This study will evaluate the clinical safety and efficacy of oral brepocitinib in participants with lichen planopilaris
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Enrollment
342
Oral
Oral
Clinical Trial Site
Phoenix, Arizona, United States
RECRUITINGClinical Trial Site
Portland, Oregon, United States
RECRUITINGClinical Trial Site
Smyrna, Tennessee, United States
RECRUITINGProportion of participants achieving IGA score 0/1 and ≥ 2-step reduction from baseline at Week 24
Time frame: Week 24
Change from baseline in LPP symptom numerical rating scale scores at Week 24
Time frame: Week 24
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Clinical Trial Site
Austin, Texas, United States
RECRUITINGClinical Trial Site
Cedar Park, Texas, United States
RECRUITING