In an observational study, >95% of people with HIV treated with LA-CAB/RPV achieved virologic suppression regardless of viremia when starting therapy.
Long-acting cabotegravir/rilpivirine (LA-CAB/RPV) was approved by the FDA in 2021 for people with HIV (PWH) who attained virologic suppression on oral antiretroviral therapy (ART), but this strategy is not currently approved for PWH unable to achieve virologic suppression with oral ART. In an observational study of PWH who started LA-CAB/RPV, investigators in San Francisco assessed virologic suppression at 48 weeks among 241 persons without viremia at treatment initiation versus 129 with viremia (overall median age, 44; 80% cisgender men; 23% Black; 40% with housing instability; 46% with reported substance use).
Among those who started LA-CAB/RPV with viremia, median viral load was 45,600 copies/mL and half had CD4 counts <200 cells/mm3. Ind…
Reviewing Author
DisclosuresGrant/Research SupportNIH/National Institute of Allergy and Infectious Diseases; NIH/National Institute on Drug Abuse
Editorial BoardsJAIDS: Journal of Acquired Immune Deficiency Syndromes; Vaccines
Leadership Positions in Professional SocietiesInternational Antiviral Society–USA (Board of Directors); Infectious Diseases Society of America (Past President)
DisclosuresGrant/Research SupportNIH/National Institute of Allergy and Infectious Diseases; NIH/National Institute on Drug Abuse
Editorial BoardsJAIDS: Journal of Acquired Immune Deficiency Syndromes; Vaccines
Leadership Positions in Professional SocietiesInternational Antiviral Society–USA (Board of Directors); Infectious Diseases Society of America (Past President)