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Dose Finding in Drug Development (Statistics for Biology and Health)


by Naitee Ting

List Price: $89.95
Price: $71.96
You Save: $17.99 (20%)
Available: Usually ships in 24 hours
Sales Rank: 969739
Studio: Springer
Binding: Hardcover
Number Of Pages: 248
Publication Date: March 07, 2006
Publisher: Springer


ACCESSORIES

Statistical Monitoring of Clinical Trials: A Unified Approach (Statistics for Biology and Health)
by Michael A. Proschan, K.K. Gordon Lan, Janet Turk Wittes

Fundamentals of Clinical Trials
by Lawrence M. Friedman, Curt D. Furberg, David L. DeMets

Analysis of Phylogenetics and Evolution with R (Use R)
by Emmanuel Paradis



EDITORIAL REVIEWS

Product Description

When you go to the pharmacy and fill a prescription, have you ever wondered if the dose of the medication is right for you? Can the dose be too low so that the drug will not work? Can the dose be too high that it may cause some potential problem? How do people learn about dosing information? This book answers some of these questions.

Dosing information on the drug label is based on discussion and agreement between the pharmaceutical manufacturer and the drug regulatory agency. A drug label is a high level summary of results obtained from many scientific experiments. Scientists with biological, chemical, medical, or statistical background working in the pharmaceutical industry designed and executed these experiments to obtain information to help understand the dosing information.

This book introduces the drug development process, the design and analysis of clinical trials. Many of the discussions are based on applications of statistical methods in the design and analysis of dose response studies. Although the book is prepared mainly for statisticians/biostatisticians, it also serves as a useful reference to a variety of professionals working for the pharmaceutical industry. The potential readers include pharmacokienticists, clinical scientists, clinical pharmacologists, pharmacists, project managers, pharmaceutical scientists, clinicians, programmers, data managers, regulatory specialists, and study report writers. This book is also a good reference for professionals working in a drug regulatory environment, for example, the FDA. Scientists and/or reviewers from both U.S. and foreign drug regulatory agencies can benefit greatly from this book. In addition, statistical and medical professionals in academia may find this book helpful in understanding the drug development process and practical concerns in selecting doses for a new drug.

From the reviews:

"The book will be of particular interest to statisticians with some pharmaceutical industry experience who find themselves working on phase II dose finding problems. It will also be valuable for clinicians and pharmacokineticists with some statistical background. All chapters in the book are extensively referenced as they each do not pretend to exhaust their subject." Journal of Biopharmaceutical Statistics, Issue #2, 2007



CUSTOMER REVIEWS (Average Customer Rating: 4.0 based on 1 review)

collection of papers covering methods to find the right dose  
In phase 2 of the drug development process after a drug has shown to satisfy proof of concept on efficacy a clinical trial is generally run with subjects randomized to a placebo or one of several dose of the drug. This is done to find the dose that is most effective but still safe for use. This book covers the various methods for accomplishing this task. The goal is often to find what is called the maximally tolerated dose (MTD, highest dose meeting safety requirements). Two of the chapters are devoted to the challenging problem of doing this for oncology trials. Methods for determining sample size requirements and the need for PK/PD studies are all considered in this book.
August 14, 2007


SIMILAR PRODUCTS

Statistical Methods for Dose-Finding Experiments (Statistics in Practice)
by Sylvie Chevret

Pharmacokinetic-Pharmacodynamic Modeling and Simulation
by Peter Bonate

Adaptive Design Methods in Clinical Trials (Biostatistics)
by Shein-Chung Chow, Mark Chang

Statistical Monitoring of Clinical Trials: A Unified Approach (Statistics for Biology and Health)
by Michael A. Proschan, K.K. Gordon Lan, Janet Turk Wittes

Modeling in Biopharmaceutics, Pharmacokinetics and Pharmacodynamics: Homogeneous and Heterogeneous Approaches (Interdisciplinary Applied Mathematics)
by Panos Macheras, Athanassios Iliadis

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