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白三烯D4受体拮抗剂ICI 204,219可缓解急性季节性变应性鼻炎的症状。

The leukotriene D4-receptor antagonist, ICI 204,219, relieves symptoms of acute seasonal allergic rhinitis.

作者信息

Donnelly A L, Glass M, Minkwitz M C, Casale T B

机构信息

Department of Internal Medicine, University of Iowa College of Medicine, Iowa City, USA.

出版信息

Am J Respir Crit Care Med. 1995 Jun;151(6):1734-9. doi: 10.1164/ajrccm.151.6.7767514.

Abstract

The efficacy and safety of single oral doses of the leukotriene D4-receptor antagonist, ICI 204,219, were tested in subjects with acute seasonal allergic rhinitis. Subjects who were enrolled in the double-blind, placebo-controlled trial spent 8 h/d for two consecutive days in a park at the peak of ragweed season (counts > 1,000 grains/m3). Subjects (n = 164) who had sufficient symptoms during a 3-h baseline period on Day 1 were randomized to treatment with 10 (n = 33), 20 (n = 33), 40 (n = 33), or 100 mg (n = 32) of ICI 204,219 or placebo (n = 33). Rhinitis symptoms (nasal congestion, sneezing, rhinorrhea, itchy nose, throat and palate, and eye symptoms) were recorded hourly in the park and three times each evening at home. Blood samples were collected twice daily to determine plasma levels of ICI 204,219. Nasal congestion improved (p < 0.01) most consistently from the evening of Day 1 through Day 2 after treatment with 20- and 40-mg doses of ICI 204,219 versus placebo. Sneezing and rhinorrhea (p < or = 0.05) also improved on Day 2 for subjects who received 20- and 40-mg doses of ICI 204,219 compared with placebo. Mean symptoms scores for the entire day showed that 20 mg of ICI 204,219 was the minimally effective dose in this trial. The onset of action for all treatment groups, including placebo, was within the first 2 h of dosing. No serious adverse events were reported during the trial. ICI 204,219 was well tolerated and relieved symptoms of acute seasonal allergic rhinitis.

摘要

对急性季节性变应性鼻炎患者进行了单剂量口服白三烯D4受体拮抗剂ICI 204,219的疗效和安全性测试。参加这项双盲、安慰剂对照试验的受试者在豚草季节高峰期(计数>1000粒/立方米)连续两天每天在公园呆8小时。在第1天3小时基线期有足够症状的受试者(n = 164)被随机分为接受10(n = 33)、20(n = 33)、40(n = 33)或100 mg(n = 32)的ICI 204,219治疗或安慰剂(n = 33)。在公园每小时记录鼻炎症状(鼻塞、打喷嚏、流涕、鼻痒、咽喉和上颚痒以及眼部症状),晚上在家记录三次。每天采集两次血样以测定ICI 204,219的血浆水平。与安慰剂相比,20 mg和40 mg剂量的ICI 204,219治疗后,从第1天晚上到第2天,鼻塞改善最为一致(p < 0.01)。接受20 mg和40 mg剂量ICI 204,219的受试者与安慰剂相比,第2天打喷嚏和流涕也有所改善(p≤0.05)。全天平均症状评分显示,20 mg的ICI 204,219是该试验中的最小有效剂量。所有治疗组(包括安慰剂)的起效时间均在给药后的前2小时内。试验期间未报告严重不良事件。ICI 204,219耐受性良好,可缓解急性季节性变应性鼻炎的症状。

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