Long-acting injectable antiretroviral therapy: will it change the future of HIV treatment?

被引:7
|
作者
Brizzi, Marisa [1 ]
Perez, Sarah E. [2 ]
Michienzi, Sarah M. [3 ,4 ]
Badowski, Melissa E. [3 ,4 ]
机构
[1] Univ Cincinnati Hlth, Cincinnati, OH USA
[2] Cook Cty Hlth, Ruth M Rothstein CORE Ctr, Chicago, IL USA
[3] Univ Illinois, Coll Pharm, Dept Pharm Practice, Chicago, IL 60607 USA
[4] Univ Illinois, Coll Pharm, Infect Dis Pharmacotherapy Sect, Chicago, IL 60607 USA
关键词
antiretroviral therapy; cabotegravir; HIV; injections; intramuscular; rilpivirine; PHASE; 2B; CABOTEGRAVIR; RILPIVIRINE; ADULTS;
D O I
10.1177/20499361221149773
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
The treatment of human immunodeficiency virus (HIV) has greatly advanced over the past few decades from complex regimens, with high toxicities, multiple daily dosing, and incomplete viral suppression to more simplified, highly effective, daily oral regimens. Although these advancements greatly improved access and tolerability, the need for daily antiretroviral (ARV) administration remained until recently. With long-acting (LA) injectable ARV options emerging, patients may choose how they want to receive treatment. By eliminating the barrier of daily medication adherence, LA injectable ARV formulations have the potential to not only improve health outcomes for the individual, but also the community by reducing HIV transmission. At the time of this writing cabotegravir/rilpivirine (LA-CAB/RPV) is the only LA injectable ARV regimen approved as a complete regimen for the treatment of HIV in adults and adolescents (> 35 kg and > 12 years of age) who are virologically suppressed. However, additional studies of LA-CAB/RPV in expanded populations, and of other LA ARVs, are underway. The goal of this article was to summarize clinical data and review pertinent clinical considerations for the use of LA-CAB/RPV in the management of HIV.
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页数:15
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