Randomized trial demonstrates continued HIV suppression with greater patient-reported satisfaction compared with oral therapy; however, a few participants developed resistance.
Oral bictegravir + emtricitabine + tenofovir alafenamide (TAF) is one of the most commonly prescribed initial therapies for HIV. Now, investigators report results of a manufacturer-sponsored open-label randomized trial comparing continuation of this oral regimen with switching to injectable cabotegravir + rilpivirine (dosed every 2 months).
Among 670 participants who were virologically suppressed on daily oral bictegravir + emtricitabine + TAF, 447 switched to injectable therapy and 223 continued their oral regimen. About 12 months later, only 1% of participants who switched to injectable therapy and 0.4% of those who continued oral therapy had HIV RNA levels >50 copies/mL. Three participants in the injectable group had (or developed) resist…
Reviewing Author
DisclosuresGrant/Research SupportNIH
Editorial BoardsUpToDate; ID Images (idimages.org); Infectious Diseases Society of America COVID-19 Treatment Guidelines; International Antiviral Society–USA (Guidelines Committee)
Leadership Positions in Professional SocietiesHIV Medicine Association; Infectious Diseases Society of America (Board of Directors)
DisclosuresGrant/Research SupportNIH
Editorial BoardsUpToDate; ID Images (idimages.org); Infectious Diseases Society of America COVID-19 Treatment Guidelines; International Antiviral Society–USA (Guidelines Committee)
Leadership Positions in Professional SocietiesHIV Medicine Association; Infectious Diseases Society of America (Board of Directors)