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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 Oct 19, 2026, 1:33 AM 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
Jan 2011 (Type not available)
Primary completion
Jul 2011 (Actual)
Completion
Mar 2012 (Actual)
Last update posted
Apr 26, 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 26, 2013 · Synced Oct 19, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01286740 live on ClinicalTrials.gov.

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