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. 2019 Dec 27;71(12):3110–3117. doi: 10.1093/cid/ciz1213

Table 3.

Participant Disposition Through Week 48

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.