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阿利卡福生用于治疗炎症性肠病。

Alicaforsen for the treatment of inflammatory bowel disease.

作者信息

Jairath Vipul, Khanna Reena, Feagan Brian G

机构信息

a Robarts Clinical Trials Inc. , University of Western Ontario , London , Ontario , Canada.

b Department of Medicine, Division of Gastroenterology , Western University , London , Canada.

出版信息

Expert Opin Investig Drugs. 2017 Aug;26(8):991-997. doi: 10.1080/13543784.2017.1349753. Epub 2017 Jul 6.

DOI:10.1080/13543784.2017.1349753
PMID:28670932
Abstract

Intracellular adhesion molecule-1 (ICAM-1), is a transmembrane glycoprotein of the immunoglobulin family, constitutively expressed on vascular endothelial cells and upregulated in inflamed colonic tissue. Alicaforsen, a 20 base ICAM-1 anti-sense oligonucleotide and highly selective ICAM-1 inhibitor, down-regulates ICAM-1 mRNA. Areas covered: We review mechanism of action, pharmacokinetics, pre-clinical, clinical and safety data of alicaforsen for the treatment of ulcerative colitis (UC), pouchitis and Crohn's disease (CD). Expert opinion: After 6 weeks of treatment, topical alicaforsen was significantly more effective than placebo in inducing remission in patients with moderate-severe distal UC, with treatment effects lasting up to 30 weeks. No difference was observed in head-head comparison with mesalamine topical enema, although alicaforsen appeared to have more durable treatment effect. Clinical trials of an intravenous formulation in Crohn's disease showed no significant treatment effect compared to placebo. An open-label trial in alicaforsen for pouchitis demonstrated encouraging results, now being assessed in a multi-national phase 3 trial. No major safety signals have been observed in UC patients treated with alicaforsen enemas. The potential as a novel therapy for pouchitis has led to orphan designation for this indication by the FDA and European Medicines Agency.

摘要

细胞间黏附分子-1(ICAM-1)是免疫球蛋白家族的一种跨膜糖蛋白,在血管内皮细胞上组成性表达,在炎症性结肠组织中上调。阿利卡福森是一种20个碱基的ICAM-1反义寡核苷酸和高度选择性的ICAM-1抑制剂,可下调ICAM-1 mRNA。涵盖领域:我们综述了阿利卡福森治疗溃疡性结肠炎(UC)、袋炎和克罗恩病(CD)的作用机制、药代动力学、临床前、临床和安全性数据。专家意见:治疗6周后,局部应用阿利卡福森在诱导中重度远端UC患者缓解方面明显比安慰剂更有效,治疗效果可持续长达30周。与美沙拉嗪局部灌肠剂进行头对头比较时未观察到差异,尽管阿利卡福森似乎具有更持久的治疗效果。在克罗恩病中静脉制剂的临床试验显示与安慰剂相比没有显著治疗效果。一项阿利卡福森治疗袋炎的开放标签试验显示了令人鼓舞的结果,目前正在一项多国3期试验中进行评估。在用阿利卡福森灌肠剂治疗的UC患者中未观察到重大安全信号。作为袋炎新疗法的潜力已导致美国食品药品监督管理局和欧洲药品管理局为此适应症指定了孤儿药地位。

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