drugset / Trial / NCT07620561

Efficacy and Speed of Response of Lebrikizumab in High-Burden Prurigo Nodularis Patients

NCT07620561

NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate the effectiveness of lebrikizumab in treating adults with moderate-to-severe Prurigo Nodularis (PN).

Timeline

Start
2026-06
Primary completion
2027-12
Completion
2028-03

Drugs

EvaluationDrugModalityDoseRoute
Subject Lebrikizumab Monoclonal antibody 250 mg Subcutaneous

Indications