Free Ebook Drug Discovery Toxicology: From Target Assessment to Translational Biomarkers From Wiley
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Drug Discovery Toxicology: From Target Assessment to Translational Biomarkers From Wiley
Free Ebook Drug Discovery Toxicology: From Target Assessment to Translational Biomarkers From Wiley
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- Sales Rank: #2178512 in Books
- Published on: 2016-04-18
- Original language: English
- Dimensions: 11.30" h x 1.40" w x 8.70" l, 1.47 pounds
- Binding: Hardcover
- 584 pages
From the Back Cover
Developing novel pharmaceuticals requires nonclinical safety studies on candidate drugs to assess general toxicology (through in vivo experiments), safety pharmacology (effects on major organ systems), and genetic toxicity tests. These data provide risk assessment data that supports progression of candidate drugs from discovery phase through clinical development, to regulatory submission and registration. Traditionally, however, less emphasis was placed on the evaluation of safety issues for projects while still in the drug design phase.
In response to this costly attrition, many pharmaceutical companies invested in “drug discovery toxicology” or “drug discovery safety” to identify hazards and take steps to design out or significantly reduce undesirable safety liabilities earlier; with the ultimate aim of enhancing the probability of success in non-clinical and clinical drug development. Because of this, there is a strong need for personnel involved with toxicology and pharmacology studies need to understand the varied tools and approaches to perform early drug discovery safety analysis.
Drug Discovery Toxicology: From Target Assessment to Translational Biomarkers serves as a valuable tool for those discovery scientists. The authors, writing from firsthand industry experience, give readers insight into the strategy and execution of predictive toxicology practices, including what experiments are possible and useful. In addition, they offer a view into the future, indicating key areas to watch for new predictive methods. Broken into different sections, the book deals with the key topics – Safety Lead Optimization Strategies, In Vitro-In Vivo Pharmacokinetics Translation, Predicting Organ Toxicity In Vitro, False Negative Space, --Omics in Predictive Toxicology, Translational Biomarkers, and Signal Investigation Rationale and Practices.
As a guide for pharmaceutical professionals to the issues and practices of drug discovery toxicology, this book integrates and reviews the strategy and application of tools and methods throughout the pre-clinical drug discovery development process.
About the Author
Yvonne Will, PhD, is a Senior Director and the Head of Science and Technology Strategy, Drug Safety Research and Development at Pfizer, Connecticut, USA. She co-edited the book Drug-Induced Mitochondrial Dysfunction, published by Wiley in 2008.
J. Eric McDuffie, PhD, is the Director of the Discovery / Investigative Toxicology and Laboratory Animal Medicine groups at Janssen Research & Development, California, USA.
Andrew J. Olaharski, PhD, is an Associate Director of Toxicology at Agios Pharmaceuticals, Massachusetts, USA.
Brandon D. Jeffy, PhD, is a Senior Principal Scientist in the Exploratory Toxicology division of Nonclinical Development at Celgene Pharmaceuticals, California, USA.
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