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NCT06813781 · ClinicalTrials.gov registry record · Phase 1

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

A Phase 1 study, sponsored by AstraZeneca.

Completed
Registry status
Phase 1
Development phase
33
Enrollment target

NCT06813781: Completed Phase 1 study, sponsored by AstraZeneca.

NCT06813781 is a Phase 1 study that has completed, run by AstraZeneca. The registered enrollment target is 33 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (45% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06813781, a Phase 1 study, has completed, sponsored by AstraZeneca.

COMPLETED
Registry status
Phase 1
Development phase
33 participants
Enrollment target

Study Summary

This is a Phase I, multicentre, single-dose, non-randomised, open-label, parallel-group study to examine the PK, safety, and tolerability of AZD5004 in male and female participants with mild, moderate, and severe hepatic impairment compared with participants with normal hepatic function.

Primary Outcome

Area under plasma concentration-time curve from zero to infinity

Interventions

  • DRUG AZD5004

Trial Details

FieldValue
Enrollment Target 33 participants
Start Date 2024-12-19
Est. Completion 2025-10-02
Phase Phase 1
AstraZeneca

1,285 total trials

What the finished NCT06813781 record still lists

NCT06813781 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 33 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (45% lower).

The record links to 0 conditions, and to 1 intervention - of which AZD5004 is the first listed.

NCT06813781 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT06813781 about?

NCT06813781 is a clinical study titled "Study to Investigate the Effect of Hepatic Impairment on the Pharmacokinetics, Safety, and Tolerability of AZD5004". This is a Phase I, multicentre, single-dose, non-randomised, open-label, parallel-group study to examine the PK, safety, and tolerability of AZD5004 in male and female participants with mild, moderate, and severe hepatic impairment compared with participants with normal hepatic function.

What is the current status of trial NCT06813781?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 33 participants. The study started on 2024-12-19. Estimated completion is 2025-10-02.

What interventions are being tested in trial NCT06813781?

The interventions under investigation include: AZD5004 (DRUG).

Who is sponsoring clinical trial NCT06813781?

This trial is sponsored by AstraZeneca, which has 1,285 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT06813781's enrollment target sits among peer trials

33 1280th of 2000 higher than 705 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT06813781, the US trial registry maintained by the National Library of Medicine. NCT06813781 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.