Mylan Pharma UK Limited, Sandwich, United Kingdom.
Roy J. and Lucille A. Carver College of Medicine, University of Iowa, Iowa City, Iowa.
J Aerosol Med Pulm Drug Deliv. 2019 Dec;32(6):352-363. doi: 10.1089/jamp.2018.1519. Epub 2019 Jun 28.
Asthma is widely treated using inhaled corticosteroid/long-acting beta agonist (LABA) combinations, for example, fluticasone propionate/salmeterol (FPS) dry powder inhaler, marketed as Advair Diskus. Some regulators require generics to demonstrate local (lung) therapeutic equivalence (LTE) for each component of the FPS reference, ideally with a dose-response within the approved FPS dose range. We sought to develop a methacholine challenge (MeCh) LTE methodology for assessing the LABA (salmeterol) component of FPS. Forty-six patients with asthma received single doses of albuterol (active control; 90 or 180 μg), FPS (100/50 or 200/100 μg), and placebo on 5 separate study days. Spirometry and MeCh were performed 1, 6, and 10 hours after study drug inhalation. Primary endpoint was provocative concentration of methacholine producing a 20% fall in forced expiratory volume in 1 second (PC). Study entry required screening PC ≤8 mg/mL, with a greater than fourfold increase (and PC ≤128 mg/mL) after 180 μg albuterol. Both albuterol (90 and 180 μg) and FPS (100/50 and 200/100 μg) significantly increased PC compared with placebo (sustained 6 and 10 hours postdose with FPS but not albuterol). The dose-response slopes (95% confidence interval) estimated 1 hour after treatment were 0.374 (-0.068 to 0.815) and 0.310 (-0.135 to 0.754) between low and high doses of albuterol and FPS, respectively, both nonsignificant. Slopes were shallower than those available in the literature for albuterol and formoterol, but similar to those for salmeterol. These data confirm that the bronchoprotective effect of FPS lasts longer than that of albuterol. The shallow dose-response slope we observed for albuterol is contrary to previous reports, probably due to the measurement of PC beginning at 1 hour postdose. The results suggest that use of MeCh to assess LTE for salmeterol formulations may be more difficult to accomplish than it is for albuterol and formoterol products.
哮喘广泛采用吸入皮质激素/长效β激动剂(LABA)联合治疗,例如丙酸氟替卡松/沙美特罗(FP S)干粉吸入剂,商品名为 Advair Diskus。一些监管机构要求仿制药证明 FP S 参考药物中每个成分的局部(肺部)治疗等效性(LTE),理想情况下,在批准的 FP S 剂量范围内具有剂量反应。我们试图开发一种用于评估 FP S 中 LABA(沙美特罗)成分的乙酰甲胆碱挑战(MeCh)LTE 方法。46 例哮喘患者在 5 个不同研究日接受沙丁胺醇(阳性对照;90 或 180μg)、FP S(100/50 或 200/100μg)和安慰剂的单次剂量。吸入研究药物后 1、6 和 10 小时进行肺活量测定和 MeCh。主要终点是引起用力呼气量下降 20%的乙酰甲胆碱浓度(PC)。研究入组要求筛选 PC ≤8mg/ml,180μg 沙丁胺醇后增加 4 倍以上(PC ≤128mg/ml)。沙丁胺醇(90 和 180μg)和 FP S(100/50 和 200/100μg)均显著增加了 PC,与安慰剂相比(FP S 在给药后 6 和 10 小时持续增加,但沙丁胺醇没有)。治疗后 1 小时估计的剂量反应斜率(95%置信区间)分别为低剂量和高剂量沙丁胺醇和 FP S 之间的 0.374(-0.068 至 0.815)和 0.310(-0.135 至 0.754),均无显著性差异。斜率比文献中报道的沙丁胺醇和福莫特罗的斜率小,但与沙美特罗的斜率相似。这些数据证实 FP S 的支气管保护作用持续时间长于沙丁胺醇。我们观察到的沙丁胺醇的浅剂量反应斜率与以前的报告相反,可能是由于在给药后 1 小时开始测量 PC。结果表明,使用 MeCh 评估沙美特罗制剂的 LTE 可能比评估沙丁胺醇和福莫特罗产品更困难。