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首页> 外文期刊>CPT: Pharmacometrics & Systems Pharmacology >Model?¢????based Meta?¢????Analysis on the Efficacy of Pharmacological Treatments for Idiopathic Pulmonary Fibrosis
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Model?¢????based Meta?¢????Analysis on the Efficacy of Pharmacological Treatments for Idiopathic Pulmonary Fibrosis

机译:基于模型的Meta分析药物治疗特发性肺纤维化疗效的分析

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Recently, the US Food and Drug Administration (FDA) approved the first two drugs (pirfenidone and nintedanib) indicated for the treatment of idiopathic pulmonary fibrosis (IPF). The purpose of this analysis was to leverage publicly available data to quantify comparative efficacy of compounds that are approved or in development. An analysis?¢????ready database was developed, and the analysis dataset is composed of summary?¢????level data from 43 arms in 20 trials, with treatment durations ranging from 8?¢????104 weeks. A hierarchical multivariable regression model with nonparametric placebo estimation was used to fit the longitudinal profile of change from baseline of percent predicted forced vital capacity (%predicted FVC) data. Pirfenidone and nintedanib were the only drugs identified to have significant estimated positive treatment effects. Model simulations were performed to further evaluate the covariate and time course of treatment effects on longitudinal change from baseline %predicted FVC to inform future trial designs and support decision making.
机译:最近,美国食品药品监督管理局(FDA)批准了前两种药物(吡非尼酮和nintedanib)用于治疗特发性肺纤维化(IPF)。该分析的目的是利用可公开获得的数据来量化已批准或正在开发的化合物的相对功效。开发了一个分析准备数据库,分析数据集由20项试验中43个小组的概要水平数据组成,治疗时间为8〜104周。使用具有非参数安慰剂估计的分层多变量回归模型来拟合预测的强制肺活量百分比(FVC预测百分比)数据相对于基线的纵向变化曲线。吡非尼酮和任他尼单抗是唯一被确定具有显着估计积极治疗效果的药物。进行了模型模拟,以进一步评估治疗效果相对于基线预测的FVC的纵向变化的协变量和时程,以为将来的试验设计和决策提供依据。

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