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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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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2002
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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. |
format | Text |
id | pubmed-149407 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2002 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT smithkendalla optimalclinicaltrialdesignsforimmunebasedtherapiesinpersistentviralinfections |