Independent directory Public ClinicalTrials.gov records United States
ClinicalTrials.gov record
Completed Phase 2 Interventional Results available

Study to Evaluate Switching From a Regimen Consisting of the Efavirenz/Emtricitabine/Tenofovir Disoproxil Fumarate Single-Tablet Regimen (STR) to the Emtricitabine/Rilpivirine/Tenofovir Disoproxil Fumarate STR

ClinicalTrials.gov ID: NCT01286740

Public ClinicalTrials.gov record NCT01286740. 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 2, 2026, 12:31 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 2B Open Label Pilot Study to Evaluate Switching From a Regimen Consisting of a Efavirenz/Emtricitabine/Tenofovir Disoproxil Fumarate (EFV/FTC/TDF) Single Tablet Regimen (STR) to Emtricitabine/Rilpivirine/Tenofovir Disoproxil Fumarate (FTC/RPV/TDF) STR in Virologically Suppressed, HIV 1 Infected Subjects

Brief summary

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

The purpose of this Phase 2b study was to evaluate the efficacy and safety of the emtricitabine/rilpivirine/tenofovir disoproxil fumarate (FTC/RPV/TDF) STR, after switching from the efavirenz (EFV)/FTC/TDF STR at baseline, in maintaining HIV-1 RNA \< 50 copies/mL at Week 12. HIV-infected patients were enrolled if they had received EFV/FTC/TDF for ≥ 3 months prior to study start, were experiencing safety or tolerability concerns (in particular, EFV-related intolerance), and wished to change to an alternate, better-tolerated regimen.

Study identification

NCT ID
NCT01286740
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Gilead Sciences
Industry
Enrollment
50 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
Dec 31, 2010
Primary completion
Jun 30, 2011
Completion
Feb 29, 2012
Last update posted
Apr 25, 2013

2011 – 2012

United States locations

U.S. sites
18
U.S. states
10
U.S. cities
15
Facility City State ZIP Site status
Living Hope Clinical Foundation Long Beach California 90814
Peter J. Ruane MD Inc Los Angeles California 90036
Anthony Mills MD, Inc. Los Angeles California 90069
La Playa Medical Group and Clinical Research San Diego California 92103
Dupont Circle Physicians Group, P.C. Washington D.C. District of Columbia 20009
Whitman Walker Clinic Washington D.C. District of Columbia 20009
Capital Medical Associates, PC Washington D.C. District of Columbia 20036
The Kinder Medical Group Miami Florida 33133
Orlando Immunology Center Orlando Florida 32803
Atlanta ID Group Atlanta Georgia 30309
Infectious Disease Specialists of Atlanta Decatur Georgia 30033
Northstar Medical Center Chicago Illinois 60657
Community Research Initiative of New England Boston Massachusetts 02215
Be Well Medical Center, P.C. Berkley Michigan 48072
Southampton Healthcare, Inc. St Louis Missouri 63139
Southwest Infectious Disease Clinical Research, Inc. Addison Texas 75001
Central Texas Clinical Research Austin Texas 78705
Peter Shalit, M.D. 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 NCT01286740, 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 25, 2013 · Synced Sep 2, 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 NCT01286740 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →