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Terminated Phase 3 Interventional Accepts healthy volunteers Results available

Study to Evaluate the Safety and Efficacy of Emtricitabine and Tenofovir Alafenamide (F/TAF) Fixed-Dose Combination Once Daily for Pre-Exposure Prophylaxis in Men and Transgender Women Who Have Sex With Men and Are At Risk of HIV-1 Infection

ClinicalTrials.gov ID: NCT02842086

Public ClinicalTrials.gov record NCT02842086. 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 26, 2026, 10:53 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, Double-blind Study to Evaluate the Safety and Efficacy of Emtricitabine and Tenofovir Alafenamide (F/TAF) Fixed-Dose Combination Once Daily for Pre-Exposure Prophylaxis in Men and Transgender Women Who Have Sex With Men and Are At Risk of HIV-1 Infection

Brief summary

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

The primary objective of this study is to assess the rates of HIV-1 infection in Men (MSM) and transgender women (TGW) who have sex with men and who are administered daily emtricitabine/tenofovir alafenamide (F/TAF) or emtricitabine/tenofovir disoproxil fumarate (F/TDF) with a minimum follow-up of 48 weeks and at least 50% of participants have 96 weeks of follow-up after randomization.

Study identification

NCT ID
NCT02842086
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Lead sponsor
Gilead Sciences
Industry
Enrollment
5,399 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Accepts healthy volunteers

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Sep 2, 2016 (Actual)
Primary completion
Jan 31, 2019 (Actual)
Completion
Jul 29, 2026 (Actual)
Last update posted
Sep 8, 2026

2016 – 2026

United States locations

U.S. sites
54
U.S. states
21
U.S. cities
41
Facility City State ZIP Site status
Not listed Beverly Hills California 90211 —
Not listed Los Angeles California 90036 —
Not listed Los Angeles California 90069 —
Not listed Newport Beach California 92663 —
Not listed Oakland California 94609 —
Not listed Sacramento California 95817 —
Not listed Sacramento California 95825 —
Not listed San Diego California 92103 —
Not listed San Francisco California 94102 —
Not listed San Francisco California 94103 —
Not listed San Francisco California 94118 —
Not listed Torrance California 90502 —
Not listed Aurora Colorado 80045 —
Not listed Denver Colorado 80209 —
Not listed New Haven Connecticut 06510 —
Not listed Washington D.C. District of Columbia 20009 —
Not listed Washington D.C. District of Columbia 20036 —
Not listed Fort Lauderdale Florida 33308 —
Not listed Fort Lauderdale Florida 33316 —
Not listed Ft. Pierce Florida 34982 —
Not listed Miami Florida 33136 —
Not listed Orlando Florida 32803 —
Not listed Pensacola Florida 32504 —
Not listed West Palm Beach Florida 33407 —
Not listed Atlanta Georgia 30308 —
Not listed Atlanta Georgia 30309 —
Not listed Atlanta Georgia 30312 —
Not listed Macon Georgia 31201 —
Not listed Chicago Illinois 60612 —
Not listed Chicago Illinois 60613 —
Not listed New Orleans Louisiana 70119 —
Not listed Boston Massachusetts 02215 —
Not listed Springfield Massachusetts 01105 —
Not listed Berkley Michigan 48072 —
Not listed Detroit Michigan 48202 —
Not listed Minneapolis Minnesota 55415 —
Not listed Las Vegas Nevada 89104 —
Not listed Somers Point New Jersey 08244 —
Not listed Santa Fe New Mexico 87505 —
Not listed New York New York 10029 —
Not listed New York New York 10032 —
Not listed New York New York 10037 —
Not listed The Bronx New York 10467 —
Not listed Chapel Hill North Carolina 27599-7215 —
Not listed Huntersville North Carolina 28078 —
Not listed Cleveland Ohio 44109 —
Not listed Philadelphia Pennsylvania 19107 —
Not listed Austin Texas 78705 —
Not listed Dallas Texas 75208 —
Not listed Dallas Texas 75246 —
Not listed Houston Texas 77098 —
Not listed Seattle Washington 98101 —
Not listed Seattle Washington 98104 —
Not listed Milwaukee Wisconsin 53226 —

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 39 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02842086, 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 8, 2026 · Synced Oct 26, 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 public registry record, listed eligibility criteria, and available contact information for NCT02842086 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →