Quantitative Decisions in Drug Development
Springer International Publishing (Verlag)
978-3-319-46075-8 (ISBN)
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The book offers useful insights to statisticians, clinicians, regulatory affairs managers and decision-makers in the pharmaceutical industry who have a basic understanding of the drug-development process and the clinical trials conducted to support drug-marketing authorization.
The authors provide software codes for select analytical approaches discussed in the book. The book includes enough technical details to allow statisticians to replicate the quantitative illustrations so that they can generate information to facilitate decision-making themselves.
Christy Chuang-Stein was Vice President and Head of the Statistical Research and Consulting Center at Pfizer prior to retirement from the company in July 2015. She has more than 30 years of experience in the pharmaceutical industry and 160 scientific publications. She is a Fellow of the American Statistical Association (ASA) and received ASA’s Founders’ Award in 2012. She was the recipient of the Distinguished Achievement Award of the International Chinese Statistical Association in 2013. Simon Kirby is Senior Director at the Statistical Research and Consulting Center at Pfizer. He has worked for Pfizer for more than 17 years after previously holding the position of Principal Lecturer in Statistics at Liverpool John Moores University. He has also previously worked as a Statistician at the Institute of Food Research in the UK, Rothamsted and Revlon Healthcare.
Clinical Testing of a New Drug.- A Frequentist Decision-making Framework.- Characteristics of a Diagnostic Test.- The Parallel Between Clinical Trials and Diagnostic Tests.- Incorporating Information from Completed Trials in Future Trial Planning.- Choosing Metrics Appropriate for Different Stages of Drug Development.- Designing Proof-of-Concept Trials with Desired Characteristics.- Designing Dose-response Studies with Desired Characteristics.- Designing Confirmatory Trials with Desired Characteristics.- Designing Phase 4 Trials.- Other Metrics That Have Been Proposed to Optimize Drug Development Decisions.- Discounting Prior Results to Account for Selection Bias.- Index.- Appendix.
"This work offers useful algorithms, classifications, and other general points to statisticians or 'quantitative scientists'. But, it is also really useful to regulatory affairs managers, clinicians, medical writers, and all kinds of decision-makers in the industry." (Andrei Myslivets, ISCB News, Vol. 68, December, 2019)
"It is presented in a concise, structured, friendly, and illustrative way that allows for a good understanding of the underlying ideas ... . the book from Chuang-Stein and Kirby is a valuable, interesting and easy read for statisticians and clinicians with some methodological background who are involved in clinical development or drug approval and who are looking for a structured way to make clinical development decisions." (Norbert Benda, Biometrical Journal, Vol. 61 (4), July, 2016)
| Erscheinungsdatum | 23.05.2017 |
|---|---|
| Reihe/Serie | Springer Series in Pharmaceutical Statistics |
| Zusatzinfo | XV, 248 p. 27 illus., 11 illus. in color. |
| Verlagsort | Cham |
| Sprache | englisch |
| Maße | 155 x 235 mm |
| Themenwelt | Mathematik / Informatik ► Mathematik |
| Medizin / Pharmazie | |
| Schlagworte | Biostatistics • Clinical Trials • drug development • Epidemiology and medical statistics • evidence-based decision • go/no go criteria • Industrial chemistry and chemical engineering • Life sciences: general issues • mathematics and statistics • metric for decision • Pharmaceutical Sciences/Technology • probability and statistics • probability of product success • probability of study success • Regulatory Affairs • Statistics for Life Sciences, Medicine, Health Sci |
| ISBN-10 | 3-319-46075-7 / 3319460757 |
| ISBN-13 | 978-3-319-46075-8 / 9783319460758 |
| Zustand | Neuware |
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