At the higher of two doses, oral tofacitinib was similar to etanercept in efficacy and safety.
A number of cytokines contribute to the pathogenesis of psoriasis. They mediate their effects by binding to receptors on target cells and, as a consequence, activate signal transduction pathways, which ultimately result in the development of psoriatic plaques. The Jak/Stat signal transduction pathway is particularly important in this regard. To evaluate the role of tofacitinib, an oral inhibitor of Jak1 and Jak3, in treating psoriasis, investigators enrolled 1106 adults with moderate-to-severe disease into a manufacturer-supported, randomized, double-blind, multicenter phase 3 trial.
There were four treatment arms: placebo, etanercept 50 mg twice weekly, tofacitinib 5 mg twice daily, and tofacitinib 10 mg twice daily. At 12 weeks, rates of ≥…
Reviewing Author
DisclosuresConsultant / Advisory board Astellas Pharmaceuticals
EquityVaxin
Grant / Research support NIH; NIH/NCI; Veteran’s Administration; Ferndale Laboratories; Kyowa Hakko Kirin Pharma, Inc.
Editorial boards Cancer Prevention Research; Photodermatology, Photoimmunology, & Photomedicine; UpToDate; eMedicine; Journal of Dermatological Sciences; JAMA Dermatology
Leadership positions in professional societies American Academy of Dermatology (Vice Chair, Committee on Science and Research); Photomedicine Society (Board of Directors)
DisclosuresConsultant / Advisory board Astellas Pharmaceuticals
EquityVaxin
Grant / Research support NIH; NIH/NCI; Veteran’s Administration; Ferndale Laboratories; Kyowa Hakko Kirin Pharma, Inc.
Editorial boards Cancer Prevention Research; Photodermatology, Photoimmunology, & Photomedicine; UpToDate; eMedicine; Journal of Dermatological Sciences; JAMA Dermatology
Leadership positions in professional societies American Academy of Dermatology (Vice Chair, Committee on Science and Research); Photomedicine Society (Board of Directors)