Sotorasib dosing and incremental cost ineffectiveness — implications and lessons for stakeholders

IF 81.1 1区 医学 Q1 ONCOLOGY
Garth W. Strohbehn, Mark J. Ratain
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引用次数: 0

Abstract

The US FDA Accelerated Approval of sotorasib required the sponsor to conduct a randomized trial that compared the safety and efficacy of the approved dose with a lower dose. These results, recently disclosed, have important implications for patients, payers, oncologists and the pharmaceutical industry.
索托拉西布剂量和增量成本无效--对利益相关者的影响和教训。
美国 FDA 加速批准索托拉西布时,要求申办方进行一项随机试验,比较获批剂量与较低剂量的安全性和有效性。最近披露的这些结果对患者、付款人、肿瘤学家和制药业具有重要意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
99.40
自引率
0.40%
发文量
114
审稿时长
6-12 weeks
期刊介绍: Nature Reviews publishes clinical content authored by internationally renowned clinical academics and researchers, catering to readers in the medical sciences at postgraduate levels and beyond. Although targeted at practicing doctors, researchers, and academics within specific specialties, the aim is to ensure accessibility for readers across various medical disciplines. The journal features in-depth Reviews offering authoritative and current information, contextualizing topics within the history and development of a field. Perspectives, News & Views articles, and the Research Highlights section provide topical discussions, opinions, and filtered primary research from diverse medical journals.
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