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Terminated Phase 2 Interventional Results available

Dose-finding Study of GSK2248761 in Antiretroviral Therapy-experienced Subjects With NNRTI-resistant HIV Infection

ClinicalTrials.gov ID: NCT01199731

Public ClinicalTrials.gov record NCT01199731. 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, 4:09 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 2b Study to Select a Once Daily Oral Dose of GSK2248761 in HIV-1 Infected Antiretroviral Therapy Experienced Adults With Non-nucleoside Reverse Transcriptase Inhibitor (NNRTI) Resistance

Brief summary

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

This 48 week, phase 2b study in 150 HIV-1 infected antiretroviral therapy experienced adult subjects consists of a dose-ranging evaluation of GSK2248761 at blinded doses of 100 mg and 200 mg once daily with a control arm of open-label etravirine (ETV) 200 mg twice daily. The background ART for all three arms will be darunavir/ritonavir (DRV/r) 600 mg/100 mg twice daily plus raltegravir (RAL) 400 mg twice daily. Antiviral activity, safety, PK, and development of viral resistance will be evaluated.

Study identification

NCT ID
NCT01199731
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
ViiV Healthcare
Industry
Enrollment
30 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
Oct 4, 2010
Primary completion
Jul 18, 2011
Completion
Jul 18, 2011
Last update posted
Nov 16, 2017

2010 – 2011

United States locations

U.S. sites
30
U.S. states
13
U.S. cities
28
Facility City State ZIP Site status
GSK Investigational Site Birmingham Alabama 35294
GSK Investigational Site Phoenix Arizona 85012
GSK Investigational Site Bakersfield California 93301
GSK Investigational Site Beverly Hills California 90211
GSK Investigational Site Fresno California 93721
GSK Investigational Site Long Beach California 90813
GSK Investigational Site Los Angeles California 90069
GSK Investigational Site San Francisco California 94115
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 33308
GSK Investigational Site Fort Lauderdale Florida 33316
GSK Investigational Site Ft. Pierce Florida 34982
GSK Investigational Site Orlando Florida 32804
GSK Investigational Site Springfield Massachusetts 01107
GSK Investigational Site Kansas City Missouri 64106
GSK Investigational Site Hillsborough New Jersey 08844
GSK Investigational Site Newark New Jersey 07102
GSK Investigational Site Santa Fe New Mexico 87505
GSK Investigational Site New York New York 10003
GSK Investigational Site Stony Brook New York 11794
GSK Investigational Site The Bronx New York 10467
GSK Investigational Site Valhalla New York 10595
GSK Investigational Site Chapel Hill North Carolina 27514
GSK Investigational Site Charlotte North Carolina 28209
GSK Investigational Site Portland Oregon 97210
GSK Investigational Site Austin Texas 78705
GSK Investigational Site Dallas Texas 75246
GSK Investigational Site Fort Worth Texas 76104
GSK Investigational Site Longview Texas 75605

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 11 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01199731, 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 Nov 16, 2017 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01199731 live on ClinicalTrials.gov.

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