559
Participants
Start Date
May 31, 2011
Primary Completion Date
December 31, 2014
Study Completion Date
June 30, 2015
ATV/r
All participants will be randomized to take ATV/r 200 mg/100 mg OD or ATV/r 300/100 mg OD. NRTIs background regimens will remain unchanged if possible. NRTIs background may include zidovudine/lamivudine, zidovudine plus ddI, ddI plus lamivudine, tenofovir plus lamivudine, tenofovir/emtricitabine, zidovudine plus tenofovir. NRTI backbone could be switched or modified due to toxicity or intolerance
HIV-NAT, Thai Red Cross AIDS Research Centre, Bangkok
Bamrasnaradura Infectious Diseases Institute, Nonthaburi
Chiang Rai Regional Hospital, Chiang Rai
ChonBuri Hospital, Chon Buri
Khon Kaen University, Khon Kaen
Sanpathong Hospital, Sanpathong
BMA Medical College and Vajira Hospital, Bangkok
Ramathibodi Hospital, Bangkok
Taksin hospital, Bangkok
Khon Kaen Hospital, Khon Kaen
Collaborators (1)
Kirby Institute
OTHER_GOV
National Health Security Office, Thailand
OTHER
The HIV Netherlands Australia Thailand Research Collaboration
OTHER