97
Participants
Start Date
September 24, 2018
Primary Completion Date
December 11, 2019
Study Completion Date
January 30, 2023
CAB LA
Administered CAB LA (600 mg) Q2M, as intramuscular injection.
RPV LA
Administered RPV LA (900 mg), Q2M, as intramuscular injection.
RPV
Oral dose of RPV 25 mg, administered once daily from Day 1 up to Month 12
DTG
Oral dose of DTG 50 mg administered once daily from Day 1 up to Month 12.
GSK Investigational Site, New York
GSK Investigational Site, New York
GSK Investigational Site, Buffalo
GSK Investigational Site, Washington D.C.
GSK Investigational Site, Washington D.C.
GSK Investigational Site, Annandale
GSK Investigational Site, Charleston
GSK Investigational Site, Macon
GSK Investigational Site, Savannah
GSK Investigational Site, Orlando
GSK Investigational Site, Fort Lauderdale
GSK Investigational Site, West Palm Beach
GSK Investigational Site, Ft. Pierce
GSK Investigational Site, Indianapolis
GSK Investigational Site, Omaha
GSK Investigational Site, Dallas
GSK Investigational Site, Austin
GSK Investigational Site, Denver
GSK Investigational Site, Phoenix
GSK Investigational Site, Las Vegas
GSK Investigational Site, Los Angeles
GSK Investigational Site, Beverly Hills
GSK Investigational Site, Long Beach
GSK Investigational Site, Bakersfield
GSK Investigational Site, Augusta
GSK Investigational Site, Vancouver
GSK Investigational Site, Toronto
GSK Investigational Site, Toronto
GSK Investigational Site, Montreal
GSK Investigational Site, Montreal
Lead Sponsor
Janssen, LP
INDUSTRY
ViiV Healthcare
INDUSTRY