Table 1.
Trial name | Study site | Intervention | Study population | Protection |
---|---|---|---|---|
iPrEx | North and South America, Thailand, South Africa | daily oral TDF-FTCa | 2499 HIV sero-negative men or transgender women who have sex with men | 44% (15% – 63%) |
FEM-PrEP | Kenya, South Africa, Tanzania | daily oral TDF-FTC | 2120 HIV negative women | halted early for lack of efficacy |
PIP | Kenya and Uganda | daily oral TDF-FTC or TDFb | 4747 HIV-1 serodiscordant heterosexual couples | 67% (44% – 81%) TDF 75%(55%–87%) TDF-FTC |
TDF2 | Botswana | daily oral TDF-FTC | 1219 HIV sero-negative men and women | 62.2% (21.5% –83.4%) |
TDF-FTC: Tenofovir and Emtricitabine combination
TDF: Tenofovir disoproxilfumarate