Preclinical Drug Development
eBook - ePub

Preclinical Drug Development

  1. 376 pages
  2. English
  3. ePUB (mobile friendly)
  4. Available on iOS & Android
eBook - ePub

Preclinical Drug Development

About this book

Preclinical Drug Development, Second Edition discusses the broad and complicated realm of preclinical drug development. Topics range from assessment of pharmacology and toxicology to industry trends and regulatory expectations to requirements that support clinical trials.

Highlights of the Second Edition include:



  • Pharmacokinetics


  • Modeling and simulation


  • Formulation and routes of administration


  • Toxicity evaluations


  • The assessment of drug absorption and metabolism


  • Interspecies scaling


  • Lead molecule selection and optimization via profiling


  • Screening using in silico and in vitro toxicity evaluations


The book also includes case studies on preclinical pharmacokinetic-pharmacodynamic modeling and simulation in drug development, a review of ICH preclinical guidelines, and experimental methods used to study membrane drug transport and metabolism. This guide is a fundamental resource for medicinal chemists, biologists, and other specialists in the drug development sciences.

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Information

Publisher
CRC Press
Year
2016
Print ISBN
9780815368496
eBook ISBN
9781040066799

Table of contents

  1. Cover
  2. Half Title
  3. Series Page
  4. Title Page
  5. Copyright Page
  6. Preface
  7. Table of Contents
  8. Contributors
  9. 1 The Scope of Preclinical Drug Development: An Introduction and Framework
  10. 2 Lead Molecule Selection: Pharmaceutical Profiling and Toxicity Assessments
  11. 3 Interspecies Differences in Physiology and Pharmacology: Extrapolating Preclinical Data to Human Populations
  12. 4 Pharmacokinetics/ADME of Small Molecules
  13. 5 Pharmacokinetics/ADME of Large Molecules
  14. 6 Preclinical Pharmacokinetic–Pharmacodynamic Modeling and Simulation in Drug Development
  15. 7 Formulation and Production Strategies for Enhancing Bioavailability of Poorly Absorbed Drugs
  16. 8 Transporters Involved in Drug Disposition, Toxicity, and Efficacy
  17. 9 Toxicity Evaluations, ICH Guidelines, and Current Practice
  18. 10 Application of Pathology in Safety Assessment
  19. 11 Utilizing the Preclinical Database to Support Clinical Drug Development
  20. Index

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Yes, you can access Preclinical Drug Development by Mark Rogge, David R. Taft, Mark Rogge,David R. Taft in PDF and/or ePUB format, as well as other popular books in Medicine & Pharmacology. We have over one million books available in our catalogue for you to explore.