
- Minimal systemic absorption: Up to 96% of patients (N=187) were below the quantifiable limit (<50 pg/mL) at week 127,8
- Low rates of treatment discontinuation: 2.8% of patients discontinued treatment due to folliculitis and 2.9% discontinued treatment due to contact dermatitis1,6
- Study discontinuation: Of those randomized to receive VTAMA cream, 1.8% and 0.9% withdrew from the study due to folliculitis, 1.5% and 2.0% withdrew due to contact dermatitis in PSOARING 1 and 2, respectively
VTAMA® (tapinarof) cream, 1% is a versatile treatment option with no label restrictions on topical, external use to the affected skin areas. It was well tolerated even on sensitive skin areas like the face, neck, intertriginous areas, inframammary areas, axillae, genitalia, and anal crux. VTAMA cream is not for oral, ophthalmic, or intravaginal use.1,4






