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Artificial Intelligence for Clinical Trial Design

Trends in Pharmacological Sciences · 2019 · Vol. 40(8) · pp. 577–591
Stefan HarrerPratik ShahBhavna AntonyJianying Hu

Abstract

Clinical trials consume the latter half of the 10 to 15 year, 1.5-2.0 billion USD, development cycle for bringing a single new drug to market. Hence, a failed trial sinks not only the investment into the trial itself but also the preclinical development costs, rendering the loss per failed clinical trial at 800 million to 1.4 billion USD. 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. We explain how recent advances in artificial intelligence (AI) can be used to reshape key steps of clinical trial design towards increasing trial success rates.

MeSH terms

Drug DevelopmentDrug DevelopmentArtificial IntelligenceClinical ProtocolsClinical Trials as TopicClinical Trials as TopicHumansPatient ComplianceResearch DesignClinical Trials, Phase III as TopicPatient Selection
Citations
609
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References
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