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Safety of aerosolized INS 365 in patients with mild to moderate cystic fibrosis: results of a phase I multi-center study.

机译:气雾化INS 365在轻度至中度囊性纤维化患者中的安全性:I期多中心研究的结果。

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Cystic fibrosis (CF) is characterized by defective cystic fibrosis transmembrane regulator (CFTR) expression and function, associated with abnormal ion transport and mucociliary clearance, and clinical lung disease. Triphosphate nucleotides such as uridine-5'-triphosphate (UTP) and INS 365, may be useful for CF through actions, mediated via P2Y(2) extracellular receptors, on chloride and liquid secretion, and ciliary beat frequency. INS 365 may offer chemical stability advantages over UTP. In a randomized, double-blind, multicenter phase I study, we studied the safety and maximally tolerated dose of escalating, single doses of aerosolized INS 365, in adult and pediatric patients with mild to moderate CF lung disease (FEV(1) > or = 45% predicted). In four successive dose cohorts of adult patients (n = 12 per cohort, age > or = 18 years) and four successive pediatric dose cohorts (n = 12 per cohort, age 5-12 years), patients were randomized 3:1 active/placebo (0.9% saline) to evaluate doses of 20, 40, 80, and 100 mg INS 365 delivered by nebulizer (Pari Star ). Sputum was collected pre- and post-dosing to obtain preliminary results on clinical efficacy. After each dose cohort, a Data Safety Monitoring Committee (DSMC) reviewed the data. Forty-eight adult and 36 pediatric patients completed the protocol (up to 100 mg for adults, 80 mg for pediatric patients). The predominant adverse events were cough, wheezing, chest tightness, and a decrease in FEV(1) (occurring in 8/48 adults, and 5/36 pediatric patients), which occurred predominantly in the 80-mg and 100-mg dose cohorts. Though a few adult patients had a tendency to increase sputum production, there was little consistent effect noted on sputum production in this acute, single-dose study. The data suggest that aerosolized INS 365 is safe when delivered at single doses of up to 40 mg in adults and children with CF, but that higher doses are unlikely to be tolerated. Copyright 2001 Wiley-Liss, Inc.
机译:囊性纤维化(CF)的特征是囊性纤维化跨膜调节剂(CFTR)的表达和功能缺陷,与异常的离子转运和粘膜纤毛清除以及临床肺部疾病有关。三磷酸核苷酸,例如尿苷5'-三磷酸(UTP)和INS 365,可通过CF2和液体分泌以及纤毛搏动频率通过P2Y(2)细胞外受体介导的作用,对CF有用。 INS 365可能比UTP具有化学稳定性优势。在一项随机,双盲,多中心I期研究中,我们研究了中度和中度CF肺病(FEV(1)>或成人)的成年和儿科患者的安全性和最大耐受剂量的单剂量雾化INS 365逐步升级=预测的45%)。在成年患者的四个连续剂量组(每组n = 12,年龄≥18岁)和四个连续的儿科剂量组(n =每组12,年龄5-12岁)中,将患者随机分为3:1活动/安慰剂(0.9%生理盐水)以评估雾化器(Pari Star)递送的20、40、80和100 mg INS 365剂量。在给药前和给药后收集痰以获得临床疗效的初步结果。在每个剂量组之后,数据安全监测委员会(DSMC)审查了数据。 48名成人和36名儿科患者完成了该方案(成人最多100 mg,小儿患者80 mg)。主要不良事件为咳嗽,喘息,胸闷和FEV(1)下降(在8/48成人和5/36儿科患者中发生),主要发生在80 mg和100 mg剂量人群中。尽管少数成年患者倾向于增加痰液的产生,但在这项急性单剂量研究中,对痰液产生的影响却很少。数据表明,雾化的INS 365在CF的成人和儿童中单次服用剂量最大为40 mg时是安全的,但更高的剂量不太可能被接受。版权所有2001 Wiley-Liss,Inc.

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