A Phase 2/3 Study of Brepocitinib in Adults With Lichen Planopilaris

Recruiting Phase 2 Phase 3 Interventional Study
Lichen Planopilaris
Pivotal Trial This treatment is in the last trial phase before FDA approval. Prior Safety Data This treatment has already been tested in at least one earlier human trial.
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At a Glance
Age
18 and older
Sex
Any
Trial phase
Phase 2/3
Study type
Interventional
Purpose
Treatment
Participants needed
342 (estimated)
Sponsor
Priovant Therapeutics, Inc. · Industry
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About This Trial

This study will evaluate the clinical safety and efficacy of oral brepocitinib in participants with lichen planopilaris

Trial Locations
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Eligibility Criteria
Inclusion Criteria: 1. Age ≥ 18 years 2. Scalp biopsy consistent with LPP 3. Active and symptomatic LPP at screening and baseline- 4. Weight \> 40 kg to \< 130 kg with BMI ≤ 45 kg/m2 Exclusion Criteria: 1. History of: Lymphoproliferative disorder; Active malignancy; History of cancer within 5 yea…
Contacts

Clinical Trial Administrator

(212) 634-9743

clinicaltrials@priovant.com

CONTACT