This guide offers an overview of the most common types of trial undertaken in early clinical development. The coverage discusses the different methodologies and the impact of new technologies, both clinical and statistical, on clinical development. Num Pages: 264 pages, Illustrations. BIC Classification: MBGR; PBT. Category: (P) Professional & Vocational. Dimension: 251 x 175 x 20. Weight in Grams: 622. . 2010. 1st Edition. Hardcover. . . . . Books ship from the US and Ireland.

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Bibliographic Details

Title: An Introduction to Statistics in Early Phase Trials
Publisher: John Wiley & Sons Inc
Publication Date: 2010
Language: English
ISBN 10: 0470059850
ISBN 13: 9780470059852
Binding: Hardcover
Condition: New

About this title

Synopsis

All new medicines and devices undergo early phase trials to assess, interpret and better understand their efficacy, tolerability and safety. An Introduction to Statistics in Early Phase Trials describes the practical design and analysis of these important early phase clinical trials and provides the crucial statistical basis for their interpretation. It clearly and concisely provides an overview of the most common types of trials undertaken in early phase clinical research and explains the different methodologies used. The impact of statistical technologies on clinical development and the statistical and methodological basis for making clinical and investment decisions are also explained.

Conveys key ideas in a concise manner understandable by non-statisticians
Explains how to optimise designs in a constrained or fixed resource setting
Discusses decision making criteria at the end of Phase II trials
Highlights practical day-to-day issues and reporting of early phase trials

An Introduction to Statistics in Early Phase Trials is an essential guide for all researchers working in early phase clinical trial development, from clinical pharmacologists and pharmacokineticists through to clinical investigators and medical statisticians. It is also a valuable reference for teachers and students of pharmaceutical medicine learning about the design and analysis of clinical trials.

About the Author

Steven A. Julious, Medical Statistics Group, School of Health and Related Research, University of Sheffield, UK.

Say-Beng Tan, Singapore Clinical Research Institute and Duke-NUS Graduate Medical School, Singapore.

David Machin, Children's Cancer and Leukaemia Group (CCLG), University of Leicester, UK.

"About this title" may belong to another edition of this title.

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