• Phase IIb EMBRACE study demonstrates N6LS (VH109), administered every four months with monthly cabotegravir, successfully maintained viral suppression in 96% of participants receiving intravenous treatment.
• The broadly neutralizing antibody was generally well-tolerated, with subcutaneous administration showing more infusion site reactions (14%) compared to intravenous delivery, which reported no such reactions.
• Based on favorable results, ViiV Healthcare is advancing development of a six-month IV formulation of N6LS combined with cabotegravir long-acting for evaluation in the next phase of the EMBRACE trial.