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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 Sep 2, 2026, 11:03 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 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 25, 2002
Primary completion
May 16, 2004
Completion
May 16, 2004
Last update posted
Mar 23, 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 23, 2020 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00046176 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →