A Study to Investigate the Effect of Hepatic Impairment on the Pharmacokinetics, Safety, and Tolerability of AZD2389

PHASE1CompletedINTERVENTIONAL
Enrollment

35

Participants

Timeline

Start Date

February 4, 2025

Primary Completion Date

September 4, 2025

Study Completion Date

September 4, 2025

Conditions
Hepatic Impairment
Interventions
DRUG

AZD2389

Single oral dose of AZD2389 in participants from all cohorts

Trial Locations (5)

32809

Research Site, Orlando

33014

Research Site, Miami Lakes

78215

Research Site, San Antonio

85225

Research Site, Chandler

92377

Research Site, Rialto

Sponsors

Lead Sponsor

All Listed Sponsors
lead

AstraZeneca

INDUSTRY