drugset / Trial / NCT06444165

Lebrikizumab Pen Ease of Use in Participants With Atopic Dermatitis

NCT06444165

Phase 3 Completed 55 enrolled Eli Lilly and Company
NaSingle-groupOpen-labelOther

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.

Timeline

Start
2024-06-04
Primary completion
2024-06-10
Completion
2024-06-10

Drugs

EvaluationDrugModalityDoseRoute
Background Lebrikizumab Monoclonal antibody 250 mg Subcutaneous

Indications