[The Identification of Critical Quality Attributes (CQAs) for the Development of Antibody Drugs]

Yakugaku Zasshi. 2018;138(12):1475-1481. doi: 10.1248/yakushi.18-00020-1.
[Article in Japanese]

Abstract

In the development of quality biopharmaceutical drugs, it is the level of knowledge gained, not the volume of data, which provides the basis for science-based submissions and their regulatory evaluation [International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH) Q8 (R2)]. The identification of critical quality attributes (CQAs) is important as the initial step for quality by design (QbD) strategies. The impact of each potential critical attribute (pCQA) is assessed by using a systematic and scientific approach with respect to bioactivity, pharmacokinetics (PK)/pharmacodynamics (PD), immunogenicity, and safety of the biopharmaceutical drugs. The purpose of this section is to introduce a strategy for identifying CQA, and new analytical methods for CQA assessment.

Keywords: biopharmaceuticals; critical quality attribute; quality by design.

Publication types

  • Review

MeSH terms

  • Antibodies, Monoclonal* / adverse effects
  • Antibodies, Monoclonal* / immunology
  • Antibodies, Monoclonal* / pharmacokinetics
  • Antibodies, Monoclonal* / pharmacology
  • Biological Products* / adverse effects
  • Biological Products* / immunology
  • Biological Products* / pharmacokinetics
  • Biological Products* / pharmacology
  • Drug Design*
  • Guidelines as Topic*
  • Quality Control*
  • Risk Assessment
  • Risk Management
  • Safety

Substances

  • Antibodies, Monoclonal
  • Biological Products