CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 334 enrolled
Drug / intervention
Emtricitabine/tenofovir disoproxil fumarate +4 moredrug
Likely dose
Emtricitabine/tenofovir disoproxil fumarate 200 mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT00851799
NCT00851799N/ACompleted

Cardiovascular, Anthropometric, and Skeletal Effects of Antiretroviral Therapy (ART) Initiation With Emtricitabine/Tenofovir Disoproxil Fumarate (FTC/TDF) Plus Atazanavir/Ritonavir (ATV/r), Darunavir/Ritonavir (DRV/r), or Raltegravir (RAL): Metabolic Substudy of A5257

Advancing Clinical Therapeutics Globally for HIV/AIDS and Other Infections·observational·Posted Feb 26, 2009·Updated Jan 13, 2016

In Brief

An observational study evaluating Emtricitabine/tenofovir disoproxil fumarate, Ritonavir, and 3 other interventions for HIV Infection. Completed, enrolled 334 participants across 26 sites.

Detailed Summary

The U.S. Department of Health and Human Services (HHS) guidelines recommend that HIV-infected people who have never received anti-HIV therapy be treated with a triple drug regimen (commonly called combination antiretroviral therapy, cART). Since the introduction of cART, morbidity and mortality among HIV-infected patients has been dramatically reduced. However, metabolic, skeletal, and cardiovascular diseases have been increasingly reported among HIV-infected patients and may be attributable, in part, to the direct effects of cART. Much of our understanding of the development of these diseases, risk factors, and consequences of these disorders has been derived from clinical studies of HIV-infected persons receiving older antiretroviral agents. A5260s was designed to examine the contributions of HIV-disease related factors and impact of newer antiretroviral drugs on the development of metabolic (such as blood vessels, blood sugar, cholesterol), skeletal, and cardiovascular diseases in people who have never received anti-HIV therapy. A5260s is a prospective substudy of a phase III randomized clinical trial A5257 (see ClinicalTrials.gov identifier: NCT00811954). A5257 was designed to look at different combinations of anti-HIV drugs that do not contain the medication efavirenz (EFV) and how well these drug combinations work to decrease the amount of HIV in the blood and to allow immune system recovery in people who have never received anti-HIV therapy. A5257 also examined drug tolerability and safety for the various drug combinations.

Study Details

Study Typeobservational
Allocation--
Masking--
Primary Purpose--
ConditionsHIV Infection
CountriesUnited States

Timeline

N/ACompletedFinished
200920102011201220132014201520162017201820192020202120222023202420252026
First PostedFeb 26, 2009
Enrollment StartJun 1, 2009
Primary CompletionJun 1, 2013
TodayJul 2, 2026
Enrollment to primary: 4 yearsPosted 17.3 years ago

Interventions

Emtricitabine/tenofovir disoproxil fumaratedrug

200 mg emtricitabine/300 mg tenofovir disoproxil fumarate taken orally daily. A combination drug of two nucleoside reverse transcriptase inhibitors (NRTIs). Other Name: TDF/FTC

Ritonavirdrug

100 mg taken orally once daily. A protease inhibitor (PI). Other Name: RTV

Atazanavirdrug

300 mg taken orally once daily. A protease inhibitor (PI). Other Name: ATV

Raltegravirdrug

400 mg taken orally twice daily. An integrase inhibitor (INI). Other Name: RAL

Darunavirdrug

100 mg taken orally once daily. A protease inhibitor (PI). Other Name: RTV