Single-dose and steady-state pharmacokinetics of clomipramine, yohimbine and clomipramine/yohimbine combination: A clinical drug-drug interaction study.

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
Amelie Leutzendorff, Valentin Al Jalali, Martin Bauer, Iris K Minichmayr, Birgit Reiter, Michael Wölfl- Duchek, Alina Nussbaumer-Pröll, Maria Weber, Sabine Eberl, Marie Spies, Maysa Sarhan, Johannes Geilen, Alexander Walther, Daniel Drai, Markus Zeitlinger
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Abstract

Aims: Clomipramine (CLOMI) has shown effectiveness in treating premature ejaculation but is linked to erectile dysfunction and reduced libido. Yohimbine (YOH), by contrast, is effective in treating erectile dysfunction and may improve libido. Combining CLOMI and YOH could potentially leverage the benefits of both drugs. This study aimed to investigate the interactions between these drugs and to evaluate their safety profile.

Methods: A prospective, open-labelled, single-centre, pharmacokinetic (PK) drug-drug interaction study was performed in 15 healthy male subjects. Single-dose and steady-state PK were investigated using noncompartmental analysis after mono- and combination therapy of the 2 orally applied drugs. Plasma sampling was performed at baseline, 0.5 (YOH), 1, 1.5 (YOH), 2, 3, 4, 5, 6, 8, 12 and 24 h (CLOMI). Differences in the area under the curve after multiple dosing (MD) were determined using an equivalence boundary of 80-125%.

Results: The geometric mean ratio of the area under the curve up to 12 h for MD CLOMI (combination vs. monotherapy) was 112% (90% confidence interval: 104-120%), whereas for MD YOH this ratio was 137% (90% confidence interval: 112-168%). The study drugs were safe and well tolerated as mono- and combination therapy, with no major adverse events reported.

Conclusion: A PK assessment of clomipramine and yohimbine indicated a clinically significant drug-drug interaction for MD YOH in combination with CLOMI. This might be explained by competitive, CLOMI-related inhibition of YOH metabolism, probably mediated by cytochrome P450 2D6. However, according to European Medicines Agency guidelines, the effect can be classified as interaction absent (<1,25 fold) or minor (>1.25-<2-fold). Given the complimentary mechanisms of action and the favourable safety profiles, the findings pave the way for future efficacy studies.

氯米帕明、育亨宾和氯米帕明/育亨宾复方制剂的单剂量和稳态药代动力学:临床药物相互作用研究。
目的:氯米帕明(CLOMI)对治疗早泄有效,但与勃起功能障碍和性欲减退有关。相比之下,育亨宾(YOH)对治疗勃起功能障碍有效,并可提高性欲。联合使用CLOMI和YOH有可能发挥两种药物的优势。本研究旨在调查这两种药物之间的相互作用,并评估其安全性:方法:在15名健康男性受试者中开展了一项前瞻性、开放标签、单中心、药代动力学(PK)药物相互作用研究。在对两种口服药物进行单药和联合用药治疗后,采用非室分析法对单药和稳态 PK 进行了研究。分别在基线、0.5 小时(YOH)、1 小时、1.5 小时(YOH)、2 小时、3 小时、4 小时、5 小时、6 小时、8 小时、12 小时和 24 小时(CLOMI)进行血浆采样。采用 80-125% 的等效边界确定多次给药后曲线下面积 (MD) 的差异:结果:MD CLOMI(联合疗法与单一疗法)12小时内曲线下面积的几何平均比值为112%(90%置信区间:104-120%),而MD YOH的这一比值为137%(90%置信区间:112-168%)。研究药物作为单一疗法和联合疗法均安全且耐受性良好,无重大不良反应报告:氯米帕明和育亨宾的 PK 评估表明,MD YOH 与 CLOMI 联用会产生临床上显著的药物相互作用。这可能是由于CLOMI对YOH代谢的竞争性抑制,可能由细胞色素P450 2D6介导。不过,根据欧洲药品管理局的指导方针,这种效应可归类为不存在相互作用(1.25- 1.25-1.25)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
7.20
自引率
4.30%
发文量
567
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