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Textbook of Clinical Trials in Oncology
Engelsk Paperback
SPAR
kr 73
Textbook of Clinical Trials in Oncology
Engelsk Paperback

There is an increasing need for educational resources for statisticians and investigators. Reflecting this, the goal of this book is to provide readers with a sound foundation in the statistical design, conduct, and analysis of clinical trials. Furthermore, it is intended as a guide for statisticians and investigators with minimal clinical trial experience who are interested in pursuing a career in this area. The advancement in genetic and molecular technologies have revolutionized drug development. In recent years, clinical trials have become increasingly sophisticated as they incorporate genomic studies, and efficient designs (such as basket and umbrella trials) have permeated the field. This book offers the requisite background and expert guidance for the innovative statistical design and analysis of clinical trials in oncology.





Key Features:







  • Cutting-edge topics with appropriate technical background






  • Built around case studies which give the work a "hands-on" approach






  • Real examples of flaws in previously reported clinical trials and how to avoid them






  • Access to statistical code on the book’s website






  • Chapters written by internationally recognized statisticians from academia and pharmaceutical companies






  • Carefully edited to ensure consistency in style, level, and approach






  • Topics covered include innovating phase I and II designs, trials in immune-oncology and rare diseases, among many others


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There is an increasing need for educational resources for statisticians and investigators. Reflecting this, the goal of this book is to provide readers with a sound foundation in the statistical design, conduct, and analysis of clinical trials. Furthermore, it is intended as a guide for statisticians and investigators with minimal clinical trial experience who are interested in pursuing a career in this area. The advancement in genetic and molecular technologies have revolutionized drug development. In recent years, clinical trials have become increasingly sophisticated as they incorporate genomic studies, and efficient designs (such as basket and umbrella trials) have permeated the field. This book offers the requisite background and expert guidance for the innovative statistical design and analysis of clinical trials in oncology.





Key Features:







  • Cutting-edge topics with appropriate technical background






  • Built around case studies which give the work a "hands-on" approach






  • Real examples of flaws in previously reported clinical trials and how to avoid them






  • Access to statistical code on the book’s website






  • Chapters written by internationally recognized statisticians from academia and pharmaceutical companies






  • Carefully edited to ensure consistency in style, level, and approach






  • Topics covered include innovating phase I and II designs, trials in immune-oncology and rare diseases, among many others


Produktdetaljer
Sprog: Engelsk
Sider: 644
ISBN-13: 9780367729578
Indbinding: Paperback
Udgave:
ISBN-10: 0367729571
Kategori: Kliniske forsøg
Udg. Dato: 18 dec 2020
Længde: 0mm
Bredde: 254mm
Højde: 178mm
Oplagsdato: 18 dec 2020
Forfatter(e):
Forfatter(e)


Kategori Kliniske forsøg


Sprog Engelsk


Indbinding Paperback


Sider 644


Udgave


Længde 0mm


Bredde 254mm


Højde 178mm

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