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阿巴西普对健康志愿者 QT 间期影响的群体药代动力学/药效学模型。

Population Pharmacokinetic/Pharmacodynamic Modeling of the Effect of Abrocitinib on QT Intervals in Healthy Volunteers.

机构信息

Pfizer Inc., Groton, Connecticut, USA.

Pfizer Inc., New York, New York, USA.

出版信息

Clin Pharmacol Drug Dev. 2022 Sep;11(9):1036-1045. doi: 10.1002/cpdd.1111. Epub 2022 May 9.

DOI:10.1002/cpdd.1111
PMID:35532896
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9835371/
Abstract

Abrocitinib is a selective Janus kinase 1 inhibitor for the treatment of moderate to severe atopic dermatitis (AD). To assess the relationship between abrocitinib plasma concentrations and heart rate (HR)-corrected QT (QTc) and HR and calculate the effect of abrocitinib on these parameters at supratherapeutic concentrations, 36 healthy volunteers received single doses of abrocitinib 600 mg, placebo, and moxifloxacin 400 mg in a 3-period crossover study. The relationship between change from baseline in Fridericia-corrected QTc (∆QTcF) values and abrocitinib plasma concentrations was modeled using a prespecified linear mixed-effects model. The 90%CIs for time-matched placebo-corrected ∆QTcF (∆∆QTcF) were calculated from model parameter estimates and assessed against the regulatory threshold (10 millisecond) at the predicted supratherapeutic concentration in patients with atopic dermatitis (2156 ng/mL). Mean (90%CI) time-matched placebo-corrected change from baseline in HR (∆∆HR) was calculated similarly. At the supratherapeutic concentration, mean (90%CI) estimates for ∆∆QTcF and ∆∆HR were 6.00 (4.52-7.49) milliseconds and 6.51 (5.23-7.80) bpm, respectively. Despite a concentration-dependent effect on ∆QTcF and ∆HR, with statistically significant slopes (90%CI) of 0.0026 (0.0018-0.0035) milliseconds/(ng/mL) and 0.0031 (0.0024-0.0038) bpm/(ng/mL), respectively, abrocitinib does not have a clinically significant effect on QTc interval or HR at supratherapeutic exposures.

摘要

阿布昔替尼是一种选择性的 Janus 激酶 1 抑制剂,用于治疗中重度特应性皮炎(AD)。为了评估阿布昔替尼血浆浓度与心率(HR)校正的 QT(QTc)和 HR 的关系,并计算超治疗浓度下阿布昔替尼对这些参数的影响,36 名健康志愿者接受了阿布昔替尼 600mg、安慰剂和莫西沙星 400mg 的单剂量 3 期交叉研究。使用预设的线性混合效应模型对 Fridericia 校正的 QTc(∆QTcF)值从基线的变化与阿布昔替尼血浆浓度之间的关系进行建模。从模型参数估计值计算了与监管阈值(10 毫秒)的 90%置信区间(90%CI),并在预测的超治疗浓度下(2156ng/mL)对特应性皮炎患者的校正 ∆QTcF(∆∆QTcF)进行了评估。类似地计算了从基线到时间匹配的安慰剂校正的 HR(∆∆HR)的平均(90%CI)时间匹配的安慰剂校正的变化。在超治疗浓度下,∆∆QTcF 和 ∆∆HR 的平均(90%CI)估计值分别为 6.00(4.52-7.49)毫秒和 6.51(5.23-7.80)bpm。尽管∆QTcF 和 ∆HR 存在浓度依赖性影响,具有统计学意义的斜率(90%CI)分别为 0.0026(0.0018-0.0035)毫秒/(ng/mL)和 0.0031(0.0024-0.0038)bpm/(ng/mL),但阿布昔替尼在超治疗暴露时对 QTc 间隔或 HR 没有临床意义的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94b9/9835371/ae45a1026e82/CPDD-11-1036-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94b9/9835371/c53fe2d27dfb/CPDD-11-1036-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94b9/9835371/0d92bd271ffc/CPDD-11-1036-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94b9/9835371/6fbde44b0bae/CPDD-11-1036-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94b9/9835371/5e9db72f2bda/CPDD-11-1036-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94b9/9835371/ae45a1026e82/CPDD-11-1036-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94b9/9835371/c53fe2d27dfb/CPDD-11-1036-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94b9/9835371/0d92bd271ffc/CPDD-11-1036-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94b9/9835371/6fbde44b0bae/CPDD-11-1036-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94b9/9835371/5e9db72f2bda/CPDD-11-1036-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94b9/9835371/ae45a1026e82/CPDD-11-1036-g004.jpg

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本文引用的文献

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Population Pharmacokinetics of Abrocitinib in Healthy Individuals and Patients with Psoriasis or Atopic Dermatitis.健康个体和银屑病或特应性皮炎患者阿布昔替尼的群体药代动力学。
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Effects of Renal Impairment on the Pharmacokinetics of Abrocitinib and Its Metabolites.
肾功能损害对阿布昔替尼及其代谢物的药代动力学的影响。
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Validation of enantioseparation and quantitation of an active metabolite of abrocitinib in human plasma.验证阿布昔替尼的一种活性代谢物在人血浆中的对映体分离和定量。
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Integrated Safety Analysis of Abrocitinib for the Treatment of Moderate-to-Severe Atopic Dermatitis From the Phase II and Phase III Clinical Trial Program.阿泊替尼治疗中重度特应性皮炎的 II 期和 III 期临床试验综合安全性分析。
Am J Clin Dermatol. 2021 Sep;22(5):693-707. doi: 10.1007/s40257-021-00618-3. Epub 2021 Aug 18.
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