Study identifier:D7930C00005
ClinicalTrials.gov identifier:NCT06846528
EudraCT identifier:N/A
CTIS identifier:N/A
An Open-label, Fixed Sequence Study in Healthy Participants to Assess the Pharmacokinetics of AZD2389 when Administered Alone and in Combination with Itraconazole
Healthy Participants
Phase 1
Yes
Itraconazole, AZD2389
All
16
Interventional
18 Years - 55 Years
Allocation: N/A
Endpoint Classification: -
Intervention Model: Sequential Assignment
Masking: -
Primary Purpose: Treatment
Verified 01 Mar 2025 by AstraZeneca
AstraZeneca
PAREXEL
The purpose of this study is to assess the pharmacokinetics (PK) of AZD2389 when administered alone and in combination with itraconazole in healthy participants.
This study will be an open-label, fixed sequence, Drug-Drug Interaction (DDI) study consisting of 3 periods. The study will comprise: • A screening period of maximum 28 days • Period 1 • Period 2 • Period 3 • A Follow-up Visit 7 to 14 days after the last PK sample has been collected.
Location
Status
Location
Brooklyn, MD, United States, 21225
Status
Recruiting
Arms | Assigned Interventions |
---|---|
Experimental: AZD2389 and Itraconazole AZD2389 is dosed on days 1 and 6. Itraconazole is dosed on days 3,4,5,6,7, with the dose on day 6 coming after AZD2389. | Drug: AZD2389 AZD2389 is administered orally |
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