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NCT06067568 · ClinicalTrials.gov registry record · Phase 1

Relative Bioavailability of Two Lutikizumab Formulations and Pharmacokinetics, Safety, and Tolerability of Lutikizumab in Chinese Participants

A Phase 1 study, sponsored by AbbVie.

Completed
Registry status
Phase 1
Development phase
50
Enrollment target

NCT06067568: Completed Phase 1 study, sponsored by AbbVie.

NCT06067568 is a Phase 1 study that has completed, run by AbbVie. The registered enrollment target is 50 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (17% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06067568, a Phase 1 study, has completed, sponsored by AbbVie.

COMPLETED
Registry status
Phase 1
Development phase
50 participants
Enrollment target

Study Summary

The purpose of this study is to compare the bioavailability of two different formulations of lutikizumab, and to assess adverse events (AEs) and how lutikizumab moves through the body in healthy Chinese participants.

Primary Outcome

Cmax of lutikizumab will be assessed.

Interventions

  • DRUG Lutikizumab Dose A
  • DRUG Lutikizumab Dose B

Trial Details

FieldValue
Enrollment Target 50 participants
Start Date 2023-09-28
Est. Completion 2024-02-26
Phase Phase 1
AbbVie

526 total trials

What the finished NCT06067568 record still lists

NCT06067568 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 50 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (17% lower).

The record links to 0 conditions, and to 2 interventions - of which Lutikizumab Dose A is the first listed.

NCT06067568 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT06067568 about?

NCT06067568 is a clinical study titled "Relative Bioavailability of Two Lutikizumab Formulations and Pharmacokinetics, Safety, and Tolerability of Lutikizumab in Chinese Participants". The purpose of this study is to compare the bioavailability of two different formulations of lutikizumab, and to assess adverse events (AEs) and how lutikizumab moves through the body in healthy Chinese participants.

What is the current status of trial NCT06067568?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 50 participants. The study started on 2023-09-28. Estimated completion is 2024-02-26.

What interventions are being tested in trial NCT06067568?

The interventions under investigation include: Lutikizumab Dose A (DRUG), Lutikizumab Dose B (DRUG).

Who is sponsoring clinical trial NCT06067568?

This trial is sponsored by AbbVie, which has 526 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT06067568's enrollment target sits among peer trials

50 973rd of 2000 higher than 984 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 NCT06067568, the US trial registry maintained by the National Library of Medicine. NCT06067568 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.