Analysis of regulatory guidance on antidrug antibody testing for therapeutic protein products

Therapeutic proteins have the potential to induce unwanted immune responses. The potential impact of immunogenicity on pharmacokinetics, pharmacodynamics, safety and efficacy are well established. Here, we analyze key aspects of current US FDA and EMA guidelines on the development and validation of antidrug antibody assays. Although FDA and EMA guidance documents are in harmony on most points, EMA allows greater leeway for scientific judgement, while FDA recommends specific approaches that may not be appropriate in some situations. Many white papers suggest approaches different from the guidance documents, however, these can conflict with each other and are themselves only scientifically valid in certain situations. Here, we indicate when alternatives to guidance may be needed and what those approaches might be.

Medienart:

E-Artikel

Erscheinungsjahr:

2019

Erschienen:

2019

Enthalten in:

Zur Gesamtaufnahme - volume:11

Enthalten in:

Bioanalysis - 11(2019), 24 vom: 25. Dez., Seite 2283-2296

Sprache:

Englisch

Beteiligte Personen:

Bano, Nazneen [VerfasserIn]
McKelvey, Troy [VerfasserIn]
Spear, Nathan [VerfasserIn]
Yang, Tong-Yuan [VerfasserIn]
Shankar, Gopi [VerfasserIn]
Schantz, Allen [VerfasserIn]

Links:

Volltext

Themen:

Antibodies
Antidrug antibody
Drug tolerance
European Medicines Agency
Food and Drug Administration Guidelines
Immunogenicity
Journal Article
Positive control
Pre-existing antibody
Proteins
Sensitivity
Therapeutic proteins

Anmerkungen:

Date Completed 21.04.2020

Date Revised 21.04.2020

published: Print

Citation Status MEDLINE

doi:

10.4155/bio-2019-0241

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM304465178