Study identifier:D7930C00006
ClinicalTrials.gov identifier:NCT06974565
EudraCT identifier:N/A
CTIS identifier:N/A
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
Advanced Chronic Liver Disease, Healthy Participants
Phase 1
Yes
AZD2389, Quinidine
All
16
Interventional
18 Years - 55 Years
Allocation: Randomized
Endpoint Classification: -
Intervention Model: Crossover Assignment
Masking: -
Primary Purpose: Treatment
Verified 01 Jul 2025 by AstraZeneca
AstraZeneca
PAREXEL
No locations available
Arms | Assigned Interventions |
---|---|
Experimental: Sequence AB Participants will receive a single dose of Treatment A (AZD2389) in Period 1 and a single dose of Treatment B (AZD2389 + quinidine) in Period 2. | Drug: AZD2389 AZD2389 will be administered orally. Drug: Quinidine Quinidine will be administered orally. |
Experimental: Sequence BA Participants will receive a single dose of Treatment B (AZD2389 + quinidine) in Period 1 and a single dose of Treatment A (AZD2389) in Period 2. | Drug: AZD2389 AZD2389 will be administered orally. Drug: Quinidine Quinidine will be administered orally. |