A Phase I Study to Investigate the Pharmacokinetics and Safety of Capivasertib in Participants With Moderate Hepatic Impairment
Recruiting now · Phase 1
Conditions studied: Moderate Hepatic Impairment
In brief
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).
Key facts
- Study ID
- NCT07343960
- Run by
- AstraZeneca
- People needed
- 20
- Starts
- 2026-01-06
- Expected to finish
- 2026-11-11
- Last updated by the study team
- 2026-07-02
Who can join
Age: 18 and older, up to 80. Sex: any. Healthy volunteers: accepted.
Where it is running
- Research Site — Rialto, California, United States (enrolling)
- Research Site — San Antonio, Texas, United States (enrolling)
Full record on ClinicalTrials.gov
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