55
Participants
Start Date
December 14, 2015
Primary Completion Date
September 29, 2017
Study Completion Date
October 15, 2019
E/C/F/TAF
150/150/200/10 mg FDC tablets administered orally once daily
B/F/TAF
50/200/25 mg FDC tablets administered orally once daily
Peter J Ruane MD Inc, Los Angeles
University of California Davis, Sacramento
Midway Immunology & Research Center, LLC, Ft. Pierce
Infectious Disease Consultants, M.D., P.A. d/b/a Orlando Immunology Center, Orlando
Triple O Research Institute PA, West Palm Beach
Medical College of Georgia, Augusta
Infectious Disease Specialists of Atlanta, Decatur
Mercer University School of Medicine, Macon
The Research Institute, Springfield
Henry Ford Health System, Detroit
Prime Health Care Services - St Michael's LLC d/b/a Saint Michael's Medical Center, Newark
University of North Carolina at Chapel Hill / UNC School of Medicine, Chapel Hill
Duke University, Durham
Wake Forest University Baptist Medical Center, Winston-Salem
University of Cincinnati Med Center, Cincinnati
MetroHealth Medical Center IRB, Cleveland
North Texas Infectious Diseases Consultants, Dallas
Trinity Health and Wellness Center, Fort Worth
Gordon E. Crofoot MD PA, Houston
Otto Wagner Spital, Vienna
Hopital Henri Mondor, Créteil
CHU de Nice-l Archet, Nice
Hopital Bichat-Claude Bernard, Paris
Hopital Saint Louis, Paris
Centre Hospitalier de Tourcoing, Tourcoing
Klinikum rechts der Isar, TUM, München
Lead Sponsor
Gilead Sciences
INDUSTRY