Literature DB >> 35449371

Machine Learning Prediction of Clinical Trial Operational Efficiency.

Kevin Wu1, Eric Wu2, Michael DAndrea3, Nandini Chitale3, Melody Lim3, Marek Dabrowski4, Klaudia Kantor4, Hanoor Rangi5, Ruishan Liu2, Marius Garmhausen6, Navdeep Pal3, Chris Harbron7, Shemra Rizzo3, Ryan Copping3, James Zou8,2.   

Abstract

Clinical trials are the gatekeepers and bottlenecks of progress in medicine. In recent years, they have become increasingly complex and expensive, driven by a growing number of stakeholders requiring more endpoints, more diverse patient populations, and a stringent regulatory environment. Trial designers have historically relied on investigator expertise and legacy norms established within sponsor companies to improve operational efficiency while achieving study goals. As such, data-driven forecasts of operational metrics can be a useful resource for trial design and planning. We develop a machine learning model to predict clinical trial operational efficiency using a novel dataset from Roche containing over 2,000 clinical trials across 20 years and multiple disease areas. The data includes important operational metrics related to patient recruitment and trial duration, as well as a variety of trial features such as the number of procedures, eligibility criteria, and endpoints. Our results demonstrate that operational efficiency can be predicted robustly using trial features, which can provide useful insights to trial designers on the potential impact of their decisions on patient recruitment success and trial duration.
© 2022. The Author(s), under exclusive licence to American Association of Pharmaceutical Scientists.

Entities:  

Keywords:  clinical trials; macxhine learning; operational efficiency

Mesh:

Year:  2022        PMID: 35449371     DOI: 10.1208/s12248-022-00703-3

Source DB:  PubMed          Journal:  AAPS J        ISSN: 1550-7416            Impact factor:   4.009


  30 in total

Review 1.  The Large Pharmaceutical Company Perspective.

Authors:  Michael Rosenblatt
Journal:  N Engl J Med       Date:  2017-01-05       Impact factor: 91.245

2.  How much do clinical trials cost?

Authors:  Linda Martin; Melissa Hutchens; Conrad Hawkins; Alaina Radnov
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3.  Strategic inclusion of regions in multiregional clinical trials.

Authors:  Seung Yeon Song; Deborah Chee; EunYoung Kim
Journal:  Clin Trials       Date:  2018-11-16       Impact factor: 2.486

Review 4.  Deconstructing the drug development process: the new face of innovation.

Authors:  K I Kaitin
Journal:  Clin Pharmacol Ther       Date:  2010-02-03       Impact factor: 6.875

5.  Estimation of clinical trial success rates and related parameters.

Authors:  Chi Heem Wong; Kien Wei Siah; Andrew W Lo
Journal:  Biostatistics       Date:  2019-04-01       Impact factor: 5.899

6.  Failure of Investigational Drugs in Late-Stage Clinical Development and Publication of Trial Results.

Authors:  Thomas J Hwang; Daniel Carpenter; Julie C Lauffenburger; Bo Wang; Jessica M Franklin; Aaron S Kesselheim
Journal:  JAMA Intern Med       Date:  2016-12-01       Impact factor: 21.873

7.  Evaluating eligibility criteria of oncology trials using real-world data and AI.

Authors:  Ruishan Liu; Shemra Rizzo; Samuel Whipple; Navdeep Pal; Arturo Lopez Pineda; Michael Lu; Brandon Arnieri; Ying Lu; William Capra; Ryan Copping; James Zou
Journal:  Nature       Date:  2021-04-07       Impact factor: 69.504

8.  Improving protocol design feasibility to drive drug development economics and performance.

Authors:  Kenneth Getz
Journal:  Int J Environ Res Public Health       Date:  2014-05-12       Impact factor: 3.390

Review 9.  Multi-regional clinical trials and global drug development.

Authors:  Premnath Shenoy
Journal:  Perspect Clin Res       Date:  2016 Apr-Jun

10.  Increasing operational and scientific efficiency in clinical trials.

Authors:  Deirdre Kelly; Anna Spreafico; Lillian L Siu
Journal:  Br J Cancer       Date:  2020-07-21       Impact factor: 7.640

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