Mon compte
Se connecter Inscription
Tous
Panier
En Vedette
Livres de fiction
Livres de non-fiction
Livres pour enfants
Livres rares
Musique
DVD et Blu-Ray
Video Games
Catégorie
Listes de favoris
Panier
Tous
Livraison gratuite
Trustpilot
Nous sommes Neutres au Carbone

Clinical Trials in Oncology, Third Edition Stephanie Green (Senior Director, Pfizer, Inc., Groton, Connecticut, USA)

Clinical Trials in Oncology, Third Edition par Stephanie Green (Senior Director, Pfizer, Inc., Groton, Connecticut, USA)

Clinical Trials in Oncology, Third Edition Stephanie Green (Senior Director, Pfizer, Inc., Groton, Connecticut, USA)

€324.00
État - Très bon état
Disponible en seulement 1 exemplaire(s)
Très bon état

Clinical Trials in Oncology, Third Edition Résumé

Clinical Trials in Oncology, Third Edition Stephanie Green (Senior Director, Pfizer, Inc., Groton, Connecticut, USA)

The third edition of the bestselling Clinical Trials in Oncology provides a concise, nontechnical, and thoroughly up-to-date review of methods and issues related to cancer clinical trials. The authors emphasize the importance of proper study design, analysis, and data management and identify the pitfalls inherent in these processes. In addition, the book has been restructured to have separate chapters and expanded discussions on general clinical trials issues, and issues specific to Phases I, II, and III. New sections cover innovations in Phase I designs, randomized Phase II designs, and overcoming the challenges of array data.

Although this book focuses on cancer trials, the same issues and concepts are important in any clinical setting. As always, the authors use clear, lucid prose and a multitude of real-world examples to convey the principles of successful trials without the need for a strong statistics or mathematics background. Armed with Clinical Trials in Oncology, Third Edition, clinicians and statisticians can avoid the many hazards that can jeopardize the success of a trial.

Clinical Trials in Oncology, Third Edition Avis

This book provides a very clear and concise overview of the main issues in the design, data management, and analysis of clinical trials. Although the examples used are from oncology trials, the principles apply to all clinical trials and so will be of use to a wide audience. The book is well written and easy to read ... recommended reading to anyone involved in the design and running of clinical trials, not just statisticians, although some familiarity with statistical terminology would help. ... a very useful and accessible reference, which covers the essential statistical elements of designing and running clinical trials all in one book, which is extensively illustrated with real examples.
-ISCB News, 57, June 2014

Praise for Previous Editions:The dedication of the authors to enhancing the quality of clinical trials in oncology is evident from this book. ... This book will be useful to students, clinical research nurses and medical statisticians involved in oncology trials. ... I also recommend it to libraries and clinical institutions.
-Clinical Trials, 2004

With over 60 years combined experience, the authors are ideally positioned to discuss the various statistical issues apparent in clinical trials, identifying alternative solutions, providing logical arguments for and against the various solutions. This book is also recommended for statisticians actively involved in the design, conduct, and analysis of clinical trial data (not only cancer clinical trials).
-Journal of Biopharmaceutical StatisticsA concise, easily readable, and thorough summary...ALL medical oncology, radiation oncology, surgical oncology, and clinical research nurse academic training programs should provide this important text to trainees on Day 1.
-Charles R. Thomas Jr., MD, University of Texas Health Science Center at San Antonio, USA

Succinct and focused...[This book] is clear, cogent, and practical. It is structured so that statisticians can use specific sections as starting point to develop shared understandings with investigators, study coordinators, and data managers...It has been useful to me and my clients, and I look forward to the second edition.
-Marlene Egger, University of Utah, USA


This book provides a very clear and concise overview of the main issues in the design, data management, and analysis of clinical trials. Although the examples used are from oncology trials, the principles apply to all clinical trials and so will be of use to a wide audience. The book is well written and easy to read ... recommended reading to anyone involved in the design and running of clinical trials, not just statisticians, although some familiarity with statistical terminology would help. ... a very useful and accessible reference, which covers the essential statistical elements of designing and running clinical trials all in one book, which is extensively illustrated with real examples.
-ISCB News, 57, June 2014

Praise for the Previous Editions:
The dedication of the authors to enhancing the quality of clinical trials in oncology is evident from this book. ... This book will be useful to students, clinical research nurses and medical statisticians involved in oncology trials. ... I also recommend it to libraries and clinical institutions.
-Clinical Trials, 2004

With over 60 years combined experience, the authors are ideally positioned to discuss the various statistical issues apparent in clinical trials, identifying alternative solutions, providing logical arguments for and against the various solutions. This book is also recommended for statisticians actively involved in the design, conduct, and analysis of clinical trial data (not only cancer clinical trials).
-Journal of Biopharmaceutical StatisticsA concise, easily readable, and thorough summary...ALL medical oncology, radiation oncology, surgical oncology, and clinical research nurse academic training programs should provide this important text to trainees on Day 1.
-Charles R. Thomas Jr., MD, University of Texas Health Science Center at San Antonio, USA

Succinct and focused...[This book] is clear, cogent, and practical. It is structured so that statisticians can use specific sections as starting point to develop shared understandings with investigators, study coordinators, and data managers...It has been useful to me and my clients, and I look forward to the second edition.
-Marlene Egger, University of Utah, USA

À propos de Stephanie Green (Senior Director, Pfizer, Inc., Groton, Connecticut, USA)

Stephanie Green, Jacqueline Benedetti

Sommaire

1. Introduction, 2. Statistical Concepts, 3. The Design of Clinical Trials, 4. Phase I and Phase I/II Trials, 5. Phase II Trials, 6. Phase III Trials, 7. Data Management and Quality Control, 8. Reporting of Results, 9. Pitfalls, 10. Exploratory Analyses, 11. Summary and Conclusions, References, Index

Informations supplémentaires

GOR013503968
9781138199118
1138199117
Clinical Trials in Oncology, Third Edition Stephanie Green (Senior Director, Pfizer, Inc., Groton, Connecticut, USA)
Stephanie Green (Senior Director, Pfizer, Inc., Groton, Connecticut, USA)
Chapman & Hall/CRC Interdisciplinary Statistics
Occasion - Très bon état
Broché
Taylor & Francis Ltd
20161014
264
N/A
La photo du livre est présentée à titre d'illustration uniquement. La reliure, la couverture ou l'édition réelle peuvent varier.
Il s'agit d'un livre d'occasion - par conséquent, il a été lu par quelqu'un d'autre et il présente des signes d'usure et d'utilisation antérieure. Dans l'ensemble, nous nous attendons à ce qu'il soit en très bon état, mais si vous n'êtes pas entièrement satisfait, veuillez prendre contact avec nous.