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Completed Phase 3 Interventional Results available

Safety and Efficacy of Switching to a FDC of B/F/TAF From E/C/F/TAF, E/C/F/TDF, or ATV+RTV+FTC/TDF in Virologically Suppressed HIV-1 Infected Women

ClinicalTrials.gov ID: NCT02652624

Public ClinicalTrials.gov record NCT02652624. 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 1, 2026, 11:09 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 3, Randomized, Open Label Study to Evaluate the Safety and Efficacy of Switching to a Fixed Dose Combination (FDC) of GS-9883/Emtricitabine/Tenofovir Alafenamide (GS-9883/F/TAF) From Elvitegravir/Cobicistat/Emtricitabine/ Tenofovir Alafenamide (E/C/F/TAF), Elvitegravir/Cobicistat/Emtricitabine/Tenofovir Disoproxil Fumarate (E/C/F/TDF) or Atazanavir + Ritonavir + Emtricitabine/Tenofovir Disoproxil Fumarate (ATV+RTV+FTC/TDF) in Virologically Suppressed HIV-1 Infected Women

Brief summary

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

The primary objective of this study is to evaluate the efficacy of switching to a fixed-dose combination (FDC) of bictegravir/emtricitabine/tenofovir alafenamide (B/F/TAF) versus continuing on a regimen consisting of elvitegravir/cobicistat/emtricitabine/tenofovir alafenamide (E/C/F/TAF), elvitegravir/cobicistat/emtricitabine/tenofovir disoproxil fumarate (E/C/F/TDF), or atazanavir (ATV) + ritonavir (RTV) + emtricitabine/tenofovir disoproxil fumarate (FTC/TDF) in virologically suppressed HIV-1 infected women.

Study identification

NCT ID
NCT02652624
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Gilead Sciences
Industry
Enrollment
472 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
Female
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 18, 2016
Primary completion
Oct 8, 2017
Completion
Nov 25, 2018
Last update posted
Mar 3, 2020

2016 – 2018

United States locations

U.S. sites
29
U.S. states
10
U.S. cities
25
Facility City State ZIP Site status
Not listed Stamford Connecticut 6902
Not listed Washington D.C. District of Columbia 20009
Not listed Washington D.C. District of Columbia 20037
Not listed Fort Lauderdale Florida 33308
Not listed Ft. Pierce Florida 34982
Not listed Miami Florida 33133
Not listed Miami Florida 33136
Not listed Orlando Florida 32803-1851
Not listed Tampa Florida 33607
Not listed Tampa Florida 33614
Not listed West Palm Beach Florida 33401
Not listed Atlanta Georgia 30308
Not listed Decatur Georgia 30033
Not listed Macon Georgia 31201
Not listed Savannah Georgia 31401
Not listed Springfield Massachusetts 01105
Not listed St Louis Missouri 63110
Not listed Newark New Jersey 07102
Not listed Great Neck New York 11021
Not listed The Bronx New York 10467
Not listed Charlotte North Carolina 28207
Not listed Durham North Carolina 27710
Not listed Huntersville North Carolina 28078
Not listed Bellaire Texas 77401
Not listed Dallas Texas 75208
Not listed Dallas Texas 75219
Not listed Fort Worth Texas 76104
Not listed Harlingen Texas 78550
Not listed Houston Texas 77004

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 27 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02652624, 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 3, 2020 · Synced Sep 1, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02652624 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →