drugset / Trial / NCT06388616

Study to Investigate the Effect of Hepatic Impairment on the Pharmacokinetics, Safety, and Tolerability of Balcinrenone

NCT06388616

Phase 1 Completed 30 enrolled AstraZeneca
Non-randomizedParallel-groupOpen-labelTreatment

Summary

This study will evaluate the pharmacokinetics (PK), safety, and tolerability of a single oral dose of balcinrenone in patients with mild and moderate hepatic impairment in comparison to a matched healthy control group.

Timeline

Start
2024-05-02
Primary completion
2024-09-05
Completion
2024-09-05

Drugs

EvaluationDrugModalityDoseRoute
Subject balcinrenone Small molecule 50 mg Oral

Indications

No indication recorded.