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COMPLETED
NCT07193875
PHASE4

Efavirenz (EFV) Intensification

Sponsor: Washington University School of Medicine

View on ClinicalTrials.gov

Summary

The goal of this clinical trial is to see if Efavirenz (EFV) intensification to a baseline combination antiretroviral regimen (cART) can help reduce the size of the latent reservoir in people living with HIV (PLWH). The main questions this study aims to address are: 1. is the addition of EFV to a cART regimen safe and well tolerated? 2. Is there a reduction in the blood and tissue HIV reservoir after intensification? Researchers will compare each participants reservoir size prior to and post EFV intensification.

Official title: Safety, Tolerability, and Efficacy of Efavirenz (EFV) Intensification on HIV-1 Reservoir Reduction

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

9

Start Date

2023-02-09

Completion Date

2024-12-16

Last Updated

2026-07-17

Healthy Volunteers

No

Conditions

Interventions

DRUG

Efavirenz 600mg

Take One pill daily for 6 months in addition to baseline combination antiretroviral therapy regimen

Locations (1)

Washington University in St Louis

St Louis, Missouri, United States