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克拉霉素与茚地那韦同时给药不会改变茚地那韦的稳态处置。

The steady-state disposition of indinavir is not altered by the concomitant administration of clarithromycin.

作者信息

Boruchoff S E, Sturgill M G, Grasing K W, Seibold J R, McCrea J, Winchell G A, Kusma S E, Deutsch P J

机构信息

Department of Medicine, University of Medicine and Dentistry of New Jersey-Robert Wood Johnson Medical School, Piscataway, NJ, USA.

出版信息

Clin Pharmacol Ther. 2000 Apr;67(4):351-9. doi: 10.1067/mcp.2000.105151.

Abstract

STUDY OBJECTIVES

To evaluate the safety and potential pharmacokinetic interaction between indinavir and clarithromycin.

STUDY METHODS

In a randomized, three-period, crossover fashion, 12 healthy adults received the following for 1 week: 800 mg oral indinavir sulfate every 8 hours with placebo, 500 mg oral clarithromycin every 12 hours with placebo, and indinavir sulfate with clarithromycin. Plasma indinavir, clarithromycin, and 14-hydroxyclarithromycin concentrations were determined after the last dose in each treatment period.

RESULTS

Administration of indinavir sulfate with clarithromycin caused a statistically significant increase in four pharmacokinetic parameters: a 58% increase in plasma indinavir concentrations at 8 hours (P = .029), a 47% increase in values for clarithromycin area under the plasma concentration versus time curve from time zero to the last measured concentration [AUC(0-12h); P = .0002], and 49% and 48% decreases in 14-hydroxyclarithromycin AUC(0-12h) and maximum plasma concentration (Cmax) values, respectively (P = .0001 and P = .0001). These effects are not considered to be clinically significant in view of the insignificant effects on the values for indinavir area under the plasma concentration versus time curve from time zero to the last measured concentration [AUC(0-8h)] and Cmax, as well as the safety profile of clarithromycin.

CONCLUSIONS

The combination of indinavir sulfate and clarithromycin is generally well tolerated and can be coadministered without dose adjustment.

摘要

研究目的

评估茚地那韦与克拉霉素之间的安全性及潜在的药代动力学相互作用。

研究方法

12名健康成年人采用随机、三周期、交叉方式,接受以下治疗1周:每8小时口服800mg硫酸茚地那韦加安慰剂;每12小时口服500mg克拉霉素加安慰剂;硫酸茚地那韦与克拉霉素联用。在每个治疗周期的最后一剂给药后,测定血浆中茚地那韦、克拉霉素及14-羟基克拉霉素的浓度。

结果

硫酸茚地那韦与克拉霉素联用时,四个药代动力学参数出现具有统计学意义的增加:8小时时血浆茚地那韦浓度增加58%(P = 0.029);从时间零点至最后一次测量浓度的血浆浓度-时间曲线下克拉霉素的面积值[AUC(0 - 12h)]增加47%(P = 0.0002);14-羟基克拉霉素的AUC(0 - 12h)和最大血浆浓度(Cmax)值分别降低49%和48%(P = 0.0001和P = 0.0001)。鉴于对从时间零点至最后一次测量浓度的血浆浓度-时间曲线下茚地那韦的面积值[AUC(0 - 8h)]和Cmax值无显著影响,以及克拉霉素的安全性,这些影响不被认为具有临床意义。

结论

硫酸茚地那韦与克拉霉素联用通常耐受性良好,无需调整剂量即可联合使用。

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