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在健康受试者中,丙磺舒和西咪替丁与米罗加巴林联合给药:一项 I 期、随机、开放标签、药物相互作用研究。

Coadministration of probenecid and cimetidine with mirogabalin in healthy subjects: A phase 1, randomized, open-label, drug-drug interaction study.

机构信息

Clinical Pharmacology Department, Daiichi Sankyo Co., Ltd., Tokyo, Japan.

Drug Metabolism and Pharmacokinetics Research Laboratories, Daiichi Sankyo Co., Ltd., Tokyo, Japan.

出版信息

Br J Clin Pharmacol. 2018 Oct;84(10):2317-2324. doi: 10.1111/bcp.13674. Epub 2018 Aug 9.

Abstract

AIMS

The primary aim of this study was to assess the individual effects of probenecid and cimetidine on mirogabalin exposure.

METHODS

This phase 1, open-label, crossover study randomized healthy adults to receive three treatment regimens, each separated by ≥5-day washout: a single oral dose of mirogabalin 15 mg on day 2, mirogabalin 15 mg on day 2 plus probenecid 500 mg every 6 h from days 1 to 4, and mirogabalin 15 mg on day 2 plus cimetidine 400 mg every 6 h from days 1 to 4.

RESULTS

Coadministration of mirogabalin with probenecid or cimetidine increased the maximum and total mirogabalin exposure. The geometric mean ratios of C and AUC (90% CI) with and without coadministration of probenecid were 128.7% (121.9-135.7%) and 176.1% (171.9-180.3%), respectively. The geometric mean ratios of C and AUC (90% CI) with and without coadministration of cimetidine were 117.1% (111.0-123.6%) and 143.7% (140.3-147.2%), respectively. Mean (standard deviation) renal clearance of mirogabalin (l h ) was substantially slower after probenecid [6.67 (1.53)] or cimetidine [7.17 (1.68)] coadministration, compared with mirogabalin alone [11.3 (2.39)]. Coadministration of probenecid or cimetidine decreased mirogabalin mean (standard deviation) apparent total body clearance [10.5 (2.33) and 12.8 (2.67) l h , respectively, vs. 18.4 (3.93) for mirogabalin alone].

CONCLUSIONS

A greater magnitude of change in mirogabalin exposure was observed when coadministered with a drug that inhibits both renal and metabolic clearance (probenecid) vs. a drug that only affects renal clearance (cimetidine). However, as the increase in exposure is not clinically significant (>2-fold), no a priori dose adjustment is recommended.

摘要

目的

本研究的主要目的是评估丙磺舒和西咪替丁对米加巴喷丁暴露的个体影响。

方法

这是一项 I 期、开放标签、交叉研究,将健康成年人随机分为 3 种治疗方案组,每组之间至少有 5 天的洗脱期:第 2 天单次口服米加巴喷丁 15mg,第 2 天给予米加巴喷丁 15mg,第 1 天至第 4 天每天每 6 小时给予丙磺舒 500mg,第 2 天给予米加巴喷丁 15mg,第 1 天至第 4 天每天每 6 小时给予西咪替丁 400mg。

结果

米加巴喷丁与丙磺舒或西咪替丁联合用药增加了米加巴喷丁的最大和总暴露量。与未联合用药相比,丙磺舒和西咪替丁分别使 C 和 AUC(90%CI)的几何均数比值增加 128.7%(121.9-135.7%)和 176.1%(171.9-180.3%)。与未联合用药相比,西咪替丁和丙磺舒使 C 和 AUC(90%CI)的几何均数比值分别增加 117.1%(111.0-123.6%)和 143.7%(140.3-147.2%)。与米加巴喷丁单药治疗相比,丙磺舒[6.67(1.53)]或西咪替丁[7.17(1.68)]联合用药后米加巴喷丁的平均(标准差)肾清除率明显减慢[分别为 11.3(2.39)、10.5(2.33)和 12.8(2.67)l/h]。丙磺舒或西咪替丁联合用药使米加巴喷丁的平均(标准差)表观全身清除率降低[分别为 10.5(2.33)和 12.8(2.67)l/h,而米加巴喷丁单药治疗为 18.4(3.93)l/h]。

结论

与仅影响肾清除率的药物(西咪替丁)相比,与同时抑制肾清除率和代谢清除率的药物(丙磺舒)联合用药时,米加巴喷丁的暴露量变化幅度更大。然而,由于暴露量的增加没有临床意义(>2 倍),因此不建议进行预先剂量调整。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac84/6138503/bfbe12fd35a0/BCP-84-2317-g001.jpg

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