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Clinical Trial Summary

The primary purpose of the study is to evaluate the efficacy of rilpivirine (RPV)-based regimen in human immunodeficiency virus type 1 (HIV-1) infected, antiretroviral (ARV) treatment-naive participants, as determined by the percentage of virologic responders defined as having HIV-1 ribonucleic acid (RNA) less than 400 copies/ milliliter (mL) at Week 24.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03563742
Study type Interventional
Source Johnson & Johnson Pte Ltd
Contact
Status Terminated
Phase Phase 3
Start date September 24, 2018
Completion date June 28, 2021

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