Features and properties of abrocitinib
Alternative names | Cibinqo®; PF 04965842; PF-4965842 |
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Class | Amines; anti-inflammatories; antipsoriatics; cyclobutanes; pyrimidines; pyrroles; skin disorder therapies; small molecules; sulfonamides |
Mechanism of action | JAK1 inhibitor |
Route of administration | Oral |
Pharmacodynamics | Selective for JAK1 over other JAKs; dose-dependently reduces markers of inflammation; reduces platelet counts and increases LDL-C, HDL-C and total cholesterol levels, in a dose-related fashion |
Pharmacokinetics | Rapidly absorbed after oral administration, reaching Cmax within 1 h; elimination half-life ≈ 5 h |
Most frequent adverse reactions | Nausea, headache, acne, herpes simplex, blood creatine phosphokinase increased > 5 × upper limit of normal, vomiting, dizziness, upper abdominal pain, herpes zoster |
ATC codes | |
WHO ATC code | D11A-H08 (abrocitinib) |
EphMRA ATC code | D11A (other dermatological preparations) |
Chemical name | N-(cis-3-(Methyl(7H-pyrrolo(2,3-d)pyrimidin-4-yl)amino)cyclobutyl)propane-1-sulfonamide |
Cmax maximum plasma concentration, HDL-C high-density lipoprotein cholesterol, JAK Janus kinase, LDL-C low-density lipoprotein cholesterol