Safety and Efficacy of Switching From Dolutegravir and ABC/3TC or ABC/DTG/3TC to B/F/TAF in HIV-1 Infected Adults Who Are Virologically Suppressed

Last updated:
2026-07-11
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View trial details

Overview

Official protocol title:

A PHASE 3, RANDOMIZED, DOUBLE-BLIND STUDY TO EVALUATE THE SAFETY AND EFFICACY OF SWITCHING FROM A REGIMEN OF DOLUTEGRAVIR AND ABC/3TC, OR A FIXED DOSE COMBINATION (FDC) OF ABC/DTG/3TC TO A FDC OF GS 9883/F/TAF IN HIV 1 INFECTED SUBJECTS WHO ARE VIROLOGICALLY SUPPRESSED

Intervention/treatment:
BICTEGRAVIR (GS-9883) -EMTRICITABINE-TENOFOVIR ALAFENAMIDE
Medical condition:
HUMAN IMMUNODEFICIENCY VIRUS (HIV)
Protocol code:
GS-US-380-1844
Control number:
189791
Status:
Closed
Approved:
December 17, 2015
Date Completed:
Trial phase:
Phase 3
For more information:
ClinicalTrials.gov - NCT02603120
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
Gilead Clinical Study Information Center
Organization
Gilead Sciences
Phone:
1-833-445-3230 (GILEAD-0)
Sponsor
GILEAD SCIENCES CANADA INC

Locations

British Columbia

Vancouver, British Columbia, V6Z 2T1

Manitoba

Winnipeg, Manitoba, R3A 1R9

Quebec

Montreal, Quebec, H2L 4P9
Montreal, Quebec, H3A 1T1
Montreal, Quebec, H4A 3J1

Results

See the results from the trial NCT02603120. This is an external link. The information is not authorized by the Government of Canada.

Date posted:
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