Type 1 diabetes prevention clinical trial simulator: Case reports of model-informed drug development tool

IF 3.1 3区 医学 Q2 PHARMACOLOGY & PHARMACY
Juan Francisco Morales, Marian Klose, Yannick Hoffert, Jagdeep T. Podichetty, Jackson Burton, Stephan Schmidt, Klaus Romero, Inish O'Doherty, Frank Martin, Martha Campbell-Thompson, Michael J. Haller, Mark A. Atkinson, Sarah Kim
{"title":"Type 1 diabetes prevention clinical trial simulator: Case reports of model-informed drug development tool","authors":"Juan Francisco Morales,&nbsp;Marian Klose,&nbsp;Yannick Hoffert,&nbsp;Jagdeep T. Podichetty,&nbsp;Jackson Burton,&nbsp;Stephan Schmidt,&nbsp;Klaus Romero,&nbsp;Inish O'Doherty,&nbsp;Frank Martin,&nbsp;Martha Campbell-Thompson,&nbsp;Michael J. Haller,&nbsp;Mark A. Atkinson,&nbsp;Sarah Kim","doi":"10.1002/psp4.13193","DOIUrl":null,"url":null,"abstract":"<p>Clinical trials seeking to delay or prevent the onset of type 1 diabetes (T1D) face a series of pragmatic challenges. Despite more than 100 years since the discovery of insulin, teplizumab remains the only FDA-approved therapy to delay progression from Stage 2 to Stage 3 T1D. To increase the efficiency of clinical trials seeking this goal, our project sought to inform T1D clinical trial designs by developing a disease progression model-based clinical trial simulation tool. Using individual-level data collected from the TrialNet Pathway to Prevention and The Environmental Determinants of Diabetes in the Young natural history studies, we previously developed a quantitative joint model to predict the time to T1D onset. We then applied trial-specific inclusion/exclusion criteria, sample sizes in treatment and placebo arms, trial duration, assessment interval, and dropout rate. We implemented a function for presumed drug effects. To increase the size of the population pool, we generated virtual populations using multivariate normal distribution and ctree machine learning algorithms. As an output, power was calculated, which summarizes the probability of success, showing a statistically significant difference in the time distribution until the T1D diagnosis between the two arms. Using this tool, power curves can also be generated through iterations. The web-based tool is publicly available: https://app.cop.ufl.edu/t1d/. Herein, we briefly describe the tool and provide instructions for simulating a planned clinical trial with two case studies. This tool will allow for improved clinical trial designs and accelerate efforts seeking to prevent or delay the onset of T1D.</p>","PeriodicalId":10774,"journal":{"name":"CPT: Pharmacometrics & Systems Pharmacology","volume":"13 8","pages":"1309-1316"},"PeriodicalIF":3.1000,"publicationDate":"2024-07-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/psp4.13193","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"CPT: Pharmacometrics & Systems Pharmacology","FirstCategoryId":"3","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/psp4.13193","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"PHARMACOLOGY & PHARMACY","Score":null,"Total":0}
引用次数: 0

Abstract

Clinical trials seeking to delay or prevent the onset of type 1 diabetes (T1D) face a series of pragmatic challenges. Despite more than 100 years since the discovery of insulin, teplizumab remains the only FDA-approved therapy to delay progression from Stage 2 to Stage 3 T1D. To increase the efficiency of clinical trials seeking this goal, our project sought to inform T1D clinical trial designs by developing a disease progression model-based clinical trial simulation tool. Using individual-level data collected from the TrialNet Pathway to Prevention and The Environmental Determinants of Diabetes in the Young natural history studies, we previously developed a quantitative joint model to predict the time to T1D onset. We then applied trial-specific inclusion/exclusion criteria, sample sizes in treatment and placebo arms, trial duration, assessment interval, and dropout rate. We implemented a function for presumed drug effects. To increase the size of the population pool, we generated virtual populations using multivariate normal distribution and ctree machine learning algorithms. As an output, power was calculated, which summarizes the probability of success, showing a statistically significant difference in the time distribution until the T1D diagnosis between the two arms. Using this tool, power curves can also be generated through iterations. The web-based tool is publicly available: https://app.cop.ufl.edu/t1d/. Herein, we briefly describe the tool and provide instructions for simulating a planned clinical trial with two case studies. This tool will allow for improved clinical trial designs and accelerate efforts seeking to prevent or delay the onset of T1D.

Abstract Image

1 型糖尿病预防临床试验模拟器:基于模型的药物开发工具案例报告。
旨在延缓或预防 1 型糖尿病(T1D)发病的临床试验面临着一系列实际挑战。尽管胰岛素的发现已有 100 多年的历史,但泰普利珠单抗仍是美国食品药品管理局批准的唯一一种可延缓 1 型糖尿病从 2 期发展到 3 期的疗法。为了提高寻求这一目标的临床试验的效率,我们的项目试图通过开发基于疾病进展模型的临床试验模拟工具,为 T1D 临床试验设计提供信息。利用从 "TrialNet Pathway to Prevention "和 "The Environmental Determinants of Diabetes in the Young "自然史研究中收集到的个体水平数据,我们之前开发了一个定量联合模型来预测 T1D 的发病时间。然后,我们应用了特定试验的纳入/排除标准、治疗组和安慰剂组的样本量、试验持续时间、评估间隔和辍学率。我们采用了假定药物效应函数。为了扩大样本库的规模,我们使用多元正态分布和 ctree 机器学习算法生成了虚拟样本。作为输出,我们计算了功率,它总结了成功的概率,显示出两组患者在确诊 T1D 之前的时间分布上存在显著的统计学差异。使用该工具,还可以通过迭代生成功率曲线。该网络工具已公开发布:https://app.cop.ufl.edu/t1d/。在此,我们将简要介绍该工具,并通过两个案例研究为模拟计划中的临床试验提供指导。该工具将有助于改进临床试验设计,加快预防或延缓 T1D 发病的进程。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
5.00
自引率
11.40%
发文量
146
审稿时长
8 weeks
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信