Research Study for Lichen Planopilaris (60 Weeks)

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
Click here to Register

For more information about this trial, please visit ClinicalTrials.gov

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