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格隆溴铵超细干粉吸入剂配方的剂量反应:随机、双盲、安慰剂对照、剂量范围研究(GlycoNEXT)。

Dose-response of an extrafine dry powder inhaler formulation of glycopyrronium bromide: randomized, double-blind, placebo-controlled, dose-ranging study (GlycoNEXT).

作者信息

Beeh Kai M, Emirova Aida, Prunier Hélène, Santoro Debora, Nandeuil Marie Anna

机构信息

Insaf Respiratory Research Institute, Wiesbaden, Germany.

Global Clinical Development, Chiesi S.A.S, Bois-Colombes, France.

出版信息

Int J Chron Obstruct Pulmon Dis. 2018 May 25;13:1701-1711. doi: 10.2147/COPD.S168493. eCollection 2018.

Abstract

INTRODUCTION

An extrafine formulation of the long-acting muscarinic antagonist, glycopyrronium bromide (GB), has been developed for delivery via the NEXThaler dry powder inhaler (DPI). This study assessed the bronchodilator efficacy and safety of different doses of this formulation in patients with COPD to identify the optimal dose for further development.

PATIENTS AND METHODS

This was a multicenter, randomized, double-blind, placebo-controlled, incomplete block, three-way crossover study, including three 28-day treatment periods, each separated by a 21-day washout period. Eligible patients had a diagnosis of COPD and post-bronchodilator forced expiratory volume in 1 s (FEV) 40%-70% predicted. Treatments administered were GB 6.25, 12.5, 25 and 50 μg or matched placebo; all were given twice daily (BID) via DPI, with spirometry assessed on Days 1 and 28 of each treatment period. The primary end point was FEV area under the curve from 0 to 12 h (AUC) on Day 28.

RESULTS

A total of 202 patients were randomized (61% male, mean age 62.6 years), with 178 (88%) completing all the three treatment periods. For the primary end point, all the four GB doses were superior to placebo (<0.001) with mean differences (95% CI) of 114 (74, 154), 125 (85, 166), 143 (104, 183) and 187 (147, 228) mL for GB 6.25, 12.5, 25 and 50 μg BID, respectively. All four GB doses were also statistically superior to placebo for all secondary efficacy end points, showing clear dose-response relationships for most of the endpoints. Accordingly, GB 25 μg BID met the criteria for the minimally acceptable dose. Adverse events were reported by 15.5, 16.2, 10.9 and 14.3% of patients receiving GB 6.25, 12.5, 25 and 50 μg BID, respectively, and 14.8% receiving placebo.

CONCLUSION

This study supports the selection of GB 25 μg BID as the minimal effective dose for patients with COPD when delivered with this extrafine DPI formulation.

摘要

引言

已开发出长效毒蕈碱拮抗剂格隆溴铵(GB)的超微粉制剂,用于通过NEXThaler干粉吸入器(DPI)给药。本研究评估了不同剂量的该制剂在慢性阻塞性肺疾病(COPD)患者中的支气管扩张疗效和安全性,以确定进一步开发的最佳剂量。

患者与方法

这是一项多中心、随机、双盲、安慰剂对照、不完全区组、三向交叉研究,包括三个28天的治疗期,每个治疗期之间有21天的洗脱期。符合条件的患者诊断为COPD,支气管扩张剂使用后第1秒用力呼气量(FEV₁)为预测值的40%-70%。给予的治疗药物为6.25、12.5、25和50μg的GB或匹配的安慰剂;所有药物均通过DPI每日两次(BID)给药,在每个治疗期的第1天和第28天进行肺功能测定。主要终点是第28天0至12小时曲线下的FEV₁面积(AUC)。

结果

共有202例患者被随机分组(男性占61%,平均年龄62.6岁),其中178例(88%)完成了所有三个治疗期。对于主要终点,所有四个GB剂量均优于安慰剂(<0.001),6.25、12.5、25和50μg BID的GB的平均差异(95%CI)分别为114(74,154)、125(85,166)、143(104,183)和187(147,228)mL。对于所有次要疗效终点而言,所有四个GB剂量在统计学上也优于安慰剂,大多数终点显示出明显的剂量反应关系。因此,25μg BID的GB符合最小可接受剂量标准。接受6.25、12.5、25和50μg BID GB治疗的患者分别有15.5%、16.2%、10.9%和14.3%报告了不良事件,接受安慰剂治疗的患者为14.8%。

结论

本研究支持选择25μg BID的GB作为使用这种超微粉DPI制剂给药时COPD患者的最小有效剂量。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f3f/5973313/358c0d06f2e9/copd-13-1701Fig1.jpg

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