Aryl Hydrocarbon Receptor (AhR) Agonist
Pregnancy: Avoid — animal studies showed no teratogenicity but insufficient human data; limit use in pregnancy unless clearly necessary
Tapinarof
Brand names: Vtama
Adult dose
Dose: 1% cream applied once daily to affected areas
Route: Topical
Frequency: Once daily
Max: No formal maximum; apply to affected areas only
Plaque psoriasis (adults); non-steroidal mechanism; apply thin layer to plaques; avoid eyes, mouth, vagina; can be used on any body site including face and intertriginous areas
Paediatric dose
Dose: Not established N/A/kg
Route: N/A
Frequency: N/A
Max: N/A
Not licensed in paediatrics; trials in adolescents ongoing
Dose adjustments
Renal
No systemic dose adjustment — topical
Hepatic
No systemic dose adjustment — topical
Paediatric weight-based calculator
Not licensed in paediatrics; trials in adolescents ongoing
Clinical pearls
- PSOARING 1 and 2 trials (Strober et al. NEJM 2021): tapinarof 1% cream achieved PGA 0/1 in 36% vs 6% vehicle at week 12 — novel non-steroidal topical mechanism; MHRA licensed 2023 for plaque psoriasis
- Novel AhR agonist mechanism: binds aryl hydrocarbon receptor in keratinocytes → upregulates skin barrier genes (filaggrin, loricrin) and downregulates IL-17A, IL-22, and IL-23 signalling; also has antioxidant effects via Nrf2 pathway; distinct from all existing topical treatments
- Remittive effect: PSOARING 3 long-term extension showed disease-free intervals (remission) lasting median 4 months after stopping treatment — unique property not seen with steroids or calcineurin inhibitors; patients may not need continuous treatment
- Folliculitis is the main tolerability concern (~23% in trials) — usually mild; treat with topical antibiotics if needed; typically does not require discontinuation; more common on trunk and intertriginous areas
- Steroid-sparing positioning: suitable for body sites where topical steroids are limited (face, genitalia, skin folds); no HPA-axis suppression, skin atrophy, or steroid rebound — useful for patients with psoriasis in sensitive locations or steroid phobia
Contraindications
- Known hypersensitivity to tapinarof
Side effects
- Folliculitis (most common — up to 23%)
- Contact dermatitis
- Pruritus at application site
- Headache
- Nasopharyngitis
- Perioral dermatitis (rare)
Interactions
- No clinically significant drug interactions — minimal systemic absorption
Monitoring
- PGA response at 4-8 weeks
- Folliculitis assessment (each visit)
- Application site reactions
Reference: BNFc; BNF 90; PSOARING 1 & 2 trials (Strober et al. NEJM 2021); PSOARING 3 long-term extension; MHRA SPC Vtama 2023; BAD Psoriasis Guideline (2017, updated 2022). Verify against your local formulary and the latest BNF before prescribing.
Related
Curated clinical cross-links plus same-class fallbacks.
Pathways
- Suspicious Pigmented Lesion — Melanoma Pathway · NICE NG14 2015 / BAD
- Cellulitis and Erysipelas · NICE NG141 2019 / CREST
- Psoriasis — Severity Assessment and Step-Up Therapy · NICE NG153 2019 / BAD
- Atopic Eczema — Assessment and Step-Up Therapy · NICE NG95 2023
- Urticaria and Angioedema · BSACI / EAACI Guidelines 2022
- Acne Vulgaris — Grading and Treatment · NICE NG198 2021 / BAD