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Clinical Trial Summary

To evaluate the safety and efficacy of ixekizumab in lichen planus and lichen planopilaris clinical response by Total Body Surface (TBS) determination, Investigator Global Assessment (IGA) Score, Lichen Planopilaris Activity Index (LPPAI), and Frontal Fibrosing Alopecia Severity Score (FFASS).


Clinical Trial Description

A proof of concept, non-randomized, one center study to explore the safety and efficacy of 16 weeks of treatment with ixekizumab in adult patients with lichen planus. The total study period will consist of 24 weeks including a 2 week screening/washout, 16 weeks of active therapy and 8 weeks of follow up. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05030415
Study type Interventional
Source University of New Mexico
Contact John R Durkin, MD MBA
Phone 5052726222
Email [email protected]
Status Recruiting
Phase Early Phase 1
Start date August 31, 2021
Completion date August 31, 2023

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