Helping you become a creative, logical thinker and skillful "simulator," Monte Carlo Simulation for the Pharmaceutical Industry: Concepts, Algorithms, and Case Studies provides broad coverage of the entire drug development process, from drug discovery to preclinical and clinical trial aspects to commercialization. It presents the theories and methods needed to carry out computer simulations efficiently, covers both descriptive and pseudocode algorithms that provide the basis for implementation of the simulation methods, and illustrates real-world problems through case studies.
The text first emphasizes the importance of analogy and simulation using examples from a variety of areas, before introducing general sampling methods and the different stages of drug development. It then focuses on simulation approaches based on game theory and the Markov decision process, simulations in classical and adaptive trials, and various challenges in clinical trial management and execution. The author goes on to cover prescription drug marketing strategies and brand planning, molecular design and simulation, computational systems biology and biological pathway simulation with Petri nets, and physiologically based pharmacokinetic modeling and pharmacodynamic models. The final chapter explores Monte Carlo computing techniques for statistical inference.
This book offers a systematic treatment of computer simulation in drug development. It not only deals with the principles and methods of Monte Carlo simulation, but also the applications in drug development, such as statistical trial monitoring, prescription drug marketing, and molecular docking.
Table of Contents
Simulation, Simulation Everywhere
Modeling and Simulation
Introductory Monte Carlo Examples
Simulations in Drug Development
Virtual Sampling Techniques
Uniform Random Number Generation
General Sampling Methods
Efficiency Improvement in Virtual Sampling
Sampling Algorithms for Specific Distributions
Overview of Drug Development
Meta-Simulation for Pharmaceutical Industry
Game Theory Basics
Prescription Drug Global Pricing
Macro-Simulation for Pharmaceutical R & D
Markov Decision Process
Pharmaceutical Decision Process
Extension of Markov Decision Process
Clinical Trial Simulation (CTS)
Classical Trial Simulation
Adaptive Trial Simulation
Clinical Trial Management and Execution
Clinical Trial Management
Patient Recruitment and Projection
Dynamic and Adaptive Drug Supply
Statistical Trial Monitoring
Prescription Drug Commercialization
Dynamics of Prescription Drug Marketing
Stock-Flow Dynamic Model for Brand Planning
Competitive Drug Marketing Strategy
Compulsory Licensing and Parallel Importation
Molecular Design and Simulation
Why Molecular Design and Simulation
Molecular Similarity Search
Overview of Molecular Docking
Small Molecule Confirmation Analysis
Disease Modeling and Biological Pathway Simulation
Computational System Biology
Biological Pathway Simulation
Overview of ADME
Physiologically Based PK Model
Way to Pharmacodynamics
Application of Pharmacodynamic Modeling
Monte Carlo for Inference and Beyond
Appendix B: K-Stage Adaptive Design Stopping Boundaries
A Summary and Exercises appear at the end of each chapter.
Mark Chang is the executive director of biostatistics and data management at AMAG Pharmaceuticals in Lexington, Massachusetts. Dr. Chang is an elected fellow of the American Statistical Association. He is the author of the best-selling Adaptive Design Theory and Implementation Using SAS and R and co-author of the best-selling Adaptive Design Methods in Clinical Trials.
Featured Author Profiles
"Overall, the book does not only cover a very broad range of different topics but manages to explain these coherently. … this book is not only of interest for scientists in the pharmaceutical industry but also for academia due to its thorough presentation."
—Frank Emmert-Streib, Statistical Methods in Medical Research, 21(6), 2012
"… well written and easy to read. … this book is worthwhile reading as a long introduction to Monte Carlo simulation and its eventual application in pharmaceutical industry. It can convince people to consider this methodology …"
—Sophie Donnet, International Statistical Review, 2012
"This is an ambitious book covering a very wide array of topics … the theoretical presentation is reliable and sophisticated … the ability of the author to condense such a broad array of topics, and to present them in a cohesive manner, is quite impressive, and means that the book will contain information of relevance to a wide audience. … Many statisticians working in the pharmaceutical industry will benefit from having access to a copy of this book. Some statisticians working outside the industry may also benefit from having access to a copy, particularly those working in areas overlapping with the pharmaceutical industry, such as clinical science and health economics."
—Ian C. Marschner, Australian & New Zealand Journal of Statistics, 2011
"For industry statisticians, scientists, and software engineers and programmers, Chang, who works for a pharmaceutical company, details concepts, theories, algorithms, and case studies for carrying out computer simulations in the drug development process, from drug discovery to clinical trial aspects to commercialization. He covers analogy and simulation using examples from different areas, general sampling methods and the different stages of drug development, simulation approaches based on game theory and the Markov decision process, simulations in classical and adaptive trials, and challenges in clinical trial management and execution. He then addresses prescription drug marketing strategies and brand planning, molecular design and simulation, computational systems biology and biological pathway simulation with Petri nets, and physiologically based pharmacokinetic modeling and pharmacodynamic models, ending with Monte Carlo computing techniques for statistical inference."
—SciTech Book News, February 2011