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STRIBILD in Non-Nucleoside Resistant Patients (SINNR STUDY) — SINNR  

HIV Clinical Trial

Official title:
STRIBILD in Non-Nucleoside Resistant Patients, An Evaluation of Safety and Efficacy in Vulnerable Population (SINNR STUDY)

Clinical Trial Summary

The SINNR study will evaluate the virologic efficacy (viral load <50 copies/mL)and safety of STRIBILD administered for 48 weeks to HIV-infected current or recent illicit drug users.

Clinical Trial Description

The SINNR study is a pilot, observational, open label study. It will evaluate the virologic efficacy (viral load <50 copies/mL), safety, and immunologic response of STRIBILD administered for 48 weeks to HIV-infected current or recent illicit drug users.

Approximately 30 HIV-infected current or recent illicit drug users (≥19y.o.,<70y.o.) from Vancouver Infectious Diseases Centre and Regina General Hospital, University of Saskatchewan will be taking an oral 1 STRIBILD tablet once a day for 48 weeks.

Additionally, adherence to STRIBILD over 48 weeks and quality of life will be measured in this population. ;

Study Design

Time Perspective: Prospective

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02306577
Study type Observational
Source Vancouver Infectious Diseases Centre
Contact Harout Tossonian, MD, PhD
Phone 604-642-6429
Email Harout.Tossonian@vidc.ca
Status Recruiting
Phase N/A
Start date November 2014
Completion date July 2016
View Details
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