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Optimal clinical trial designs for immune-based therapies in persistent viral infections

There is now effective therapy for infection by the Human Immunodeficiency Virus (HIV), but there is no cure. Consequently, antiviral drugs must be administered continuously to suppress viral replication. Recently, a large phase III international immune-based therapy trial was discontinued because i...

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Autor principal: Smith, Kendall A
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2002
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC149407/
https://www.ncbi.nlm.nih.gov/pubmed/12459051
http://dx.doi.org/10.1186/1476-9433-1-4
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author Smith, Kendall A
author_facet Smith, Kendall A
author_sort Smith, Kendall A
collection PubMed
description There is now effective therapy for infection by the Human Immunodeficiency Virus (HIV), but there is no cure. Consequently, antiviral drugs must be administered continuously to suppress viral replication. Recently, a large phase III international immune-based therapy trial was discontinued because it is difficult to measure clinical endpoints while antivirals are administered. Since the immune system has evolved under the selective force of microbial infections, the immune reaction is antiviral. This commentary explores the rationale of using "Diagnostic Treatment Interruptions" of antiviral therapies to determine efficacies of immune-based therapies.
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spelling pubmed-1494072003-02-25 Optimal clinical trial designs for immune-based therapies in persistent viral infections Smith, Kendall A Med Immunol Commentary There is now effective therapy for infection by the Human Immunodeficiency Virus (HIV), but there is no cure. Consequently, antiviral drugs must be administered continuously to suppress viral replication. Recently, a large phase III international immune-based therapy trial was discontinued because it is difficult to measure clinical endpoints while antivirals are administered. Since the immune system has evolved under the selective force of microbial infections, the immune reaction is antiviral. This commentary explores the rationale of using "Diagnostic Treatment Interruptions" of antiviral therapies to determine efficacies of immune-based therapies. BioMed Central 2002-11-21 /pmc/articles/PMC149407/ /pubmed/12459051 http://dx.doi.org/10.1186/1476-9433-1-4 Text en Copyright © 2002 Smith; licensee BioMed Central Ltd. This is an Open Access article: verbatim copying and redistribution of this article are permitted in all media for any purpose, provided this notice is preserved along with the article's original URL.
spellingShingle Commentary
Smith, Kendall A
Optimal clinical trial designs for immune-based therapies in persistent viral infections
title Optimal clinical trial designs for immune-based therapies in persistent viral infections
title_full Optimal clinical trial designs for immune-based therapies in persistent viral infections
title_fullStr Optimal clinical trial designs for immune-based therapies in persistent viral infections
title_full_unstemmed Optimal clinical trial designs for immune-based therapies in persistent viral infections
title_short Optimal clinical trial designs for immune-based therapies in persistent viral infections
title_sort optimal clinical trial designs for immune-based therapies in persistent viral infections
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC149407/
https://www.ncbi.nlm.nih.gov/pubmed/12459051
http://dx.doi.org/10.1186/1476-9433-1-4
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