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Recommendations for Clinical Pathology Data Generation, Interpretation, and Reporting in Target Animal Safety Studies for Veterinary Drug Development.

作者信息

Siska William, Gupta Aradhana, Tomlinson Lindsay, Tripathi Niraj, von Beust Barbara

机构信息

1 Charles River Laboratories, Inc, Reno, NV, USA.

2 Boehringer Ingelheim, Duluth, GA, USA.

出版信息

Int J Toxicol. 2017 Jul/Aug;36(4):293-302. doi: 10.1177/1091581817711876. Epub 2017 Jun 6.

Abstract

Clinical pathology testing is routinely performed in target animal safety studies in order to identify potential toxicity associated with administration of an investigational veterinary pharmaceutical product. Regulatory and other testing guidelines that address such studies provide recommendations for clinical pathology testing but occasionally contain outdated analytes and do not take into account interspecies physiologic differences that affect the practical selection of appropriate clinical pathology tests. Additionally, strong emphasis is often placed on statistical analysis and use of reference intervals for interpretation of test article-related clinical pathology changes, with limited attention given to the critical scientific review of clinically, toxicologically, or biologically relevant changes. The purpose of this communication from the Regulatory Affairs Committee of the American Society for Veterinary Clinical Pathology is to provide current recommendations for clinical pathology testing and data interpretation in target animal safety studies and thereby enhance the value of clinical pathology testing in these studies.

摘要

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