HealthDay News—Monotherapy with UB-421 antibody, which blocks the HIV virus-binding site on human CD4+ T-cells, maintains viral suppression for up to 16 weeks in HIV-infected persons undergoing analytic treatment interruption, according to a study published in the April 18 issue of the New England Journal of Medicine.

Chang-Yi Wang, PhD, from United Biomedical in Hauppauge, New York, and colleagues conducted a nonrandomized, open-label, phase 2 clinical study assessing the safety, pharmacokinetics, and antiviral activity of UB-421 monotherapy in HIV-infected persons undergoing analytic treatment interruption. At the screening visit, all participants had undetectable plasma viremia. After antiretroviral therapy (ART) discontinuation, they received 8 intravenous infusions of UB-421 at 10 mg/kg body weight/week (cohort 1; 14 participants) or 25 mg/kg body weight every 2 weeks (cohort 2; 15 participants).

The researchers found that during analytic treatment interruption, administration of UB-421 maintained virologic suppression in all participants (94.5% of measurements at study visits 2 through 9) during analytic treatment interruption. Intermittent viral blips were observed in eight participants (28 percent). None of the participants had plasma viral rebound to more than 400 copies/mL. Throughout the study, CD4+ T-cell counts remained stable. Rash was a common and transient adverse event, which resulted in one participant discontinuing the study drug.

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“Future studies are warranted to determine the longer-term safety and efficacy of UB-421 in HIV-infected persons,” the authors write.

Several authors disclosed financial ties to United Biomedical, United Biomedical Asia, and United BioPharma, all of which funded the study.

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