A Phase I Study to Investigate the Pharmacokinetics and Safety of Capivasertib in Participants With Moderate Hepatic Impairment
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).
Body weight of at least 50 kg and Body Mass Index (BMI) of between ≥ 18 up to ≤... [+7]
Any evidence of diseases (such as severe or uncontrolled systemic diseases, incl... [+14]