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[临床III期研究的原理与实践]

[Principle and practice of clinical phase III studies].

作者信息

Morant Rudolf

机构信息

Tumorzentrum ZeTuP St.Gallen und Chur, St. Gallen, Schweiz.

出版信息

Onkologie. 2008;31 Suppl 2:53-7. doi: 10.1159/000113032. Epub 2008 Apr 18.

Abstract

Randomized phase III studies compare new treatments with standard therapy according to defined guidelines and legal rules. Large international randomized phase III studies are some of the most complex and expensive medical experiments. The results of such trials will decide about the future of new drugs and are the basis of evidence-based medicine and the development of clinical guidelines. This contribution discusses randomization, endpoints, inclusion and exclusion criteria of phase III trials as well as further challenges when developing and conducting phase III studies in oncology.

摘要

随机III期研究根据既定指南和法律规则,将新疗法与标准疗法进行比较。大型国际随机III期研究是一些最复杂且成本高昂的医学实验。此类试验的结果将决定新药的未来走向,并且是循证医学和临床指南制定的基础。本文探讨了III期试验的随机化、终点、纳入和排除标准,以及在肿瘤学领域开展III期研究时面临的其他挑战。

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