Encouraging results in the Nucleosides and Darunavir/Dolutegravir in Africa (NADIA) trial extend to 96 weeks.
In the NADIA (Nucleosides and Darunavir/Dolutegravir in Africa) trial, conducted in three sub-Saharan African countries, individuals who had virologic failure on a nonnucleoside reverse-transcriptase inhibitor (NNRTI)–based regimen were randomized to receive dolutegravir or ritonavir-boosted darunavir in combination with either tenofovir/lamivudine or zidovudine/lamivudine. The investigators previously reported on the proportion of patients with HIV-1 RNA <400 copies/mL at 48 weeks (the primary outcome; NEJM JW Infect Dis Sep 2021 and N Engl J Med 2021; 385:330). Now, they report the proportion of patients with such virologic suppression at 96 weeks.
Among 484 participants, rates of virologic suppression were:
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)