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Overcoming Obstacles to Drug Repositioning in Japan

Drug repositioning (DR) is the process of identifying new indications for existing drugs. DR usually focuses on drugs that have cleared phase-I safety trials but has yet to show efficacy for the intended indication. Therefore, DR can probably skip the preclinical and phase-I study, which can reduce...

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Autores principales: Nishimura, Yuhei, Tagawa, Masaaki, Ito, Hideki, Tsuruma, Kazuhiro, Hara, Hideaki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5641581/
https://www.ncbi.nlm.nih.gov/pubmed/29075191
http://dx.doi.org/10.3389/fphar.2017.00729
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author Nishimura, Yuhei
Tagawa, Masaaki
Ito, Hideki
Tsuruma, Kazuhiro
Hara, Hideaki
author_facet Nishimura, Yuhei
Tagawa, Masaaki
Ito, Hideki
Tsuruma, Kazuhiro
Hara, Hideaki
author_sort Nishimura, Yuhei
collection PubMed
description Drug repositioning (DR) is the process of identifying new indications for existing drugs. DR usually focuses on drugs that have cleared phase-I safety trials but has yet to show efficacy for the intended indication. Therefore, DR can probably skip the preclinical and phase-I study, which can reduce the cost throughout drug development. However, the expensive phase-II/III trials are required to establish efficacy. The obstacles to DR include identification of new indications with a high success rate in clinical studies, obtaining funding for clinical studies, patent protection, and approval systems. To tackle these obstacles, various approaches have been applied to DR worldwide. In this perspective, we provide representative examples of DR and discuss the ongoing efforts to overcome obstacles to DR in Japan.
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spelling pubmed-56415812017-10-26 Overcoming Obstacles to Drug Repositioning in Japan Nishimura, Yuhei Tagawa, Masaaki Ito, Hideki Tsuruma, Kazuhiro Hara, Hideaki Front Pharmacol Pharmacology Drug repositioning (DR) is the process of identifying new indications for existing drugs. DR usually focuses on drugs that have cleared phase-I safety trials but has yet to show efficacy for the intended indication. Therefore, DR can probably skip the preclinical and phase-I study, which can reduce the cost throughout drug development. However, the expensive phase-II/III trials are required to establish efficacy. The obstacles to DR include identification of new indications with a high success rate in clinical studies, obtaining funding for clinical studies, patent protection, and approval systems. To tackle these obstacles, various approaches have been applied to DR worldwide. In this perspective, we provide representative examples of DR and discuss the ongoing efforts to overcome obstacles to DR in Japan. Frontiers Media S.A. 2017-10-11 /pmc/articles/PMC5641581/ /pubmed/29075191 http://dx.doi.org/10.3389/fphar.2017.00729 Text en Copyright © 2017 Nishimura, Tagawa, Ito, Tsuruma and Hara. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Nishimura, Yuhei
Tagawa, Masaaki
Ito, Hideki
Tsuruma, Kazuhiro
Hara, Hideaki
Overcoming Obstacles to Drug Repositioning in Japan
title Overcoming Obstacles to Drug Repositioning in Japan
title_full Overcoming Obstacles to Drug Repositioning in Japan
title_fullStr Overcoming Obstacles to Drug Repositioning in Japan
title_full_unstemmed Overcoming Obstacles to Drug Repositioning in Japan
title_short Overcoming Obstacles to Drug Repositioning in Japan
title_sort overcoming obstacles to drug repositioning in japan
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5641581/
https://www.ncbi.nlm.nih.gov/pubmed/29075191
http://dx.doi.org/10.3389/fphar.2017.00729
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