<図書>
Adaptive design methods in clinical trials
責任表示 | Shein-Chung Chow, Mark Chang |
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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
状態 | 巻次 | 所蔵場所 | 請求記号 | 刷年 | 文庫名称 | 資料番号 | コメント | 予約・取寄 | 複写申込 | 自動書庫 |
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理系図3F 数理独自 | CHOW/25/3 | 2007 |
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023212006007443 |
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書誌詳細
一般注記 | Includes bibliographical references (p. [255]-267) and index |
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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 |