Selective TYK2 Inhibition in the Treatment of Moderate to Severe Chronic Plaque Psoriasis

Skin Therapy Lett. 2022 Nov;27(6):1-5.

Abstract

Moderate to severe chronic plaque psoriasis may be difficult to control using current therapies, which has led to development of a novel class of therapy, selective tyrosine kinase 2 (TYK2) inhibitors, to address this unmet need. Oral deucravacitinib is a first-inclass selective TYK2 inhibitor, which has shown efficacy in moderate to severe chronic plaque psoriasis from two phase III pivotal trials (POETYK PSO-1 and PSO-2), whereby response rates were significantly higher with deucravacitinib vs. placebo or apremilast for Psoriasis Area Severity Index (PASI) 75 and static Physician's Global Assessment (sPGA) 0/1. Deucravacitinib was generally well tolerated and safe compared to placebo and apremilast. Although deucravacitinib is a type of Janus kinase (JAK) inhibitor, it only blocks specific cytokine-driven responses, potentially reducing off-target effects more commonly associated with other JAK inhibitors on the market. Incidence rates of serious adverse events, such as serious infections, malignancies, thrombosis, cardiovascular events, creatinine kinase elevation, hematologic changes, and lipid profile abnormalities were absent or low.

MeSH terms

  • Humans
  • Janus Kinase Inhibitors* / adverse effects
  • Psoriasis* / drug therapy
  • Psoriasis* / pathology
  • Severity of Illness Index
  • TYK2 Kinase / therapeutic use
  • Thalidomide / adverse effects
  • Treatment Outcome

Substances

  • apremilast
  • TYK2 Kinase
  • Thalidomide
  • Janus Kinase Inhibitors
  • TYK2 protein, human