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Clinical Trial Summary

This study seeks to assess the virologic effectiveness of dual therapy (lopinavir/ ritonavir (LPV/r) + lamivudine (3TC)) in treatment-experienced human immunodeficiency virus 1 (HIV-1) infected participants with an undetectable plasma HIV-1 (ribonucleic acid) RNA level (for at least 6 months) at the 48 week time point of treatment in the routine clinical settings of the Russian Federation.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02581202
Study type Observational
Source AbbVie
Contact
Status Completed
Phase
Start date December 21, 2015
Completion date May 27, 2017

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