Merck & Co., Inc., Kenilworth, New Jersey, USA.
Celerion, Tempe, Arizona, USA.
Clin Pharmacol Drug Dev. 2021 Feb;10(2):198-206. doi: 10.1002/cpdd.852. Epub 2020 Jul 22.
Letermovir is a prophylactic agent for cytomegalovirus infection and disease in adult cytomegalovirus-seropositive recipients of allogeneic hematopoietic stem cell transplant. As the antifungal agent fluconazole is administered frequently in transplant recipients, a drug-drug interaction study was conducted between oral letermovir and oral fluconazole. A phase 1 open-label, fixed-sequence study was performed in healthy females (N = 14, 19-55 years). In Period 1, a single dose of fluconazole 400 mg was administered. Following a 14-day washout, a single dose of letermovir 480 mg was administered (Period 2), and after a 7-day washout, single doses of fluconazole 400 mg and letermovir 480 mg were coadministered in Period 3. Pharmacokinetics and safety were evaluated. The pharmacokinetics of fluconazole and letermovir were not meaningfully changed following coadministration. Fluconazole geometric mean ratio (GMR; 90% confidence interval [CI]) with letermovir for area under the concentration-versus-time curve from time 0 to infinity (AUC ) was 1.03 (0.99-1.08); maximum concentration (C ) was 0.95 (0.92-0.99). Letermovir AUC GMR (90%CI) was 1.11 (1.01-1.23), and C was 1.06 (0.93-1.21) following coadministration with fluconazole. Coadministration of fluconazole and letermovir was generally well tolerated.
乐特韦是一种预防巨细胞病毒感染和疾病的药物,用于接受异基因造血干细胞移植的巨细胞病毒血清阳性成人受者。由于抗真菌药物氟康唑在移植受者中经常使用,因此进行了口服乐特韦和口服氟康唑之间的药物相互作用研究。在健康女性中进行了一项 1 期开放标签、固定序列研究(N=14,19-55 岁)。在第 1 期,给予单剂量氟康唑 400mg。洗脱期 14 天后,给予单剂量乐特韦 480mg(第 2 期),洗脱期 7 天后,在第 3 期同时给予单剂量氟康唑 400mg 和乐特韦 480mg。评估药代动力学和安全性。氟康唑和乐特韦的药代动力学在联合用药后没有明显改变。氟康唑与乐特韦的几何均数比值(GMR;90%置信区间[CI])的 AUC 从 0 到无穷大(AUC)为 1.03(0.99-1.08);C 最大值为 0.95(0.92-0.99)。乐特韦与氟康唑联合使用时,AUC 的 GMR(90%CI)为 1.11(1.01-1.23),C 为 1.06(0.93-1.21)。氟康唑和乐特韦联合使用通常具有良好的耐受性。