Feng Hwa-Ping, Caro Luzelena, Fandozzi Christine M, Guo Zifang, Talaty Jennifer, Wolford Dennis, Panebianco Deborah, Iwamoto Marian, Butterton Joan R, Yeh Wendy W
Merck & Co., Inc., Kenilworth, NJ, USA.
J Clin Pharmacol. 2018 May;58(5):666-673. doi: 10.1002/jcph.1052. Epub 2018 Jan 12.
Elbasvir (EBR)/grazoprevir (GZR) may be coadministered with immunosuppressant drugs in posttransplant people who are infected with hepatitis C virus. The aim of the present study was to assess the safety and pharmacokinetic interactions between EBR and GZR and single doses of cyclosporine, tacrolimus, mycophenolate mofetil (MMF), and prednisone. This was a 4-part, open-label study in 58 healthy volunteers. Participants received single doses of cyclosporine 400 mg, tacrolimus 2 mg, MMF 1 g, or prednisone 40 mg alone or in the presence of once-daily EBR 50 mg/GZR 200 mg. Multiple oral doses of EBR + GZR had no significant effect on cyclosporine. However, in the presence of cyclosporine, the 24-hour area under the concentration-time curve of GZR was increased by approximately 15-fold (geometric mean ratio [90%CI] 15.21 [12.83; 18.04]); the concentration of EBR was increased approximately 2-fold in the presence of cyclosporine. Coadministration of EBR/GZR and tacrolimus did not affect the pharmacokinetics of EBR or GZR, but resulted in an increase in tacrolimus AUC (geometric mean ratio [90%CI] 1.43 [1.24; 1.64]). There were no clinically relevant interactions between EBR/GZR and either MMF or prednisone. Data from the present study indicate that EBR/GZR may be coadministered in people receiving tacrolimus, MMF, and prednisolone. EBR/GZR is contraindicated in people receiving cyclosporine because the significantly higher concentrations of GZR may increase the risk of transaminase elevations.
艾尔巴韦(EBR)/格拉瑞韦(GZR)可与丙型肝炎病毒感染的移植后患者的免疫抑制剂联合使用。本研究的目的是评估EBR和GZR与单剂量环孢素、他克莫司、吗替麦考酚酯(MMF)和泼尼松之间的安全性和药代动力学相互作用。这是一项针对58名健康志愿者的4部分开放标签研究。参与者单独或在每日一次的EBR 50 mg/GZR 200 mg存在的情况下接受单剂量的环孢素400 mg、他克莫司2 mg、MMF 1 g或泼尼松40 mg。多次口服EBR + GZR对环孢素无显著影响。然而,在环孢素存在的情况下,GZR浓度-时间曲线下的24小时面积增加了约15倍(几何平均比值[90%CI] 15.21 [12.83; 18.04]);在环孢素存在的情况下,EBR的浓度增加了约2倍。EBR/GZR与他克莫司联合使用不影响EBR或GZR的药代动力学,但导致他克莫司AUC增加(几何平均比值[90%CI] 1.43 [1.24; 1.64])。EBR/GZR与MMF或泼尼松之间均无临床相关相互作用。本研究数据表明,EBR/GZR可与接受他克莫司、MMF和泼尼松龙的患者联合使用。接受环孢素的患者禁用EBR/GZR,因为GZR浓度显著升高可能会增加转氨酶升高的风险。