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ClinicalTrials.gov record
Completed Not applicable Interventional

Dolutegravir Expanded Access Study

ClinicalTrials.gov ID: NCT01536873

Public ClinicalTrials.gov record NCT01536873. 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 Jul 21, 2026, 5:27 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 Dolutegravir Open Label Protocol for HIV Infected, Adult and Adolescent Patients With Integrase Resistance

Study identification

NCT ID
NCT01536873
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
ViiV Healthcare
Industry
Enrollment
200 participants

Conditions and interventions

Interventions

  • Dolutegravir Drug

Drug

Eligibility (public fields only)

Age range
12 Years to 99 Years
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
Jun 13, 2012
Primary completion
Sep 22, 2016
Completion
Sep 22, 2016
Last update posted
Sep 29, 2020

2012 – 2016

United States locations

U.S. sites
24
U.S. states
13
U.S. cities
20
Facility City State ZIP Site status
GSK Investigational Site Phoenix Arizona 85012
GSK Investigational Site San Francisco California 94115
GSK Investigational Site Denver Colorado 80218
GSK Investigational Site Fort Lauderdale Florida 33311
GSK Investigational Site Fort Lauderdale Florida 33316
GSK Investigational Site Orlando Florida 32803
GSK Investigational Site St. Petersburg Florida 33701
GSK Investigational Site Vero Beach Florida 32960
GSK Investigational Site Atlanta Georgia 30322
GSK Investigational Site Chicago Illinois 60612
GSK Investigational Site Chicago Illinois 60613
GSK Investigational Site Chicago Illinois 60657
GSK Investigational Site Topeka Kansas 66606
GSK Investigational Site St Louis Missouri 63139
GSK Investigational Site Omaha Nebraska 68198
GSK Investigational Site New York New York 10011
GSK Investigational Site The Bronx New York 1057
GSK Investigational Site Chapel Hill North Carolina 27599-7215
GSK Investigational Site Lancaster Pennsylvania 17604
GSK Investigational Site Philadelphia Pennsylvania 19107
GSK Investigational Site Austin Texas 78705
GSK Investigational Site Dallas Texas 75204
GSK Investigational Site Houston Texas 77004
GSK Investigational Site Houston Texas 77098

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 50 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01536873, 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 Sep 29, 2020 · Synced Jul 21, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01536873 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →