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. 2022 Mar 18;15:1935–1941. doi: 10.2147/JIR.S356316

Table 1.

The Application of Baricitinib in Dermatology. vIGA-AD (0, 1): Validated Investigator’s Global Assessment of AD (Complete or Almost Complete Removal of Lesions)

Diseases Signaling Pathway and Cytokines Latest Trials Effective Dose Effects Adverse Events
Atopic dermatitis (AD) TH2axis, TH17/TH22/TH1;14 IL-14, IL-5, IL-13, IL-22, IL-3137 Randomized clinical trial Phase 337,38 Oral 2mg/4mg once daily38 11.4% for baricitinib 2mg and 16.8% for baricitinib 4 mg achieved vIGA-AD (0, 1) at week 16; 2 mg baricitinib group achieved EASI75 in week-1637,38 Nasopharyngitis, upper respiratory tract infections, and folliculitis37
Psoriasis IL-23/Th17 axis15 Randomized clinical trial phase218 Oral 8mg/10mg once daily18 8mg or 10mg barbitinib group achieved index (PASI)-75 after 12 weeks18 No serious adverse events18
Vitiligo CXCR3+ CD8+ T; IFN-γ21 Randomized clinical trial phase221 Oral 4mg once daily (no result yet)21 No result yet21 No result yet21
Alopecia areata (AA) CD8 + NKG2D + T cells; IFN-γ, IL-15, IL-2, IL-722 Randomized clinical trial phase229 Oral 2mg/4mg once daily29 33.3% for baricitinib 2mg and 51.9% for baricitinib 4 mg achieved a severity of alopecia tool score of <20 at 36 weeks29 No serious adverse events29