Novel Designs of Early Phase Trials for Cancer Therapeutics
Language: English
Published by Elsevier Science, 2018
- Softcover
- New

Seller: AHA-BUCH GmbH, Einbeck, GermanyAHA-BUCH GmbH
AbeBooks seller since August 14, 2006
Condition: New
£ 137.47
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Add to basketItem description from seller
nach der Bestellung gedruckt Neuware - Printed after ordering - Novel Designs of Early Phase Trials for Cancer Therapeutics provides a comprehensive review by leaders in the field of the process of drug development, the integration of molecular profiling, the changes in early phase trial designs, and endpoints to optimally develop a new generation of cancer therapeutics. The book discusses topics such as statistical perspectives on cohort expansions, the role and application of molecular profiling and how to integrate biomarkers in early phase trials. Additionally, it discusses how to incorporate patient reported outcomes in phase one trials. This book is a valuable resource for medical oncologists, basic and translational biomedical scientists, and trainees in oncology and pharmacology who are interested in learning how to improve their research by using early phase trials.
Seller Inventory # 9780128125120
- Title
- Novel Designs of Early Phase Trials for Cancer Therapeutics
- Author
- Shivaani Kummar
- Publisher
- Elsevier Science
- Publication year
- 2018
- Condition
- Neu
- Binding
- Taschenbuch
- Language
- English
- ISBN 10
- 0128125128
- ISBN 13
- 9780128125120
- Item weight
- 494 grams
- Dimensions
- 232x191x11 mm
Novel Designs of Early Phase Trials for Cancer Therapeutics provides a comprehensive review by leaders in the field of the process of drug development, the integration of molecular profiling, the changes in early phase trial designs, and endpoints to optimally develop a new generation of cancer therapeutics. The book discusses topics such as statistical perspectives on cohort expansions, the role and application of molecular profiling and how to integrate biomarkers in early phase trials. Additionally, it discusses how to incorporate patient reported outcomes in phase one trials.
This book is a valuable resource for medical oncologists, basic and translational biomedical scientists, and trainees in oncology and pharmacology who are interested in learning how to improve their research by using early phase trials.
"Synopsis" may belong to another edition of this title.
About the Author
Chris Takimoto did his undergraduate training in Chemistry at Stanford University before receiving his M.D. and Ph.D. in Pharmacology from Yale University. He subsequently completed fellowships in Medical Oncology at the National Cancer Institute (NCI) and Clinical Pharmacology at the Uniformed Services University and he then served as a Senior Investigator in the NCI’s Medicine Branch. While at the NCI, Takimoto worked in the GI tumor group focusing on translational research and early phase clinical trials. In 2000, he became an Associate Professor at the University of Texas Health Science Center San Antonio (UTHSCSA), where he also held the Zachry Chair for Translational Research at the Institute for Drug Development/Cancer Therapy & Research Center. At the time, the CTRC was home to the largest oncology Phase 1 program in the world. Takimoto was also a Professor (Adjunct) of Pharmacology at UTHSCSA, and in 2007, he helped to found an independent Phase 1 oncology clinical research center called South Texas Accelerated Research Therapeutics (START). While in San Antonio he was a principal or co-investigator on over 250 early phase oncology clinical trials. In 2008, Takimoto moved to Johnson & Johnson ultimately becoming Vice President of Experimental Medicine Early Development for Oncology at Janssen R&D where he oversaw all the early phase clinical trials for the oncology portfolio. In 2016, he joined a new, clinical stage biotechnology company called Forty Seven, Inc. as Chief Medical Officer.
"About the title" may belong to another edition of this title.
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