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Titlebook: Innovative Designs and Analyses for Small Population Clinical Trials; Development Strategi Jingjing Ye,Lei Nie Book 2024 The Editor(s) (if

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發(fā)表于 2025-3-21 17:37:35 | 只看該作者 |倒序?yàn)g覽 |閱讀模式
書(shū)目名稱(chēng)Innovative Designs and Analyses for Small Population Clinical Trials
副標(biāo)題Development Strategi
編輯Jingjing Ye,Lei Nie
視頻videohttp://file.papertrans.cn/477/476156/476156.mp4
概述Offers coverage and discussion on a relatively new topic in the clinical trial space.Features successful and precedent-setting examples.Promotes the importance of interdisciplinary collaboration
叢書(shū)名稱(chēng)ICSA Book Series in Statistics
圖書(shū)封面Titlebook: Innovative Designs and Analyses for Small Population Clinical Trials; Development Strategi Jingjing Ye,Lei Nie Book 2024 The Editor(s) (if
描述This book discusses a multidisciplinary and multi-stakeholder collaborative approach to small population clinical trials. It provides and illustrates a systematic framework that depends upon a collaborative infrastructure between the patient community, patient advocacy groups, researchers and investigators, pharmaceutical companies, global regulatory agencies, and customers. The book also highlights the considerations of natural history and patient registry, diagnostic criteria determination, identification of clinically meaningful endpoints, and global regulatory guidance. The authors detail the nuances of clinical trial design as specific to small population disease, drawing from real examples.
出版日期Book 2024
關(guān)鍵詞rare disease; pediatric; patient registry; enrichment design; master protocol; Bayesian analysis; adaptive
版次1
doihttps://doi.org/10.1007/978-3-031-60843-8
isbn_softcover978-3-031-60845-2
isbn_ebook978-3-031-60843-8Series ISSN 2199-0980 Series E-ISSN 2199-0999
issn_series 2199-0980
copyrightThe Editor(s) (if applicable) and The Author(s), under exclusive license to Springer Nature Switzerl
The information of publication is updating

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發(fā)表于 2025-3-21 20:34:11 | 只看該作者
Master Protocol,e described in detail, separately for exploratory and confirmatory settings. The master protocol has been implemented successfully and improved the patient care in treating patients with rare cancers and pediatric cancers. One of those successful examples is discussed in the chapter.
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發(fā)表于 2025-3-22 00:27:12 | 只看該作者
Operation and Other Considerations,sease classification, and patient monitoring. Additionally, translational relevance of preclinical models to pediatric and rare diseases and potential pharmacodynamic endpoints are included in the considerations.
地板
發(fā)表于 2025-3-22 07:23:51 | 只看該作者
Case Studies,ents who receive lung transplants. The third case is Belimumab’s approval that has applied Bayesian analysis to borrow adult data into pediatric to support approval in children with system lupus erythematosus (SLE).
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發(fā)表于 2025-3-22 10:23:09 | 只看該作者
Book 2024a systematic framework that depends upon a collaborative infrastructure between the patient community, patient advocacy groups, researchers and investigators, pharmaceutical companies, global regulatory agencies, and customers. The book also highlights the considerations of natural history and patie
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發(fā)表于 2025-3-23 05:07:25 | 只看該作者
Diagnostic Criteria and Endpoint,tive multi-stake holders’ collaboration to best utilize the available information or generate the fit-for-purpose evidence. The statistical evaluation of the diagnosis and the endpoints are provided. Successful implementations in case studies are included.
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發(fā)表于 2025-3-23 06:42:39 | 只看該作者
Introduction,que rare diseases, affecting 300?million people worldwide, about 72% of which are genetic and about 70% of which are exclusively pediatric onset. More than 90% of rare diseases are without an FDA-approved treatment. Rare diseases are numerous, heterogenous in nature, and geographically disparate. Gi
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