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Active, not recruiting Phase 3 Interventional Results available

Attachment Inhibitor Comparison in Heavily Treatment Experienced Patients

ClinicalTrials.gov ID: NCT02362503

Public ClinicalTrials.gov record NCT02362503. 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 22, 2026, 8:57 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 Multi-arm, Phase 3, Randomized, Placebo Controlled, Double Blind Clinical Trial to Investigate the Efficacy and Safety of Fostemsavir (BMS-663068/GSK3684934) in Heavily Treatment Experienced Subjects Infected With Multi-drug Resistant HIV-1 (BRIGHTE Study)

Study identification

NCT ID
NCT02362503
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 3
Lead sponsor
ViiV Healthcare
Industry
Enrollment
371 participants

Conditions and interventions

Conditions

Interventions

  • BMS-663068 Drug
  • Placebo Other

Drug · Other

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
Feb 22, 2015
Primary completion
Aug 17, 2016
Completion
Jan 27, 2027
Last update posted
Jun 16, 2026

2015 – 2027

United States locations

U.S. sites
39
U.S. states
18
U.S. cities
30
Facility City State ZIP Site status
GSK Investigational Site Los Angeles California 90008
GSK Investigational Site Los Angeles California 90027
GSK Investigational Site Los Angeles California 90033
GSK Investigational Site Los Angeles California 90069
GSK Investigational Site Palm Springs California 92262
GSK Investigational Site San Francisco California 94115
GSK Investigational Site Denver Colorado 80262
GSK Investigational Site New Haven Connecticut 06510
GSK Investigational Site Washington D.C. District of Columbia 20007
GSK Investigational Site Washington D.C. District of Columbia 20009
GSK Investigational Site Ft. Pierce Florida 34982
GSK Investigational Site Orlando Florida 32801
GSK Investigational Site West Palm Beach Florida 33407
GSK Investigational Site Wilton Manors Florida 33306
GSK Investigational Site Atlanta Georgia 30308
GSK Investigational Site Atlanta Georgia 30312
GSK Investigational Site Savannah Georgia 31401
GSK Investigational Site Chicago Illinois 60612
GSK Investigational Site Chicago Illinois 60613
GSK Investigational Site Indianapolis Indiana 46202
GSK Investigational Site Baltimore Maryland 21201
GSK Investigational Site Baltimore Maryland 21287
GSK Investigational Site Boston Massachusetts 211
GSK Investigational Site Southfield Michigan 48075
GSK Investigational Site Hillsborough New Jersey 08844
GSK Investigational Site Newark New Jersey 07102
GSK Investigational Site Manhasset New York 11030
GSK Investigational Site New York New York 10010
GSK Investigational Site New York New York 10029
GSK Investigational Site The Bronx New York 10467
GSK Investigational Site Chapel Hill North Carolina 27599
GSK Investigational Site Durham North Carolina 27710
GSK Investigational Site Cincinnati Ohio 45267-0405
GSK Investigational Site Tulsa Oklahoma 74135
GSK Investigational Site Philadelphia Pennsylvania 19104
GSK Investigational Site Bellaire Texas 77401
GSK Investigational Site Dallas Texas 75235
GSK Investigational Site Dallas Texas 75246
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 100 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02362503, 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 Jun 16, 2026 · Synced Jul 22, 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 NCT02362503 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →