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Trends in Artificial Intelligence Applications in Clinical Trials: An analysis of ClinicalTrials.gov

임상시험에서 인공지능의 활용에 대한 분석 및 고찰: ClinicalTrials.gov 분석

  • Jeong Min Go (School of Pharmacy, Jeonbuk National University) ;
  • Ji Yeon Lee (School of Pharmacy, Jeonbuk National University) ;
  • Yun-Kyoung Song (College of Pharmacy, The Catholic University of Korea) ;
  • Jae Hyun Kim (School of Pharmacy, Jeonbuk National University)
  • Received : 2024.05.24
  • Accepted : 2024.06.12
  • Published : 2024.06.30

Abstract

Background: Increasing numbers of studies and research about artificial intelligence (AI) and machine learning (ML) have led to their application in clinical trials. The purpose of this study is to analyze computer-based new technologies (AI/ML) applied on clinical trials registered on ClinicalTrials.gov to elucidate current usage of these technologies. Methods: As of March 1st, 2023, protocols listed on ClinicalTrials.gov that claimed to use AI/ML and included at least one of the following interventions-Drug, Biological, Dietary Supplement, or Combination Product-were selected. The selected protocols were classified according to their context of use: 1) drug discovery; 2) toxicity prediction; 3) enrichment; 4) risk stratification/management; 5) dose selection/optimization; 6) adherence; 7) synthetic control; 8) endpoint assessment; 9) postmarketing surveillance; and 10) drug selection. Results: The applications of AI/ML were explored in 131 clinical trial protocols. The areas where AI/ML was most frequently utilized in clinical trials included endpoint assessment (n=80), followed by dose selection/optimization (n=15), risk stratification/management (n=13), drug discovery (n=4), adherence (n=4), drug selection (n=1) and enrichment (n=1). Conclusion: The most frequent application of AI/ML in clinical trials is in the fields of endpoint assessment, where the utilization is primarily focuses on the diagnosis of disease by imaging or video analyses. The number of clinical trials using artificial intelligence will increase as the technology continues to develop rapidly, making it necessary for regulatory associates to establish proper regulations for these clinical trials.

Keywords

Acknowledgement

본 연구는 2023년 식품의약품안전처의 지원을 받아 수행되었으며(23212한임평226) 이에 감사드립니다.

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