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Artificial Intelligence for Clinical Trial Design

机译:临床试验设计的人工智能

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Artificial intelligence (AI) technologies have advanced to a level of maturity that allows them to be employed under real-life conditions to assist human decision-makers. AI has the potential to transform key steps of clinical trial design from study preparation to execution towards improving trial success rates, thus lowering the pharma R&D burden. Suboptimal patient cohort selection and recruiting techniques, paired with the inability to monitor patients effectively during trials, are two of the main causes for high trial failure rates: only one of 10 compounds entering a clinical trial reaches the market. This session will explain in layman's terms some of the foundations of AI methodology, such as Machine Learning and Deep Learning, highlighting how recent advances can be applied at specific stages of the clinical trial design process to improve cohort composition, patient recruitment, medication compliance and patient retention. A special focus will be given to describing how patients in neurology trials could be monitored more efficiently through Digital Disease Diaries, which use wearable devices, machine learning at the edge and cloud technology to automatically detect and log disease episodes and patient adherence to trial protocols. Like all technical revolutions, this comes with challenges and risks, both technical and regulatory. In particular, we will discuss scalability, data encryption and patient privacy.
机译:人工智能(AI)技术已经发展到成熟的水平,使他们能够在现实条件下使用,以帮助人类决策者。 AI有可能改变的临床试验设计的关键步骤的研究准备执行对改善试验的成功率,从而降低药品R&d负担的潜力。次优患者群的选择和招聘技术,有效期间用的审判无法监测病人配对,是对高试验失败率的主要原因之二:只有在进入临床试验10种化合物中的一个达到了市场。本次会议将在通俗地说解释一些AI方法论基础,如机器学习和深入学习,突出的进步如何近期可以在临床试验设计过程的特定阶段被应用到改善人群组成,招募患者,服药依从性和病人保留。特别注重将给予描述如何患者在神经学试验,可以通过数字病日记,它使用可穿戴设备,机器学习在边缘和云技术,自动检测和记录疾病发作和患者坚持试验方案更有效地监控。像所有的技术革命,这种带有挑战和风险,技术和监管。特别是,我们将讨论的可扩展性,数据加密和病人的隐私。

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