Switch to Doravirine/Islatravir (DOR/ISL) in Human Immunodeficiency Virus 1 (HIV-1) Participants Treated With Bictegravir/Emtricitabine/Tenofovir Alafenamide (BIC/FTC/TAF) (MK-8591A-018)

Last updated:
2026-07-11
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View trial details

Overview

Official protocol title:

A PHASE 3, RANDOMIZED, ACTIVE-CONTROLLED, DOUBLE-BLIND CLINICAL STUDY TO EVALUATE A SWITCH TO DORAVIRINE/ISLATRAVIR (DOR/ISL) ONCE-DAILY IN PARTICIPANTS WITH HIV-1 VIROLOGICALLY SUPPRESSED ON BICTEGRAVIR/EMTRICITABINE/TENOFOVIR ALAFENAMIDE (BIC/FTC/TAF)

Intervention/treatment:
DORAVIRINE-ISLATRAVIR (MK-8591A)
Medical condition:
HUMAN IMMUNODEFICIENCY VIRUS (HIV)
Protocol code:
MK-8591A-018
Control number:
233479
Status:
Closed
Approved:
December 13, 2019
Date Completed:
Trial phase:
Phase 3
For more information:
ClinicalTrials.gov - NCT04223791
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
Senior Vice President, Global Clinical Development
Organization
Merck Sharp & Dohme LLC
Phone:
1-800-672-6372
Sponsor
MERCK CANADA INC

Locations

British Columbia

Vancouver ID Research and Care Centre Society ( Site 2800)
Vancouver, British Columbia, V6Z 2C7

Ontario

Hamilton Health Sciences ( Site 2803)
Hamilton, Ontario, L8L 2X2

Quebec

Clinique de Medecine Urbaine du Quartier Latin ( Site 2804)
Montreal, Quebec, H2L 4E9
Clinique Medicale L Actuel ( Site 2814)
Montreal, Quebec, H2L 4P9

Results

See the results from the trial NCT04223791. This is an external link. The information is not authorized by the Government of Canada.

Date posted:
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