225 An oral, selective inhibitor of tyrosine kinase 2, BMS-986165, improves molecular, cellular, and clinical biomarkers associated with efficacy in moderate to severe psoriasis. (April 2019)

• Record Type: Journal Article
• Authors: Catlett, Ian; Hu, Sarah; Banerjee, Subhashis; Gordon, Kenneth; Krueger, James
• Is Part Of: Lupus science & medicine. Volume 6(2019)supplement 1
• Page Start: A169
• Page End: A169
• Publication Date: 2019-04
• Subjects: Systemic lupus erythematosus -- Periodicals; 616.772005
• DOI: 10.1136/lupus-2019-lsm.225
• Languages: English
• ISSNs: 2398-8851

Abstract

Abstract : Background: Psoriasis, a chronic immune-mediated inflammatory disease dependent upon the interleukin (IL)−23/TH17 pathway, is thought to be initiated through plasmacytoid dendritic cell activation and induction of type I interferons. BMS-986165 is a novel tyrosine kinase 2 (TYK2) inhibitor that blocks signal transduction of IL-23, IL-12, and type I interferons. BMS-986165 selectivity for TYK2, compared with Janus kinases (JAKs) 13, is driven by binding to its pseudokinase domain, rather than the conserved kinase domain. Methods: BMS-986165 was evaluated in a randomized, placebo-controlled, dose-ranging trial in 267 patients with moderate to severe psoriasis. Dose- and time-dependent effects on laboratory parameters indicative of non-selective inhibition of JAKs 13 were assessed. In an optional substudy, 37 patients provided biopsies, which were assessed from healthy-appearing skin on Day 1 and from lesional skin on Days 1, 15, and 85 for changes in the IL-23, IL-12, and type I interferon pathways by QRTPCR, RNA sequencing, and immunohistochemistry. Results: All BMS-986165 treatment groups, except 3 mg every other day (QOD), achieved superiority versus placebo in the proportion of patients achieving Psoriasis Area and Severity Index 75 after 12 weeks of treatment (primary endpoint): 3 mg QOD, 9.1%; 3 mg daily (QD), 38.6%; 3 mg twice daily (BID), 68.9%; 6 mg BID, 66.7%; and 12 mg QD, 75.0% vs 6.7% with placebo. Mean levels of factors impacted with JAK 13 inhibition, including hemoglobin, total cholesterol, neutrophils, platelets, total lymphocytes, natural killer, and B cells, were not affected by BMS-986165. Markers of the IL-23 pathway including IL-17(A/F), S100A8/9, IL-22, and -defensin returned to non-lesion levels dose-dependently. Interferon and IL-12 pathway genes were normalized; keratinocyte dysregulation markers keratin-16 and 10, and late cornified envelope genes, returned toward non-lesion levels with effective doses. Conclusions: Clinical efficacy with BMS-986165 was associated with decreases in IL-23/TH17 and interferon pathway markers. TYK2 selectivity was confirmed by lack of effect on clinical biomarkers of JAK 13 inhibition. BMS-986165 has promising efficacy in psoriasis, and a distinct selectivity profile that warrants further investigation. Funding Source(s): Bristol-Myers Squibb