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Bayesian Applications in Pharmaceutical Development [Kõva köide]

  • Formaat: Hardback, 532 pages, kõrgus x laius: 234x156 mm, kaal: 1140 g
  • Sari: Chapman & Hall/CRC Biostatistics Series
  • Ilmumisaeg: 11-Oct-2019
  • Kirjastus: CRC Press
  • ISBN-10: 1138296767
  • ISBN-13: 9781138296763
Teised raamatud teemal:
  • Formaat: Hardback, 532 pages, kõrgus x laius: 234x156 mm, kaal: 1140 g
  • Sari: Chapman & Hall/CRC Biostatistics Series
  • Ilmumisaeg: 11-Oct-2019
  • Kirjastus: CRC Press
  • ISBN-10: 1138296767
  • ISBN-13: 9781138296763
Teised raamatud teemal:
The cost for bringing new medicine from discovery to market has nearly doubled in the last decade and has now reached 2.6 billion. There is an urgent need to make drug development less time-consuming and less costly. Innovative trial designs/analyses such as the Bayesian approach are essential to meet this need. This book will be the first to provide comprehensive coverage of Bayesian applications across the span of drug development, from discovery, to clinical trial, to manufacturing with practical examples. This book will have a wide appeal to statisticians, scientists, and physicians working in drug development who are motivated to accelerate and streamline the drug development process, as well as students who aspire to work in this field. The advantages of our book are as follows:Provides motivating, worked, practical case examples with easy to grasp models, technical details, and computational codes to run the analysesBalances practical examples with best practices on trial simulation and reporting, as well as regulatory perspectivesChapters written by authors who are individual contributors in their respective topicsDr. Mani Lakshminarayanan is currently working as Vice-President, Clinical and Database Studies at Complete Health Economics Outcomes and Research Solutions (CHEORS). He has over 30 years of experience in the pharmaceutical industry. He has volunteered his time to the American Statistical Association (ASA) in various positions and to the DIA Bayesian Scientific Working Group (BSWG). He has a PhD in Statistics from Southern Methodist University, Dallas, Texas and is an ASA Fellow.Dr. Fanni Natanegara has over 15 years of pharmaceutical experience and is currently Principal Research Scientist and Group Leader for the Early Phase Neuroscience Statistics team at Eli Lilly and Company. She played a key role in the Advanced Analytics team to provide Bayesian education and statistical consultation at Eli Lilly. Dr. Natanegara is the chair of the cross industry-regulatory-academic DIA BSWG to ensure that Bayesian methods are appropriately utilized for design and analysis throughout the drug-development process.

Arvustused

'This is not a book that you should breeze through. Sure, you can. However, the reader should read at a pace that is appropriate to extract all the juice out of it. It will not be an exaggeration to say that you can explore the book like a treasure trove. I highly recommended it for those who want to challenge their minds and wouldn't mind rethinking and relearning.'

- Enayet Raheem, International Society for Clinical Biostatistics, 71, June 2021

Preface vii
Editors xi
Contributors xiii
1 Introduction
1(16)
Mani Lakshminarayanan
Fanni Natanegara
2 Incorporation of Historical Control Data in Analysis of Clinical Trials
17(32)
G. Frank Liu
Wen Li
A. Lawrence Gould
3 Practical Considerations for Building Priors for Confirmatory Studies
49(12)
Guochen Song
John Zhong
Stacy Lindborg
Baoguang Han
4 The Practice of Prior Elicitation
61(32)
Timothy H. Montague
Karen L. Price
John W. Seaman Jr.
5 Bayesian Examples in Preclinical In Vivo Research
93(32)
John Sherington
Phil Stanley
Ros Walley
6 Planning a Model-Based Bayesian Dose Response Study
125(16)
Neal Thomas
7 Novel Designs for Early Phase Drug-Combination Trials
141(28)
Ying Yuan
Ruitao Lin
8 Executing and Reporting Clinical Trial Simulations: Practical Recommendations for Best Practices
169(18)
Cory R. Heilmann
Fanni Natanegara
Maria J. Costa
Matilde Sanchez-Kam
John W. Seaman Jr.
9 Reporting of Bayesian Analyses in Clinical Research: Some Recommendations
187(38)
Melvin Munsaka
Mani Lakshminarayanan
10 Handling Missing Data in Clinical Trials with Bayesian and Prequentist Approaches
225(22)
Xin Zhao
Baoguang Han
John Zhong
Stacy Lindborg
Neal Thomas
G. Frank Liu
11 Bayesian Probability of Success for Go/No-Go Decision Making
247(20)
Qi Tang
12 Simulation for Bayesian Adaptive Designs---Step-by-Step Guide for Developing the Necessary R. Code
267(20)
J. Kyle Wathen
13 Power Priors for Sample Size Determination in the Process Validation Life Cycle
287(20)
Paul Fay a
John W. Seaman Jr.
James D. Stamey
14 Bayesian Approaches in the Regulation of Medical Products
307(22)
Telba Irony
Lei Huang
15 Computational Tools
329(46)
David Kahle
Michael Sonksen
16 Software for Bayesian Computation---An Overview of Some Currently Available Tools
375(34)
Melvin Munsaka
Mani Lakshminarayanan
17 Considerations and Bayesian Applications in Pharmaceutical Development for Rare Diseases
409(18)
Freda Cooner
18 Extrapolation Process in Pediatric Drug Development and Corresponding Bayesian Implementation for Validating Clinical Efficacy
427(56)
Margaret Gamalo-Siebers
Simin Baygani
19 A Brief Guide to Bayesian Model Checking
483(20)
John W. Seaman Jr.
James D. Stamey
David J. Kahle
Somer Blair
Index 503
Dr. Mani Lakshminarayanan is a researcher and statistical consultant with more than 30 years of experience in the pharmaceutical industry. He has published over 50 articles, technical reports, and book chapters besides serving as a referee for several journals. He has a Ph.D. in Statistics from Southern Methodist University, Dallas, Texas and is a Fellow of the American Statistical Association.

Dr. Fanni Natanegara has over 15 years of pharmaceutical experience and is currently Principal Research Scientist and Group Leader for the Early Phase Neuroscience Statistics team at Eli Lilly and Company. She played a key role in the Advanced Analytics team to provide Bayesian education and statistical consultation at Eli Lilly. Dr. Natanegara is the chair of the cross industry-regulatory-academic DIA BSWG to ensure that Bayesian methods are appropriately utilized for design and analysis throughout the drug-development process.