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A Study to Investigate the Pharmacokinetics of AZD2389 When Administered Alone and in Combination With Itraconazole in Healthy Participants

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NCT06846528

Sponsored by AstraZeneca (industry) · AZN — their whole pipeline →. With Parexel.

Phase
Phase 1
Status
Completed
Study type
Interventional
Design
Na · None · Treatment
Enrollment
16actual
Sites
1
Country
United States

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2025-02-26actualWhen the study began enrolling
Primary completion2025-04-23actualThe date the last participant is measured for the primary outcome — the readout window
Study completion2025-04-23actualThe whole study's end, after follow-up
First posted2025-02-26actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2025-04-29actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Healthy Participants

Interventions

  • Drug: AZD2389
  • Drug: Itraconazole

Primary outcomes

what the primary-completion date above is the date OF
Maximum observed drug concentration (Cmax) of AZD2389
measured Day 1 to Day 8
Area under concentration-timecurve from time zero to infinity (AUCinf) of AZD2389
measured Day 1 to Day 8
Area under concentration-curve from time 0 to the last quantifiable concentration (AUClast) of AZD2389
measured Day 1 to Day 8

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