Skip to content
KStart free
AI InfrastructureDefenseQuantumAll studies →

Study to Investigate the Effect of Hepatic Impairment on the Pharmacokinetics, Safety, and Tolerability of AZD5004

← catalyst calendar

NCT06813781

Sponsored by AstraZeneca (industry) · AZN — their whole pipeline →. With Fortrea Clinical Research Unit Inc..

Phase
Phase 1
Status
Completed
Study type
Interventional
Design
Non randomized · None · Treatment
Enrollment
33actual
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
DateFiledBasisWhat it is
Start2024-12-19actualWhen the study began enrolling
Primary completion2025-10-02actualThe date the last participant is measured for the primary outcome — the readout window
Study completion2025-10-02actualThe whole study's end, after follow-up
First posted2025-02-07actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2025-10-15actualThe 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: AZD5004 — also filed as ECC5004, Dose 1

Primary outcomes

what the primary-completion date above is the date OF
AUCinf
measured Day 1 to Day 6
AUClast
measured Day 1 to Day 6
Cmax
measured Day 1 to Day 6

Permalink · AZN's whole pipeline · Catalyst calendar · Every registered study · What changed