24 February 2021 - ViiV Healthcare announced today the submission of a supplemental new drug application to the US FDA for the expanded use of Cabenuva (cabotegravir, rilpivirine).
The supplemental new drug application seeks to expand Cabenuva’s label to include every 2 month dosing for the treatment of HIV-1 infection in virologically suppressed adults (HIV-1 RNA less than 50 copies/mL) on a stable regimen, with no history of treatment failure, and with no known or suspected resistance to either cabotegravir or rilpivirine.