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Completed Phase 3 Interventional

A HIV Study Of A Fixed-Dose Combination Tablet In Antiretroviral Experienced Patients

ClinicalTrials.gov ID: NCT00046176

Public ClinicalTrials.gov record NCT00046176. 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 17, 2026, 4:06 PM 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 Phase III, 48-Week, Open-Label, Randomized, Multicenter Study of the Safety and Efficacy of the Abacavir/Lamivudine Fixed-Dose Combination Tablet Administered QD Versus Abacavir + Lamivudine Administered BID in Combination With a PI or NNRTI in Antiretroviral Experienced Patients.

Brief summary

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

This study is a 48-week study designed to evaluate the safety and efficacy of a fixed-dose combination tablet administered once-a-day versus the individual tablets administered twice-a-day within 3-drug combination regimens in ART (antiretroviral)-experienced HIV-1 infected patients.

Study identification

NCT ID
NCT00046176
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
ViiV Healthcare
Industry
Enrollment
240 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
Aug 26, 2002 (Actual)
Primary completion
May 17, 2004 (Actual)
Completion
May 17, 2004 (Actual)
Last update posted
Mar 24, 2020

2002 – 2004

United States locations

U.S. sites
52
U.S. states
18
U.S. cities
37
Facility City State ZIP Site status
GSK Investigational Site Phoenix Arizona 85006 —
GSK Investigational Site Fountain Valley California 92708 —
GSK Investigational Site Long Beach California 90813 —
GSK Investigational Site Los Angeles California 90028 —
GSK Investigational Site Los Angeles California 90033 —
GSK Investigational Site Sacramento California 95825 —
GSK Investigational Site San Francisco California 94115-1931 —
GSK Investigational Site Torrance California 90502 —
GSK Investigational Site Denver Colorado 80205 —
GSK Investigational Site Denver Colorado 80220 —
GSK Investigational Site Washington D.C. District of Columbia 20007 —
GSK Investigational Site Washington D.C. District of Columbia 20009 —
GSK Investigational Site Fort Lauderdale Florida 33145 —
GSK Investigational Site Fort Lauderdale Florida 33308 —
GSK Investigational Site Fort Lauderdale Florida 33316 —
GSK Investigational Site Fort Myers Florida 33901 —
GSK Investigational Site Jacksonville Florida 32206 —
GSK Investigational Site Miami Florida 33133 —
GSK Investigational Site Miami Florida 33136 —
GSK Investigational Site Orlando Florida 32804 —
GSK Investigational Site Orlando Florida 32806 —
GSK Investigational Site Plantation Florida 33317 —
GSK Investigational Site Tampa Florida 33602 —
GSK Investigational Site Tampa Florida 33614 —
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 Wichita Kansas 67214 —
GSK Investigational Site Baltimore Maryland 21201 —
GSK Investigational Site Hillsborough New Jersey 08844 —
GSK Investigational Site Somers Point New Jersey 08244 —
GSK Investigational Site New York New York 10011 —
GSK Investigational Site New York New York 10014 —
GSK Investigational Site New York New York 10019 —
GSK Investigational Site Stony Brook New York 11794 —
GSK Investigational Site Charlotte North Carolina 28209 —
GSK Investigational Site Durham North Carolina 27710 —
GSK Investigational Site Greenville North Carolina 27858 —
GSK Investigational Site Akron Ohio 44304 —
GSK Investigational Site Tulsa Oklahoma 74127 —
GSK Investigational Site Hershey Pennsylvania 17033 —
GSK Investigational Site Reading Pennsylvania 19601 —
GSK Investigational Site Columbia South Carolina 29206-4713 —
GSK Investigational Site Knoxville Tennessee 37916 —
GSK Investigational Site Dallas Texas 75204 —
GSK Investigational Site Dallas Texas 75208 —
GSK Investigational Site Dallas Texas 75219 —
GSK Investigational Site Dallas Texas 75246 —
GSK Investigational Site Houston Texas 77004 —
GSK Investigational Site Houston Texas 77027 —
GSK Investigational Site Hampton Virginia 23666 —

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 4 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00046176, 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 Mar 24, 2020 · Synced Oct 17, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00046176 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →