...
首页> 外文期刊>Journal of aerosol medicine and pulmonary drug delivery >Clinical Bioequivalence of Wixela Inhub and Advair Diskus in Adults With Asthma
【24h】

Clinical Bioequivalence of Wixela Inhub and Advair Diskus in Adults With Asthma

机译:Wixela Inhub和Advair Diskus患有哮喘的临床生物等效性

获取原文
获取原文并翻译 | 示例
           

摘要

Background: Wixela (R) Inhub (R) is a dry powder inhaler approved as a generic equivalent to Advair (R) Diskus (R) (fluticasone propionate [FP]/salmeterol fixed-dose combination) for patients with asthma or chronic obstructive pulmonary disease (COPD). This study aimed at confirming the local (lung) therapeutic equivalence of both the FP and salmeterol components of Wixela Inhub (test [T]) to Advair Diskus (reference [R]) after inhalation. Methods: This randomized, double-blind, double-dummy, placebo-controlled, parallel-group study in patients >= 18 years with mild-to-moderate persistent asthma compared the local therapeutic equivalence (using forced expiratory volume in 1 second [FEV1]) of FP/salmeterol (100/50 mu g) after inhaled delivery via T and R. Results: Randomized patients (N = 1127) received T (n = 512), R (n = 512), or placebo (n = 103). T and R significantly increased day 1 FEV1 area under the effect curve over 12 hours of the change from baseline (AUC([0-12])) and day 29 trough FEV1 over placebo, indicating that these endpoints were sufficiently sensitive for evaluation of bioequivalence. On day 1, T and R each increased FEV1 AUC((0-12)) over placebo (3.134 L center dot h [T], 2.677 L center dot h [R]; each p < 0.0001). Following twice-daily dosing for 28 days, T and R also each increased trough FEV1 (measured on day 29) over placebo (235 mL [T], 215 mL [R]; each p < 0.0001). Least-squares mean T/R ratios (90% confidence intervals) for day 1 FEV1 AUC((0-12)) and day 29 trough FEV1 were 1.120 (1.016-1.237) and 1.069 (0.938-1.220), respectively, indicating that T and R were bioequivalent for both co-primary endpoints. FP/salmeterol was well tolerated when administered via either T or R. Conclusions: These results demonstrate that the therapeutic effects of Wixela Inhub are bioequivalent to Advair Diskus in the lung. Wixela Inhub represents a therapeutically equivalent new FP/salmeterol treatment option for use in the treatment of asthma and COPD.
机译:背景:Wixela(R)Inhub(R)是一种批准的干粉吸入器,作为哮喘或慢性阻塞性肺部患者的伴随(r)Diskus(r)(丙酮丙酮[fp] / salmeterol固定剂组合)的通用等同物疾病(COPD)。本研究旨在确认威克斯拉Inhub的FP和Salmeterol组分的局部(肺)治疗当量(测试[T])以在吸入后的辅导下(参考[R])。方法:这种随机,双盲,双伪,安慰剂控制,平行群体研究> = 18年,患有轻度至中度持续的哮喘,比较局部治疗当量(在1秒内使用强制呼气量[FEV1通过T和R.结果:随机患者(n = 1127)接受T(n = 512),R(n = 512),r(n = 512)或安慰剂(n = 103)。 T和R显着增加了在基线(AUC([0-12])的变化的效果曲线下的第1天FEV1面积(AUC([0-12]))和第29天槽FEV1,表明这些终点对于评估生物等效性足够敏感。在第1,T和R各自增加FEV1 AUC((0-12)),通过安慰剂(3.134 L中心点H [T],2.677 L中心点H [R];每个P <0.0001)。在每日28天的每日剂量后,T和R也增加了槽FEV1(在第29天测量)过安慰剂(235ml [T],215mL [R];每个P <0.0001)。第1天的最小二乘意味着T / R比(90%置信区间)FEV1 AUC((0-12))和第29天槽FEV1分别为1.120(1.016-1.237)和1.069(0.938-1.220),表明这一点对于共同初级终点,T和R是生物等效性。通过T或R或R.结论施用时,FP / Salmeterol良好耐受:这些结果表明,Wixela Inhub的治疗效果是对肺中的伴随的Diskus生物等效。 Wixela Inhub代表治疗等效的新型FP / Salmeterol治疗选择,用于治疗哮喘和COPD。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号