000			03524nam a2200241Ia 4500
003			NULRC
005			20250520094822.0
008			250520s9999 xx 000 0 und d
020			_a9780853697145
040			_cNULRC
050			_aR 853 .D87 2008
100			_aDurham, Todd A. _eauthor
245		0	_aIntroduction to statistics in pharmaceutical clinical trials / _cTodd A. Durham and J. Rick Turner
260			_aLondon, United Kingdom : _bPharmaceutical Press, _cc2008
300			_axiii, 226 pages : _billustrations ; _c25 cm.
365			_bUSD3595
504			_aIncludes index.
505			_a1. The discipline of statistics: introduction and terminology 2. The role of clinical trials in new drug development 3. Research questions and research hypotheses 4. Study design and experimental methodology 5. Data, central tendency and variation 6. Probability, hypothesis testing and estimation 7. Early phase clinical trials 8. Confirmatory clinical trials: safety data 1 9. Confirmatory clinical trials: safety data II 10. Confirmatory clinical trials: analysis of categorical efficacy data 11. Confirmatory clinical trials: analysis of continuous efficacy data 12. Additional statistical considerations in clinical trials 13. Concluding remarks Appendices
520			_aA self-contained introduction to Statistics, presented in the context of clinical trials and pharmaceutical drug development. This title focuses on the statistical analyses most commonly used in drug development. It emphasises the importance of descriptive statistics as well as inferential statistics. This book is a self-contained introduction to Statistics, presented in the context of clinical trials and pharmaceutical drug development. It focuses on the statistical analyses most commonly used in drug development and is therefore an ideal introduction to pharmaceutical statistics. Instead of introducing a series of statistical techniques, the book's organizational structure follows the order in which numerical information and statistical analyses are used in trials and new drug development.All students taking classes in pharmaceutical sciences and clinical research need a solid knowledge and understanding of the nature, methods, application and importance of Statistics. They need to understand:why, and how data are collected in clinical trials; how these data are summarized and analyzed; what the results mean in the context of the clinical research question; and, how the results are communicated to regulatory agencies and to scientific and medical communities.This title therefore adopts a unique approach and concept in organization of the content. It begins with an introduction to statistical theory, analysis and interpretation. This is followed by a discussion of t-tests and confidence intervals. Readers are then taken through the whole process of new drug development (using one specific example throughout) that is meaningful in the context of their broader studies. Throughout this process, statistical techniques and analyses are introduced in the order in which they are employed during the process. The book's realistic scientific and progressive organization from pre-clinical trials to clinical pharmacology through clinical trials is novel, meaningful and educationally powerful. The book emphasizes the importance of descriptive statistics as well as inferential statistics, something that is rarely done.
650			_aCLINICAL TRIALS AS TOPIC
700			_aTurner, J. Rick. _eco-author
942			_2lcc _cBK
999			_c3461 _d3461