A Phase I Study to Investigate the Effect of Hepatic Impairment of AZD9550 and AZD6234
A Phase I, Multicentre, Single-Dose, Non-Randomised, Open-Label, Parallel-Group Study to Investigate the Effect of Hepatic Impairment on the Pharmacokinetics, Safety, and Tolerability of AZD9550 and AZD6234
AstraZeneca
28 participants
Mar 20, 2026
INTERVENTIONAL
Conditions
Summary
The purpose of this study is to examine the safety and tolerability of AZD6234 and AZD9550 in participants with hepatic impairment and participants with normal hepatic function.
Eligibility
Plain Language Summary
Simplified for easier understanding
This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.
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Interventions
Single subcutaneous dose of AZD6234 in participants from all groups
Single subcutaneous dose of AZD9550 in participants from all groups
Locations(4)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT07546760