A little boy and woman playing with blocks A little boy and woman playing with blocks
Not actual patients/caregiver.

Powerful skin clearance

VTAMA cream delivers a safe and well-tolerated formulation for patients with atopic dermatitis down to 2 years of age.2

Not actual patients/caregiver.

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

VTAMA cream was studied for up to 56 weeks in 2 identical pivotal studies and an open-label long-term extension (LTE) study. ~50% of study population were patients with skin of color.2

Powerful skin clearance

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 cream 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.2

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

55.8% and 59.1% of patients on VTAMA cream 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.2

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 8.2

vIGA-AD Success at Week 82
Up to 46% of patients achieved clear or almost clear skin
*P<0.0001.

View Study Design

Visible results*

Primary Endpoint Success†7
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

Validated Investigator Global Assessment for Atopic Dermatitis (vIGA-AD): measure of AD severity with scores ranging from 0 (clear) to 4 (severe). vIGA-AD is a trademark of Eli Lilly and Co.
Eczema Area and Severity Index (EASI): 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.
Patient Oriented Eczema Measure (POEM): 7-item questionnaire to measure eczema severity focusing on the disease as experienced by the patient. Scores range from 0 to 28, with higher scores indicating more severe disease.
Peak Pruritus-Numeric Rating Scale (PP-NRS): patients are asked to rate their worst itch in the past 24 hours on a scale of 0 (no itch) to 10 (worst itch imaginable).

*Please note that these photographs are representative of one target lesion on individual patients treated with VTAMA cream during the pivotal clinical studies.

Primary endpoint success defined as vIGA-AD score of 0 (clear) or 1 (almost clear) and ≥2-grade improvement from baseline at Week 8.2

Rapid itch relief

See how VTAMA cream may provide rapid itch relief2-4

IMPORTANT SAFETY INFORMATION

Indications: VTAMA® (tapinarof) cream, 1% is an aryl hydrocarbon receptor agonist indicated for:

Adverse Events: In plaque psoriasis, the most common adverse reactions (incidence ≥1%) were: red raised bumps around the hair pores (folliculitis), pain or swelling in the nose and throat (nasopharyngitis), skin rash or irritation, including itching and redness, peeling, burning, or stinging (contact dermatitis), headache, itching (pruritus), and flu (influenza).
Adverse Events: In atopic dermatitis, the most common adverse reactions (incidence ≥1%) were: upper respiratory tract infection, red raised bumps around the hair pores (folliculitis), lower respiratory tract infection, headache, asthma, vomiting, ear infection, pain in extremity, and stomach-area (abdominal) pain.

You are encouraged to report negative side effects of prescription drugs to the FDA. Visit www.fda.gov/medwatch or call 1-800-FDA-1088.

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