drugset / Trial / NCT07343960

A Phase I Study to Investigate the Pharmacokinetics and Safety of Capivasertib in Participants With Moderate Hepatic Impairment

NCT07343960

Phase 1 Recruiting 20 enrolled AstraZeneca Parexel · collab
Non-randomizedParallel-groupOpen-labelBasic science

Summary

The purpose of this study is to measure the pharmacokinetics (PK), safety, and tolerability of capivasertib in participants with moderate hepatic impairment and participants with normal hepatic function (as control).

Timeline

Start
2026-01-06
Primary completion
2026-11-11
Completion
2026-11-11

Drugs

EvaluationDrugModalityDoseRoute
Subject Capivasertib Small molecule Oral

Indications

No indication recorded.