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吸入长效β-肾上腺素能受体激动剂PF-00610355对志愿者和慢性阻塞性肺疾病患者心率的预测影响。

Predicted heart rate effect of inhaled PF-00610355, a long acting β-adrenoceptor agonist, in volunteers and patients with chronic obstructive pulmonary disease.

作者信息

Diderichsen Paul Matthias, Cox Eugène, Martin Steven W, Cleton Adriaan, Ribbing Jakob

机构信息

Quantitative Solutions BV, Breda, the Netherlands.

出版信息

Br J Clin Pharmacol. 2013 Nov;76(5):752-62. doi: 10.1111/bcp.12080.

Abstract

AIM

To assess the cardiovascular effects of a new inhaled long-acting β-adrenoceptor agonist PF-00610355 in COPD patients.

METHODS

Thirteen thousand and sixty-two heart rate measurements collected in 10 clinical studies from 579 healthy volunteers, asthma and COPD patients were analyzed. The relationship between heart rate profiles and predicted plasma concentration profiles, patient status, demographics and concomitant medication was evaluated using non-linear mixed-effects models. The median heart rate increase in COPD patients for doses of PF-00610355 up to 280 μg once daily was simulated with the final pharmacokinetic/pharmacodynamic (PKPD) model.

RESULTS

An Emax model accounting for delayed on-and off-set of the PF-00610355-induced change in heart rate was developed. The predicted potency in COPD patients was three-fold lower compared with healthy volunteers, while no difference in maximum drug effect was identified. Simulations suggested a maximum placebo-corrected increase of 2.7 (0.90-4.82) beats min(-1) in COPD patients for a PF-00610355 dose of 280 μg once daily, with 19% subjects experiencing a heart rate increase of more than 20 beats min(-1) compared with 8% in the placebo group.

CONCLUSIONS

This PKPD analysis supports the clinical observation that no relevant effects of PF-00610355 on heart rate in COPD patients should be expected for doses up to 280 μg once daily.

摘要

目的

评估新型吸入长效β-肾上腺素受体激动剂PF-00610355对慢性阻塞性肺疾病(COPD)患者心血管系统的影响。

方法

分析了从579名健康志愿者、哮喘和COPD患者的10项临床研究中收集的13062次心率测量数据。使用非线性混合效应模型评估心率变化曲线与预测血浆浓度曲线、患者状态、人口统计学特征及合并用药之间的关系。采用最终的药代动力学/药效学(PKPD)模型模拟了COPD患者每日一次给予剂量高达280μg的PF-00610355时的心率中位数增加情况。

结果

建立了一个Emax模型,该模型考虑了PF-00610355引起的心率变化的延迟起效和消退。COPD患者的预测效价相比健康志愿者低三倍,而最大药物效应未发现差异。模拟结果表明,对于COPD患者,每日一次给予280μg的PF-00,610355,安慰剂校正后的心率最大增加为2.7(0.90 - 4.82)次/分钟,19%的受试者心率增加超过20次/分钟,而安慰剂组为8%。

结论

该PKPD分析支持临床观察结果,即对于COPD患者,每日一次给予剂量高达280μg的PF-00610355,预计对心率无相关影响。

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