAMA® (tapinarof) cream, 1% is an aryl hydrocarbon receptor (AhR) agonist indicated for the topical treatment of atopic dermatitis in adults and pediatric patients 2 years of age and older.

SELECTED SAFETY INFORMATION

Adverse Events: In atopic dermatitis, the most common adverse reactions (incidence ≥1%) were: upper respiratory tract infection, folliculitis, lower respiratory tract infection, headache, asthma, vomiting, ear infection, pain in extremity, and abdominal pain.

Before prescribing VTAMA cream, please read the Prescribing Information.

References: 1. Silverberg JI, Eichenfield LF, Hebert AA, et al. Tapinarof cream 1% once daily: significant efficacy in the treatment of moderate to severe atopic dermatitis in adults and children down to 2 years of age in the pivotal phase 3 ADORING trials. J Am Acad Dermatol. 2024;91(3):457-465. 2. Organon DOF. ADORING Patient Images. 2024.

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