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Discontinued Drugs for the Treatment of Cardiovascular Disease from 2016 to 2018
Cardiovascular drug research and development (R&D) has been in active state and continuously attracts attention from the pharmaceutical industry. However, only one individual drug can eventually reach the market from about the 10,000 compounds tested. It would be useful to learn from these failu...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6769515/ https://www.ncbi.nlm.nih.gov/pubmed/31547243 http://dx.doi.org/10.3390/ijms20184513 |
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author | Li, Tingting Jiang, Sida Ni, Bingwei Cui, Qiuji Liu, Qinan Zhao, Hongping |
author_facet | Li, Tingting Jiang, Sida Ni, Bingwei Cui, Qiuji Liu, Qinan Zhao, Hongping |
author_sort | Li, Tingting |
collection | PubMed |
description | Cardiovascular drug research and development (R&D) has been in active state and continuously attracts attention from the pharmaceutical industry. However, only one individual drug can eventually reach the market from about the 10,000 compounds tested. It would be useful to learn from these failures when developing better strategies for the future. Discontinued drugs were identified from a search performed by Thomson Reuters Integrity. Additional information was sought through PubMed, ClinicalTrials.gov, and pharmaceutical companies search. Twelve compounds discontinued for cardiovascular disease treatment after reaching Phase I–III clinical trials from 2016 to 2018 are detailed in this manuscript, and the reasons for these failures are reported. Of these, six candidates (MDCO-216, TRV027, ubenimex, sodium nitrite, losmapimod, and bococizumab) were dropped for lack of clinical efficacy, the other six for strategic or unspecified reasons. In total, three candidates were discontinued in Phase I trials, six in Phase II, and three in Phase III. It was reported that the success rate of drug R&D utilizing selection biomarkers is higher. Four candidate developments (OPC-108459, ONO-4232, GSK-2798745, and TAK-536TCH) were run without biomarkers, which could be used as surrogate endpoints in the 12 cardiovascular drugs discontinued from 2016 to 2018. This review will be useful for those involved in the field of drug discovery and development, and for those interested in the treatment of cardiovascular disease. |
format | Online Article Text |
id | pubmed-6769515 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-67695152019-10-30 Discontinued Drugs for the Treatment of Cardiovascular Disease from 2016 to 2018 Li, Tingting Jiang, Sida Ni, Bingwei Cui, Qiuji Liu, Qinan Zhao, Hongping Int J Mol Sci Review Cardiovascular drug research and development (R&D) has been in active state and continuously attracts attention from the pharmaceutical industry. However, only one individual drug can eventually reach the market from about the 10,000 compounds tested. It would be useful to learn from these failures when developing better strategies for the future. Discontinued drugs were identified from a search performed by Thomson Reuters Integrity. Additional information was sought through PubMed, ClinicalTrials.gov, and pharmaceutical companies search. Twelve compounds discontinued for cardiovascular disease treatment after reaching Phase I–III clinical trials from 2016 to 2018 are detailed in this manuscript, and the reasons for these failures are reported. Of these, six candidates (MDCO-216, TRV027, ubenimex, sodium nitrite, losmapimod, and bococizumab) were dropped for lack of clinical efficacy, the other six for strategic or unspecified reasons. In total, three candidates were discontinued in Phase I trials, six in Phase II, and three in Phase III. It was reported that the success rate of drug R&D utilizing selection biomarkers is higher. Four candidate developments (OPC-108459, ONO-4232, GSK-2798745, and TAK-536TCH) were run without biomarkers, which could be used as surrogate endpoints in the 12 cardiovascular drugs discontinued from 2016 to 2018. This review will be useful for those involved in the field of drug discovery and development, and for those interested in the treatment of cardiovascular disease. MDPI 2019-09-12 /pmc/articles/PMC6769515/ /pubmed/31547243 http://dx.doi.org/10.3390/ijms20184513 Text en © 2019 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Li, Tingting Jiang, Sida Ni, Bingwei Cui, Qiuji Liu, Qinan Zhao, Hongping Discontinued Drugs for the Treatment of Cardiovascular Disease from 2016 to 2018 |
title | Discontinued Drugs for the Treatment of Cardiovascular Disease from 2016 to 2018 |
title_full | Discontinued Drugs for the Treatment of Cardiovascular Disease from 2016 to 2018 |
title_fullStr | Discontinued Drugs for the Treatment of Cardiovascular Disease from 2016 to 2018 |
title_full_unstemmed | Discontinued Drugs for the Treatment of Cardiovascular Disease from 2016 to 2018 |
title_short | Discontinued Drugs for the Treatment of Cardiovascular Disease from 2016 to 2018 |
title_sort | discontinued drugs for the treatment of cardiovascular disease from 2016 to 2018 |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6769515/ https://www.ncbi.nlm.nih.gov/pubmed/31547243 http://dx.doi.org/10.3390/ijms20184513 |
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