A Phase IIIb Study of the Safety, Efficacy, and Tolerability of Switching to a Fixed-dose Combination of Abacavir/Dolutegravir/ Lamivudine From Current Antiretroviral Regimen

Last updated:
2026-07-11
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View trial details

Overview

Official protocol title:

A PHASE IIIB, RANDOMIZED, OPEN-LABEL STUDY OF THE SAFETY, EFFICACY, AND TOLERABILITY OF SWITCHING TO A FIXED-DOSE COMBINATION OF ABACAVIR/DOLUTEGRAVIR/LAMIVUDINE FROM CURRENT ANTIRETROVIRAL REGIMEN COMPARED WITH CONTINUATION OF THE CURRENT ANTIRETROVIRAL REGIMEN IN HIV-1 INFECTED ADULTS WHO ARE VIROLOGICALLY SUPPRESSED

Intervention/treatment:
GSK2619619
Medical condition:
HUMAN IMMUNODEFICIENCY VIRUS (HIV)
Protocol code:
ING201147
Control number:
172945
Status:
Closed
Approved:
April 03, 2014
Date Completed:
Trial phase:
Phase 3
For more information:
ClinicalTrials.gov - NCT02105987
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 ULC

Locations

Alberta

GSK Investigational Site
Calgary, Alberta, T2R 0X7

British Columbia

GSK Investigational Site
Vancouver, British Columbia, V6Z 2C7
GSK Investigational Site
Vancouver, British Columbia, V6Z 2T1
GSK Investigational Site
Victoria, British Columbia, V8W 1M8

Manitoba

GSK Investigational Site
Winnipeg, Manitoba, R3A 1R9

Ontario

GSK Investigational Site
Toronto, Ontario, M4N 3M5
GSK Investigational Site
Toronto, Ontario, M4T 3A7
GSK Investigational Site
Toronto, Ontario, M5G 1K2
GSK Investigational Site
Toronto, Ontario, M5G 2N2

Quebec

GSK Investigational Site
Montreal, Quebec, H2L 4P9
GSK Investigational Site
Montreal, Quebec, H2L 5B1
GSK Investigational Site
Montreal, Quebec, H3A 1T1

Results

See the results from the trial NCT02105987. This is an external link. The information is not authorized by the Government of Canada.

Date posted:
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