Pharmaceutical Sciences, Merck & Co., Inc., West Point, Pennsylvania, USA
Pharmaceutical Sciences, Merck & Co., Inc., West Point, Pennsylvania, USA.
Antimicrob Agents Chemother. 2018 Sep 24;62(10). doi: 10.1128/AAC.01058-18. Print 2018 Oct.
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.
方案依从性仍然是每日口服药物治疗和预防人类免疫缺陷病毒(HIV)感染方案成功的主要障碍。需要较少频繁给药的长效药物制剂提供了改善依从性的机会,并允许在错过剂量时有更宽容的选择。在临床环境中给予长效制剂使医疗保健提供者能够直接跟踪依从性。MK-8591(4'-乙炔基-2-氟-2'-脱氧腺苷[EFdA])是一种正在研究的核苷逆转录酶易位抑制剂(NRTTI)候选药物,作为 HIV 治疗方案的一部分进行研究,具有作为暴露前预防(PrEP)单一药物的潜在用途。MK-8591 的活性三磷酸酯(MK-8591-TP)表现出延长的细胞内持久性,并且与 MK-8591 的效力一起支持其考虑用于延长给药时间。为此,设计了载药植入装置以提供延长的 MK-8591 释放,并在啮齿动物和非人灵长类动物中研究了皮下给予的植入物,以建立 MK-8591 的药代动力学和细胞内 MK-8591-TP 水平。这些数据与药代动力学和药效动力学模型以及在 Ph1a 和 Ph1b 临床研究中每周口服一次给予 MK-8591 生成的数据进行了评估。在动物单次给药后,MK-8591 植入物达到了临床相关的药物暴露和持续的药物释放,血浆水平维持超过 6 个月,与有效的 MK-8591-TP 水平相对应,导致病毒载量降低 1.6 对数。需要进一步研究 MK-8591 植入物用于 HIV 治疗和预防。