Regimen Switch to Dolutegravir/Lamivudine Fixed Dose Combination From Current Antiretroviral Regimen in HIV-1 Infected and Virologically Suppressed Adults (SALSA)

Last updated:
2026-07-11
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View trial details

Overview

Official protocol title:

A PHASE III, RANDOMIZED, MULTICENTER, OPEN-LABEL, NON-INFERIORITY STUDY EVALUATING THE EFFICACY, SAFETY AND TOLERABILITY OF SWITCHING TO DOLUTEGRAVIR/LAMIVUDINE FIXED DOSE COMBINATION IN HIV-1 INFECTED ADULTS WHO ARE VIROLOGICALLY SUPPRESSED

Intervention/treatment:
LAMIVUDINE-DOLUTEGRAVIR (GSK3515864)
Medical condition:
HUMAN IMMUNODEFICIENCY VIRUS (HIV)
Protocol code:
208090
Control number:
227747
Status:
Closed
Approved:
June 07, 2019
Date Completed:
Trial phase:
Phase 3
For more information:
ClinicalTrials.gov - NCT04021290
This is an external link. The information is not authorized by the Government of Canada.

Eligibility

Sex: ALL
Age
18 Years and older
Accepts healthy volunteers: No

Contacts and locations

Contact
Name
GSK Response Center
Organization
GlaxoSmithKline
Phone:
866-435-7343
Sponsor
VIIV HEALTHCARE UK LIMITED

Locations

British Columbia

GSK Investigational Site
Vancouver, British Columbia, V6Z 2T1

Manitoba

GSK Investigational Site
Winnipeg, Manitoba, R3A 1R9

Ontario

GSK Investigational Site
Ottawa, Ontario, K1H 8L6
GSK Investigational Site
Toronto, Ontario, M5G 2N2

Quebec

GSK Investigational Site
Montreal, Quebec, H2L 4E9
GSK Investigational Site
Montreal, Quebec, H4A 3J1

Saskatchewan

GSK Investigational Site
Regina, Saskatchewan, S4P 0W5

Results

See the results from the trial NCT04021290. This is an external link. The information is not authorized by the Government of Canada.

Date posted:
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