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Current drug resistance testing takes 3 weeks to deliver results. There is a need for an antiviral efficacy test that delivers results as quickly as possible.
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Objective
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The
purpose of this study is to determine the efficacy of an experimental antiviral efficacy device called SpectraPoint. If the new system works as planned, results of the test could be obtained as quickly as 24 hours. The hope is that in many cases patients would receive clinical benefit from faster data delivery to inform their treatment decisions.
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This
study involves one blood draw and a second visit to receive their drug resistance results.
This
study will compare current phenotypic resistance tests with the experimental SpectraPoint testing device.
Study volunteers will receive free phenotypic testing and will be compensated $25 for their time and inconvenience.
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Inclusion
Criteria
(partial
list)
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HIV-positive adult male or female
Have documented
previous drug resistance test with current viral load greater than
500 OR failing HAART triple therapy with viral current viral load greater than 10,000
Not have active Hepatitis B infection
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Status
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Enrolling
--
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For
more information about participating in this study in
the Los Angeles area, please call 310.358.2429 or e-mail
Corie Castro at
ccastro@aidsresearch.org
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We
encourage participation by women and people of color
This
ad was reviewed and approved by the AIDS Research Alliance
Institutional Review Board in April, 2005.
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