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Completed Phase 2 Interventional Results available

Safety and Efficacy of Bictegravir + Emtricitabine/Tenofovir Alafenamide Versus Dolutegravir + Emtricitabine/Tenofovir Alafenamide in HIV-1 Infected, Antiretroviral Treatment-Naive Adults

ClinicalTrials.gov ID: NCT02397694

Public ClinicalTrials.gov record NCT02397694. 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, 7:23 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 2, Randomized, Double-Blinded Study of the Safety and Efficacy of GS-9883 + Emtricitabine/Tenofovir Alafenamide Versus Dolutegravir + Emtricitabine/Tenofovir Alafenamide in HIV-1 Infected, Antiretroviral Treatment-Naive Adults

Brief summary

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

This study will evaluate the efficacy, safety and tolerability of bictegravir (BIC) + emtricitabine/tenofovir alafenamide (F/TAF) fixed dose combination (FDC) versus dolutegravir (DTG) + F/TAF in HIV-1 Infected, antiretroviral treatment-naive adults. This study will also evaluate the pharmacokinetic (PK) profile of BIC, emtricitabine and TAF.

Study identification

NCT ID
NCT02397694
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Gilead Sciences
Industry
Enrollment
98 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
Mar 22, 2015
Primary completion
Nov 29, 2015
Completion
Feb 26, 2019
Last update posted
Apr 6, 2020

2015 – 2019

United States locations

U.S. sites
21
U.S. states
11
U.S. cities
18
Facility City State ZIP Site status
Not listed Phoenix Arizona 85012
Not listed Los Angeles California 90036
Not listed Los Angeles California 90069
Not listed Sacramento California 95817
Not listed Washington D.C. District of Columbia 20009
Not listed Washington D.C. District of Columbia 20036
Not listed Fort Lauderdale Florida 33316
Not listed Orlando Florida 32803
Not listed West Palm Beach Florida 33401
Not listed Atlanta Georgia 30312
Not listed Decatur Georgia 30033
Not listed Boston Massachusetts 02115
Not listed Berkley Michigan 48072
Not listed Newark New Jersey 07102
Not listed Austin Texas 78705
Not listed Dallas Texas 75208
Not listed Houston Texas 77004
Not listed Houston Texas 77098
Not listed Longview Texas 75605
Not listed Annandale Virginia 22003
Not listed Seattle Washington 98104

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02397694, 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 Apr 6, 2020 · Synced Sep 1, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02397694 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →