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Completed Phase 4 Interventional Results available

Abacavir/Lamivudine Versus Emtricitabine/Tenofovir Both In Combination With Lopinavir/Ritonavir For The Treatment Of HIV

ClinicalTrials.gov ID: NCT00244712

Public ClinicalTrials.gov record NCT00244712. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 23, 2026, 8:45 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A 96-Week, Phase IV, Randomized, Double-Blind, Multicenter Study of the Safety and Efficacy of EPZICOM Versus TRUVADA Administered in Combination With KALETRA in Antiretroviral-Naive HIV-1 Infected Subjects

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This study was designed to test the safety and effectiveness of EPZICOM(abacavir/lamivudine) and TRUVADA (emtricitabine/tenofovir) for the treatment of HIV infection when both are used in combination with KALETRA (lopinavir/ritonavir) over 96 weeks

Study identification

NCT ID
NCT00244712
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
688 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jul 2005 (Type not available)
Primary completion
Apr 2008 (Actual)
Completion
Apr 2008 (Actual)
Last update posted
Jun 8, 2010

2005 – 2008

United States locations

U.S. sites
72
U.S. states
22
U.S. cities
55
Facility City State ZIP Site status
GSK Investigational Site Phoenix Arizona 85006 —
GSK Investigational Site Phoenix Arizona 85012 —
GSK Investigational Site Tucson Arizona 85745 —
GSK Investigational Site Beverly Hills California 90210 —
GSK Investigational Site Fountain Valley California 92708 —
GSK Investigational Site Garden Grove California 92845 —
GSK Investigational Site Long Beach California 90813 —
GSK Investigational Site Los Angeles California 90069 —
GSK Investigational Site Newport Beach California 92663 —
GSK Investigational Site Oakland California 94602 —
GSK Investigational Site Oakland California 94609 —
GSK Investigational Site Denver Colorado 80204 —
GSK Investigational Site Denver Colorado 80205 —
GSK Investigational Site Denver Colorado 80220 —
GSK Investigational Site Glastonbury Connecticut 06033 —
GSK Investigational Site Norwalk Connecticut 06851 —
GSK Investigational Site Washington D.C. District of Columbia 20007 —
GSK Investigational Site Washington D.C. District of Columbia 20009 —
GSK Investigational Site Washington D.C. District of Columbia 20037 —
GSK Investigational Site Fort Lauderdale Florida 33306 —
GSK Investigational Site Fort Lauderdale Florida 33308 —
GSK Investigational Site Fort Lauderdale Florida 33316 —
GSK Investigational Site Fort Myers Florida 33901 —
GSK Investigational Site Key West Florida 33040 —
GSK Investigational Site Miami Florida 33136 —
GSK Investigational Site Plantation Florida 33317 —
GSK Investigational Site Port Saint Lucie Florida 34952 —
GSK Investigational Site Sarasota Florida 34239 —
GSK Investigational Site Sarasota Florida 34243 —
GSK Investigational Site Tampa Florida 33602 —
GSK Investigational Site Tampa Florida 33614 —
GSK Investigational Site Atlanta Georgia 30308/30309 —
GSK Investigational Site Atlanta Georgia 30308 —
GSK Investigational Site Atlanta Georgia 30339 —
GSK Investigational Site Augusta Georgia 30912 —
GSK Investigational Site Decatur Georgia 30033 —
GSK Investigational Site Chicago Illinois 60612 —
GSK Investigational Site Chicago Illinois 60637 —
GSK Investigational Site Chicago Illinois 60657 —
GSK Investigational Site Maywood Illinois 60153 —
GSK Investigational Site Lexington Kentucky 40536 —
GSK Investigational Site Louisville Kentucky 40202 —
GSK Investigational Site Baltimore Maryland 21201 —
GSK Investigational Site St Louis Missouri 63108 —
GSK Investigational Site Las Vegas Nevada 89102 —
GSK Investigational Site Hillsborough New Jersey 08844 —
GSK Investigational Site Newark New Jersey 07102 —
GSK Investigational Site Somers Point New Jersey 08244 —
GSK Investigational Site New York New York 10011 —
GSK Investigational Site New York New York 10065 —
GSK Investigational Site Rochester New York 14604 —
GSK Investigational Site Charlotte North Carolina 28209 —
GSK Investigational Site Greenville North Carolina 27834 —
GSK Investigational Site Toledo Ohio 43614 —
GSK Investigational Site Portland Oregon 97219 —
GSK Investigational Site Philadelphia Pennsylvania 19140 —
GSK Investigational Site West Reading Pennsylvania 19611 —
GSK Investigational Site Columbia South Carolina 29206 —
GSK Investigational Site Austin Texas 78751 —
GSK Investigational Site Dallas Texas 75208 —
GSK Investigational Site Dallas Texas 75246 —
GSK Investigational Site Fort Worth Texas 76104 —
GSK Investigational Site Harlingen Texas 78550 —
GSK Investigational Site Houston Texas 77027 —
GSK Investigational Site Houston Texas 77030 —
GSK Investigational Site Longview Texas 75604 —
GSK Investigational Site Tyler Texas 75708 —
GSK Investigational Site Annandale Virginia 22003 —
GSK Investigational Site Charlottesville Virginia 22908 —
GSK Investigational Site Hampton Virginia 23666 —
GSK Investigational Site Lynchburg Virginia 24501 —
GSK Investigational Site Milwaukee Wisconsin 53226 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 2 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00244712, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jun 8, 2010 · Synced Oct 23, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00244712 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →