drugset / Trial / NCT05112419

A Study to Assess Zibotentan Pharmacokinetics in Participants With Moderate Hepatic and Moderate Renal Impairment

NCT05112419

Phase 1 Completed 12 enrolled AstraZeneca
Non-randomizedParallel-groupOpen-labelTreatment

Summary

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

Timeline

Start
2021-11-10
Primary completion
2021-12-15
Completion
2021-12-15

Drugs

EvaluationDrugModalityDoseRoute
Subject Zibotentan Small molecule 5 mg