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Biomarkers and Surrogate Endpoints: How and When might They Impact Drug Development?

As the pharmaceutical industry starts developing novel molecules developed based on molecular biology principles and a better understanding of the human genome, it becomes increasingly important to develop early indicators of activity and/or toxicity. Biomarkers are measurements based on molecular p...

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Detalles Bibliográficos
Autor principal: Lathia, Chetan D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: IOS Press 2002
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3850863/
https://www.ncbi.nlm.nih.gov/pubmed/12364814
http://dx.doi.org/10.1155/2002/438745
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author Lathia, Chetan D.
author_facet Lathia, Chetan D.
author_sort Lathia, Chetan D.
collection PubMed
description As the pharmaceutical industry starts developing novel molecules developed based on molecular biology principles and a better understanding of the human genome, it becomes increasingly important to develop early indicators of activity and/or toxicity. Biomarkers are measurements based on molecular pharmacology and/or pathophysiology of the disease being evaluated that may assist with decision-making in various phases of drug development. The utility of biomarkers in the development of drugs is described in this review. Additionally, the utility of pharmacokinetic data in drug development is described. Development of biomarkers may help reduce the cost of drug development by allowing key decisions earlier in the drug development process. Additionally, biomarkers may be used to select patients who have a high likelihood of benefit or they could be used by clinicians to evaluate the potential for efficacy after start of treatment.
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spelling pubmed-38508632014-02-03 Biomarkers and Surrogate Endpoints: How and When might They Impact Drug Development? Lathia, Chetan D. Dis Markers Other As the pharmaceutical industry starts developing novel molecules developed based on molecular biology principles and a better understanding of the human genome, it becomes increasingly important to develop early indicators of activity and/or toxicity. Biomarkers are measurements based on molecular pharmacology and/or pathophysiology of the disease being evaluated that may assist with decision-making in various phases of drug development. The utility of biomarkers in the development of drugs is described in this review. Additionally, the utility of pharmacokinetic data in drug development is described. Development of biomarkers may help reduce the cost of drug development by allowing key decisions earlier in the drug development process. Additionally, biomarkers may be used to select patients who have a high likelihood of benefit or they could be used by clinicians to evaluate the potential for efficacy after start of treatment. IOS Press 2002 2002-10-21 /pmc/articles/PMC3850863/ /pubmed/12364814 http://dx.doi.org/10.1155/2002/438745 Text en Copyright © 2002 Hindawi Publishing Corporation.
spellingShingle Other
Lathia, Chetan D.
Biomarkers and Surrogate Endpoints: How and When might They Impact Drug Development?
title Biomarkers and Surrogate Endpoints: How and When might They Impact Drug Development?
title_full Biomarkers and Surrogate Endpoints: How and When might They Impact Drug Development?
title_fullStr Biomarkers and Surrogate Endpoints: How and When might They Impact Drug Development?
title_full_unstemmed Biomarkers and Surrogate Endpoints: How and When might They Impact Drug Development?
title_short Biomarkers and Surrogate Endpoints: How and When might They Impact Drug Development?
title_sort biomarkers and surrogate endpoints: how and when might they impact drug development?
topic Other
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3850863/
https://www.ncbi.nlm.nih.gov/pubmed/12364814
http://dx.doi.org/10.1155/2002/438745
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