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Biomarkers in Drug Development: A Handbook of Practice, Application, and Strategy - ISBN 9780470169278

Biomarkers in Drug Development: A Handbook of Practice, Application, and Strategy

ISBN 9780470169278

Autor: Michael R. Bleavins, Claudio Carini, Mallé Jurima–Romet, Ramin Rahbari

Wydawca: Wiley

Dostępność: 3-6 tygodni

Cena: 893,55 zł

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ISBN13:      

9780470169278

ISBN10:      

0470169273

Autor:      

Michael R. Bleavins, Claudio Carini, Mallé Jurima–Romet, Ramin Rahbari

Oprawa:      

Hardback

Rok Wydania:      

2010-03-05

Ilość stron:      

784

Wymiary:      

244x166

Tematy:      

MJ


Discover how biomarkers can boost the success rate of drug development efforts
As pharmaceutical companies struggle to improve the success rate and cost–effectiveness of thedrug development process, biomarkers have emerged as a valuable tool. This book synthesizes and reviews the latest efforts to identify, develop, and integrate biomarkers as a key strategy in translational medicine and the drug development process. Filled with case studies, the book demonstrates how biomarkers can improve drug development timelines, lower costs, facilitate better compound selection, reduce late–stage attrition, and open the door to personalized medicine.
Biomarkers in Drug Development is divided into eight parts:
Part One offers an overview of biomarkers and their role in drug development.
Part Two highlights important technologies to help researchers identify new biomarkers.
Part Three examines the characterization and validation process for both drugs and diagnostics, and provides practical advice on appropriate statistical methods to ensure that biomarkers fulfill their intended purpose.
Parts Four through Six examine the application of biomarkers in discovery, preclinical safety assessment, clinical trials, and translational medicine.
Part Seven focuses on lessons learned and the practical aspects of implementing biomarkers in drug development programs.
Part Eight explores future trends and issues, including data integration, personalized medicine, and ethical concerns.
Each of the thirty–eight chapters was contributed by one or more leading experts, including scientists from biotechnology and pharmaceutical firms, academia, and the U.S. Food and Drug Administration. Their contributions offer pharmaceutical and clinical researchers the most up–to–date understanding of the strategies used for and applications of biomarkers in drug development.

< b>Spis treści:
Part 1 – What is a Biomarker and Role in Drug Development.
1. Biomarkers are Not New (Ian Dews).
2. Biomarkers: Facing the Challenges at the Crossroads of Research and Health Care (Gregory J. Downing).
3. Enabling Go/No–Go Decisions (J. Fred Pritchard and Mallé Jurima–Romet).
Part 2 – Identifying New Biomarkers: Technology Approaches .
4. Imaging as a Localized Biomarker: Opportunities and Challenges (Jonathan Moody, Philip S. Murphy, Edward P. Ficaro).
5. Protein Biomarker Discovery Using Mass Spectrometry Based Proteomics (Joanna M. Hunter and Daniel Chelsky).
6. Quantitative Multiplexed Patterning of Immune–Related Biomarkers (Dominic Eisinger, Ralph McDade, and Thomas Joos).
7. Gene Expression Profiles as Preclinical and Clinical Cancer Biomarkers of Prognosis, Drug Response, and Drug Toxicity (Jason A. Sprowl and Amadeo M. Parissenti).
8. The Use of High Through–Put Proteomic Arrays for the Discovery of Disease–Associated Molecules (Douglas M. Molina, W. John W. Morrow, and Xiaowu Liang).
Part 3 – Characterization and Validation.
9. Characterization and Validation Biomarkers in Drug Development: A Regulatory Perspective (Federico Goodsaid).
10. "Fit for Purpose" Method Validation and Assays for Biomarker Characterization to Support Drug Development (Jean W. Lee, Yuling Wu, and Jin Wang).
11. Molecular Biomarkers from a Diagnostic Perspective (Klaus Lindpaintner).
12. Strategies for the Co–Development of Drugs and Diagnostics – An FDA Perspective on Diagnostics Regulation (Francis Kalush and Steven Gutman).
13. Importance of Statistics in the Qualification and Application of Biomarkers (Mary Zacour).
Part 4 – Biomarkers in Discovery and Pre–Clinical Safety.
14. Qualification of Safety Biomark ers for Application to Early Drug Development (William B. Mattes and Frank D. Sistare).
15. Development of Serum Calcium and Phosphorus as Clinical Biomarkers for Drug–Induced Systemic Mineralization: Case Study with a MEK Inhibitor (Alan P. Brown).
16. Biomarkers for the Immunogenicity of Therapeutic Proteins and its Clinical Consequences (Claire Cornips and Huub Shellekens).
17. New Markers of Kidney Injury (Sven Beushausen).
Part 5 – Translating From Pre–Clinical Results to Clinical and Back.
18. Translational Medicine – A Paradigm Shift in Modern Drug Discovery and Development: The Role of Biomarkers (Giora Z. Feuerstein, Salvatore Alesci, Frank L. Walsh, J. Lynn Rutkowski, Robert R. Ruffolo, Jr.).
19. Clinical Validation and Biomarker Translation (David Lin, Andreas Scherer, Raymond Ng, Robert Balshaw, Shawna Flynn, Paul Keown, Rob McMaster, and Bruce McManus).
20. Predicting and Assessing an Inflammatory Disease and Its Complications – An Example from Rheumatoid Arthritis (Christina Trollmo and Lars Klareskog).
21. Pharmacokinetic and Pharmacodynamic Biomarker Correlations (Jean–Francois Marier and Keith Gallicano).
22. Validating In Vitro Toxicity Biomarkers Against Clinical Endpoints (Calvert Louden and Ruth Roberts).
Part 6 – Biomarkers in Clinical Trials.
23. Opportunities and Pitfalls Associated with Early Utilization of Biomarkers: A Case Study in Anticoagulant Development (Kay A. Criswell).
24. Integrating Molecular Testing into Clinical Applications (Anthony A. Killeen).
25. Biomarkers for Lysosomal Storage Disorders (Ari Zimran, Candida Fratazzi, and Deborah Elstein).
26. The Value Chain in the Development of Biomarkers for Disease Targets (Charles W. Richard III, Arthur O. Tzianabos, Whaijen Soo).
Part 7 – Lessons Learned: Practical Aspects of Biomarke r Implementation.
27. Biomarkers in Pharmaceutical Development – The Essential Role of Project Management and Teamwork (Lena King, Nita Ichhpurani, and Mall‚ Jurima–Romet).
28. Integrating Academic Laboratories Into Pharmaceutical Development (Peter A. Ward and Kent J. Johnson).
29. Funding Biomarker Research and Development Through the Small Business Innovative Research (SBIR) Program (James Varani).
30. Novel and Traditional Nonclinical Biomarker Utilization in the Estimation of Pharmaceutical Therapeutic Indices (Bruce D. Car, Brian Gemzik, and William R. Foster).
31. The Anti–Unicorn Principle: Appropriate Biomarkers Don’t Need to be Rare or Hard to Find (Michael R. Bleavins and Ramin Rahbari).
32. Biomarker Patent Strategies – Opportunities and Risks (Cynthia M. Bott and Eric J. Baude).
Part 8 – Where Are We Heading/What Do We Really Need.
33. IT Supporting Biomarker–Enabling Drug Development (Michael Heheberger).
34. Redefining Disease and Pharmaceutical Targets Through Molecular Definitions and Personalized Medicine (Craig P. Webb, John F. Thompson and Bruce H. Littman).
35. Ethics of Biomarkers: Where are the Borders of Investigative Research, Informed Consent, and Patient Protection (Heather Walmsley, Michael Burgess, Jacqui Brinkman, Richard Hegele, Janet Wilson–McManus, Bruce McManus).
36. Pathodynamics: Improving Biomarker Selection By Getting More Information From Changes Over Time (Donald C. Trost).
37. Optimizing the Use of Biomarkers for Drug Development: A Clinician Perspective (Alberto Gimona).
38. Nanotechnology–Based Biomarker Detection (Joshua Reinke).

Nota biograficzna:

MICHAEL R. BLEAVINS, PhD, is cofounder of Michigan Technology and Research Institute. He retired from Pfizer/Warner–Lambert/Parke–Davis in 2006 and has t wenty–three years of experience in pharmaceutical research, development, and biomarkers with more than sixty–five peer–reviewed publications.
CLAUDIO CARINI, MD, PhD, FRCPath, is Chief Medical Officer and Vice President for Clinical Research at Fresenius. Previously, Claudio served as Global Head of Translational Medicine at MDS and Global Head of Biomarkers at Hoffmann–La Roche. Claudio has more than twenty years of experience in the field of immunology and biomarkers and has authored more than 200 publications in international and domestic peer–reviewed journals.
MALLÉ JURIMA–ROMET, PhD, is Senior Director for Development and Regulatory Services at MDS Pharma Services, where she provides strategic and scientific consulting to pharmaceutical and biotech sponsors, and leads drug development program teams. Mallé has authored over forty peer–reviewed publications and is an adjunct professor at the University of Montreal.
RAMIN RAHBARI, MS, is cofounder and Senior Consultant at Innovative Scientific Management. Previously, Ramin has held positions at Pfizer, Synaptic, and Parke–Davis pharmaceutical companies, leading cross–functional biomarker teams.

Okładka tylna:

Discover how biomarkers can boost the success rate of drug development efforts
As pharmaceutical companies struggle to improve the success rate and cost–effectiveness of thedrug development process, biomarkers have emerged as a valuable tool. This book synthesizes and reviews the latest efforts to identify, develop, and integrate biomarkers as a key strategy in translational medicine and the drug development process. Filled with case studies, the book demonstrates how biomarkers can improve drug development timelines, lower costs, facilitate better compound selection, reduce late–stage attrition, and open the door to personalized medicine.
Biomarkers in Drug Development is divided into eight parts:
Part One offers an overview of biomarkers and their role in drug development.
Part Two highlights important technologies to help researchers identify new biomarkers.
Part Three examines the characterization and validation process for both drugs and diagnostics, and provides practical advice on appropriate statistical methods to ensure that biomarkers fulfill their intended purpose.
Parts Four through Six examine the application of biomarkers in discovery, preclinical safety assessment, clinical trials, and translational medicine.
Part Seven focuses on lessons learned and the practical aspects of implementing biomarkers in drug development programs.
Part Eight explores future trends and issues, including data integration, personalized medicine, and ethical concerns.
Each of the thirty–eight chapters was contributed by one or more leading experts, including scientists from biotechnology and pharmaceutical firms, academia, and the U.S. Food and Drug Administration. Their contributions offer pharmaceutical and clinical researchers the most up–to–date understanding of the strategies used for and applications of biomarkers in drug development.

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