A study to investigate the pharmacokinetics of AZD2389 in healthy participants when administered alone and in combination with quinidine

Study identifier:D7930C00006

ClinicalTrials.gov identifier:NCT06974565

EudraCT identifier:N/A

CTIS identifier:N/A

Study Complete

Official Title

An open-label, randomized, cross-over, single dose study in healthy participants to assess the pharmacokinetics of AZD2389 when administered alone and in combination with quinidine

Medical condition

Advanced Chronic Liver Disease, Healthy Participants

Phase

Phase 1

Healthy volunteers

Yes

Study drug

AZD2389, Quinidine

Sex

All

Actual Enrollment

16

Study type

Interventional

Age

18 Years - 55 Years

Date

Study Start Date: 12 May 2025
Primary Completion Date: 18 Jul 2025
Study Completion Date: 18 Jul 2025

Study design

Allocation: Randomized
Endpoint Classification: -
Intervention Model: Crossover Assignment
Masking: -
Primary Purpose: Treatment

Verification:

Verified 01 Jul 2025 by AstraZeneca

Sponsors

AstraZeneca

Collaborators

PAREXEL

Inclusion and exclusion criteria