Overview

This trial is active, not recruiting.

Condition hiv infection
Treatment all licensed antiretroviral medications
Phase phase 4
Sponsor University of Minnesota - Clinical and Translational Science Institute
Collaborator National Institute of Allergy and Infectious Diseases (NIAID)
Start date March 2009
End date December 2016
Trial size 4688 participants
Trial identifier NCT00867048, 0603M83587, 2008-006439-12, NCT00821171, U01AI068641

Summary

Objectives:

- To find out if the chance of developing a serious illness or of getting AIDS is less if patients start taking HIV medicines at a time when their cluster-of-differentiation-4 (CD4)+ cell count is still fairly high, instead of waiting until the CD4+ count is at the level where there is good evidence for starting medicines.

- To learn more about how a strategy of starting HIV medicines early might affect other aspects of care, such as the chances of developing other illnesses or resistance to HIV medicines, the frequency of doctor visits, the cost of medical care, and general health and satisfaction.

United States No locations recruiting
Other Countries No locations recruiting

Study Design

Allocation randomized
Endpoint classification safety/efficacy study
Intervention model parallel assignment
Masking open label
Primary purpose treatment
Arm
(Experimental)
Initiate ART immediately following randomization
all licensed antiretroviral medications
In both arms, participants may be prescribed any licensed antiretroviral medication, in accordance with national treatment guidelines. The nature of the intervention is the timing of when to begin treatment with these medications, as described in the two treatment arms.
(Active Comparator)
Defer ART until the CD4+ count declines to <350 cells/cu mm or AIDS develops
all licensed antiretroviral medications
In both arms, participants may be prescribed any licensed antiretroviral medication, in accordance with national treatment guidelines. The nature of the intervention is the timing of when to begin treatment with these medications, as described in the two treatment arms.

Primary Outcomes

Measure
Composite endpoint of AIDS, serious non-AIDS diagnoses, and all-cause mortality
time frame: 4.5 years

Secondary Outcomes

Measure
Components of the composite primary outcome measure
time frame: 4.5 years
Specific non-AIDS diagnoses
time frame: 4.5 years
Adverse events
time frame: 4.5 years
Hospitalization, health-care utilization, quality of life
time frame: 4.5 years
HIV drug resistance and transmission risk behavior
time frame: 4.5 years
Change in neurocognitive function (in a subset of participants)
time frame: 4.5 years
Obtain a whole blood sample from which DNA will be extracted to study validated genetic variants that determine the risk of the various primary and secondary outcomes assessed in START (in a subset of participants)
time frame: Blood taken at study entry and stored in a central repository indefinitely
Evaluate understanding of study information and satisfaction with the consent process among START participants, after receiving information from either a standard or a concise consent form (at a subset of sites)
time frame: Before randomization into START
Large and small artery elasticity (in a subset of participants)
time frame: 4.5 years
Rate of lung function decline (in a subset of participants)
time frame: 4.5 years
Changes in bone mineral density (in a subset of participants)
time frame: 4.5 years

Eligibility Criteria

Male or female participants at least 18 years old.

INCLUSION CRITERIA: - Signed informed consent - HIV infection documented by a plasma HIV RNA viral load, rapid HIV test or any licensed* ELISA test; and confirmed by another test using a different method including but not limited to a rapid HIV test, Western Blot, HIV culture, HIV antigen, or HIV pro-viral DNA at any time prior to study entry. - Age greater than or equal to 18 years - Karnofsky performance score greater than or equal to 80 (an indication that the participant can perform normal activities) - Perceived life expectancy of at least 6 months - For women of child-bearing potential, willingness to use contraceptives as described in the product information of the ART drugs they are prescribed - Two CD4+ cell counts greater than 500 cells/mm(3) at least 2 weeks apart within 60 days before randomization - The term licensed refers to an FDA-approved kit or, for sites located in countries other than the United States, a kit that has been certified or licensed by an oversight body within that country. Confirmation of the initial test result must use a test method that is different than the one used for the initial assessment. EXCLUSION CRITERIA: - Any previous use of ART or interleukin-2 (IL-2) - Diagnosis of any clinical AIDS event before randomization (including esophageal candidiasis and chronic Herpes simplex infection) - Presence of HIV progression such as oral thrush, unexplained weight loss, or unexplained fever - Cardiovascular event (myocardial infarction, angioplasty, coronary-artery bypass grafting, stroke) within 6 months before randomization - Non-AIDS-defining cancer, excluding basal and squamous cell skin cancer, within 6 months before randomization - Dialysis within 6 months before randomization - Diagnosis of decompensated liver disease before randomization - Current imprisonment, or compulsory detention (involuntary incarceration) for treatment of a psychiatric or physical illness - Current pregnancy or breastfeeding (a negative serum or urine pregnancy test is required within 14 days before randomization for women of child-bearing potential)

Additional Information

Official title Strategic Timing of AntiRetroviral Treatment
Principal investigator James D Neaton, PhD
Description Background: - Most guidelines agree that if the number of your CD4+ cells (cells in your blood which help fight infection) drops below 350 cells/mm3, or if you have symptoms of AIDS, you should start taking HIV medicines. There are randomized trials that support this recommendation. (Randomized trials are usually considered the strongest form of evidence to support treatment decisions. Other studies, like observational studies, provide evidence too, but the evidence is often considered to be weaker than evidence from randomized trials. A randomized trial gives the most certain information about how well a treatment works because randomization makes sure each group is similar except for the treatment they receive.) Some experts believe that HIV treatment should be started even when the number of CD4+ cells is above 350 cells/mm3. For example, guidelines issued in the US in December 2009 include a new recommendation for starting HIV medicines if your CD4+ cell count is between 350 and 500 cells/mm3. However, this recommendation is based on information from observational studies, not randomized trials. We are doing this study to find out if the chances of getting a serious illness or of getting AIDS are less if people start taking HIV medicines at a time when their CD4+ cell counts are still fairly high, instead of waiting to take HIV medicines at a CD4+ count where there is good evidence for starting medicines. Objectives: - To find out if the chance of developing a serious illness or of getting AIDS is less if patients start taking HIV medicines at a time when their CD4+ cell count is still fairly high, instead of waiting until the CD4+ count is at the level where there is good evidence for starting medicines. - To learn more about how a strategy of starting HIV medicines early might affect other aspects of care, such as the chances of developing other illnesses or resistance to HIV medicines, the frequency of doctor visits, the cost of medical care, and general health and satisfaction. Eligibility: - Patients 18 years of age and older who are infected with HIV, have CD4+ cell counts of greater than 500 cells/mm3, and who have never had antiretroviral therapy to treat HIV. Design: - Initial screening visits (2) to draw blood for CD4+ cell counts and provide a full medical history - Patients will be randomly split into two groups: Early: Patients will begin receiving HIV medications from the start of the study. Deferred: Patients will begin to take HIV medications when the CD4 drops below 350 cells/mm3, or they develop AIDS or other symptoms of HIV infection. - HIV medications for each patient will be determined by the study doctors. - Evaluations during the treatment period: - Physical examination, including vital signs and body weight checks, and pregnancy test for women who can become pregnant. - Questions about daily life, including sexual behaviors. - Blood and urine tests. - Heart tests with electrocardiogram. - Patients will return for evaluations at 1 and 4 months after randomization, and every 4 months thereafter for the duration of the study. Substudies will take advantage of the START randomization to compare outcomes in people starting ART early vs. later. The purpose of this randomized study is to determine whether immediate initiation of antiretroviral treatment (ART) is superior to deferral of ART until the CD4+ declines below 350 cells/mm(3) in terms of morbidity and mortality in HIV-1 (subsequently referred to as HIV) infected persons who are antiretroviral naive with a CD4+ count above 500 cells/mm(3). The study will enroll an estimated 4,000 participants. Participants will be followed for at least 3 years after enrollment, to a common closing date. Substudies will take advantage of the START randomization to compare outcomes in people starting ART early vs. later. These will measure outcomes that do not require the entire sample size of START to determine whether early ART is related to a difference in these outcomes over the course of the study.
Trial information was received from ClinicalTrials.gov and was last updated in January 2015.
Information provided to ClinicalTrials.gov by University of Minnesota - Clinical and Translational Science Institute.