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last updated on 08/02/2026
JAK Inhibitor
Baricitinib: in adult patients and children from 2 years of age
Baricitinib is a selective and reversible JAK1 and JAK2 inhibitor administered orally. Baricitinib has Marketing Authorization (MA) and is reimbursed in France for adults in the treatment of moderate-to-severe AD.
A European MA authorized baricitinib in October 2023 for children from 2 years of age with AD requiring systemic treatment.
This treatment is not reimbursed in France for children and adolescents at the time of writing these recommendations.
Recommended dose:
- 4 mg per day for adults or 2 mg per day for at-risk patientsor after achieving prolonged remission on 4 mg/day.
ANSM Recommendations (March 2023): JAK inhibitors should only be used in the absence of appropriate therapeutic alternatives in patients who are: aged 65 and over; smokers or long-term former smokers; presenting other cardiovascular risk factors or malignant tumors. Use with caution in patients with venous thromboembolic risk factors. Dosage recommendations are adjusted for certain groups of patients with risk factors.
The most common reported AEs for baricitinib: an increase in LDL cholesterol levels, upper respiratory tract infections, and headaches. Acneiform eruption is less frequent than with other JAK inhibitors. The frequency of HSV infections is higher in the 4 mg group compared to the 2 mg groups.
Concomitant use of emollients, TCS, and TCIs is possible.
➜ Upadacitinib
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