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Effects of ketoconazole and carbamazepine on lapatinib pharmacokinetics in healthy subjects.

机译:酮康唑和卡马西平对健康受试者中拉帕替尼药代动力学的影响。

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AIMS: To characterize the impact of potent CYP3A4 inhibition and induction on lapatinib pharmacokinetics. METHODS: Two studies were conducted in healthy subjects. One study examined the effect of ketoconazole 200 mg b.i.d. for 7 days on a single 100-mg dose of lapatinib in 22 healthy subjects. The other study examined the effect of carbamazepine titrated up to 200 mg b.i.d. over 20 days on a single 250-mg dose of lapatinib in 24 healthy subjects. RESULTS: Ketoconazole altered lapatinib AUC, C(max) and half-life, with geometric mean [95% confidence interval (CI)] increases of 3.57-fold (3.07, 4.15), 2.14-fold (1.74, 2.64) and 1.66-fold (1.50, 1.84), respectively, but had no effect on absorption rate. Carbamazepine altered lapatinib AUC, C(max) and absorption rate, with geometric mean (95% CI) decreases of 72% (68, 77), 59% (49, 66) and 28% (4, 46), respectively, but had no effect on half-life. CONCLUSIONS: Systemic exposure to lapatinib was significantly altered by potent inhibition and induction of CYP3A4. Dose adjustments may be required when lapatinib is administered with orally administered drugs that potently alter the activity of this enzyme.
机译:目的:表征强效CYP3A4抑制和诱导对拉帕替尼药代动力学的影响。方法:在健康受试者中进行了两项研究。一项研究检查了200 mg b.i.d酮康唑的作用。在22位健康受试者中以单剂量100毫克拉帕替尼治疗7天。另一项研究检查了卡马西平滴定至200 mg b.i.d.在24位健康受试者中,以单剂量250毫克的拉帕替尼治疗20天以上。结果:酮康唑改变了拉帕替尼的AUC,C(max)和半衰期,几何平均数[95%置信区间(CI)]分别提高了3.57倍(3.07,4.15),2.14倍(1.74,2.64)和1.66。分别为1.50、1.84倍,但对吸收速率没有影响。卡马西平改变了拉帕替尼的AUC,C(最大)和吸收率,几何平均数(95%CI)分别降低了72%(68、77),59%(49、66)和28%(4、46),但是对半衰期没有影响。结论:强效抑制和诱导CYP3A4显着改变了拉帕替尼的全身暴露。当拉帕替尼与有效改变该酶活性的口服药物一起给药时,可能需要调整剂量。

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