A snapshot of biologic drug development

Author:

Andrews L1,Ralston S2,Blomme E3,Barnhart K4

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

Since the approval of insulin as the first recombinant therapeutic protein, the prominence of biologic therapies in drug development has grown significantly. Many modalities beyond traditional biologics are now being developed or explored for various indications with significant unmet medical needs. From early traditional replacement proteins to more recent, highly engineered antibodies, oligonucleotides, fusion proteins, and gene constructs, biologic agents have delivered life-changing therapies, despite often having scientifically and technically challenging development programs. This brief review outlines some of the major biotherapeutic classes and identifies the advantages and challenges with the development of these products.

Publisher

SAGE Publications

Subject

Health, Toxicology and Mutagenesis,Toxicology,General Medicine

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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