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From Basic Immunology to Clinical Practice: Bio-Originators versus Bio-Similars

Biologic agents are macromolecules, and as such, they have a high level of structural heterogeneity. Treatment with such agents has been extremely expensive limiting thus their availability to increasing numbers of patients; therefore, many manufacturers chose to develop biologics that are highly si...

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Detalles Bibliográficos
Autores principales: Liossis, Stamatis-Nick C., Konstantopoulou, Georgia M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Mediterranean Journal of Rheumatology (MJR) 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7280872/
https://www.ncbi.nlm.nih.gov/pubmed/32524078
http://dx.doi.org/10.31138/mjr.30.1.54
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author Liossis, Stamatis-Nick C.
Konstantopoulou, Georgia M.
author_facet Liossis, Stamatis-Nick C.
Konstantopoulou, Georgia M.
author_sort Liossis, Stamatis-Nick C.
collection PubMed
description Biologic agents are macromolecules, and as such, they have a high level of structural heterogeneity. Treatment with such agents has been extremely expensive limiting thus their availability to increasing numbers of patients; therefore, many manufacturers chose to develop biologics that are highly similar to the originators, the biosimilars. The immunological properties of both products should therefore be characterized and compared. The biosimilar developers must have a complete qualitative documentation, appropriate preclinical pharmacodynamic and pharmacokinetic studies, and finally comparative studies with the originator to define the relative similarity in terms of biologic activity, quality characteristics, efficacy and safety. Immunogenicity assessment of the biosimilars continues through clinical trials and pharmacovigilance programs.
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spelling pubmed-72808722020-06-09 From Basic Immunology to Clinical Practice: Bio-Originators versus Bio-Similars Liossis, Stamatis-Nick C. Konstantopoulou, Georgia M. Mediterr J Rheumatol Review Biologic agents are macromolecules, and as such, they have a high level of structural heterogeneity. Treatment with such agents has been extremely expensive limiting thus their availability to increasing numbers of patients; therefore, many manufacturers chose to develop biologics that are highly similar to the originators, the biosimilars. The immunological properties of both products should therefore be characterized and compared. The biosimilar developers must have a complete qualitative documentation, appropriate preclinical pharmacodynamic and pharmacokinetic studies, and finally comparative studies with the originator to define the relative similarity in terms of biologic activity, quality characteristics, efficacy and safety. Immunogenicity assessment of the biosimilars continues through clinical trials and pharmacovigilance programs. The Mediterranean Journal of Rheumatology (MJR) 2019-05-31 /pmc/articles/PMC7280872/ /pubmed/32524078 http://dx.doi.org/10.31138/mjr.30.1.54 Text en © 2019 The Mediterranean Journal of Rheumatology (MJR) http://creativecommons.org/licenses/by/4.0/ This work is licensed under and Creative Commons Attribution-NonCommercial 4.0 International License.
spellingShingle Review
Liossis, Stamatis-Nick C.
Konstantopoulou, Georgia M.
From Basic Immunology to Clinical Practice: Bio-Originators versus Bio-Similars
title From Basic Immunology to Clinical Practice: Bio-Originators versus Bio-Similars
title_full From Basic Immunology to Clinical Practice: Bio-Originators versus Bio-Similars
title_fullStr From Basic Immunology to Clinical Practice: Bio-Originators versus Bio-Similars
title_full_unstemmed From Basic Immunology to Clinical Practice: Bio-Originators versus Bio-Similars
title_short From Basic Immunology to Clinical Practice: Bio-Originators versus Bio-Similars
title_sort from basic immunology to clinical practice: bio-originators versus bio-similars
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7280872/
https://www.ncbi.nlm.nih.gov/pubmed/32524078
http://dx.doi.org/10.31138/mjr.30.1.54
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