Open-Label Pilot Study to Evaluate Switching From a Regimen Consisting of Raltegravir Plus Emtricitabine/Tenofovir DF Fixed-Dose Combination to the Elvitegravir/Cobicistat/Emtricitabine/Tenofovir DF Single-Tablet Regimen in Virologically Suppressed, HIV-1 Infected Patients

PHASE3CompletedINTERVENTIONAL
Enrollment

48

Participants

Timeline

Start Date

January 31, 2012

Primary Completion Date

November 30, 2012

Study Completion Date

July 31, 2013

Conditions
Acquired Immunodeficiency SyndromeHIV Infections
Interventions
DRUG

Stribild

Elvitegravir (EVG) 150 mg/cobicistat (COBI) 150 mg/emtricitabine (FTC) 200 mg/tenofovir disoproxil fumarate (TDF) 300 mg single-tablet regimen (STR) administered orally once daily with food

Trial Locations (9)

20009

Dupont Circle Physician's Group, Washington D.C.

20036

Capital Medical Associates, PC, Washington D.C.

32803

Orlando Immunology Center, Orlando

77098

Gordon E. Crofoot, MD, PA, Houston

78705

Central Texas Clinical Research, Austin

90027

Kaiser Permanente Los Angeles, Los Angeles

90036

Peter J. Ruane, MD, Inc., Los Angeles

90069

Anthony Mills MD, Inc, Los Angeles

02215

Community Research Initiative of New England, Boston

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Gilead Sciences

INDUSTRY