SCYNEXIS, Inc., Jersey City, NJ, USA.
Riverside Consulting, Wilmington, DE, USA.
Clin Pharmacol Drug Dev. 2019 Jan;8(1):60-69. doi: 10.1002/cpdd.588. Epub 2018 Jun 27.
SCY-078 is an orally bioavailable triterpenoid glucan synthase inhibitor in clinical development as an intravenous and oral treatment of fungal infections caused by Candida and Aspergillus species. This was a sequential, single-center, open-label phase 1 study to assess the drug-drug interaction potential between SCY-078 and tacrolimus during concomitant administration in healthy subjects. In cohort 1, period 1, subjects received a single oral dose of tacrolimus 2 mg in the fasted state. In period 2 after a ≥15 day washout, subjects received a single loading dose of SCY-078 1250 mg on day 1 followed by maintenance doses of SCY-780 750 mg on days 2 through 8. On day 3 of period 2, subjects also received a single dose of tacrolimus 2 mg concurrent with SCY-078. In cohort 2, subjects received a loading dose of SCY-078 1250 mg on day 1 followed by maintenance doses of SCY-780 750 mg on days 2 and 3. Pharmacokinetic (PK) parameters were compared to assess both the impact of steady-state SCY-078 on tacrolimus and the impact of tacrolimus on the PK of steady-state SCY-078. The concurrent coadministration of tacrolimus and SCY-078 had no effect on the maximum blood levels of tacrolimus, as evidenced by no change in maximum concentration of drug in blood plasma and a 1.4-fold increase in total area under the plasma drug concentration-time curve. The concurrent coadministration of tacrolimus and SCY-078 resulted in a weaker interaction than typically observed with the azole class of antifungals. The current data indicate that an initial dose adjustment for tacrolimus may not be warranted when combined with SCY-078, as the modest increase in exposure is less than the therapeutic window, although tacrolimus monitoring, as with addition of any new medication, is recommended. These results support the coadministration of SCY-078 and tacrolimus.
SCY-078 是一种在研的可口服生物利用三萜类葡聚糖合酶抑制剂,可作为静脉注射和口服制剂,用于治疗念珠菌和曲霉菌引起的真菌感染。这是一项序贯、单中心、开放性的 1 期研究,旨在评估健康受试者中同时使用时 SCY-078 与他克莫司的药物相互作用潜力。在队列 1 的第 1 期,受试者空腹单次口服他克莫司 2mg。在第 1 期的第 2 期洗脱期≥15 天后,第 1 天给予 SCY-078 单剂量负荷 1250mg,随后第 2 至 8 天给予 SCY-780 维持剂量 750mg。第 2 期第 2 天,受试者还同时给予单剂量他克莫司 2mg。在队列 2 中,受试者第 1 天给予 SCY-078 负荷剂量 1250mg,随后第 2 和第 3 天给予 SCY-780 维持剂量 750mg。比较药代动力学(PK)参数,以评估稳态 SCY-078 对他克莫司的影响以及他克莫司对稳态 SCY-078 PK 的影响。同时给予他克莫司和 SCY-078 对他克莫司的最大血药水平没有影响,这表现在血浆中药物最大浓度没有变化,药物总浓度-时间曲线下面积增加了 1.4 倍。同时给予他克莫司和 SCY-078 的相互作用比通常观察到的唑类抗真菌药物的相互作用弱。目前的数据表明,当与 SCY-078 联合使用时,他克莫司可能不需要进行初始剂量调整,因为暴露的适度增加小于治疗窗,尽管与添加任何新药物一样,建议进行他克莫司监测。这些结果支持 SCY-078 和他克莫司的联合用药。