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Alternative Routes of Administration for Therapeutic Antibodies—State of the Art

Background: For the past two decades, there has been a huge expansion in the development of therapeutic antibodies, with 6 to 10 novel entities approved each year. Around 70% of these Abs are delivered through IV injection, a mode of administration allowing rapid and systemic delivery of the drug. H...

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Autores principales: Pitiot, Aubin, Heuzé-Vourc’h, Nathalie, Sécher, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9495858/
https://www.ncbi.nlm.nih.gov/pubmed/36134952
http://dx.doi.org/10.3390/antib11030056
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author Pitiot, Aubin
Heuzé-Vourc’h, Nathalie
Sécher, Thomas
author_facet Pitiot, Aubin
Heuzé-Vourc’h, Nathalie
Sécher, Thomas
author_sort Pitiot, Aubin
collection PubMed
description Background: For the past two decades, there has been a huge expansion in the development of therapeutic antibodies, with 6 to 10 novel entities approved each year. Around 70% of these Abs are delivered through IV injection, a mode of administration allowing rapid and systemic delivery of the drug. However, according to the evidence presented in the literature, beyond the reduction of invasiveness, a better efficacy can be achieved with local delivery. Consequently, efforts have been made toward the development of innovative methods of administration, and in the formulation and engineering of novel Abs to improve their therapeutic index. Objective: This review presents an overview of the routes of administration used to deliver Abs, different from the IV route, whether approved or in the clinical evaluation stage. We provide a description of the physical and biological fundamentals for each route of administration, highlighting their relevance with examples of clinically-relevant Abs, and discussing their strengths and limitations. Methods: We reviewed and analyzed the current literature, published as of the 1 April 2022 using MEDLINE and EMBASE databases, as well as the FDA and EMA websites. Ongoing trials were identified using clinicaltrials.gov. Publications and data were identified using a list of general keywords. Conclusions: Apart from the most commonly used IV route, topical delivery of Abs has shown clinical successes, improving drug bioavailability and efficacy while reducing side-effects. However, additional research is necessary to understand the consequences of biological barriers associated with local delivery for Ab partitioning, in order to optimize delivery methods and devices, and to adapt Ab formulation to local delivery. Novel modes of administration for Abs might in fine allow a better support to patients, especially in the context of chronic diseases, as well as a reduction of the treatment cost.
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spelling pubmed-94958582022-09-23 Alternative Routes of Administration for Therapeutic Antibodies—State of the Art Pitiot, Aubin Heuzé-Vourc’h, Nathalie Sécher, Thomas Antibodies (Basel) Review Background: For the past two decades, there has been a huge expansion in the development of therapeutic antibodies, with 6 to 10 novel entities approved each year. Around 70% of these Abs are delivered through IV injection, a mode of administration allowing rapid and systemic delivery of the drug. However, according to the evidence presented in the literature, beyond the reduction of invasiveness, a better efficacy can be achieved with local delivery. Consequently, efforts have been made toward the development of innovative methods of administration, and in the formulation and engineering of novel Abs to improve their therapeutic index. Objective: This review presents an overview of the routes of administration used to deliver Abs, different from the IV route, whether approved or in the clinical evaluation stage. We provide a description of the physical and biological fundamentals for each route of administration, highlighting their relevance with examples of clinically-relevant Abs, and discussing their strengths and limitations. Methods: We reviewed and analyzed the current literature, published as of the 1 April 2022 using MEDLINE and EMBASE databases, as well as the FDA and EMA websites. Ongoing trials were identified using clinicaltrials.gov. Publications and data were identified using a list of general keywords. Conclusions: Apart from the most commonly used IV route, topical delivery of Abs has shown clinical successes, improving drug bioavailability and efficacy while reducing side-effects. However, additional research is necessary to understand the consequences of biological barriers associated with local delivery for Ab partitioning, in order to optimize delivery methods and devices, and to adapt Ab formulation to local delivery. Novel modes of administration for Abs might in fine allow a better support to patients, especially in the context of chronic diseases, as well as a reduction of the treatment cost. MDPI 2022-08-26 /pmc/articles/PMC9495858/ /pubmed/36134952 http://dx.doi.org/10.3390/antib11030056 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Pitiot, Aubin
Heuzé-Vourc’h, Nathalie
Sécher, Thomas
Alternative Routes of Administration for Therapeutic Antibodies—State of the Art
title Alternative Routes of Administration for Therapeutic Antibodies—State of the Art
title_full Alternative Routes of Administration for Therapeutic Antibodies—State of the Art
title_fullStr Alternative Routes of Administration for Therapeutic Antibodies—State of the Art
title_full_unstemmed Alternative Routes of Administration for Therapeutic Antibodies—State of the Art
title_short Alternative Routes of Administration for Therapeutic Antibodies—State of the Art
title_sort alternative routes of administration for therapeutic antibodies—state of the art
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9495858/
https://www.ncbi.nlm.nih.gov/pubmed/36134952
http://dx.doi.org/10.3390/antib11030056
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