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Managing risks in drug discovery: reproducibility of published findings

In spite of tremendous advances in biopharmaceutical science and technology, the productivity of pharmaceutical research and development has been steadily declining over the last decades. The reasons for this decline are manifold and range from improved standard of care that is more and more difficu...

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Detalles Bibliográficos
Autores principales: Kannt, Aimo, Wieland, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4785199/
https://www.ncbi.nlm.nih.gov/pubmed/26883784
http://dx.doi.org/10.1007/s00210-016-1216-8
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author Kannt, Aimo
Wieland, Thomas
author_facet Kannt, Aimo
Wieland, Thomas
author_sort Kannt, Aimo
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description In spite of tremendous advances in biopharmaceutical science and technology, the productivity of pharmaceutical research and development has been steadily declining over the last decades. The reasons for this decline are manifold and range from improved standard of care that is more and more difficult to top to inappropriate management of technical and translational risks along the R&D value chain. In this short review, major types of risks in biopharmaceutical R&D and means to address them will be described. A special focus will be on a risk, i.e., the lack of reproducibility of published information, that has so far not been fully appreciated and systematically analyzed. Measures to improve reproducibility and trust in published information will be discussed.
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spelling pubmed-47851992016-04-09 Managing risks in drug discovery: reproducibility of published findings Kannt, Aimo Wieland, Thomas Naunyn Schmiedebergs Arch Pharmacol Review In spite of tremendous advances in biopharmaceutical science and technology, the productivity of pharmaceutical research and development has been steadily declining over the last decades. The reasons for this decline are manifold and range from improved standard of care that is more and more difficult to top to inappropriate management of technical and translational risks along the R&D value chain. In this short review, major types of risks in biopharmaceutical R&D and means to address them will be described. A special focus will be on a risk, i.e., the lack of reproducibility of published information, that has so far not been fully appreciated and systematically analyzed. Measures to improve reproducibility and trust in published information will be discussed. Springer Berlin Heidelberg 2016-02-17 2016 /pmc/articles/PMC4785199/ /pubmed/26883784 http://dx.doi.org/10.1007/s00210-016-1216-8 Text en © The Author(s) 2016 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Review
Kannt, Aimo
Wieland, Thomas
Managing risks in drug discovery: reproducibility of published findings
title Managing risks in drug discovery: reproducibility of published findings
title_full Managing risks in drug discovery: reproducibility of published findings
title_fullStr Managing risks in drug discovery: reproducibility of published findings
title_full_unstemmed Managing risks in drug discovery: reproducibility of published findings
title_short Managing risks in drug discovery: reproducibility of published findings
title_sort managing risks in drug discovery: reproducibility of published findings
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4785199/
https://www.ncbi.nlm.nih.gov/pubmed/26883784
http://dx.doi.org/10.1007/s00210-016-1216-8
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