Repurposing of medications for pulmonary arterial hypertension
This manuscript on drug repurposing incorporates the broad experience of members of the Pulmonary Vascular Research Institute’s Innovative Drug Development Initiative as an open debate platform for academia, the pharmaceutical industry and regulatory experts surrounding the future design of clinical...
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2020-10-01
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Series: | Pulmonary Circulation |
Online Access: | https://doi.org/10.1177/2045894020941494 |
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doaj-0f4edbcf1f6f4b4e9233a1b02eef07a72020-11-25T04:02:08ZengSAGE PublishingPulmonary Circulation2045-89402020-10-011010.1177/2045894020941494Repurposing of medications for pulmonary arterial hypertensionMark Toshner0Edda Spiekerkoetter1Harm Bogaard2Georg Hansmann3Sylvia Nikkho4Kurt W. Prins5Department of Medicine, University of Cambridge, Cambridge, UKDepartment of Medicine, Stanford University School of Medicine, Stanford, CA, USADepartment of Pulmonary Medicine, Vrije Universiteit Amsterdam, Amsterdam, NetherlandsDepartment of Pediatric Cardiology and Critical Care, Hannover Medical School, Hannover, GermanyBayer Pharmaceuticals, Clinical Development Pulmonology, Berlin, GermanyLillehei Heart Institute, University of Minnesota, Minneapolis, MN, USAThis manuscript on drug repurposing incorporates the broad experience of members of the Pulmonary Vascular Research Institute’s Innovative Drug Development Initiative as an open debate platform for academia, the pharmaceutical industry and regulatory experts surrounding the future design of clinical trials in pulmonary hypertension. Drug repurposing, use of a drug in a disease for which it was not originally developed, in pulmonary arterial hypertension has been a remarkable success story, as highlighted by positive large phase 3 clinical trials using epoprostenol, bosentan, iloprost, and sildenafil. Despite the availability of multiple therapies for pulmonary arterial hypertension, mortality rates have modestly changed. Moreover, pulmonary arterial hypertension patients are highly symptomatic and frequently end up on parental therapy and lung transplant waiting lists. Therefore, an unmet need for new treatments exists and drug repurposing may be an important avenue to address this problem.https://doi.org/10.1177/2045894020941494 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Mark Toshner Edda Spiekerkoetter Harm Bogaard Georg Hansmann Sylvia Nikkho Kurt W. Prins |
spellingShingle |
Mark Toshner Edda Spiekerkoetter Harm Bogaard Georg Hansmann Sylvia Nikkho Kurt W. Prins Repurposing of medications for pulmonary arterial hypertension Pulmonary Circulation |
author_facet |
Mark Toshner Edda Spiekerkoetter Harm Bogaard Georg Hansmann Sylvia Nikkho Kurt W. Prins |
author_sort |
Mark Toshner |
title |
Repurposing of medications for pulmonary arterial hypertension |
title_short |
Repurposing of medications for pulmonary arterial hypertension |
title_full |
Repurposing of medications for pulmonary arterial hypertension |
title_fullStr |
Repurposing of medications for pulmonary arterial hypertension |
title_full_unstemmed |
Repurposing of medications for pulmonary arterial hypertension |
title_sort |
repurposing of medications for pulmonary arterial hypertension |
publisher |
SAGE Publishing |
series |
Pulmonary Circulation |
issn |
2045-8940 |
publishDate |
2020-10-01 |
description |
This manuscript on drug repurposing incorporates the broad experience of members of the Pulmonary Vascular Research Institute’s Innovative Drug Development Initiative as an open debate platform for academia, the pharmaceutical industry and regulatory experts surrounding the future design of clinical trials in pulmonary hypertension. Drug repurposing, use of a drug in a disease for which it was not originally developed, in pulmonary arterial hypertension has been a remarkable success story, as highlighted by positive large phase 3 clinical trials using epoprostenol, bosentan, iloprost, and sildenafil. Despite the availability of multiple therapies for pulmonary arterial hypertension, mortality rates have modestly changed. Moreover, pulmonary arterial hypertension patients are highly symptomatic and frequently end up on parental therapy and lung transplant waiting lists. Therefore, an unmet need for new treatments exists and drug repurposing may be an important avenue to address this problem. |
url |
https://doi.org/10.1177/2045894020941494 |
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