Oncology Clinical Trials

Successful Design, Conduct, and Analysis

By: William Kevin Kelly (Editor), Susan Halabi (Editor)

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Hardcover | 30 May 2018 | Edition Number 2

At a Glance

Hardcover
550 Pages

Edition Type
Revised

Dimensions(cm)
27.9 x 21.6 x 2.5

Hardcover

RRP $344.00

$263.75

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The second edition of Oncology Clinical Trials has been thoroughly revised and updated and now contains the latest designs and methods of conducting and analyzing cancer clinical trials in the era of precision medicine with biologic agents - including trials investigating the safety and efficacy of targeted therapies, immunotherapies, and combination therapies as well as novel radiation therapy modalities. Now divided into five sections this revamped book provides the necessary background and expert guidance from the principles governing oncology clinical trials to the innovative statistical design methods permeating the field; from conducting trials in a safe and effective manner, analyzing and interpreting the data, to a forward-looking assessment and discussion of regulatory issues impacting domestic, international, and global clinical trials. Considered by many as the gold standard reference on oncology clinical trials in the field, the second edition continues to provide examples of real-life flaws and real-world examples for how to successfully design, conduct and analyze quality clinical trials and interpret them. With chapters written by oncologists, researchers, biostatisticians, clinical research administrators, and industry and FDA representatives, this volume provides a comprehensive guide in the design, conduct, monitoring, analysis, and reporting of clinical trials in oncology. New to this Edition:

Outlines how to design clinical trials with and without biomarker testingÎ"¶including genomics-based Î"£basket'©'?'
? trials, and adaptive trials for all phases during treatment and quality-of-life trials
Includes new chapters on immunotherapy trials, radiation therapy trials, multi-arm trials, meta-analysis and adaptive design, use of genomics, dose modifications and use of ancillary treatments in investigational studies, establishing surrogate endpoints, practical issues with correlative studies, cost-effectiveness analysis, and more
Comprehensively covers all regulatory aspects in the pursuit of global oncology trials
Digital Access to the eBook included

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