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Chapter 6 Drug development and clinical trial via artificial intelligence

  • Rishabha Malviya , Shristy Verma , Sonali Sundram and Harshil Shah
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Abstract

Clinical trials and medication development have been profoundly impacted by artificial intelligence (AI), with deep learning techniques outperforming traditional machine learning tactics. Though its potential and accessibility are limited, highthroughput virtual screening (HTVS) has been proposed as an alternative to expensive and time-consuming methods. The chapter overviews computational drug development techniques that identify drug targets, validate drugs, and conduct clinical trials using artificial intelligence (AI). Additionally, by simply acquiring the governing equations from data, a novel deep learning technique has been described that is designed to build PK/PD models that can forecast patient response times and simulate the impact of unknown dosage regimens. The technique keeps the dose-concentration effect pharmacologically sound while enabling the model to predict treatment outcomes and replicate the patient’s dosage schedule. Drug target interactions (DTIs) are essential for locating possible drugs and offering information on side effects and drug mechanisms. Additionally, ethical issues about social gaps, security of data, informed consent, medical consultation, empathy, as well as sympathy, are raised in the last section and affect AI-enabled clinical trials in the healthcare industry.

Abstract

Clinical trials and medication development have been profoundly impacted by artificial intelligence (AI), with deep learning techniques outperforming traditional machine learning tactics. Though its potential and accessibility are limited, highthroughput virtual screening (HTVS) has been proposed as an alternative to expensive and time-consuming methods. The chapter overviews computational drug development techniques that identify drug targets, validate drugs, and conduct clinical trials using artificial intelligence (AI). Additionally, by simply acquiring the governing equations from data, a novel deep learning technique has been described that is designed to build PK/PD models that can forecast patient response times and simulate the impact of unknown dosage regimens. The technique keeps the dose-concentration effect pharmacologically sound while enabling the model to predict treatment outcomes and replicate the patient’s dosage schedule. Drug target interactions (DTIs) are essential for locating possible drugs and offering information on side effects and drug mechanisms. Additionally, ethical issues about social gaps, security of data, informed consent, medical consultation, empathy, as well as sympathy, are raised in the last section and affect AI-enabled clinical trials in the healthcare industry.

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