For condition: Lichen Planopilaris
Research Study for Lichen Planopilaris (60 Weeks)
Study Summary
Who Can Participate?
Individuals 18+ with lichen planopilaris (LPP) may be eligible to participate.
Inclusion Criteria
- Males and females aged 18+
- Have active LPP (moderate to severe)
- Are experiencing scalp symptoms (itch, burning, pain, tingling and/or tenderness)
- Weigh between 40kg and 130kg and have a body mass index (BMI) at least 45 kg/m2 or less
- Do not have any active skin diseases of the scalp other than LPP that may interfere with the assessment of the study disease or require
treatment with prohibited medications
Participant Information
- Participate and receive study treatment at no cost
- Regular visits with study doctors who specialize in treating LPP
- Will receive either an investigative oral treatment (active study drug) or a placebo
- Reimbursement for study-related expenses will be provided
How Long Will The Study Last?
- Participation will last about 60 weeks and involve about 13 visits to the study research site
For more information about this trial, please visit ClinicalTrials.gov
