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Nemolizumab to Treat Lichen Planopilaris, a Noncontrolled, Prospective, Pilot Study.

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 4
SUMMARY

Lichen planopilaris (LPP) is a primary lymphocytic cicatricial alopecia characterized by progressive, permanent hair loss and scalp symptoms such as pruritus and burning. Current treatments-including topical and intralesional corticosteroids, hydroxychloroquine, and immunosuppressants-are often inadequate, with limited evidence for efficacy and frequent treatment switching or discontinuation due to side effects or lack of response.1,2 Recent systematic reviews and meta-analyses highlight the need for new, targeted therapies. 3,4 Nemolizumab, an IL-31 receptor antagonist, FDA-approved for prurigo nodularis and atopic dermatitis, has demonstrated efficacy in pruritic and fibrosing dermatoses, making it a rational candidate for LPP.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Age ≥18 years.

• Clinical and/or histopathologic diagnosis of LPP.

• Presence of scalp pruritus.

• Average Peak Pruritus Numerical Rating Scale (PP-NRS) score ≥4 in the 7 days prior to Day 1.

• Ability and willingness to provide written informed consent and comply with study procedures.

• Willingness to undergo optional scalp biopsy for research purposes.

Locations
United States
New York
The Skin Center Dermatology Group
RECRUITING
New City
Contact Information
Primary
Peter Friedman, MD PhD
drfriedman@skincenterderm.com
8453520500
Time Frame
Start Date: 2026-02-01
Estimated Completion Date: 2027-06
Participants
Target number of participants: 10
Treatments
Experimental: Patients receive nemolizumab injections every 4 weeks, weight based dosing
Sponsors
Leads: The Skin Center Dermatology Group

This content was sourced from clinicaltrials.gov

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