Fixed-Dose Combination of Bictegravir/Emtricitabine/Tenofovir Alafenamide Taken as 5 Days Per Week

This protocol describes an open-label, single-center study to evaluate the safety and efficacy of 5/7 intermittent therapy versus 7/7 continuous therapy of coformulated BIC/FTC/TAF FDC in PLWH who are virologically suppressed. The study is comprised of two periods as shown in Figure 1. The first period is an observational 2-week run-in period during which participants who meet the screening criteria will receive daily oral dose of BIC/FTC/TAF. The second study period is a 48-week treatment period (defined as the time the first dose of study drug is administered on Day 1 after randomization through completion of Week 48 assessments) which will evaluate the PK, efficacy, and safety of 5 consecutive days on treatment (typically Monday through Friday) followed by 2 days off treatment (five-on, two-off or 5/7 treatment schedule) regimen compared to continuous therapy (or 7/7) regimen in virologically suppressed HIV-1-infected patients. The study will include Screening of up to 30 days to determine eligibility of participants and to complete disease-related assessments. A self-reported adherence diary will be given to all participants to record whether they take ART during the study period. If the participants in the 5/7 regimen group miss doses during the 5-on days, the missed doses could be taken during the 2-off days to complete the 5 doses a week. Participants will provide written informed consent and visit the study site to complete the screening assessment during the screening period. If the participants are women, contraception is required during study period.

Following successful screening, the 2-week run-in period will commence, during which participants will receive daily coformulated BIC/FTC/TAF dose and only participants with 100% compliance will be eligible to be enrolled in 52-week treatment period. Upon confirmation of eligibility, participants will be randomized in a 1:1 ratio to received 5 days on and 2 days off regimen (5/7 regimen) or continuous therapy (7/7 regimen). Approximately 60 subjects are planned to be randomized. Participants excluded before randomization will be replaced at Screening. After randomization (baseline +/- 1 week), participants will return to the study site at week 4 (+/- 2 weeks) and subsequently every 12 weeks (+/- 3 months) until Week 52 (+/- 1 month) (Table 1). To assess the drug compliance of the study subjects, it is required for them to fill in the paper or online electronic diary cards. Pharmacological study (PK), efficacy and safety assessment will be conducted at Weeks 4, 28 and 52; and QoL will be assessed at baseline and 52 by the electronic form of SF-36v2. The primary endpoint will be assessed at Weeks 4, 28 and 52. Once subjects completed 52-week treatment period, subjects will return to the study site for safety follow-up visit 30 days +/- 3 days after the last dose. If PLWH on 5/7 regimen had virological failure (>1,000 copies/mL) at week 4, 28, or 52, they would be withdrawn from the study. Their HIV isolates would be sent for resistant testing. They would start daily regimen, and their PVL would be checked every 3 months until their PVL return to be suppressed (<200 copies/mL). After Week 52, the participants in continuous therapy (or 7/7) regimen will be invited to change to 5 consecutive days on treatment (typically Monday through Friday) followed by 2 days off treatment (five-on, two-off or 5/7 treatment schedule) regimen. All participants will be followed for 2 years after the enrollment.