Welch M J, Nelson H S, Paull B R, Smith J A, Feiss G, Tobey R E
Allergy and Asthma Medical Group and Research Center, San Diego, California.
Ann Allergy. 1994 Apr;72(4):348-52.
RG 12525 is a new oral leukotriene D4 (LTD4) antagonist with proven activity in animal and human models of leukotriene-induced bronchoconstriction. In this randomized, double-blind, parallel-group, placebo-controlled study the bronchodilator effects of single oral doses of RG 12525 of 25 and 200 mg or placebo were evaluated in 62 adult asthmatic patients. All patients had previously demonstrated 20% reversibility of FEV1 with an inhaled beta-agonist. They had an unmedicated FEV1 less than 80% of predicted value at the time of the study. Bronchodilator activity was assessed by spirometry before and at multiple time points after dosing for eight hours. A single 200-mg dose of RG 12525 of mg resulted in statistically significantly greater increases in mean maximum change above baseline for FEV1 and FEF25-75% than placebo. The peak effect was observed four to five hours after dosing. The RG 12525 dose of 25 mg dose induced better bronchodilation than placebo but the differences were not significant. Adverse clinical experiences or laboratory abnormalities were not noted.
RG 12525是一种新型口服白三烯D4(LTD4)拮抗剂,在白三烯诱导的支气管收缩的动物和人体模型中已证实具有活性。在这项随机、双盲、平行组、安慰剂对照研究中,对62名成年哮喘患者评估了单次口服25毫克和200毫克RG 12525或安慰剂的支气管扩张作用。所有患者此前吸入β受体激动剂后FEV1均有20%的可逆性。在研究时,他们未用药时的FEV1低于预测值的80%。通过在给药后8小时的多个时间点进行肺活量测定来评估支气管扩张活性。单次口服200毫克RG 12525导致FEV1和FEF25-75%较基线的平均最大变化在统计学上显著大于安慰剂。在给药后4至5小时观察到峰值效应。25毫克剂量的RG 12525诱导的支气管扩张优于安慰剂,但差异不显著。未观察到不良临床事件或实验室异常。