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<図書>
Adaptive design methods in clinical trials

責任表示 Shein-Chung Chow, Mark Chang
データ種別 図書
出版情報 Boca Raton : Chapman & Hall/CRC , c2007
本文言語 英語
大きさ 277 p. : ill. ; 24 cm
概要 Adapting the trial and/or statistical procedure of on-going clinical trials based on accrued data--for example all the subjects dying--has been common practice for years, but regulators look a little ...skance at it. Chow (medicine, Duke U. and National Cheng-Kung U., Taiwan) and Chang, with a Massachusetts pharmaceutical company, suggest that if the trial were designed from the beginning to be adapted, the US Food and Drug Administration might be less skeptical. They explain how to incorporate into trial design possible adaptation in such areas as protocol, group sequence, sample size, and treatment switching. Annotation ©2007 Book News, Inc., Portland, OR (booknews.com) 続きを見る

所蔵情報



理系図3F 数理独自 CHOW/25/3 2007
023212006007443

書誌詳細

一般注記 Includes bibliographical references (p. [255]-267) and index
著者標目 *Chow, Shein-Chung, 1955-
Chang, Mark
件 名 LCSH:Clinical trials
LCSH:Adaptive sampling (Statistics)
LCSH:Experimental design
LCSH:Clinical trials -- Statistical methods  全ての件名で検索
分 類 LCC:R853.C55
DC22:610.7/4
書誌ID 1001243226
ISBN 1584887761
NCID BA79804854
巻冊次 ISBN:1584887761 ; XISBN:9781584887768
登録日 2009.09.18
更新日 2009.11.02

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