PO.ET07.02 · 实验与分子治疗

InVEST44™是一种具有成本效益的体外安全性检测组合,可在早期药物发现中识别脱靶效应

InVEST44™ is a cost-effective in vitro safety panel that identifies off-target effects in early-stage drug discovery

编号 3150 展板 18 时间 4/20 02:00–05:00 区域 Section 18 主讲 Julian Wooltorton
分会场 Pharmacogenomics and Translational Biomarkers for Precision Cancer Therapy
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作者与单位 Authors & Affiliations

Julian R. Wooltorton, Afsara Ahona, Nicole Barbacane, Alex D'Andrea, Justin Lansberry, Cindy Lay, Paige Miller, John Ries, Jamin Steffen, Patricia Valentine

Reaction Biology Corporation, Malvern, PA

摘要 Abstract

中文摘要
药物开发成本超过1.72亿美元,若将临床试验失败考虑在内则增至超过5亿美元(Sertkaya 2024, DOI: 10.1001/jamanetworkopen.2024.15445)。将一种药物推向市场可能需要20年,因此在发现过程早期识别安全性隐患至关重要,以确保宝贵的时间和金钱不会被投入到临床前和临床试验中。体外安全性检测组合,如InVEST44™,可在早期药物开发过程中以具有成本效益的方式识别药物的潜在毒性。这一点尤为相关,因为在2006年至2023年间,风险投资在早期药物发现中的投资比例从50%下降到16%,而在后期阶段则从20%增加到54%(The Biopharma Industry Investment Report 2015. Biotechnology Innovation Organization; Larka 2024, Trends in Venture Capital Funding for Biopharma Startups. GlobalData)。这凸显了一种趋势,即转向昂贵、高风险但潜在利润丰厚的临床试验,而远离早期药物发现。目标是证明早期体外安全性检测组合在药物开发中是财务和科学上关键的步骤,可在药物推进到动物试验和临床试验之前识别脱靶效应。InVEST44™是一种体外安全性检测组合,旨在识别肿瘤学和其他治疗领域先导化合物在早期药物开发中的脱靶效应,确保从发现到临床试验的更高效路径。它包含44个基于Bowes等人(2012; DOI: 10.1038/nrd3845)的行业标准高风险靶点,包括GPCRs、转运体、离子通道、核受体和酶。采用了多种检测类型,包括放射性配体结合、荧光偏振、酶活性、细胞报告基因、钙动员和电生理检测。我们从2001年至2025年间17项失败的临床肿瘤学试验中识别出20个候选药物,这些试验均因报告的严重不良反应而终止(clinicaltrials.org)。这些药物在InVEST44™中以10 μM进行筛选:17种药物在至少1个靶点上产生了>50%的效应,包括8种具有4个及以上靶点相互作用的药物和1种与15个安全性靶点相互作用的药物。本研究通过在进行耗时且昂贵的动物试验和可能失败的临床试验之前识别先导化合物的脱靶效应,证明了体外安全性检测组合(如InVEST44™)的重要性。此类检测组合的数据正越来越多地被提供以增强IND申请(Scott, 2022, DOI: 10.1016/j.vascn.2022.107205)。总之,通过提供具有成本效益的早期先导化合物脱靶效应识别,体外安全性检测组合(如InVEST44™)已成为药物发现不可或缺的组成部分,值得在未来给予更多的早期考虑和投资。
查看英文原文 English abstract
Drug development costs exceed $172m and increase to over $500m when clinical trial failures are considered (Sertkaya 2024, DOI: 10.1001/jamanetworkopen.2024.15445). It can take 20 years to bring a drug to market so it is critical to identify safety liabilities early in the discovery process to ensure valuable time and money are not invested in preclinical and clinical trials. In vitro safety panels, such as InVEST44™, can identify potential toxicities of drugs cost-effectively during early-stage drug development. This is particularly relevant as, between 2006 and 2023, the proportion of venture capital investments in early-stage drug discovery has decreased from 50% to 16% while increasing for later stage from 20 to 54% ( The Biopharma Industry Investment Report 2015 . Biotechnology Innovation Organization; Larka 2024, Trends in Venture Capital Funding for Biopharma Startups . GlobalData). This highlights a trend towards expensive, high-risk but potentially lucrative, clinical trials and away from early drug discovery. The goal is to demonstrate that early-stage in vitro safety panels are fiscally and scientifically critical steps in drug development to identify off-target effects before advancing drugs to animal testing and clinical trials. InVEST44™ is an in vitro safety panel designed to identify off-target effects of lead compounds for oncology and other therapeutic areas in early-stage drug development, ensuring a more efficient path from discovery to clinical trials. It comprises 44 industry standard, high risk targets based on Bowes et al. (2012; DOI: 10.1038/nrd3845), including GPCRs, transporters, ion channels, nuclear receptors and enzymes. Various assay types are utilized, including radioligand binding, fluorescence polarization, enzymatic activity, cell reporter, calcium mobilization and electrophysiology assays. We identified 20 drug candidates from 17 failed clinical oncology trials between 2001 and 2025, all terminated because of reported severe adverse effects (clinicaltrials.org). These were screened at 10 µM in InVEST44™: 17 drugs elicited >50% effect on at least 1 target, including 8 with 4+ target interactions and one interacting with 15 safety targets. This study demonstrates the importance of in vitro safety panels, such as InVEST44™, by identifying off-targets effect of lead compounds before pursuing time-consuming and expensive animal testing and potentially failed clinical trials. Data from such panels are increasingly being provided to enhance IND applications (Scott, 2022, DOI: 10.1016/j.vascn.2022.107205). In summary, by providing cost-efficient, early-stage identification of off-target effects by lead compounds, in vitro safety panels, such as InVEST44™, have become integral components of drug discovery and warrant increased early-stage consideration and investment in the future.
利益披露 Disclosure
J. R. Wooltorton, None.. A. Ahona, None.. N. Barbacane, None.. A. D'Andrea, None.. J. Lansberry, None.. C. Lay, None.. P. Miller, None.. J. Ries, None.. J. Steffen, None.. P. Valentine, None.

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