Lenacapavir Reduces Viral Load in Multidrug-Resistant HIV-1 Infection

Reduction in viral load from baseline greater with lenacapavir versus placebo among those with multidrug-resistant HIV-1 infection

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THURSDAY, May 12, 2022 (HealthDay News) -- Patients with multidrug-resistant HIV-1 infection receiving the capsid inhibitor lenacapavir have a greater reduction in viral load than those receiving placebo, according to a study published in the May 12 issue of the New England Journal of Medicine.

Sorana Segal-Maurer, M.D., from NewYork/Presbyterian Queens in Flushing, and colleagues enrolled patients with multidrug-resistant HIV-1 infection in two cohorts, according to the change in the plasma HIV-1 RNA level between screening and cohort-selection visits in a phase 3 trial. In cohort 1, patients were first randomly assigned to receive oral lenacapavir or placebo for 14 days; the lenacapavir group then received subcutaneous lenacapavir once every six months, while the placebo group received oral lenacapavir followed by subcutaneous lenacapavir; both groups also received optimized background therapy. In cohort 2, all patients received open-label oral lenacapavir on days 1 through 14 with optimized background therapy, then received subcutaneous lenacapavir. Seventy-two patients were enrolled: 36 in each cohort.

The researchers observed a decrease of at least 0.5 log10 copies/mL in the viral load by day 15 in 88 and 17 percent of patients in the lenacapavir and placebo groups, respectively, in cohort 1. At week 26, 81 and 83 percent of patients in cohorts 1 and 2, respectively, reported a viral load of less than 50 copies/mL, with a least-squares mean increase of 75 and 104 cells/mm3 in the CD4+ count, respectively. There were no serious adverse events related to lenacapavir reported.

"Lenacapavir led to a significant decrease in viral load as functional monotherapy," the authors write.

The study was funded by Gilead Sciences, the manufacturer of lenacapavir.

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Physician’s Briefing Staff

Physician’s Briefing Staff

Published on May 12, 2022

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