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Terminated Phase 2 Interventional

GW873140 In Combination With Kaletra In HIV Infected Subjects

ClinicalTrials.gov ID: NCT00102778

Public ClinicalTrials.gov record NCT00102778. 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 21, 2026, 6:22 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 IIb, 96 Week, Randomized, Open-label Multicenter, Parallel Group, Repeat Dose Study to Evaluate the Safety, Tolerability, PK and Antiviral Effect of Different Doses and Regimens of GW873140 in Combination With Kaletra (Lopinavir and Ritonavir) in HIV-1 Infected Antiretroviral Therapy naïve Subjects

Brief summary

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

This study is a 96-week study designed to evaluate the safety and efficacy of GW873140 in combination with Kaletra in HIV infected, untreated subjects.

Study identification

NCT ID
NCT00102778
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
ViiV Healthcare
Industry
Enrollment
175 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
Dec 2004 (Type not available)
Primary completion
Sep 2007 (Actual)
Completion
Sep 2007 (Actual)
Last update posted
May 30, 2017

2004 – 2007

United States locations

U.S. sites
32
U.S. states
16
U.S. cities
26
Facility City State ZIP Site status
GSK Investigational Site Phoenix Arizona 85006 —
GSK Investigational Site Tucson Arizona 85745 —
GSK Investigational Site Fountain Valley California 92708 —
GSK Investigational Site Long Beach California 90813 —
GSK Investigational Site Los Angeles California 90027 —
GSK Investigational Site Los Angeles California 90069 —
GSK Investigational Site San Francisco California 94115-1931 —
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 20036 —
GSK Investigational Site Bradenton Florida 34205 —
GSK Investigational Site Fort Lauderdale Florida 33306 —
GSK Investigational Site Fort Lauderdale Florida 33308 —
GSK Investigational Site Fort Myers Florida 33901 —
GSK Investigational Site Orlando Florida 32804 —
GSK Investigational Site Tampa Florida 33614 —
GSK Investigational Site West Palm Beach Florida 33408 —
GSK Investigational Site Atlanta Georgia 30308 —
GSK Investigational Site Atlanta Georgia 30339 —
GSK Investigational Site Chicago Illinois 60613 —
GSK Investigational Site Chicago Illinois 60657 —
GSK Investigational Site New Orleans Louisiana 70115 —
GSK Investigational Site New Orleans Louisiana 70127-0800 —
GSK Investigational Site Jackson Mississippi 39202 —
GSK Investigational Site Santa Fe New Mexico 87505 —
GSK Investigational Site New York New York 10014 —
GSK Investigational Site Charlotte North Carolina 28209 —
GSK Investigational Site Portland Oregon 97209 —
GSK Investigational Site Allentown Pennsylvania 18103 —
GSK Investigational Site Philadelphia Pennsylvania 19102 —
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 38 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00102778, 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 May 30, 2017 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00102778 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →