Table 3.
Disposition | D/C/F/TAF (N = 109) |
---|---|
Completed | 97 (89) |
Discontinueda | 12 (11) |
Baseline resistance | 0 (0) |
Safety stopping rules | 3 (3) |
Adverse event | 1 (<1) |
Lost to follow-up | 4 (4) |
Protocol violation | 1 (<1) |
Withdrawal of consent | 1 (<1) |
Otherb | 2 (2) |
Data are presented as no. (%).
Abbreviations: D/C/F/TAF, darunavir/cobicistat/emtricitabine/tenofovir alafenamide.
aOf the 11 participants who prematurely discontinued treatment, retention in care assessment was completed for 7 (64%) participants; among these participants, 6 (86%) had a documented clinical visit within 90 days of discontinuing D/C/F/TAF. One participant withdrew consent and no follow-up effort was made, while 1 participant was lost to follow-up (the site attempted a follow-up that yielded no information [failed attempt]).
bOther reasons were participant incarceration and switch to another antiretroviral due to D/C/F/TAF food requirements.