Scientific and Regulatory Policy Committee Points-to-consider Paper*

Author:

Frazier Kendall S.1,Engelhardt Jeffery A.2,Fant Pierluigi3,Guionaud Silvia4,Henry Scott P.2,Leach Michael W.5,Louden Calvert6,Scicchitano Marshall S.1,Weaver James L.7,Zabka Tanja S.8

Affiliation:

1. GlaxoSmithKline—Safety Assessment, King of Prussia, Pennsylvania, USA

2. ISIS Pharmaceuticals, Carlsbad, California, USA

3. WIL Research Europe, Saint-Germain-Nuelles, France

4. MedImmune, Cambridge, UK

5. Pfizer—Drug Safety Research and Development, Andover, Massachusetts, USA

6. Raritan, Somerset, New Jersey, USA

7. FDA, CDER, Silver Spring, Maryland, USA

8. Genentech, South San Francisco, California, USA

Abstract

Drug-induced vascular injury (DIVI) is a recurrent challenge in the development of novel pharmaceutical agents. Although DIVI in laboratory animal species has been well characterized for vasoactive small molecules, there is little available information regarding DIVI associated with biotherapeutics such as peptides/proteins or antibodies. Because of the uncertainty about whether DIVI in preclinical studies is predictive of effects in humans and the lack of robust biomarkers of DIVI, preclinical DIVI findings can cause considerable delays in or even halt development of promising new drugs. This review discusses standard terminology, characteristics, and mechanisms of DIVI associated with biotherapeutics. Guidance and points to consider for the toxicologist and pathologist facing preclinical cases of biotherapeutic-related DIVI are outlined, and examples of regulatory feedback for each of the mechanistic types of DIVI are included to provide insight into risk assessment.

Publisher

SAGE Publications

Subject

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

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