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Accelerating target discovery using pre-competitive open science—patients need faster innovation more than anyone else

We are experiencing a new era enabled by unencumbered access to high quality data through the emergence of open science initiatives in the historically challenging area of early stage drug discovery. At the same time, many patient-centric organisations are taking matters into their own hands by part...

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Detalles Bibliográficos
Autores principales: Low, Eric, Bountra, Chas, Lee, Wen Hwa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cancer Intelligence 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4990051/
https://www.ncbi.nlm.nih.gov/pubmed/27594912
http://dx.doi.org/10.3332/ecancer.2016.ed57
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author Low, Eric
Bountra, Chas
Lee, Wen Hwa
author_facet Low, Eric
Bountra, Chas
Lee, Wen Hwa
author_sort Low, Eric
collection PubMed
description We are experiencing a new era enabled by unencumbered access to high quality data through the emergence of open science initiatives in the historically challenging area of early stage drug discovery. At the same time, many patient-centric organisations are taking matters into their own hands by participating in, enabling and funding research. Here we present the rationale behind the innovative partnership between the Structural Genomics Consortium (SGC)—an open, pre-competitive pre-clinical research consortium and the research-focused patient organisation Myeloma UK to create a new, comprehensive platform to accelerate the discovery and development of new treatments for multiple myeloma.
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spelling pubmed-49900512016-09-02 Accelerating target discovery using pre-competitive open science—patients need faster innovation more than anyone else Low, Eric Bountra, Chas Lee, Wen Hwa Ecancermedicalscience Editorial We are experiencing a new era enabled by unencumbered access to high quality data through the emergence of open science initiatives in the historically challenging area of early stage drug discovery. At the same time, many patient-centric organisations are taking matters into their own hands by participating in, enabling and funding research. Here we present the rationale behind the innovative partnership between the Structural Genomics Consortium (SGC)—an open, pre-competitive pre-clinical research consortium and the research-focused patient organisation Myeloma UK to create a new, comprehensive platform to accelerate the discovery and development of new treatments for multiple myeloma. Cancer Intelligence 2016-08-03 /pmc/articles/PMC4990051/ /pubmed/27594912 http://dx.doi.org/10.3332/ecancer.2016.ed57 Text en © the authors; licensee ecancermedicalscience. http://creativecommons.org/licenses/by/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Editorial
Low, Eric
Bountra, Chas
Lee, Wen Hwa
Accelerating target discovery using pre-competitive open science—patients need faster innovation more than anyone else
title Accelerating target discovery using pre-competitive open science—patients need faster innovation more than anyone else
title_full Accelerating target discovery using pre-competitive open science—patients need faster innovation more than anyone else
title_fullStr Accelerating target discovery using pre-competitive open science—patients need faster innovation more than anyone else
title_full_unstemmed Accelerating target discovery using pre-competitive open science—patients need faster innovation more than anyone else
title_short Accelerating target discovery using pre-competitive open science—patients need faster innovation more than anyone else
title_sort accelerating target discovery using pre-competitive open science—patients need faster innovation more than anyone else
topic Editorial
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4990051/
https://www.ncbi.nlm.nih.gov/pubmed/27594912
http://dx.doi.org/10.3332/ecancer.2016.ed57
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