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Risk in CNS drug discovery: focus on treatment of Alzheimer's Disease

Despite rapid progress in our understanding of disease mechanisms and an exploding list of new targets for therapeutic intervention, drug discovery and development remains a highly risky business. Understanding the risk involved requires appreciation of the differing perspectives of risk held by the...

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Autor principal: Pritchard, J Fred
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2604886/
https://www.ncbi.nlm.nih.gov/pubmed/19090998
http://dx.doi.org/10.1186/1471-2202-9-S3-S1
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author Pritchard, J Fred
author_facet Pritchard, J Fred
author_sort Pritchard, J Fred
collection PubMed
description Despite rapid progress in our understanding of disease mechanisms and an exploding list of new targets for therapeutic intervention, drug discovery and development remains a highly risky business. Understanding the risk involved requires appreciation of the differing perspectives of risk held by the various stakeholders involved in drug research. Risk can be reduced by thoughtful management of drug candidate selection, careful planning and program execution by a team of engaged experts, and disciplined decision making. Drug development is particularly challenging for treatments of neurodegenerative diseases such as Alzheimer's disease, in which translation from animal models of efficacy to human success is poor or unknown, the timelines for clinical study are long, and the markers of efficacy are still evolving. Despite this there are several therapies in clinical development that hold the promise of influencing this disease through novel and possibly synergistic mechanisms.
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spelling pubmed-26048862008-12-18 Risk in CNS drug discovery: focus on treatment of Alzheimer's Disease Pritchard, J Fred BMC Neurosci Review Despite rapid progress in our understanding of disease mechanisms and an exploding list of new targets for therapeutic intervention, drug discovery and development remains a highly risky business. Understanding the risk involved requires appreciation of the differing perspectives of risk held by the various stakeholders involved in drug research. Risk can be reduced by thoughtful management of drug candidate selection, careful planning and program execution by a team of engaged experts, and disciplined decision making. Drug development is particularly challenging for treatments of neurodegenerative diseases such as Alzheimer's disease, in which translation from animal models of efficacy to human success is poor or unknown, the timelines for clinical study are long, and the markers of efficacy are still evolving. Despite this there are several therapies in clinical development that hold the promise of influencing this disease through novel and possibly synergistic mechanisms. BioMed Central 2008-12-10 /pmc/articles/PMC2604886/ /pubmed/19090998 http://dx.doi.org/10.1186/1471-2202-9-S3-S1 Text en Copyright © 2008 Pritchard; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Pritchard, J Fred
Risk in CNS drug discovery: focus on treatment of Alzheimer's Disease
title Risk in CNS drug discovery: focus on treatment of Alzheimer's Disease
title_full Risk in CNS drug discovery: focus on treatment of Alzheimer's Disease
title_fullStr Risk in CNS drug discovery: focus on treatment of Alzheimer's Disease
title_full_unstemmed Risk in CNS drug discovery: focus on treatment of Alzheimer's Disease
title_short Risk in CNS drug discovery: focus on treatment of Alzheimer's Disease
title_sort risk in cns drug discovery: focus on treatment of alzheimer's disease
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2604886/
https://www.ncbi.nlm.nih.gov/pubmed/19090998
http://dx.doi.org/10.1186/1471-2202-9-S3-S1
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