Use of Animal Models of Human Disease for Nonclinical Safety Assessment of Novel Pharmaceuticals

Author:

Morgan Sherry J.1,Elangbam Chandikumar S.2,Berens Shawn3,Janovitz Evan4,Vitsky Allison5,Zabka Tanja6,Conour Laura7

Affiliation:

1. Abbott Laboratories, Preclinical Safety, Abbott Park, Illinois, USA

2. GlaxoSmithKline, Safety Assessment, Research Triangle Park, North Carolina, USA

3. Allergan, Drug Safety Evaluation, Irvine, California, USA

4. Bristol-Myers Squibb, Discovery Toxicology Research, Princeton, New Jersey, USA

5. Pfizer, Drug Safety Research and Development, San Diego, California, USA

6. Genentech Safety Assessment, San Francisco, California, USA

7. Princeton University, Princeton, New Jersey, USA

Abstract

Animal models of human disease are commonly utilized to gain insight into the potential efficacy and mode of action of novel pharmaceuticals. However, conventional (healthy) rodent and nonrodent models are generally utilized in nonclinical safety testing. Animal models of human disease may be helpful in understanding safety risks of compounds in nonclinical or clinical development, with their greatest value being in targeted or hypothesis-driven studies to help understand the mechanism of a particular toxicity. Limitations of animal models of disease in nonclinical safety testing include a lack of historical control, heterogeneity in disease expression, a limited life span, and confounding effects of the disease. In most instances, animal models of human disease should not be utilized to supplant testing in conventional animal models. While of potential benefit, testing in an animal model of human disease should only be taken after adequate consideration of relevance along with benefits and limitations of the proposed model.

Publisher

SAGE Publications

Subject

Cell Biology,Toxicology,Molecular Biology,Pathology and Forensic Medicine

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