Muirhead G J, Harness J, Holt P R, Oliver S, Anziano R J
Department of Clinical Research, Pfizer Central Research, Sandwich, Kent, UK.
Br J Clin Pharmacol. 2000;49 Suppl 1(Suppl 1):49S-56S. doi: 10.1046/j.1365-2125.2000.00153.x.
To determine whether multiple doses of ziprasidone alter the steady-state pharmacokinetics of the component steroids, ethinyloestradiol and levonorgestrel, of an oral contraceptive; to evaluate the tolerability of a co-administered combined oral contraceptive and ziprasidone; and to compare plasma concentrations of prolactin in subjects taking a combined oral contraceptive with placebo or ziprasidone.
Nineteen women taking a combined oral contraceptive (ethinyloestradiol 30 microg day(-1) and levonorgestrel 150 microg day(-1)) were enrolled into a double-blind, placebo-controlled, two-way crossover study. They received ziprasidone 40 mg day- 1 in two divided daily doses or placebo for 8 days (days 8-15) in one of two 21 day treatment periods separated by a 7 day washout period. Venous blood samples were collected immediately before and up to 24 h after the morning dose of oral contraceptive and ziprasidone or placebo on day 15 of each 21 day treatment period. These were assayed for ethinyloestradiol and levonorgestrel and the resulting data used to derive pharmacokinetic data for these steroids. Additional samples were collected immediately before and 4 h after the morning dose of oral contraceptive and ziprasidone or placebo on day 15 of each 21 day treatment period for prolactin assay. All observed and volunteered adverse events were recorded throughout the study.
The mean AUC(0,24 h), Cmax and tmax for ethinyloestradiol and the mean AUC(0, 24 h) and Cmax for levonorgestrel during ziprasidone co-administration were not statistically significantly different from corresponding values occurring during placebo co-administration. The tmax for levonorgestrel was approximately 0.5 h longer. Concomitant therapy with a combined oral contraceptive and ziprasidone did not result in adverse events not previously seen with either preparation alone.
The findings of this study suggest that, based on pharmacokinetic and tolerability data, ziprasidone may be co-administered with ethinyloestradiol and levonorgestrel without loss of contraceptive efficacy or increased risk of adverse events.
确定多次服用齐拉西酮是否会改变口服避孕药中雌激素炔雌醇和孕激素左炔诺孕酮的稳态药代动力学;评估联合服用复方口服避孕药和齐拉西酮的耐受性;并比较服用复方口服避孕药的受试者与服用安慰剂或齐拉西酮的受试者的催乳素血浆浓度。
19名服用复方口服避孕药(炔雌醇30μg/天和左炔诺孕酮150μg/天)的女性被纳入一项双盲、安慰剂对照、双向交叉研究。在两个21天治疗期之一中,她们接受齐拉西酮40mg/天,分两次服用,或服用安慰剂,共8天(第8 - 15天),两个治疗期之间有7天的洗脱期。在每个21天治疗期的第15天,于早晨服用口服避孕药和齐拉西酮或安慰剂之前及之后长达24小时采集静脉血样。对这些血样进行炔雌醇和左炔诺孕酮检测,并将所得数据用于推导这些甾体激素的药代动力学数据。在每个21天治疗期的第15天,于早晨服用口服避孕药和齐拉西酮或安慰剂之前及之后4小时额外采集血样用于催乳素检测。在整个研究过程中记录所有观察到的和受试者自发报告的不良事件。
在合用齐拉西酮期间,炔雌醇的平均AUC(0,24 h)、Cmax和tmax以及左炔诺孕酮的平均AUC(0,24 h)和Cmax与合用安慰剂期间的相应值相比,差异无统计学意义。左炔诺孕酮的tmax约长0.5小时。复方口服避孕药与齐拉西酮联合治疗未导致单独使用任何一种制剂时未曾出现的不良事件。
本研究结果表明,基于药代动力学和耐受性数据,齐拉西酮可与炔雌醇和左炔诺孕酮联合使用,而不会降低避孕效果或增加不良事件风险。