A Study to Investigate the Effect of Hepatic Impairment on the Pharmacokinetics, Safety, and Tolerability of AZD2389
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Phase
Phase 1
Status
Completed
Study type
Interventional
Design
Non randomized · None · Other
Enrollment
35actual
Sites
5
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| Date | Filed | Basis | What it is |
|---|---|---|---|
| Start | 2025-02-04 | actual | When the study began enrolling |
| Primary completion | 2025-09-04 | actual | The date the last participant is measured for the primary outcome — the readout window |
| Study completion | 2025-09-04 | actual | The whole study's end, after follow-up |
| First posted | 2025-02-06 | actual | When this record first appeared on the registry |
| Results posted | — | When the sponsor posted results to the registry | |
| Record updated | 2025-09-24 | actual | The sponsor's own last edit to this record — every projection above is as current as this date |
What it studies
Condition
- Hepatic Impairment
Intervention
- Drug: AZD2389
Primary outcomes
what the primary-completion date above is the date OFPlasma PK parameter Cmax
measured pre-dose to 48 hours post-dose
Plasma PK parameter AUCinf
measured pre-dose to 48 hours post-dose
Plasma PK parameter AUClast
measured pre-dose to 48 hours post-dose
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