GSK-1605786, a selective small-molecule antagonist of the CCR9 chemokine receptor for the treatment of Crohn's disease.

Idrugs Pub Date : 2010-07-01
Bertus Eksteen, David H Adams
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引用次数: 0

Abstract

GSK-1605786 (CCX-282; Traficet-EN), a selective antagonist of the CC chemokine receptor (CCR9), is being developed by GlaxoSmithKline plc under license from ChemoCentryx Inc for the potential treatment of inflammatory bowel disease, including Crohn's disease and celiac disease. CCR9 is a tissue-specific lymphocyte trafficking molecule that selectively attracts both B- and T-cells to the small gut. Inhibition of CCR9 by GSK-1605786 may inhibit B- and T-cell entry to the small gut and ameliorate inflammation while leaving immune function at other anatomical sites unaffected. GSK-1605786 was assessed as a treatment for moderate-to-severe Crohn's disease in the phase II/III PROTECT-1 trial and as a treatment for celiac disease in a phase II trial. Data suggest that GSK-1605786 is efficacious in patients with Crohn's disease with the advantage of being orally bioavailable.

GSK-1605786, CCR9趋化因子受体的选择性小分子拮抗剂,用于治疗克罗恩病。
gsk - 1605786 (ccx - 282;Traficet-EN是一种CC趋化因子受体(CCR9)的选择性拮抗剂,由葛兰素史克公司根据ChemoCentryx公司的许可开发,用于治疗炎症性肠病,包括克罗恩病和乳糜泻。CCR9是一种组织特异性淋巴细胞运输分子,可选择性地将B细胞和t细胞吸引到小肠。GSK-1605786抑制CCR9可能会抑制B细胞和t细胞进入小肠并改善炎症,同时不影响其他解剖部位的免疫功能。GSK-1605786在II/III期PROTECT-1试验中被评估为中度至重度克罗恩病的治疗药物,在II期试验中被评估为乳糜泻的治疗药物。数据显示GSK-1605786对克罗恩病患者有效,具有口服生物利用度的优势。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Idrugs
Idrugs 医学-药学
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