Bioequivalence and statistics in clinical pharmacology
著者
書誌事項
Bioequivalence and statistics in clinical pharmacology
（Chapman & Hall/CRC biostatistics series）（A Chapman & Hall book）
CRC, c2017
2nd ed
- : hardback
大学図書館所蔵 件 / 全2件
-
該当する所蔵館はありません
- すべての絞り込み条件を解除する
注記
Includes bibliographical references (p. 343-430) and index
内容説明・目次
内容説明
Maintaining a practical perspective, Bioequivalence and Statistics in Clinical Pharmacology, Second Edition explores statistics used in day-to-day clinical pharmacology work. The book is a starting point for those involved in such research and covers the methods needed to design, analyze, and interpret bioequivalence trials; explores when, how, and why these studies are performed as part of drug development; and demonstrates the methods using real world examples.
Drawing on knowledge gained directly from working in the pharmaceutical industry, the authors set the stage by describing the general role of statistics. Once the foundation of clinical pharmacology drug development, regulatory applications, and the design and analysis of bioequivalence trials are established, including recent regulatory changes in design and analysis and in particular sample-size adaptation, they move on to related topics in clinical pharmacology involving the use of cross-over designs. These include, but are not limited to, safety studies in Phase I, dose-response trials, drug interaction trials, food-effect and combination trials, QTc and other pharmacodynamic equivalence trials, proof-of-concept trials, dose-proportionality trials, and vaccines trials.
This second edition addresses several recent developments in the field, including new chapters on adaptive bioequivalence studies, scaled average bioequivalence testing, and vaccine trials.
Purposefully designed to be instantly applicable, Bioequivalence and Statistics in Clinical Pharmacology, Second Edition provides examples of SAS and R code so that the analyses described can be immediately implemented. The authors have made extensive use of the proc mixed procedures available in SAS.
目次
Bioequivalence & Biopharmaceutical Development
Drug Development and Clinical Pharmacology
Aims of This Book
Biopharmaceutical Development
Clinical Pharmacology
Statistics in Clinical Pharmacology
Structure of the Book
History and Regulation of Bioequivalence
When and How BE Studies Are Performed
Why Are BE Studies Performed?
Deciding When Formulations Are Bioequivalent
Potential Issues with TOST Bioequivalent
Current International Regulation
Some Practical Notes
Testing for Average Bioequivalence
Background
Linear Model for 2 x 2 Data
Applying the TOST Procedure
Carry-over, Sequence, and Interaction Effects
Checking Assumptions Made about the Linear Model
Power and Sample Size for ABE in the 2 x 2 Design
Example Where Test and Reference Are Not ABE
Nonparametric Analysis
BE Studies with More Than Two Periods
Background
Three-period Designs
Within-subject Variability
Robust Analyses for Three Period Designs
Four-period Designs
Designes with More Than Two Treatments
Adjusting for Multiple Testing
Nonparametric Analyses of Tmax
Technical appendix: Efficiency
Tables of Data
Special Topics in Bioequivalence
Dealing with Special BE Challenges
Restricted Maximum Likelihood Modelling
Failing BE and the DER Assessment
Simulation
Data-based Simulation
Carry-over
Optimal Designs
Determining Trial Size
What Outliers Are and How to Handle Their Data
Bayesian BE Assessment
Adaptive Bioequivalence Trials
Background
Two-stage design for testing for ABE
TOST using the standard combination test
Example of using the standard combination test
The maximum combination test
Example of using the maximum combination test
Conditional errors and conditional power
Algorithm for sample size re-estimation
Operating characteristics
Conclusions
Techniccal Appendix: R code
Scaled Average Bioequivalence Testing
Background
Scaled Average Bioequivalence in Europe
Scaled Average Bioequivalence in USA
Discussion and Cautions
Clinical Pharmacology
Clinical Pharmacology Safety Studies
Background
First-time-in-humans
Sub-chronic Dosing Studies
Food-Effect Assessment and DDIs
Dose-Proportionality
Technical Appendix
QTc
Background
Modelling of QTc Data
Interpreting the QTc Modelling Findings
Design of a Thorough QTc Study in the Future
Clinical Pharmacology Efficacy Studies
Background
Sub-chronic Dosing
Phase IIa and the Proof of Concept
Population Pharmacokinetics
Population and Pharmacokinetics
Absolute and Relative Bioavailability
Age and Gender Pharmacokinetic Studies
Ethnicity
Liver Disease
Kidney Disease
Technical Appendix
Vaccines & Epilogue
Vaccine Trials
Brief Introduction to Vaccine Research and Development
Phase I Vaccine Studies
Proof of Concept and Phase II
Lot Consistency
Concomitant Vaccination
Cross-over Trials in Vaccines
Epilogue
Bibliography
Index
「Nielsen BookData」 より