AGPred: An End-to-End Deep Learning Model for Predicting Drug Approvals in Clinical Trials Based on Molecular Features

One of the major challenges in drug development is maintaining acceptable levels of efficacy and safety throughout the various stages of clinical trials and successfully bringing the drug to market. However, clinical trials are time-consuming and expensive. While there are computational methods designed to predict the likelihood of a drug passing clinical trials and reaching the market, these methods heavily rely on manual feature engineering and cannot automatically learn drug molecular representations, resulting in relatively low model performance. In this study, we propose AGPred, an attention-based deep Graph Neural Network (GNN) designed to predict drug approval rates in clinical trials accurately. Unlike the few existing studies on drug approval prediction, which only use predicted targets of compounds, our novel approach employs a GNN module to extract high-potential features of compounds based on their molecular graphs. Additionally, a cross-attention-based fusion module is utilized to learn molecular fingerprint features, enhancing the model's representation of chemical structures. Meanwhile, AGPred integrates the physicochemical properties of drugs to provide a comprehensive description of the molecules. Experimental results indicate that AGPred outperforms four state-of-the-art models on both benchmark and independent datasets. The study also includes several ablation experiments and visual analyses to demonstrate the effectiveness of our method in predicting drug approval during clinical trials.

Authors

Institutions

Publication Details

Journal
IEEE Journal of Biomedical and Health Informatics
Published
2025-03-06
DOI
https://doi.org/10.1109/jbhi.2025.3547315
Citations
1
Primary Topic
Computational Drug Discovery Methods
Type
article
Field-Weighted Citation Impact
1.50
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

AGPred: An End-to-End Deep Learning Model for Predicting Drug Approvals in Clinical Trials Based on Molecular Features

Xiao Liang, Haochen Zhao, Shaokai Wang, Chenliang Xie
1 citations
IEEE Journal of Biomedical and Health Informatics
Computational Drug Discovery Methods
1.50
article

AGPred: An End-to-End Deep Learning Model for Predicting Drug Approvals in Clinical Trials Based on Molecular Features

Xiao Liang, Haochen Zhao, Shaokai Wang, Chenliang Xie
article en
1 citations

Abstract

One of the major challenges in drug development is maintaining acceptable levels of efficacy and safety throughout the various stages of clinical trials and successfully bringing the drug to market. However, clinical trials are time-consuming and expensive. While there are computational methods designed to predict the likelihood of a drug passing clinical trials and reaching the market, these methods heavily rely on manual feature engineering and cannot automatically learn drug molecular representations, resulting in relatively low model performance. In this study, we propose AGPred, an attention-based deep Graph Neural Network (GNN) designed to predict drug approval rates in clinical trials accurately. Unlike the few existing studies on drug approval prediction, which only use predicted targets of compounds, our novel approach employs a GNN module to extract high-potential features of compounds based on their molecular graphs. Additionally, a cross-attention-based fusion module is utilized to learn molecular fingerprint features, enhancing the model's representation of chemical structures. Meanwhile, AGPred integrates the physicochemical properties of drugs to provide a comprehensive description of the molecules. Experimental results indicate that AGPred outperforms four state-of-the-art models on both benchmark and independent datasets. The study also includes several ablation experiments and visual analyses to demonstrate the effectiveness of our method in predicting drug approval during clinical trials.

IEEE Journal of Biomedical and Health InformaticsVol. 29(11)
Central South University (CN), Hong Kong University of Science and Technology (HK)
Good health and well-being
Openalex Percentile: Top 19%
Computational Drug Discovery Methods
1.50
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

AGPred: An End-to-End Deep Learning Model for Predicting Drug Approvals in Clinical Trials Based on Molecular Features — Xiao Liang, Haochen Zhao, et al. · IEEE Journal of Biomedical and Health Informatics (2025) | TGRS Research Map | TGRS