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25 years of maturation: A systematic review of RNAi in the clinic

The year 2023 marks the 25th anniversary of the discovery of RNAi. RNAi-based therapeutics enable sequence-specific gene knockdown by eliminating target RNA molecules through complementary base-pairing. A systematic review of published and ongoing clinical trials was performed. Web of Science, PubMe...

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Autores principales: Corydon, Ida Juhl, Fabian-Jessing, Bjørn Kristensen, Jakobsen, Thomas Stax, Jørgensen, Asbjørn Cortnum, Jensen, Emilie Grarup, Askou, Anne Louise, Aagaard, Lars, Corydon, Thomas Juhl
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society of Gene & Cell Therapy 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10424002/
https://www.ncbi.nlm.nih.gov/pubmed/37583575
http://dx.doi.org/10.1016/j.omtn.2023.07.018
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author Corydon, Ida Juhl
Fabian-Jessing, Bjørn Kristensen
Jakobsen, Thomas Stax
Jørgensen, Asbjørn Cortnum
Jensen, Emilie Grarup
Askou, Anne Louise
Aagaard, Lars
Corydon, Thomas Juhl
author_facet Corydon, Ida Juhl
Fabian-Jessing, Bjørn Kristensen
Jakobsen, Thomas Stax
Jørgensen, Asbjørn Cortnum
Jensen, Emilie Grarup
Askou, Anne Louise
Aagaard, Lars
Corydon, Thomas Juhl
author_sort Corydon, Ida Juhl
collection PubMed
description The year 2023 marks the 25th anniversary of the discovery of RNAi. RNAi-based therapeutics enable sequence-specific gene knockdown by eliminating target RNA molecules through complementary base-pairing. A systematic review of published and ongoing clinical trials was performed. Web of Science, PubMed, and Embase were searched from January 1, 1998, to December 30, 2022 for clinical trials using RNAi. Following inclusion, data from the articles were extracted according to a predefined protocol. A total of 90 trials published in 81 articles were included. In addition, ongoing clinical trials were retrieved from ClinicalTrials.gov, resulting in the inclusion of 48 trials. We investigated how maturation of RNAi-based therapeutics and developments in delivery platforms, administration routes, and potential targets shape the current landscape of clinically applied RNAi. Notably, most contemporary clinical trials used either N-acetylgalactosamine delivery and subcutaneous administration or lipid nanoparticle delivery and intravenous administration. In conclusion, RNAi therapeutics have gained great momentum during the past decade, resulting in five approved therapeutics targeting the liver for treatment of severe diseases, and the trajectory depicted by the ongoing trials emphasizes that even more RNAi-based medicines also targeting extra-hepatic tissues are likely to be available in the years to come.
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spelling pubmed-104240022023-08-15 25 years of maturation: A systematic review of RNAi in the clinic Corydon, Ida Juhl Fabian-Jessing, Bjørn Kristensen Jakobsen, Thomas Stax Jørgensen, Asbjørn Cortnum Jensen, Emilie Grarup Askou, Anne Louise Aagaard, Lars Corydon, Thomas Juhl Mol Ther Nucleic Acids Review The year 2023 marks the 25th anniversary of the discovery of RNAi. RNAi-based therapeutics enable sequence-specific gene knockdown by eliminating target RNA molecules through complementary base-pairing. A systematic review of published and ongoing clinical trials was performed. Web of Science, PubMed, and Embase were searched from January 1, 1998, to December 30, 2022 for clinical trials using RNAi. Following inclusion, data from the articles were extracted according to a predefined protocol. A total of 90 trials published in 81 articles were included. In addition, ongoing clinical trials were retrieved from ClinicalTrials.gov, resulting in the inclusion of 48 trials. We investigated how maturation of RNAi-based therapeutics and developments in delivery platforms, administration routes, and potential targets shape the current landscape of clinically applied RNAi. Notably, most contemporary clinical trials used either N-acetylgalactosamine delivery and subcutaneous administration or lipid nanoparticle delivery and intravenous administration. In conclusion, RNAi therapeutics have gained great momentum during the past decade, resulting in five approved therapeutics targeting the liver for treatment of severe diseases, and the trajectory depicted by the ongoing trials emphasizes that even more RNAi-based medicines also targeting extra-hepatic tissues are likely to be available in the years to come. American Society of Gene & Cell Therapy 2023-07-18 /pmc/articles/PMC10424002/ /pubmed/37583575 http://dx.doi.org/10.1016/j.omtn.2023.07.018 Text en © 2023 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Review
Corydon, Ida Juhl
Fabian-Jessing, Bjørn Kristensen
Jakobsen, Thomas Stax
Jørgensen, Asbjørn Cortnum
Jensen, Emilie Grarup
Askou, Anne Louise
Aagaard, Lars
Corydon, Thomas Juhl
25 years of maturation: A systematic review of RNAi in the clinic
title 25 years of maturation: A systematic review of RNAi in the clinic
title_full 25 years of maturation: A systematic review of RNAi in the clinic
title_fullStr 25 years of maturation: A systematic review of RNAi in the clinic
title_full_unstemmed 25 years of maturation: A systematic review of RNAi in the clinic
title_short 25 years of maturation: A systematic review of RNAi in the clinic
title_sort 25 years of maturation: a systematic review of rnai in the clinic
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10424002/
https://www.ncbi.nlm.nih.gov/pubmed/37583575
http://dx.doi.org/10.1016/j.omtn.2023.07.018
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