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

Phase 1 Completed NCT06367153

ConditionHealthy
PhasePhase 1
SponsorBoehringer Ingelheim
StatusCompleted
Enrollment18 participants
InterventionsBI 1569912, Repaglinide, Midazolam, Bupropion
Start dateMay 15, 2024
Completion dateAug 20, 2024
Results postedMay 22, 2026

Summary

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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