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早期批准后确认药物有效性的挑战。

Challenges in confirming drug effectiveness after early approval.

机构信息

University of Pennsylvania, Philadelphia, PA, USA.

Boston University, Boston, MA, USA.

出版信息

Science. 2021 Dec 3;374(6572):1205-1207. doi: 10.1126/science.abk3495. Epub 2021 Dec 2.

DOI:10.1126/science.abk3495
PMID:34855490
Abstract

Reform requires clarity about whether, when, and how meaningful postapproval trials are possible.

摘要

改革需要明确在何时以及如何进行有意义的批准后试验。

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Challenges in confirming drug effectiveness after early approval.早期批准后确认药物有效性的挑战。
Science. 2021 Dec 3;374(6572):1205-1207. doi: 10.1126/science.abk3495. Epub 2021 Dec 2.
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Impact of Postapproval Evidence Generation on the Biopharmaceutical Industry.批准后证据生成对生物制药行业的影响。
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Preparing for safety issues following drug approval: pre-approval risk management considerations.药物批准后的安全性问题准备:批准前的风险管理考虑因素。
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Patient burden and clinical advances associated with postapproval monotherapy cancer drug trials: a retrospective cohort study.与批准后单药癌症药物试验相关的患者负担和临床进展:一项回顾性队列研究。
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Accelerated approval of oncology products: the food and drug administration experience.肿瘤学产品的加速审批:美国食品和药物管理局的经验。
J Natl Cancer Inst. 2011 Apr 20;103(8):636-44. doi: 10.1093/jnci/djr062. Epub 2011 Mar 21.
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Assessing the safety and effectiveness of devices after US Food and Drug Administration approval: FDA-mandated postapproval studies.评估美国食品和药物管理局批准后设备的安全性和有效性:FDA 强制要求的上市后研究。
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Is patient exposure preapproval and postapproval a determinant of the timing and frequency of occurrence of safety issues?患者暴露的预先批准和事后批准是否是安全问题发生时间和频率的一个决定因素?
Pharmacoepidemiol Drug Saf. 2018 Feb;27(2):168-173. doi: 10.1002/pds.4359. Epub 2017 Dec 26.

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