Oral Brepocitinib
DrugOral
NCT Number: NCT07532603
This study will evaluate the clinical safety and efficacy of oral brepocitinib in participants with lichen planopilaris
Interested in participating?
Request Info18 year and older
All sexes
Interventional
Phase 2 / Phase 3
Clinical Trial Site, Adelaide, Australia
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Oral
Oral
Time frame: Week 24
Time frame: Week 24
Contact information is provided by the study sponsor or research team.
Priovant Therapeutics, Inc.
Industry
A Phase 2/3 Randomized, Double-Blind, Placebo-Controlled Study to Investigate the Safety and Efficacy of Oral Brepocitinib in Adults With Lichen Planopilaris
Acronym: ALPINE
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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