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Completed Phase 3 Interventional Results available

Study to Evaluate the Safety and Efficacy of Switching From Regimens Consisting of Boosted Atazanavir or Darunavir Plus Either Emtricitabine/Tenofovir or Abacavir/Lamivudine to Bictegravir/Emtricitabine/Tenofovir Alafenamide in Virologically Suppressed HIV-1 Infected Adults

ClinicalTrials.gov ID: NCT02603107

Public ClinicalTrials.gov record NCT02603107. 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 24, 2026, 5:19 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 From Regimens Consisting of Boosted Atazanavir or Darunavir Plus Either Emtricitabine/Tenofovir or Abacavir/Lamivudine to GS-9883/Emtricitabine/Tenofovir Alafenamide in Virologically Suppressed HIV-1 Infected Adults

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 boosted atazanavir (ATV) or darunavir (DRV) plus either emtricitabine/tenofovir disoproxil fumarate (FTC/TDF) or abacavir/lamivudine (ABC/3TC) in HIV-1 infected adults who are virologically suppressed.

Study identification

NCT ID
NCT02603107
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Gilead Sciences
Industry
Enrollment
578 participants

Conditions and interventions

Interventions

Drug

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
Nov 20, 2015 (Actual)
Primary completion
May 15, 2017 (Actual)
Completion
Dec 23, 2019 (Actual)
Last update posted
Dec 29, 2020

2015 – 2019

United States locations

U.S. sites
63
U.S. states
23
U.S. cities
52
Facility City State ZIP Site status
Not listed Phoenix Arizona 85012 —
Not listed Phoenix Arizona 85015 —
Not listed Los Angeles California 90027 —
Not listed Los Angeles California 90036 —
Not listed Los Angeles California 90069 —
Not listed Newport Beach California 92663 —
Not listed Oakland California 94602 —
Not listed Sacramento California 95825 —
Not listed San Diego California 92103 —
Not listed San Francisco California 94102 —
Not listed San Leandro California 94577 —
Not listed Torrance California 90502 —
Not listed Aurora Colorado 80045 —
Not listed Washington D.C. District of Columbia 20017 —
Not listed Washington D.C. District of Columbia 20036 —
Not listed DeLand Florida 32720 —
Not listed Fort Lauderdale Florida 33316 —
Not listed Ft. Pierce Florida 34982 —
Not listed Miami Florida 33133 —
Not listed Miami Florida 33136 —
Not listed Orlando Florida 32803-1851 —
Not listed Pensacola Florida 32504 —
Not listed Tampa Florida 33614 —
Not listed Vero Beach Florida 32960 —
Not listed West Palm Beach Florida 33401 —
Not listed Wilton Manors Florida 33305 —
Not listed Atlanta Georgia 30312 —
Not listed Augusta Georgia 30912 —
Not listed Macon Georgia 31201 —
Not listed Honolulu Hawaii 96813 —
Not listed Chicago Illinois 60613 —
Not listed Chicago Illinois 60657 —
Not listed Chicago Illinois — —
Not listed Kansas City Kansas 66160 —
Not listed Louisville Kentucky 40202 —
Not listed New Orleans Louisiana 70112 —
Not listed Boston Massachusetts 01211 —
Not listed Springfield Massachusetts 1105 —
Not listed Berkley Michigan 48072 —
Not listed Minneapolis Minnesota 55407 —
Not listed Kansas City Missouri 64111 —
Not listed St Louis Missouri 63139 —
Not listed Buffalo New York 14215 —
Not listed The Bronx New York 10467 —
Not listed The Bronx New York — —
Not listed Chapel Hill North Carolina 27599-7080 —
Not listed Charlotte North Carolina 28209 —
Not listed Durham North Carolina 27710 —
Not listed Greenville North Carolina 27834 —
Not listed Huntersville North Carolina 28078 —
Not listed Philadelphia Pennsylvania 19107 —
Not listed Columbia South Carolina 29203 —
Not listed Memphis Tennessee 38105 —
Not listed Austin Texas 78705 —
Not listed Dallas Texas 75215 —
Not listed Dallas Texas 75219 —
Not listed Dallas Texas 75246 —
Not listed Houston Texas 77004 —
Not listed Houston Texas 77098 —
Not listed Longview Texas 75605 —
Not listed Annandale Virginia 22003-7313 —
Not listed Seattle Washington 98104 —
Not listed Spokane Washington 99204 —

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 56 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02603107, 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 Dec 29, 2020 · Synced Oct 24, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02603107 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →