Doravirine/Islatravir (DOR/ISL) in Heavily Treatment-Experienced (HTE) Participants for Human Immunodeficiency Virus Type 1 (HIV-1) Infection (MK-8591A-019)

Last updated:
2026-07-11
Language and content disclaimer

The content and search results on this site are collected from or provided by third parties. As such some of the information may only be available in the language originally submitted by the sponsor of the trial. Learn more about the information on the search portal.

Linking to Non-Government of Canada Websites

Links to websites not under the control of the Government of Canada, including those to our social media accounts, and to clinical trial records in international registries are provided solely for the convenience of our website visitors. We are not responsible for the accuracy, currency or reliability of the content of such websites. The Government of Canada does not offer any guarantee in that regard and is not responsible for the information found through these links, nor does it endorse the sites and their content.

Visitors should also be aware that information offered by non-Government of Canada sites to which this website links is not subject to the Privacy Act or the Official Languages Act and may not be accessible to persons with disabilities. The information offered may be available only in the language(s) used by the sites in question. With respect to privacy, visitors should research the privacy policies of these non-government websites before providing personal information.

View trial details

Overview

Official protocol title:

A PHASE 3, RANDOMIZED, CLINICAL STUDY IN HIV-1-INFECTED HEAVILY TREATMENT-EXPERIENCED PARTICIPANTS EVALUATING THE ANTIRETROVIRAL ACTIVITY OF BLINDED ISLATRAVIR (ISL), DORAVIRINE (DOR), AND DORAVIRINE/ISLATRAVIR (DOR/ISL), EACH COMPARED TO PLACEBO, AND THE ANTIRETROVIRAL ACTIVITY, SAFETY, AND TOLERABILITY OF OPEN-LABEL DOR/ISL [MK-8591A-019-00]

Intervention/treatment:
DORAVIRINE-ISLATRAVIR (MK-8591A) / ISLATRAVIR (MK-8591)/ DORAVIRINE (MK-1439)
Medical condition:
HUMAN IMMUNODEFICIENCY VIRUS (HIV)
Protocol code:
MK-8591A-019
Control number:
235381
Status:
Closed
Approved:
February 19, 2020
Date Completed:
Trial phase:
Phase 3
For more information:
ClinicalTrials.gov - NCT04233216
This is an external link. The information is not authorized by the Government of Canada.

Eligibility

Sex: ALL
Age
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 4100)
Vancouver, British Columbia, V6Z 2C7

Ontario

Hamilton Health Sciences ( Site 4115)
Hamilton, Ontario, L8L 2X2
Ottawa Hospital Research Institute ( Site 4111)
Ottawa, Ontario, K1H 8L6
Toronto General Hospital - University Health Network ( Site 4105)
Toronto, Ontario, M5G 2N2

Quebec

McGill University Health Center - Research Institute-CVIS Clinical Research Unit ( Site 4102)
Montreal, Quebec, H4A 3J1

Results

See the results from the trial NCT04233216. This is an external link. The information is not authorized by the Government of Canada.

Date posted:
Did you find what you were looking for?