A Phase 2 Study of the Safety and Efficacy of Brepocitinib in Adults With Cutaneous Sarcoidosis (BEACON)
Recruiting now · Phase 2 · Has a placebo group
Conditions studied: Cutaneous Sarcoidosis
In brief
This study will evaluate the clinical safety and efficacy of oral brepocitinib in participants with cutaneous sarcoidosis.
Key facts
- Study ID
- NCT06978725
- Run by
- Priovant Therapeutics, Inc.
- People needed
- 28
- Starts
- 2025-04-09
- Expected to finish
- 2026-12-01
- Last updated by the study team
- 2025-05-18
Who can join
Age: 18 and older, up to 75. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Adults subjects (18-74)
- Cutaneous sarcoidosis with characteristic skin biopsy histology
- A CSAMI activity score ≥ 10
- Weight > 40 kg to < 130 kg with BMI < 40 kg/m2 .
You may not qualify if…
- History of
- Lymphoproliferative disorder
- Active malignancy;
- History of cancer within 5 years prior to baseline (exceptions for basal cell carcinoma, squamous cell carcinoma, or carcinoma in situ of the uterine cervix).
- High risk of thrombosis or cardiovascular disease
- High risk of herpes zoster
- Active or recent infection
Where it is running
- Clinical Trial Site — San Francisco, California, United States (enrolling)
- Clinical Trial Site — Durham, North Carolina, United States (enrolling)
- Clinical Trial Site — Philadelphia, Pennsylvania, United States (enrolling)
- Clinical Trial Site — Madison, Wisconsin, United States (enrolling)
Full record on ClinicalTrials.gov
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