Source:http://linkedlifedata.com/resource/pubmed/id/11306153
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
2001-4-18
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pubmed:abstractText |
ACTG (AIDS Clinical Trials Group) 384 is designed to evaluate different strategies for antiretroviral treatment in HIV-1-infected individuals with no previous exposure to antiretroviral treatment. The study is a randomized, partially double-blinded, controlled trial with 980 subjects at 81 centers in the United States and Italy. The study has a factorial design that addresses the following scientific questions: (1) Does the best initial choice of therapy include both a protease inhibitor (PI) and non-nucleoside reverse transcriptase inhibitor (NNRTI) in a four-drug combination with nucleoside analogue (NRTI) drugs, or should these agents be used sequentially in three-drug combinations?; (2) Which sequence is best in a three-drug regimen-PI followed by NNRTI or NNRTI followed by PI ?; (3) Which is the best sequence of dual NRTI combinations-zidovudine plus lamivudine followed by didanosine plus stavudine, or the converse? Subjects in the three-drug combination arms are offered a salvage regimen after failure of their second regimen; subjects in the four-drug combination arm are offered a salvage regimen after failure of their first regimen. The primary endpoint of the study is the time until salvage; secondary endpoints include time to virological failure and time to toxicity-related discontinuation of therapy. A Division of AIDS Data and Safety Monitoring Board will review the trial for safety and efficacy. Control Clin Trials 2001;22:142-159
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pubmed:grant | |
pubmed:commentsCorrections | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Apr
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pubmed:issn |
0197-2456
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
22
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
142-59
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pubmed:dateRevised |
2007-11-15
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pubmed:meshHeading |
pubmed-meshheading:11306153-Adolescent,
pubmed-meshheading:11306153-Adult,
pubmed-meshheading:11306153-Aged,
pubmed-meshheading:11306153-Double-Blind Method,
pubmed-meshheading:11306153-Female,
pubmed-meshheading:11306153-HIV Infections,
pubmed-meshheading:11306153-HIV-1,
pubmed-meshheading:11306153-Humans,
pubmed-meshheading:11306153-Italy,
pubmed-meshheading:11306153-Male,
pubmed-meshheading:11306153-Middle Aged,
pubmed-meshheading:11306153-Multicenter Studies as Topic,
pubmed-meshheading:11306153-Protease Inhibitors,
pubmed-meshheading:11306153-Randomized Controlled Trials as Topic,
pubmed-meshheading:11306153-Reverse Transcriptase Inhibitors,
pubmed-meshheading:11306153-Salvage Therapy,
pubmed-meshheading:11306153-United States
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pubmed:year |
2001
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pubmed:articleTitle |
ACTG (AIDS Clinical Trials Group) 384: a strategy trial comparing consecutive treatments for HIV-1.
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pubmed:affiliation |
Center for Biostatistics in AIDS Research, Harvard School of Public Health, 651 Huntington Avenue, Francois-Xavier Bagnound Building, Boston, MA 02115-6017, USA. smeaton@sdac.harvard.edu
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pubmed:publicationType |
Journal Article,
Clinical Trial,
Comparative Study,
Research Support, U.S. Gov't, P.H.S.,
Randomized Controlled Trial
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