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Clinical Trial Summary

The purpose of this study is to investigate a combined set of parameters deemed to impact the quality of CMI analyses in terms of the proportion of viable lymphocytes in antiretroviral therapy-naïve HIV-1 infected subjects.


Clinical Trial Description

This study will address the respective and combined impact of (i) timing between blood collection and peripheral blood mononuclear cells (PBMC) processing ["time-to-process"] and (ii) timing of PBMC resting before stimulation ["resting -time"]. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT01610427
Study type Interventional
Source GlaxoSmithKline
Contact
Status Completed
Phase N/A
Start date June 25, 2012
Completion date October 30, 2012

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