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A Randomized Controlled Trial of a Weekly Schedule of Five Consecutive Days on Treatment With Efavirenz, Tenofovir, and Emtricitabine Followed by Two Days Off Treatment (5/2 Intermittent Treatment Schedule) Versus Continuous Treatment in Individuals With Virologic Suppression on This Combination
For people with HIV who are currently taking specific medications (including Sustiva (efavirenz)) and have no detectable viral load, this study tracks how patients do if they take their medications for five days of the week compared with seven days of the week.
The purpose of this study is to evaluate virologic control of a weekly schedule of 5 days of treatment followed by two days off treatment versus continuous treatment with the same regimen. This is a larger study based on the results of our successful pilot study using the same protocol. The 48 week, phase IV trial addresses the issues of the high cost of HIV treatment, adherence problems associated with daily treatment, and cumulative toxicities. Virologic and immunologic parameters, drug levels of efavirenz, adherence, and toxicity will be measured. Subjects will have to be seen at CRI for 6 visits after randomization. Subjects randomized to daily therapy will cross over to 5/2 therapy at 24 weeks if their viral load remains undetectable.
Age
18 - 65 years
Sex
ALL
Healthy Volunteers
No
Whitman-Walker Clinic
Washington D.C., District of Columbia, United States
CARE-ID
Washington D.C., District of Columbia, United States
Steinhart Medical Associates
Miami, Florida, United States
Orlando Immunology Center
Orlando, Florida, United States
Treasure Chest Infectious Disease
Vero Beach, Florida, United States
Community Research Initiative of New England - Boston
Boston, Massachusetts, United States
Community Research Initiative of New England - West
Springfield, Massachusetts, United States
Start Date
August 1, 2006
Primary Completion Date
December 1, 2009
Completion Date
December 1, 2009
Last Updated
September 25, 2017
60
ACTUAL participants
Intermitent Dosing
DRUG
Lead Sponsor
Community Research Initiative of New England
Collaborators
NCT06694805
NCT04142047
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT07428330