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NCT06444165 · ClinicalTrials.gov registry record · Phase 3

Lebrikizumab Pen Ease of Use in Participants With Atopic Dermatitis

A Phase 3 study, sponsored by Eli Lilly and Company.

Completed
Registry status
Phase 3
Development phase
55
Enrollment target

NCT06444165: Completed Phase 3 study, sponsored by Eli Lilly and Company.

NCT06444165 is a Phase 3 study that has completed, run by Eli Lilly and Company. The registered enrollment target is 55 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (93% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06444165, a Phase 3 study, has completed, sponsored by Eli Lilly and Company.

COMPLETED
Registry status
Phase 3
Development phase
55 participants
Enrollment target

Study Summary

The purpose of this study is to assess the ease of use of the lebrikizumab pen. Participants will use a practice pad to simulate administration of a dose. Participants will complete the modified Subcutaneous Administration Assessment Questionnaire (mSQAAQ) following the simulated injection. This study involves one study visit.

Primary Outcome

mSQAAQ: This modified, short questionnaire is an instrument that includes 10 questions about the ease of use and confidence in using the lebrikizumab pen. Questions: 1) Easy for me to learn how to use, 2) Easy for me to unlock, 3) Easy to hold in my hand when I inject my dose, 4) Easy to inject my dose, 5) Easy to know that my dose is complete, 7) Easy to remove needle shield/cover, 8) Easy to pick up, 9) Overall, easy to use, 11) I am confident in my ability to use the device, and 12) I am conf

Interventions

  • DRUG Lebrikizumab Pen

Trial Details

FieldValue
Enrollment Target 55 participants
Start Date 2024-06-04
Est. Completion 2024-06-10
Phase Phase 3
Eli Lilly and Company

1,341 total trials

What the finished NCT06444165 record still lists

NCT06444165 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 55 participants, a relatively small participant target, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (93% lower).

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

NCT06444165 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT06444165 about?

NCT06444165 is a clinical study titled "Lebrikizumab Pen Ease of Use in Participants With Atopic Dermatitis". The purpose of this study is to assess the ease of use of the lebrikizumab pen. Participants will use a practice pad to simulate administration of a dose. Participants will complete the modified Subcutaneous Administration Assessment Questionnaire (mSQAAQ) following the simulated injection. This st...

What is the current status of trial NCT06444165?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 55 participants. The study started on 2024-06-04. Estimated completion is 2024-06-10.

What interventions are being tested in trial NCT06444165?

The interventions under investigation include: Lebrikizumab Pen (DRUG).

Who is sponsoring clinical trial NCT06444165?

This trial is sponsored by Eli Lilly and Company, which has 1,341 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT06444165's enrollment target sits among peer trials

55 1834th of 2000 higher than 163 of 2,000 other Phase 3 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 3 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 NCT06444165, the US trial registry maintained by the National Library of Medicine. NCT06444165 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.