drugset / Trial / NCT05731908

A Study to Test How BI 690517 is Taken up in the Body of People With and Without Liver Problems

NCT05731908

Phase 1 Completed 28 enrolled Boehringer Ingelheim IQVIA global CRO · collab
Non-randomizedParallel-groupOpen-labelTreatment

Summary

The main objective of this trial is to assess the effect of mild and moderate hepatic impairment (Child-Pugh classification A and B) on the pharmacokinetics, safety, and tolerability of BI 690517 in comparison with a control group with normal hepatic function.

Timeline

Start
2023-02-21
Primary completion
2023-04-13
Completion
2023-04-13

Drugs

EvaluationDrugModalityDoseRoute
Subject Vicadrostat Small molecule

Indications