Study of Doravirine/Islatravir (DOR/ISL 100 mg/0.75 mg) to Evaluate the Antiretroviral Activity, Safety, and Tolerability in Treatment-Naïve Participants With Human Immunodeficiency Virus Type 1 (HIV-1) Infection (MK-8591A-020)

Last updated:
2026-08-01
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, ACTIVE-CONTROLLED, DOUBLE-BLIND CLINICAL STUDY TO EVALUATE THE ANTIRETROVIRAL ACTIVITY, SAFETY, AND TOLERABILITY OF DORAVIRINE/ISLATRAVIR ONCE-DAILY IN HIV-1 INFECTED TREATMENT-NAÏVE PARTICIPANTS

Intervention/treatment:
DORAVIRINE-ISLATRAVIR (MK-8591A)
Medical condition:
HUMAN IMMUNODEFICIENCY VIRUS (HIV)
Protocol code:
MK-8591A-020
Control number:
235224
Status:
Closed
Approved:
February 13, 2020
Date Completed:
Trial phase:
Phase 3
For more information:
ClinicalTrials.gov - NCT04233879
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

Ontario

Hamilton Health Sciences- Urgent Care Centre-SIS Clinic ( Site 5703)
Hamilton, Ontario, L8S 14K
Toronto General Hospital - University Health Network ( Site 5705)
Toronto, Ontario, M5G 2N2

Quebec

Clinique Medicale L Actuel ( Site 5714)
Montreal, Quebec, H2L 4P9
McGill University Health Center - Research Institute-CVIS Clinical Research Unit ( Site 5702)
Montreal, Quebec, H4A 3J1

Results

See the results from the trial NCT04233879. 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?