ZW Howe, S Norman, AF Lueken… - … : The Journal of …, 2021 - Wiley Online Library
Abstract Cabotegravir/rilpivirine (CAB/RPV) was recently approved by the US Food and Drug Administration (FDA) as the first complete parenteral antiretroviral (ART) regimen for …
L Fletcher, SAB Burrowes, GK Khan, L Sabin… - Harm Reduction …, 2023 - Springer
Introduction Adherence to daily oral antiretroviral therapy (ART) and regular clinic appointments can be challenging for individuals who experience adverse social …
A Mantsios, M Murray, TS Karver, W Davis… - BMC health services …, 2021 - Springer
Background Long-acting injectable antiretroviral therapy (LA ART) has been shown to be non-inferior to daily oral ART, with high patient satisfaction and preference to oral standard …
JG O'Shea, P Cholli, EL Heil, K Buchacz - AIDS, 2023 - journals.lww.com
People with HIV (PWH) can now enjoy longer, healthier lives due to safe and highly effective antiretroviral therapy (ART), and improved care and prevention strategies. New drug …
L Slama, R Porcher, F Linard, C Chakvetadze… - BMC infectious …, 2023 - Springer
Background The use of long acting injectable (LAA) antiretroviral drugs may be an alternative option for HIV treatment and prevention. Our study focused on patient …
Background Long-acting injectable cabotegravir plus rilpivirine (LAI CAB/RPV) has several potential benefits over daily oral formulations for HIV treatment, including the potential to …
Advancements in long-acting (LA) HIV treatment and cure research with analytical treatment interruptions (ATIs) have generated important scientific and implementation questions …
E Kokori, G Olatunji, IJ Ogieuhi, TC Olusakin… - Discover Public …, 2024 - Springer
Abstract Human Immunodeficiency Virus (HIV) and Acquired Immunodeficiency Syndrome (AIDS) represent a global public health challenge that has persisted for decades. While …
Long-acting injectable (LAI) antiretroviral therapy (ART) is a novel HIV treatment option for people with HIV. The first LAI ART regimen for HIV treatment received regulatory approval in …