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Discovery of Lanraplenib (GS-9876): A Once-Daily Spleen Tyrosine Kinase Inhibitor for Autoimmune Diseases

机译:Lanraplenib的发现(GS-9876):用于自身免疫疾病的曾经每日脾脏酪氨酸激酶抑制剂

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Spleen tyrosine kinase (SYK) is a critical regulator of signaling in a variety of immune cell types such as B-cells, monocytes, and macrophages. Accordingly, there have been numerous efforts to identify compounds that selectively inhibit SYK as a means to treat autoimmune and inflammatory diseases. We previously disclosed GS-9973 (entospletinib) as a selective SYK inhibitor that is under clinical evaluation in hematological malignancies. However, a BID dosing regimen and drug interaction with proton pump inhibitors (PPI) prevented development of entospletinib in inflammatory diseases. Herein, we report the discovery of a second-generation SYK inhibitor, GS-9876 (lanraplenib), which has human pharmacokinetic properties suitable for once-daily administration and is devoid of any interactions with PPI. Lanraplenib is currently under clinical evaluation in multiple autoimmune indications.
机译:脾酪氨酸激酶(SYK)是一种在各种免疫细胞类型中的信号传导的临界调节因子,例如B细胞,单核细胞和巨噬细胞。 因此,有许多努力鉴定选择性地抑制Syk作为治疗自身免疫和炎症性疾病的手段的化合物。 我们之前公开了GS-9973(EntoSpletinib)作为在血液恶性肿瘤临床评价下的选择性SYK抑制剂。 然而,与质子泵抑制剂(PPI)的出价调节剂和药物相互作用阻止了炎症性疾病中Entospletinib的发育。 在此,我们报告了第二代SYK抑制剂GS-9876(LANRAPLENIB)的发现,其具有适合于每日施用的人类药代动力学性质,并且没有与PPI的任何相互作用。 Lanraplenib目前在多种自身免疫指示中临床评估。

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