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首页> 外文期刊>Genetic Engineering & Biotechnology News: The Information Source of the Biotechnology Industry >Compel Data to PredictHigh-Perf ormance Clinical Trial Sites:To Reduce Guesswork over Rate of Recruitment and Other Metrics, Use a Platform-Based Approach
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Compel Data to PredictHigh-Perf ormance Clinical Trial Sites:To Reduce Guesswork over Rate of Recruitment and Other Metrics, Use a Platform-Based Approach

机译:将数据强制到redichrigh-perf ormance临床试验站点:减少估计和其他指标的猜测,使用基于平台的方法

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摘要

Drug development has been vexed by the following metrics for decades: 5% of eligible patients participate in a clinical trial, 25% of sites do not enroll any patients, and 80% of trials are delayed because of patient recruitment.Despite increased access to data (EMR, claims, registries, feasibility, CTMS, etc.) and advances in analytical techniques (that is, artificial intelligence, machine learning; AI-ML) over the past several years, the aforementioned metrics haven't moved much in the industry. A high degree of reliability in predicting site performance (that is, patient recruitment) and, in turn, trial outcomes, specifically rate of recruitment (RoR), remains elusive. Getting these predictions correct are crucial as net present value calculations and investments in new trials are often contingent on these numbers being reliable and accurate.
机译:据药物发展已经被以下数十年来烦恼:5%的符合条件的患者参与临床试验,25%的网站没有注册任何患者,而80%的试验因患者招聘而延迟。分别增加了对数据的访问 (EMR,索赔,注册机构,可行性,CTMS等)和分析技术的进步(即人工智能,机器学习; AI-ML)在过去几年中,上述指标在该行业中没有移动过多 。 在预测现场性能(即患者招聘)和反过来,试验结果,特别是招聘费率(ROR)的程度高度可靠性仍然难以捉摸。 获得这些预测正确是至关重要的,因为净目前的价值计算和新试验的投资往往是这些数字可靠和准确的。

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