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

PHASE2CompletedINTERVENTIONAL
Enrollment

50

Participants

Timeline

Start Date

January 31, 2011

Primary Completion Date

July 31, 2011

Study Completion Date

March 31, 2012

Conditions
HIV-1 Infection
Interventions
DRUG

FTC/RPV/TDF

Emtricitabine (FTC) 200 mg/rilpivirine (RPV) 25 mg/tenofovir disoproxil fumarate (tenofovir DF; TDF) 300 mg single-tablet regimen (STR) administered orally with a meal once daily

Trial Locations (18)

20009

Dupont Circle Physicians Group, P.C., Washington D.C.

Whitman Walker Clinic, Washington D.C.

20036

Capital Medical Associates, PC, Washington D.C.

30033

Infectious Disease Specialists of Atlanta, Decatur

30309

Atlanta ID Group, Atlanta

32803

Orlando Immunology Center, Orlando

33133

The Kinder Medical Group, Miami

48072

Be Well Medical Center, P.C., Berkley

60657

Northstar Medical Center, Chicago

63139

Southampton Healthcare, Inc., St Louis

75001

Southwest Infectious Disease Clinical Research, Inc., Addison

78705

Central Texas Clinical Research, Austin

90036

Peter J. Ruane MD Inc, Los Angeles

90069

Anthony Mills MD, Inc., Los Angeles

90814

Living Hope Clinical Foundation, Long Beach

92103

La Playa Medical Group and Clinical Research, San Diego

98104

Peter Shalit, M.D., Seattle

02215

Community Research Initiative of New England, Boston

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Gilead Sciences

INDUSTRY