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Clinical Trial Summary

Switch patients from Atripla to Stribild will be evaluated to see if patients have less sleep disturbances.


Clinical Trial Description

Stribild is a preferred regimen in the Department of Health and Human Services guidelines and has demonstrated non-inferiority to Atripla in treatment naïve patients out to 144 weeks (GS-102). Stribild also has statistically significant less Central Nervous System side effects, sleep disturbances and lipid elevations compared to Atripla. This study will evaluate the efficacy, safety, changes in Central Nervous System abnormalities and sleep disorders following a switch from virologically suppressed subjects on Atripla to Stribild. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02477527
Study type Interventional
Source Midtown Medical Center, Tampa, FL
Contact
Status Completed
Phase Phase 4
Start date February 2015
Completion date January 2016

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