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Genotoxicity and Carcinogenicity Tes...
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Graziano, Michael J.
Genotoxicity and Carcinogenicity Testing of Pharmaceuticals
Record Type:
Language materials, printed : Monograph/item
Title/Author:
Genotoxicity and Carcinogenicity Testing of Pharmaceuticals/ edited by Michael J. Graziano, David Jacobson-Kram.
other author:
Graziano, Michael J.
Description:
X, 206 p. 15 illus., 8 illus. in color.online resource. :
Contained By:
Springer Nature eBook
Subject:
Cancer research. -
Online resource:
https://doi.org/10.1007/978-3-319-22084-0
ISBN:
9783319220840
Genotoxicity and Carcinogenicity Testing of Pharmaceuticals
Genotoxicity and Carcinogenicity Testing of Pharmaceuticals
[electronic resource] /edited by Michael J. Graziano, David Jacobson-Kram. - 1st ed. 2015. - X, 206 p. 15 illus., 8 illus. in color.online resource.
Introduction -- History and Current Regulatory Requirements -- Genotoxicity Testing of API and Impurities -- New Emerging Genotoxicity Tests -- Carcinogenicity Testing of Small Molecules -- Alternatives to the 2-Year Rodent Studies -- Addressing Positive Findings in Carcinogenicity Studies -- Investigating Tumor Signals in Clinical Trials -- Tumor Promoters -- Carcinogenicity Testing of Biologics -- In Silico Predictive Tests.
This book provides an overview of the nonclinical testing strategies that are used to asses and de-risk the genotoxicity and carcinogenicity properties of human pharmaceuticals. It includes a review of relevant ICH guidelines, numerous case studies where follow-up studies were conducted to further investigate positive findings, and practical considerations for the use of alternative and emerging tests. With contributions from recognized experts in the pharmaceutical industry and health authorities, this volume presents a balanced view on the interpretation and application of genotoxicity and carcinogenicity regulatory guidances. Genotoxicity and Carcinogenicity Testing of Pharmaceuticals is a valuable resource for scientists, regulators, and consultants that are engaged in the conduct, reporting, and review of nonclinical studies. This book will also help academicians better understand and appreciate the complexity of the regulations and breadth of toxicology research that are necessary to support the development and marketing of new drugs.
ISBN: 9783319220840
Standard No.: 10.1007/978-3-319-22084-0doiSubjects--Topical Terms:
1253664
Cancer research.
LC Class. No.: RC261-271
Dewey Class. No.: 614.5999
Genotoxicity and Carcinogenicity Testing of Pharmaceuticals
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Introduction -- History and Current Regulatory Requirements -- Genotoxicity Testing of API and Impurities -- New Emerging Genotoxicity Tests -- Carcinogenicity Testing of Small Molecules -- Alternatives to the 2-Year Rodent Studies -- Addressing Positive Findings in Carcinogenicity Studies -- Investigating Tumor Signals in Clinical Trials -- Tumor Promoters -- Carcinogenicity Testing of Biologics -- In Silico Predictive Tests.
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This book provides an overview of the nonclinical testing strategies that are used to asses and de-risk the genotoxicity and carcinogenicity properties of human pharmaceuticals. It includes a review of relevant ICH guidelines, numerous case studies where follow-up studies were conducted to further investigate positive findings, and practical considerations for the use of alternative and emerging tests. With contributions from recognized experts in the pharmaceutical industry and health authorities, this volume presents a balanced view on the interpretation and application of genotoxicity and carcinogenicity regulatory guidances. Genotoxicity and Carcinogenicity Testing of Pharmaceuticals is a valuable resource for scientists, regulators, and consultants that are engaged in the conduct, reporting, and review of nonclinical studies. This book will also help academicians better understand and appreciate the complexity of the regulations and breadth of toxicology research that are necessary to support the development and marketing of new drugs.
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Biomedical and Life Sciences (R0) (SpringerNature-43708)
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