Extended-Duration MK-8591-Eluting Implant as a Candidate for HIV Treatment and Prevention

Regimen adherence remains a major hurdle to the success of daily oral drug regimens for the treatment and prevention of human immunodeficiency virus (HIV) infection. Long-acting drug formulations requiring less-frequent dosing offer an opportunity to improve adherence and allow for more forgiving op...

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Veröffentlicht in:Antimicrobial agents and chemotherapy 2018-10, Vol.62 (10)
Hauptverfasser: Barrett, Stephanie E, Teller, Ryan S, Forster, Seth P, Li, Li, Mackey, Megan A, Skomski, Daniel, Yang, Zhen, Fillgrove, Kerry L, Doto, Gregory J, Wood, Sandra L, Lebron, Jose, Grobler, Jay A, Sanchez, Rosa I, Liu, Zhen, Lu, Bing, Niu, Tao, Sun, Li, Gindy, Marian E
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Sprache:eng
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Zusammenfassung:Regimen adherence remains a major hurdle to the success of daily oral drug regimens for the treatment and prevention of human immunodeficiency virus (HIV) infection. Long-acting drug formulations requiring less-frequent dosing offer an opportunity to improve adherence and allow for more forgiving options with regard to missed doses. The administration of long-acting formulations in a clinical setting enables health care providers to directly track adherence. MK-8591 (4'-ethynyl-2-fluoro-2'-deoxyadenosine [EFdA]) is an investigational nucleoside reverse transcriptase translocation inhibitor (NRTTI) drug candidate under investigation as part of a regimen for HIV treatment, with potential utility as a single agent for preexposure prophylaxis (PrEP). The active triphosphate of MK-8591 (MK-8591-TP) exhibits protracted intracellular persistence and, together with the potency of MK-8591, supports its consideration for extended-duration dosing. Toward this end, drug-eluting implant devices were designed to provide prolonged MK-8591 release and Implants, administered subcutaneously, were studied in rodents and nonhuman primates to establish MK-8591 pharmacokinetics and intracellular levels of MK-8591-TP. These data were evaluated against pharmacokinetic and pharmacodynamic models, as well as data generated in phase 1a (Ph1a) and Ph1b clinical studies with once-weekly oral administration of MK-8591. After a single administration in animals, MK-8591 implants achieved clinically relevant drug exposures and sustained drug release, with plasma levels maintained for greater than 6 months that correspond to efficacious MK-8591-TP levels, resulting in a 1.6-log reduction in viral load. Additional studies of MK-8591 implants for HIV treatment and prevention are warranted.
ISSN:0066-4804
1098-6596
DOI:10.1128/AAC.01058-18