A snapshot of biologic drug development
Author:
Affiliation:
1. Preclinical Safety, AbbVie Research Center, Worcester, MA, USA
2. Preclinical Safety, AbbVie, Lake County, IL, USA
3. Comparative and Molecular Toxicology, AbbVie, Lake County, IL, USA
4. Department of Pathology, AbbVie, Lake County, IL, USA
Abstract
Publisher
SAGE Publications
Subject
Health, Toxicology and Mutagenesis,Toxicology,General Medicine
Link
http://journals.sagepub.com/doi/pdf/10.1177/0960327115603594
Reference64 articles.
1. U.S. Department of Health and Human Services, Food and Drug Administration Center for Drug Evaluation and Research (CDER), and Center for Biologics Evaluation and Research (CBER). Guidance for Industry: ICH S6 Addendum to Preclinical Safety Evaluation of Biotechnology-Derived Pharmaceuticals, July 1997.
2. U.S. Department of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research (CDER), and Center for Biologics Evaluation and Research (CBER). Guidance for Industry: ICH S6 Addendum to Preclinical Safety Evaluation of Biotechnology-Derived Pharmaceuticals, May 2012.
3. U.S. Department of Health and Human Services, Food and Drug Administration Center for Drug Evaluation and Research (CDER), and Center for Biologics Evaluation and Research (CBER). Guidance for Industry: ICH S9 Addendum to Nonclinical Evaluation for Anticancer Pharmaceuticals, March 2010.
4. Monoclonal antibody TGN1412 trial failure explained by species differences in CD28 expression on CD4+ effector memory T-cells
5. Preclinical safety testing of monoclonal antibodies: the significance of species relevance
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