Improving Risk Assessment in Clinical Trials: Toward a Systematic Risk-Based Monitoring Approach

ABSTRACT: Regulatory authorities have encouraged the usage of a monitoring (RBM) system in clinical trials before trial initiation for detection of potential risks and inclusion of a mitigation plan in the monitoring strategy. Several RBM tools were developed after the International Council for Harm...

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Main Authors: Firas Fneish, Frank Schaarschmidt, Gerhard Fortwengel
Format: Article
Language:English
Published: Elsevier 2021-01-01
Series:Current Therapeutic Research
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S0011393X21000217
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spelling doaj-16a288bef9964419a300e6b003e1feb32021-10-05T04:18:24ZengElsevierCurrent Therapeutic Research0011-393X2021-01-0195100643Improving Risk Assessment in Clinical Trials: Toward a Systematic Risk-Based Monitoring ApproachFiras Fneish0Frank Schaarschmidt1Gerhard Fortwengel2Institute of Cell Biology and Biophysics, Department of Biostatistics, Leibniz University Hannover, 30419 Hannover, Germany; Address correspondence to: Firas Fneish, Institute of Cell Biology and Biophysics, Department of Biostatistics, Leibniz University Hannover, Hannover, Germany.Institute of Cell Biology and Biophysics, Department of Biostatistics, Leibniz University Hannover, 30419 Hannover, GermanyFaculty III Media Information and Design, Hochschule Hannover, 30539 Hannover, GermanyABSTRACT: Regulatory authorities have encouraged the usage of a monitoring (RBM) system in clinical trials before trial initiation for detection of potential risks and inclusion of a mitigation plan in the monitoring strategy. Several RBM tools were developed after the International Council for Harmonization gave sponsors the flexibility to initiate an approach to enhance quality management in a clinical trial. However, various studies have demonstrated the need for improvement of the available RBM tools as each does not provide a comprehensive overview of the characteristics, focus, and application.This research lays out a rationale for a risk methodology assessment (RMA) within the RBM system. The core purpose of RMA is to deliver a scientifically based evaluation and decision of any potential risk in a clinical trial. Thereby, a monitoring plan can be developed to elude prior identified risk outcome.To demonstrate RMA's theoretical approach in practice, a Shiny web application (R Foundation for Statistical Computing) was designed to describe the assessment process of risk analysis and visualization tools that eventually aid in focusing monitoring activities.RMA focuses on the identification of an individual risk and visualizes its weight on the trial. The scoring algorithm of the presented approach computes the assessment of the individual risk in a radar plot and computes the overall score of the trial. Moreover, RMA's novelty lies in its ability to decrease biased decision making during risk assessment by categorizing risk influence and detectability; a characteristic pivotal to serve RBM in assessing risks, and in contributing to a better understanding in the monitoring technique necessary for developing a functional monitoring plan.Future research should focus on validating the power of RMAs to demonstrate its efficiency. This would facilitate the process of characterizing the strengths and weaknesses of RMA in practice.http://www.sciencedirect.com/science/article/pii/S0011393X21000217Clinical trialsICH-GCPMitigation planRisk-based monitoringRisk methodology assessment
collection DOAJ
language English
format Article
sources DOAJ
author Firas Fneish
Frank Schaarschmidt
Gerhard Fortwengel
spellingShingle Firas Fneish
Frank Schaarschmidt
Gerhard Fortwengel
Improving Risk Assessment in Clinical Trials: Toward a Systematic Risk-Based Monitoring Approach
Current Therapeutic Research
Clinical trials
ICH-GCP
Mitigation plan
Risk-based monitoring
Risk methodology assessment
author_facet Firas Fneish
Frank Schaarschmidt
Gerhard Fortwengel
author_sort Firas Fneish
title Improving Risk Assessment in Clinical Trials: Toward a Systematic Risk-Based Monitoring Approach
title_short Improving Risk Assessment in Clinical Trials: Toward a Systematic Risk-Based Monitoring Approach
title_full Improving Risk Assessment in Clinical Trials: Toward a Systematic Risk-Based Monitoring Approach
title_fullStr Improving Risk Assessment in Clinical Trials: Toward a Systematic Risk-Based Monitoring Approach
title_full_unstemmed Improving Risk Assessment in Clinical Trials: Toward a Systematic Risk-Based Monitoring Approach
title_sort improving risk assessment in clinical trials: toward a systematic risk-based monitoring approach
publisher Elsevier
series Current Therapeutic Research
issn 0011-393X
publishDate 2021-01-01
description ABSTRACT: Regulatory authorities have encouraged the usage of a monitoring (RBM) system in clinical trials before trial initiation for detection of potential risks and inclusion of a mitigation plan in the monitoring strategy. Several RBM tools were developed after the International Council for Harmonization gave sponsors the flexibility to initiate an approach to enhance quality management in a clinical trial. However, various studies have demonstrated the need for improvement of the available RBM tools as each does not provide a comprehensive overview of the characteristics, focus, and application.This research lays out a rationale for a risk methodology assessment (RMA) within the RBM system. The core purpose of RMA is to deliver a scientifically based evaluation and decision of any potential risk in a clinical trial. Thereby, a monitoring plan can be developed to elude prior identified risk outcome.To demonstrate RMA's theoretical approach in practice, a Shiny web application (R Foundation for Statistical Computing) was designed to describe the assessment process of risk analysis and visualization tools that eventually aid in focusing monitoring activities.RMA focuses on the identification of an individual risk and visualizes its weight on the trial. The scoring algorithm of the presented approach computes the assessment of the individual risk in a radar plot and computes the overall score of the trial. Moreover, RMA's novelty lies in its ability to decrease biased decision making during risk assessment by categorizing risk influence and detectability; a characteristic pivotal to serve RBM in assessing risks, and in contributing to a better understanding in the monitoring technique necessary for developing a functional monitoring plan.Future research should focus on validating the power of RMAs to demonstrate its efficiency. This would facilitate the process of characterizing the strengths and weaknesses of RMA in practice.
topic Clinical trials
ICH-GCP
Mitigation plan
Risk-based monitoring
Risk methodology assessment
url http://www.sciencedirect.com/science/article/pii/S0011393X21000217
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