BENITIONSClinical Trial Intelligence

A Study in Healthy Men and Women to Test Whether BI 1569912 Influences the Amount of Repaglinide, Midazolam and Bupropion in the Blood

1期 已完成 NCT06367153

适应症Healthy
分期1期
申办方Boehringer Ingelheim
状态已完成
受试者人数18 人
干预(药物)BI 1569912, Repaglinide, Midazolam, Bupropion
开始日期2024年5月15日
完成日期2024年8月20日
结果公布日2026年5月22日

摘要

The main objective of this trial is to investigate the effect of multiple oral doses of BI 1569912 on the pharmacokinetics of a single oral dose of repaglinide, midazolam and bupropion (i.e. sensitive CYP2C8, CYP3A4 and CYP2B6 substrates).

Area Under the Concentration-time Curve of Repaglinide in Plasma Over the Time Interval From 0 Extrapolated to Infinity (AUC0-∞)

Within 3 hours (h) before repaglinide administration and 0.25, 0.5, 0.75, 1, 1.5, 2, 3, 4, 6, 8, 10 and 12 h thereafter. · hour*picomole/liter

Repaglinide 0.5 mg (R1)21882.61 ± NA hour*picomole/liter
Repaglinide 0.5 mg + BI 1569912 (T1)27332.41 ± NA hour*picomole/liter
Adjusted gMean ratio [%]124.90 (95% CI 115.78–134.75)

Area Under Concentration-time Curve of Midazolam in Plasma Over the Time Interval From 0 Extrapolated to Infinity (AUC0-∞)

Within 3 hours (h) before midazolam administration and 0.25, 0.5, 0.75, 1, 1.5, 2, 3, 4, 6, 8, 10 and 12 h thereafter. · hour*picomole/liter

Midazolam 2 mg (R2)57471.40 ± NA hour*picomole/liter
Midazolam 2 mg + BI 1569912 (T2)69127.73 ± NA hour*picomole/liter
Adjusted gMean ratio [%]120.28 (95% CI 108.66–133.15)

Area Under the Concentration-time Curve of S-bupropion in Plasma Over the Time Interval From 0 Extrapolated to Infinity (AUC0-∞)

Within 3 hours (h) before bupropion administration and 1, 2, 3, 4, 5, 6, 8, 10, 12, 24, 48, 72, 96, 120 h thereafter. · hour*nanomole/liter

Bupropion 150 mg (R3)302.02 ± NA hour*nanomole/liter
Bupropion 150 mg + BI 1569912 (T3)312.11 ± NA hour*nanomole/liter
Adjusted gMean ratio [%]103.34 (95% CI 93.98–113.64)

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本页整理自 ClinicalTrials.gov 的公开数据,不构成医疗建议,也不构成投资建议。请务必咨询专业医师。