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Main description:
concerns within the pharmaceutical industry about generating data that might be difficult to interpret in a regulated environment. There is also a growing apprec- tion for the challenges in translating this new information into clinical utility, including scientific, commercial, ethical, and policy challenges. Pharmacogenomics and Personalized Medicine, which is part of the Methods in Pharmacology and Toxicology series, comprises chapters on selected aspects of pharmacogenomics and personalized medicine. Our overall intent is to assist both novice and experienced investigators in understanding the current scientific ch- lenges in applying PGx to discovery and clinical development and in making app- priate decisions to engage in and interpret PGx research. Designed to share the experiences of leading experts in the field, the book is a useful guide for conducting PGx research--from discovery to the market, but we also aim to present a realistic perspective on the challenges, practicalities, and obstacles in applying pharmac- enomics. Generally, the book avoids statements such as "Pharmacogenomics is going to revolutionize the practice of medicine," which are neither realistic nor particularly useful to anyone. The book presents an industry perspective on the implementation of PGx in research and development, in drug discovery, and in clinical trials, including rec- mendations for a systematic approach for assessing the feasibility and added value of PGx studies in clinical trials.
Contents:
Preface Contributors    Challenges, Opportunities and Evolving Landscape in Pharmacogenomics 
and Personalized Medicine: An Industry Perspective
Nadine Cohen and Theresa Frangiosa     Considerations for Sample Collections Intended for Pharmacogenomic analyses: The Pharmacogenomics protocol and informed consent form 
Deborah Ricci and Monique Franc    Pharmacogenomics: The Regulatory Environment and Labeling Implication
Myong-Jin Kim, Shiew-Mei Huang, Atiqur Rahman, Felix W. Frueh, 
Lawrence J. Lesko    Applications of Pharmacogenomics in Drug Discovery
Duncan McHale    Applications of Pharmacogenomics in Clinical Trials
Monique Franc     Pharmacogenomics applications in drug metabolism: from genotyping to drug
label-challenges?
Ann K. Daly     The Genetics of Adverse Drug Reactions - Promises and Problems
Martin Armstrong     Strategies and resources for marker selection and genotyping in genetic 
association studies
Nicole Soranzo, Dong-Jing Fu and Qingqin S. Li     Study Design and Statistical Methods in Pharmacogenomics Research: From 
Candidate Genes to Genome Wide Screens
Nicholas J. Schork, Nathalie Malo, Eric J. Topol 
 Holy SNP, Batman! 
Reyna Favis    Use of Predictive Biomarker Classifiers in the Design of Pivotal Clinical 
Trials
Richard Simon     Translation of biomarkers into clinical utility 
William Trepicchio and George Mulligan     Pharmacogenomic Study Feasibility Assessment and Pharmaceutical Business 
Decision-Making
Monique Franc and Theresa Frangiosa     Co-development of drugs andPharmacogenomics based Diagnostics in Oncology Jeffrey Ross    Pharmacogenomics applications in Epilepsy 
Chantal Depondt     Pharmacogenomics in Alzheimer's Disease
Ramon Cacabelos     Pharmacogenomics applications in Psychiatric disorders 
Todd Lencz and Anil K. Malhotra    Pharmacogenomics in HIV Disease
Amalio Telenti    Pharmacogenomics and Cardiovascular Drugs 
Gerard Siest, Hind Berrahmoune, Jean-Brice Marteau,
and Sophie Visvikis-Siest
 Pharmacogenomic applications in Children 
Struan F.A. Grant and Hakon Hakonarson  Pharmacogenomics of rare and monogenic disorders 
Paul Maher
PRODUCT DETAILS
Publisher: Springer (Humana Press Inc.)
Publication date: September, 2008
Pages: 528
Weight: 949g
Availability: Available
Subcategories: General Practice, Genetics, Pharmacology
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