Join our mailing list
Get exclusive deals and learn about new products!
Reliable shipping
Flexible returns
This book provides a comprehensive view of the methodologies used for the study of liver toxicity encountered throughout the whole life cycle of a drug, from drug discovery, to clinical trial, post-marketing, and even clinical practice. Organized into six sections, the first section introduces the mechanisms contributing to drug-induced liver toxicity. The second and third section explore in silico and in vitro approaches used to help mitigate hepatotoxicity liability at the early stages of drug development. The fourth section describes methodologies applied in regulatory processes, including preclinical studies, clinical trials, and post-marketing surveillance. The fifth section discusses clinical hepatotoxicity. Emerging technologies are examined in the final section. As a volume in the Methods in Pharmacology and Toxicology series, chapters include the kind of expert advice that will lead to optimal results.
Published by: Humana
Publication Date: 2018-03-21
Format: Hardcover
ISBN-13: 9781493976768
DOI: 10.1007/978-1-4939-7677-5
Dimensions: 254cm x178cm
Pages: 667