CI

At a glance

ClinicalIndex Comparison Record
Phase 1Completed· 18 enrolled
Drug / intervention
BI 1569912 +3 moredrug
Likely dose
Repaglinide 0.5 mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT06367153
NCT06367153Phase 1Completed

The Effect of Multiple Doses of BI 1569912 on the Single-dose Pharmacokinetics of Repaglinide, Midazolam and Bupropion Following Oral Administration in Healthy Male and Female Subjects (an Open-label, 2-period Fixed-sequence Trial)

Boehringer Ingelheim·interventional·Posted Apr 16, 2024·Updated May 22, 2026

In Brief

A Phase 1 clinical trial evaluating BI 1569912, Repaglinide, and 2 other interventions for Healthy. Completed, enrolled 18 participants across 1 site.

Detailed 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).

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsHealthy
CountriesBelgium
Collaborators--

Timeline

Phase 1CompletedFinished
20252026
First PostedApr 16, 2024
Enrollment StartMay 15, 2024
Primary CompletionAug 20, 2024
TodayJul 2, 2026
Enrollment to primary: 3 monthsPosted 2.2 years ago

Interventions

BI 1569912drug

Intended dose of BI 1569912

Repaglinidedrug

0.5 mg tablet

Midazolamdrug

2 mg solution for injection

Bupropiondrug

150 mg extended-release tablet