52
Participants
Start Date
January 10, 2014
Primary Completion Date
June 19, 2016
Study Completion Date
June 19, 2016
Lopinavir/ritonavir
Participants received two 200 mg/50 mg tablets of lopinavir/ritonavir orally twice daily.
Emtricitabine/tenofovir disoproxil fumarate
Participants received one 200 mg/300 mg tablet of Emtricitabine/tenofovir disoproxil fumarate orally once daily.
Efavirenz
Participants received one 600 mg tablet of efavirenz orally once daily.
Nevirapine
If unable to take efavirenz, participants received on 200 mg tablet of nevirapine orally once daily.
Trimethoprim/sulfamethoxazole
Participants received one 160 mg/800 mg tablet of trimethoprim/sulfamethoxazole orally once daily.
Walter Reed Project - Kenya Med. Research Institute Kericho CRS (12501), Kericho
AMPATH at Moi Univ. Teaching Hosp. Eldoret CRS (12601), Eldoret
Kisumu Crs (31460), Kisumu
College of Med. JHU CRS (30301), Blantyre
Joint Clinical Research Centre (JCRC) (12401), Kampala
National Institute of Allergy and Infectious Diseases (NIAID)
NIH
Advancing Clinical Therapeutics Globally for HIV/AIDS and Other Infections
NETWORK