A Randomized Clinical Trial to Evaluate Solutions for the Management of Virologic Failure on TLD in Sub-Saharan Africa

Recruiting N/A Interventional Study
HIV Infections AIDS Virologic Failure
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
15 and older
Sex
Any
Study type
Interventional
Purpose
Treatment
Participants needed
648 (estimated)
Sponsor
Massachusetts General Hospital · Other
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About This Trial
The RESOLVE trial is an open, parallel arm, randomized clinical trial which aims to determine the optimal strategy for management of virologic failure on antiretroviral therapy (ART) with tenofovir, lamivudine, and dolutegravir (TLD) in sub-Saharan Africa. The primary outcome of interest will be viral suppression to \<50 copies/mL at 48 weeks using the FDA snapshot definition. The study will be co…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Age 15 years and above * Enrolled in HIV care at one of the study clinics * History of two HIV-1 RNA viral load measurements \>1,000 copies/mL while on TLD * On TLD for at least 12 months * Lives within 100 kilometers of study clinic * Pregnant women are eligible for enroll…
Contacts

Suzanne McCluskey, MD

617-726-9488

smccluskey@mgh.harvard.edu

CONTACT