AbbVie Inc, North Chicago, IL, USA.
Clin Pharmacol Drug Dev. 2016 Jul;5(4):269-77. doi: 10.1002/cpdd.246. Epub 2016 Jan 24.
Paritaprevir (administered with low-dose ritonavir), ombitasvir, and dasabuvir are direct-acting antiviral agents administered as combination regimens for the treatment of chronic hepatitis C virus infection. Drug-drug interactions between 2D (ombitasvir/paritaprevir/ritonavir) or 3D (ombitasvir/paritaprevir/ritonavir and dasabuvir) regimens and omeprazole, a CYP2C19 substrate and acid-reducing agent, were evaluated in 24 healthy volunteers. Subjects received omeprazole (40 mg once daily) on day 1 and days 20-24 and the 2D or 3D regimen (ombitasvir/paritaprevir/ritonavir 25/150/100 mg once daily ± dasabuvir 250 mg twice daily) on days 6-24. Compared with omeprazole alone, coadministration with the 2D or 3D regimen decreased omeprazole geometric mean Cmax and AUCt values by 40% to 50%. Ombitasvir, dasabuvir, and ritonavir mean exposures showed <10% change, and paritaprevir mean exposures showed <20% change when the 2D or 3D regimen was administered with omeprazole compared with administration without omeprazole. Although no a priori dose adjustment is needed, a higher omeprazole dose should be considered if clinically indicated when coadministered with the 2D or 3D regimen. No dose adjustment is required for the 2D or 3D regimen when administered with omeprazole, other acid-reducing agents, or CYP2C19 inhibitors.
帕利瑞韦(与低剂量利托那韦合用)、奥比他韦、达塞布韦均为直接作用抗病毒药物,联合用于治疗慢性丙型肝炎病毒感染。在 24 名健康志愿者中评估了 2D(奥比他韦/帕利瑞韦/利托那韦)或 3D(奥比他韦/帕利瑞韦/利托那韦和达塞布韦)方案与奥美拉唑(一种 CYP2C19 底物和抑酸剂)之间的药物相互作用。受试者在第 1 天和第 20-24 天服用奥美拉唑(40mg 每日 1 次),在第 6-24 天服用 2D 或 3D 方案(奥比他韦/帕利瑞韦/利托那韦 25/150/100mg 每日 1 次±达塞布韦 250mg 每日 2 次)。与单独使用奥美拉唑相比,与 2D 或 3D 方案合用使奥美拉唑的几何均数 Cmax 和 AUCt 值降低 40%至 50%。与不使用奥美拉唑相比,当与奥美拉唑合用 2D 或 3D 方案时,奥比他韦、达塞布韦和利托那韦的平均暴露量变化<10%,帕利瑞韦的平均暴露量变化<20%。当与奥美拉唑、其他抑酸剂或 CYP2C19 抑制剂合用时,2D 或 3D 方案无需调整剂量。