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A Phase 2 Randomized, Double-Blind, Placebo-Controlled, Dose-Ranging Study to Investigate the Safety and Efficacy of Oral Brepocitinib in Adults With Cutaneous Sarcoidosis
This study will evaluate the clinical safety and efficacy of oral brepocitinib in participants with cutaneous sarcoidosis.
Age
18 - 75 years
Sex
ALL
Healthy Volunteers
No
Clinical Trial Site
San Francisco, California, United States
Clinical Trial Site
Durham, North Carolina, United States
Clinical Trial Site
Philadelphia, Pennsylvania, United States
Clinical Trial Site
Madison, Wisconsin, United States
Start Date
April 9, 2025
Primary Completion Date
December 1, 2026
Completion Date
December 1, 2026
Last Updated
May 18, 2025
28
ESTIMATED participants
Oral Brepocitinib
DRUG
Oral Placebo
DRUG
Lead Sponsor
Priovant Therapeutics, Inc.
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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