Cabotegravir: a novel HIV integrase inhibitor combined with rilpivirine as the first long-acting injectable program for the treatment of HIV infection

被引:1
|
作者
Zeuli, John D. [1 ,2 ,4 ]
Rivera, Christina G. [1 ,2 ]
Smith, Bradley L. [3 ]
Otto, Ashley [2 ]
Temesgen, Zelalem [1 ]
机构
[1] Mayo Clin, HIV Program, Div Infect Dis, Rochester, MN USA
[2] Mayo Clin, Dept Pharm, Rochester, MN USA
[3] Grady Hlth Syst, Dept Pharm, Atlanta, GA USA
[4] Mayo Clin, Dept Pharm, 200 First St SW, Rochester, MN 55905 USA
关键词
Cabotegravir; Rilpivirine; HIV integrase; inhibitors; - Anti-HIV drugs; Treatment of HIV infection; STRAND TRANSFER; ANTIVIRAL ACTIVITY; PLUS RILPIVIRINE; NAIVE ADULTS; PHASE; 2B; PHARMACOKINETICS; GSK1265744; RESISTANCE; RALTEGRAVIR; PREVENTION;
D O I
10.1358/dot.2022.58.12.3448340
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Cabotegravir, a novel HIV integrase inhibitor, shares structural similarity with dolutegravir and bictegravir. Its oral half-life is 32 hours, but cabotegravir nanosus-pension for intramuscular injection yields half-lives ranging from 25 to54 days, enabling extended interval dosing. Drug interactions are minimal, although oral doses require spacing from polyvalent cations, and potent uridine glucuronosyltransferase induction (e.g., rifampin, carbamazepine) requires avoidance due to anticipated subtherapeutic cabotegravir exposure thro-ugh extended intervals. Randomized clinical trials combined cabotegravir treatment with rilpivirine to demonstrate treatment efficacy in patients living with HIV who had attained virologic suppression, lacked known/suspected mutations to either component, and had not experienced prior HIV treatment failure. Together, oral cabotegravir and rilpivirine maintained viral suppression in the LATTE study while the combi-nation, given intramuscularly, performed compara-bly to conventional oral therapy in LATTE-2. FLAIR and ATLAS, respectively, demonstrated HIV suppression maintenance for monthly injections in treatment-naive participants and treatment-experienced patients, with ATLAS-2M supporting the efficacy of injections given every 2 months. Investigations to date show an excellent safety profile. Injectable cabotegravir causes short-lived, mild injection site reactions (primarily adminis-tration site pain/soreness) that decrease in frequency over time, produce attributable discontinuation rates <= 2%, and generate satisfaction scores that favor inject-able therapy over oral therapy. Virologic failure with resistance development is rare, primarily occurs in the first year of therapy, and is associated with baseline proviral DNA mutations to coadministered rilpivir-ine. A key component of the first U.S. Food and Drug Administration (FDA)-approved injectable mainte-nance treatment program for HIV, injectable cabote-gravir heralds a new era in HIV treatment innovation. Here we provide a detailed review of the clinical phar-macology, administration and available formulations of the novel HIV integrase inhibitor cabotegravir with in-depth analysis of the clinical trial data, safety, sat-isfaction and viral resistance development when com-bined with rilpivirine as the first long-acting injectable program for the treatment of HIV infection.
引用
收藏
页码:555 / 576
页数:22
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