U.S., June 3 -- ClinicalTrials.gov registry received information related to the study (NCT07620561) titled 'Efficacy and Speed of Response of Lebrikizumab in High-Burden Prurigo Nodularis Patients' on May 26.
Brief Summary: The purpose of this study is to evaluate the effectiveness of lebrikizumab in treating adults with moderate-to-severe Prurigo Nodularis (PN).
Study Start Date: June, 2026
Study Type: INTERVENTIONAL
Condition:
Prurigo Nodularis (PN)
Intervention:
DRUG: Lebrikizumab
Participants will receive subcutaneous injections of Lebrikizumab every two weeks for 24 weeks. The first two doses will be 500 mg, and following doses will be 250 mg.
Recruitment Status: NOT_YET_RECRUITING
Sponsor: University of Maryland, Baltimore
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