Table 1.
Parent study |
Study week |
ART regimen |
Last missed Doses During study |
Genital HIV RNA (copies/ml) |
Plasma HIV RNA* (copies/ml) |
CMV DNA (copies/ml) |
HSV DNA (copies/ml) |
Gonorrhea RNA |
Chlamydia RNA |
---|---|---|---|---|---|---|---|---|---|
ASPIRE #1 | 48 | RPV/TDF/FTC | 1–2 weeks | 42 | 179 | Not detected | Not detected | Not detected | Not detected |
ASPIRE #2** |
36 | DTG+3TC | > 3 months | 488 | <20 | 314607 | Not detected | Not detected | Not detected |
48 | DTG+3TC | Never | 79 | 31 | 86090 | Not detected | Not detected | Not detected | |
A5353 | 24 | DTG+3TC | Never | 48 | <40 | NA*** | NA*** | Not detected | Not detected |
Legend: RPV: Rilpivirine, TDF: Tenofovir, FTC: Emtricitabine, DTG: Dolutegravir, 3TC: Lamivudine. NA: Not Available.
Plasma HIV RNA collected at the same time as genital HIV RNA shedding
ASPIRE participant #2 had detectable HIV RNA at two consecutive time-points (weeks 36 and 48)
Genital HSV and CMV testing could not be completed in one participant with HIV genital shedding because there was not enough seminal plasma to perform this analysis.